File Changes for mspeir

v502_preview to v502_preview2 (2026-07-27 to 2026-08-04) v502

• docs/tutorials/customTrackTutorial.md
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    981342c978baf2d56a1ddad178b100138b55298c Sat Aug 1 20:58:19 2026 -0700
    Fix pandoc rendering of tutorial step text inside the walkthrough columns Indented markdown that ran directly into a closing </div> was being folded into the raw-HTML block, so Step 1 paragraphs lost their <p> wrapper (and hugged the heading) and two Table Browser lists did not close cleanly. Added the blank line pandoc needs before </div> in the affected columns. refs #37355 Co-Authored-By: Claude Opus 4.8 (1M context) <noreply@anthropic.com>
• docs/tutorials/gb101.md
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    fd37b0cc737fd221a94034202db5458d954614eb Mon Aug 3 14:50:37 2026 -0700
    Fix mismatched heading tag in gb101 tutorial The Interactive Tutorial panel opened an <h3> but closed with </h4>. refs #37355 Co-Authored-By: Claude Opus 4.8 (1M context) <noreply@anthropic.com>
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    93ee577eacf6c0ec157f11aee34085f34d476b72 Mon Aug 3 15:30:22 2026 -0700
    Add Recommended Track Sets and Share a link sections to gb101 tutorial Document two features now on the RR that the intro page did not cover: the Recommended Track Sets dialog (curated, pre-configured track groups) and the Share a link button for short, permanent view links. Adds a screenshot of each dialog and notes Recommended Track Sets in the Genome Browser menu list. refs #37355 Co-Authored-By: Claude Opus 4.8 (1M context) <noreply@anthropic.com>
• docs/tutorials/tableBrowserTutorial.md
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    981342c978baf2d56a1ddad178b100138b55298c Sat Aug 1 20:58:19 2026 -0700
    Fix pandoc rendering of tutorial step text inside the walkthrough columns Indented markdown that ran directly into a closing </div> was being folded into the raw-HTML block, so Step 1 paragraphs lost their <p> wrapper (and hugged the heading) and two Table Browser lists did not close cleanly. Added the blank line pandoc needs before </div> in the affected columns. refs #37355 Co-Authored-By: Claude Opus 4.8 (1M context) <noreply@anthropic.com>
• src/hg/htdocs/images/recommendedTrackSets.png
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    93ee577eacf6c0ec157f11aee34085f34d476b72 Mon Aug 3 15:30:22 2026 -0700
    Add Recommended Track Sets and Share a link sections to gb101 tutorial Document two features now on the RR that the intro page did not cover: the Recommended Track Sets dialog (curated, pre-configured track groups) and the Share a link button for short, permanent view links. Adds a screenshot of each dialog and notes Recommended Track Sets in the Genome Browser menu list. refs #37355 Co-Authored-By: Claude Opus 4.8 (1M context) <noreply@anthropic.com>
• src/hg/htdocs/images/shareLinkExample.png
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    93ee577eacf6c0ec157f11aee34085f34d476b72 Mon Aug 3 15:30:22 2026 -0700
    Add Recommended Track Sets and Share a link sections to gb101 tutorial Document two features now on the RR that the intro page did not cover: the Recommended Track Sets dialog (curated, pre-configured track groups) and the Share a link button for short, permanent view links. Adds a screenshot of each dialog and notes Recommended Track Sets in the Genome Browser menu list. refs #37355 Co-Authored-By: Claude Opus 4.8 (1M context) <noreply@anthropic.com>
• src/hg/htdocs/images/tutorialImages/hgCustomAnnotated_pt1.png
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    91df4233e1ec4523f20367104bbdebd932f6e640 Sat Aug 1 20:45:29 2026 -0700
    Reposition and enlarge call-outs on the Add Custom Tracks annotated image Moved the red 'Send the data...' call-out to the empty page area right of the Submit button, dropped the blue documentation call-out down next to the Optional track documentation input, aligned the purple call-out with the paste box, and enlarged the call-out text so it matches the pt2 image on the page. refs #37355 Co-Authored-By: Claude Opus 4.8 (1M context) <noreply@anthropic.com>
• src/hg/makeDb/doc/hg38/singleCellSignalsPeaks.txt
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    d0632693bee08bf61b7990e0c6a1de8c050e337f Sat Aug 1 20:53:09 2026 -0700
    singleCellSignalsPeaks: color by cell class, harmonize labels and facets (hg38) Overhaul of the hg38 track and the shared build scripts it and the mm10 track are generated from: - Color every subtrack by broad cell class from one colorblind-conscious palette (shared with the mm10 track, so a class is the same color on both assemblies); add a color legend to the description page. - Add a "Cell class" facet; the fine cell type becomes a searchable table column. Group subtracks by class via priority; every subtrack is off by default. - Paper-curated cell-type names, redundant-synonym merges, QC-cluster drop, and per-collection tissue/life-stage/condition (including the SEA-AD region and ADNC neuropathology level, from Gabitto 2024 and Hawrylycz 2024). - Rebuild the longLabels from the harmonized cell type + facets, so the cryptic source short labels decode. - Reclassify 10 mislabeled interaction bigBeds out of the signal/peaks composite, retype a narrowPeak-format bigBed, and drop deprecated *.old data (936 -> 925 subtracks). - Archive the curation with the scripts: build_celltype_crosswalks.py and celltype-crosswalks/ (per-collection crosswalks, palette, class map, and the paper-decode source tables). refs #37914 Co-Authored-By: Claude Opus 4.8 (1M context) <noreply@anthropic.com>
  • lines changed 20, context: html, text, full: html, text
    b914d581f876d486caf9404e715e4f61ada38195 Mon Aug 3 16:19:44 2026 -0700
    singleCellSignalsPeaks: make every subtrack label unique, fix cell-class regressions The harmonized labels were not distinguishing tracks. build_long_label composed from cell type + condition + tissue, but the upstream steps discard the discriminators on purpose to keep the facets compact, so hg38 had 925 subtracks sharing only 401 distinct longLabels and mm10 629 sharing 359. Worst case: cortex-atac's MACS, enhancer and cell-type-specific peak sets all read "Astrocytes and oligodendrocytes (Cortex ATAC)", with the peak method surviving only in the raw shortLabel. Labels are now built from the harmonized cell type plus a variant descriptor that recovers what was dropped (peak method, grouping level, cohort, signal vs peaks), and anything still colliding is qualified with its source cluster code. shortLabels are rebuilt too -- the old ones were raw source strings up to 50 chars with underscores, ArchR filename tails and R-mangled names -- abbreviated through a curated word table to 22 chars, with compact tokens where the longLabel distinction would otherwise be invisible (SEA-AD region + ADNC, CATLAS aging age). All 925/587 longLabels are now unique; no shortLabel exceeds 22 chars or contains an underscore. Also fixed, found while verifying the above: - Correcting source misspellings in the cell types broke the curated lookups, which are keyed on those same misspelled strings, and 16 hg38 tracks silently lost their Cell_class and color. The class map and the hub_config tables now normalize their keys on load, and a cell type with no broad class is reported instead of becoming "unknown". - Nephron progenitor was classed as Neural progenitor: the decode tables give it the bare broad class "Progenitor" and that was blanket-mapped to neural. It is Six2+ kidney cap mesenchyme, so it is now Stromal. The HTML legend had been worded to match the bug. - The plural/case merge picked the most frequent form, which was inconsistent -- singular for 15 of 17 merged groups but plural for Megakaryocytes/Oligodendrocytes. It now prefers the singular. - Removed 42 byte-identical Allen basal-ganglia bigWigs (md5-verified) that were served from four grouping directories and rendered as four indistinguishable mm10 subtracks, freeing 4.4 GB. Where the four copies genuinely differ all are kept and told apart by the grouping-level descriptor. mm10 goes 629 -> 587 subtracks. - Corrected five stale per-dataset subtrack counts in the description pages and spelled out what ADNC means, noting that it grades neuropathology rather than symptoms. - The SEA-AD Dataset facet link used the collection name, which is not a served Cell Browser slug; it now points at sea-ad-mtg+cohort. - Dropped a dead placeholder variable and made the hardcoded hub-build path overridable. refs #37914 Co-Authored-By: Claude Opus 5 (1M context) <noreply@anthropic.com>
• src/hg/makeDb/doc/mm10/singleCellSignalsPeaks.txt
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    0abed78024d40b506c2b2e3a49ad483045bc5e1d Sat Aug 1 20:53:25 2026 -0700
    singleCellSignalsPeaks: add native mm10 track mm10 counterpart of the hg38 track: 629 single-cell ATAC signal (bigWig) and peak (bigNarrowPeak) subtracks from 9 Cell Browser datasets, re-parented under one faceted composite in the regulation group. Colored by broad cell class from the same palette as hg38, grouped by class, off by default; cell types are paper-curated and the facets/longLabels are harmonized (see the makeDoc). Data lives in /hive/data/genomes/mm10/bed/singleCellSignalsPeaks and is served via the /gbdb/mm10/bbi symlink; the .ra is regenerated by makeSingleCellSignalsPeaksRa.py from the Cell Browser hub build. Included in mm10 trackDb.ra (alpha). refs #37914 Co-Authored-By: Claude Opus 4.8 (1M context) <noreply@anthropic.com>
  • lines changed 90, context: html, text, full: html, text
    b914d581f876d486caf9404e715e4f61ada38195 Mon Aug 3 16:19:44 2026 -0700
    singleCellSignalsPeaks: make every subtrack label unique, fix cell-class regressions The harmonized labels were not distinguishing tracks. build_long_label composed from cell type + condition + tissue, but the upstream steps discard the discriminators on purpose to keep the facets compact, so hg38 had 925 subtracks sharing only 401 distinct longLabels and mm10 629 sharing 359. Worst case: cortex-atac's MACS, enhancer and cell-type-specific peak sets all read "Astrocytes and oligodendrocytes (Cortex ATAC)", with the peak method surviving only in the raw shortLabel. Labels are now built from the harmonized cell type plus a variant descriptor that recovers what was dropped (peak method, grouping level, cohort, signal vs peaks), and anything still colliding is qualified with its source cluster code. shortLabels are rebuilt too -- the old ones were raw source strings up to 50 chars with underscores, ArchR filename tails and R-mangled names -- abbreviated through a curated word table to 22 chars, with compact tokens where the longLabel distinction would otherwise be invisible (SEA-AD region + ADNC, CATLAS aging age). All 925/587 longLabels are now unique; no shortLabel exceeds 22 chars or contains an underscore. Also fixed, found while verifying the above: - Correcting source misspellings in the cell types broke the curated lookups, which are keyed on those same misspelled strings, and 16 hg38 tracks silently lost their Cell_class and color. The class map and the hub_config tables now normalize their keys on load, and a cell type with no broad class is reported instead of becoming "unknown". - Nephron progenitor was classed as Neural progenitor: the decode tables give it the bare broad class "Progenitor" and that was blanket-mapped to neural. It is Six2+ kidney cap mesenchyme, so it is now Stromal. The HTML legend had been worded to match the bug. - The plural/case merge picked the most frequent form, which was inconsistent -- singular for 15 of 17 merged groups but plural for Megakaryocytes/Oligodendrocytes. It now prefers the singular. - Removed 42 byte-identical Allen basal-ganglia bigWigs (md5-verified) that were served from four grouping directories and rendered as four indistinguishable mm10 subtracks, freeing 4.4 GB. Where the four copies genuinely differ all are kept and told apart by the grouping-level descriptor. mm10 goes 629 -> 587 subtracks. - Corrected five stale per-dataset subtrack counts in the description pages and spelled out what ADNC means, noting that it grades neuropathology rather than symptoms. - The SEA-AD Dataset facet link used the collection name, which is not a served Cell Browser slug; it now points at sea-ad-mtg+cohort. - Dropped a dead placeholder variable and made the hardcoded hub-build path overridable. refs #37914 Co-Authored-By: Claude Opus 5 (1M context) <noreply@anthropic.com>
• src/hg/makeDb/scripts/singleCellSignalsPeaks/build_celltype_crosswalks.py
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    d0632693bee08bf61b7990e0c6a1de8c050e337f Sat Aug 1 20:53:09 2026 -0700
    singleCellSignalsPeaks: color by cell class, harmonize labels and facets (hg38) Overhaul of the hg38 track and the shared build scripts it and the mm10 track are generated from: - Color every subtrack by broad cell class from one colorblind-conscious palette (shared with the mm10 track, so a class is the same color on both assemblies); add a color legend to the description page. - Add a "Cell class" facet; the fine cell type becomes a searchable table column. Group subtracks by class via priority; every subtrack is off by default. - Paper-curated cell-type names, redundant-synonym merges, QC-cluster drop, and per-collection tissue/life-stage/condition (including the SEA-AD region and ADNC neuropathology level, from Gabitto 2024 and Hawrylycz 2024). - Rebuild the longLabels from the harmonized cell type + facets, so the cryptic source short labels decode. - Reclassify 10 mislabeled interaction bigBeds out of the signal/peaks composite, retype a narrowPeak-format bigBed, and drop deprecated *.old data (936 -> 925 subtracks). - Archive the curation with the scripts: build_celltype_crosswalks.py and celltype-crosswalks/ (per-collection crosswalks, palette, class map, and the paper-decode source tables). refs #37914 Co-Authored-By: Claude Opus 4.8 (1M context) <noreply@anthropic.com>
  • lines changed 15, context: html, text, full: html, text
    b914d581f876d486caf9404e715e4f61ada38195 Mon Aug 3 16:19:44 2026 -0700
    singleCellSignalsPeaks: make every subtrack label unique, fix cell-class regressions The harmonized labels were not distinguishing tracks. build_long_label composed from cell type + condition + tissue, but the upstream steps discard the discriminators on purpose to keep the facets compact, so hg38 had 925 subtracks sharing only 401 distinct longLabels and mm10 629 sharing 359. Worst case: cortex-atac's MACS, enhancer and cell-type-specific peak sets all read "Astrocytes and oligodendrocytes (Cortex ATAC)", with the peak method surviving only in the raw shortLabel. Labels are now built from the harmonized cell type plus a variant descriptor that recovers what was dropped (peak method, grouping level, cohort, signal vs peaks), and anything still colliding is qualified with its source cluster code. shortLabels are rebuilt too -- the old ones were raw source strings up to 50 chars with underscores, ArchR filename tails and R-mangled names -- abbreviated through a curated word table to 22 chars, with compact tokens where the longLabel distinction would otherwise be invisible (SEA-AD region + ADNC, CATLAS aging age). All 925/587 longLabels are now unique; no shortLabel exceeds 22 chars or contains an underscore. Also fixed, found while verifying the above: - Correcting source misspellings in the cell types broke the curated lookups, which are keyed on those same misspelled strings, and 16 hg38 tracks silently lost their Cell_class and color. The class map and the hub_config tables now normalize their keys on load, and a cell type with no broad class is reported instead of becoming "unknown". - Nephron progenitor was classed as Neural progenitor: the decode tables give it the bare broad class "Progenitor" and that was blanket-mapped to neural. It is Six2+ kidney cap mesenchyme, so it is now Stromal. The HTML legend had been worded to match the bug. - The plural/case merge picked the most frequent form, which was inconsistent -- singular for 15 of 17 merged groups but plural for Megakaryocytes/Oligodendrocytes. It now prefers the singular. - Removed 42 byte-identical Allen basal-ganglia bigWigs (md5-verified) that were served from four grouping directories and rendered as four indistinguishable mm10 subtracks, freeing 4.4 GB. Where the four copies genuinely differ all are kept and told apart by the grouping-level descriptor. mm10 goes 629 -> 587 subtracks. - Corrected five stale per-dataset subtrack counts in the description pages and spelled out what ADNC means, noting that it grades neuropathology rather than symptoms. - The SEA-AD Dataset facet link used the collection name, which is not a served Cell Browser slug; it now points at sea-ad-mtg+cohort. - Dropped a dead placeholder variable and made the hardcoded hub-build path overridable. refs #37914 Co-Authored-By: Claude Opus 5 (1M context) <noreply@anthropic.com>
• src/hg/makeDb/scripts/singleCellSignalsPeaks/celltype-crosswalks/allen-basal-ganglia-atac.tsv
  • lines changed 46, context: html, text, full: html, text
    d0632693bee08bf61b7990e0c6a1de8c050e337f Sat Aug 1 20:53:09 2026 -0700
    singleCellSignalsPeaks: color by cell class, harmonize labels and facets (hg38) Overhaul of the hg38 track and the shared build scripts it and the mm10 track are generated from: - Color every subtrack by broad cell class from one colorblind-conscious palette (shared with the mm10 track, so a class is the same color on both assemblies); add a color legend to the description page. - Add a "Cell class" facet; the fine cell type becomes a searchable table column. Group subtracks by class via priority; every subtrack is off by default. - Paper-curated cell-type names, redundant-synonym merges, QC-cluster drop, and per-collection tissue/life-stage/condition (including the SEA-AD region and ADNC neuropathology level, from Gabitto 2024 and Hawrylycz 2024). - Rebuild the longLabels from the harmonized cell type + facets, so the cryptic source short labels decode. - Reclassify 10 mislabeled interaction bigBeds out of the signal/peaks composite, retype a narrowPeak-format bigBed, and drop deprecated *.old data (936 -> 925 subtracks). - Archive the curation with the scripts: build_celltype_crosswalks.py and celltype-crosswalks/ (per-collection crosswalks, palette, class map, and the paper-decode source tables). refs #37914 Co-Authored-By: Claude Opus 4.8 (1M context) <noreply@anthropic.com>
• src/hg/makeDb/scripts/singleCellSignalsPeaks/celltype-crosswalks/catlas-mouse-aging.tsv
  • lines changed 234, context: html, text, full: html, text
    d0632693bee08bf61b7990e0c6a1de8c050e337f Sat Aug 1 20:53:09 2026 -0700
    singleCellSignalsPeaks: color by cell class, harmonize labels and facets (hg38) Overhaul of the hg38 track and the shared build scripts it and the mm10 track are generated from: - Color every subtrack by broad cell class from one colorblind-conscious palette (shared with the mm10 track, so a class is the same color on both assemblies); add a color legend to the description page. - Add a "Cell class" facet; the fine cell type becomes a searchable table column. Group subtracks by class via priority; every subtrack is off by default. - Paper-curated cell-type names, redundant-synonym merges, QC-cluster drop, and per-collection tissue/life-stage/condition (including the SEA-AD region and ADNC neuropathology level, from Gabitto 2024 and Hawrylycz 2024). - Rebuild the longLabels from the harmonized cell type + facets, so the cryptic source short labels decode. - Reclassify 10 mislabeled interaction bigBeds out of the signal/peaks composite, retype a narrowPeak-format bigBed, and drop deprecated *.old data (936 -> 925 subtracks). - Archive the curation with the scripts: build_celltype_crosswalks.py and celltype-crosswalks/ (per-collection crosswalks, palette, class map, and the paper-decode source tables). refs #37914 Co-Authored-By: Claude Opus 4.8 (1M context) <noreply@anthropic.com>
• src/hg/makeDb/scripts/singleCellSignalsPeaks/celltype-crosswalks/catlas-mouse-brain.tsv
  • lines changed 160, context: html, text, full: html, text
    d0632693bee08bf61b7990e0c6a1de8c050e337f Sat Aug 1 20:53:09 2026 -0700
    singleCellSignalsPeaks: color by cell class, harmonize labels and facets (hg38) Overhaul of the hg38 track and the shared build scripts it and the mm10 track are generated from: - Color every subtrack by broad cell class from one colorblind-conscious palette (shared with the mm10 track, so a class is the same color on both assemblies); add a color legend to the description page. - Add a "Cell class" facet; the fine cell type becomes a searchable table column. Group subtracks by class via priority; every subtrack is off by default. - Paper-curated cell-type names, redundant-synonym merges, QC-cluster drop, and per-collection tissue/life-stage/condition (including the SEA-AD region and ADNC neuropathology level, from Gabitto 2024 and Hawrylycz 2024). - Rebuild the longLabels from the harmonized cell type + facets, so the cryptic source short labels decode. - Reclassify 10 mislabeled interaction bigBeds out of the signal/peaks composite, retype a narrowPeak-format bigBed, and drop deprecated *.old data (936 -> 925 subtracks). - Archive the curation with the scripts: build_celltype_crosswalks.py and celltype-crosswalks/ (per-collection crosswalks, palette, class map, and the paper-decode source tables). refs #37914 Co-Authored-By: Claude Opus 4.8 (1M context) <noreply@anthropic.com>
• src/hg/makeDb/scripts/singleCellSignalsPeaks/celltype-crosswalks/catlas-paired-tag.tsv
  • lines changed 21, context: html, text, full: html, text
    d0632693bee08bf61b7990e0c6a1de8c050e337f Sat Aug 1 20:53:09 2026 -0700
    singleCellSignalsPeaks: color by cell class, harmonize labels and facets (hg38) Overhaul of the hg38 track and the shared build scripts it and the mm10 track are generated from: - Color every subtrack by broad cell class from one colorblind-conscious palette (shared with the mm10 track, so a class is the same color on both assemblies); add a color legend to the description page. - Add a "Cell class" facet; the fine cell type becomes a searchable table column. Group subtracks by class via priority; every subtrack is off by default. - Paper-curated cell-type names, redundant-synonym merges, QC-cluster drop, and per-collection tissue/life-stage/condition (including the SEA-AD region and ADNC neuropathology level, from Gabitto 2024 and Hawrylycz 2024). - Rebuild the longLabels from the harmonized cell type + facets, so the cryptic source short labels decode. - Reclassify 10 mislabeled interaction bigBeds out of the signal/peaks composite, retype a narrowPeak-format bigBed, and drop deprecated *.old data (936 -> 925 subtracks). - Archive the curation with the scripts: build_celltype_crosswalks.py and celltype-crosswalks/ (per-collection crosswalks, palette, class map, and the paper-decode source tables). refs #37914 Co-Authored-By: Claude Opus 4.8 (1M context) <noreply@anthropic.com>
• src/hg/makeDb/scripts/singleCellSignalsPeaks/celltype-crosswalks/celltype-class.tsv
  • lines changed 342, context: html, text, full: html, text
    d0632693bee08bf61b7990e0c6a1de8c050e337f Sat Aug 1 20:53:09 2026 -0700
    singleCellSignalsPeaks: color by cell class, harmonize labels and facets (hg38) Overhaul of the hg38 track and the shared build scripts it and the mm10 track are generated from: - Color every subtrack by broad cell class from one colorblind-conscious palette (shared with the mm10 track, so a class is the same color on both assemblies); add a color legend to the description page. - Add a "Cell class" facet; the fine cell type becomes a searchable table column. Group subtracks by class via priority; every subtrack is off by default. - Paper-curated cell-type names, redundant-synonym merges, QC-cluster drop, and per-collection tissue/life-stage/condition (including the SEA-AD region and ADNC neuropathology level, from Gabitto 2024 and Hawrylycz 2024). - Rebuild the longLabels from the harmonized cell type + facets, so the cryptic source short labels decode. - Reclassify 10 mislabeled interaction bigBeds out of the signal/peaks composite, retype a narrowPeak-format bigBed, and drop deprecated *.old data (936 -> 925 subtracks). - Archive the curation with the scripts: build_celltype_crosswalks.py and celltype-crosswalks/ (per-collection crosswalks, palette, class map, and the paper-decode source tables). refs #37914 Co-Authored-By: Claude Opus 4.8 (1M context) <noreply@anthropic.com>
  • lines changed 6, context: html, text, full: html, text
    b914d581f876d486caf9404e715e4f61ada38195 Mon Aug 3 16:19:44 2026 -0700
    singleCellSignalsPeaks: make every subtrack label unique, fix cell-class regressions The harmonized labels were not distinguishing tracks. build_long_label composed from cell type + condition + tissue, but the upstream steps discard the discriminators on purpose to keep the facets compact, so hg38 had 925 subtracks sharing only 401 distinct longLabels and mm10 629 sharing 359. Worst case: cortex-atac's MACS, enhancer and cell-type-specific peak sets all read "Astrocytes and oligodendrocytes (Cortex ATAC)", with the peak method surviving only in the raw shortLabel. Labels are now built from the harmonized cell type plus a variant descriptor that recovers what was dropped (peak method, grouping level, cohort, signal vs peaks), and anything still colliding is qualified with its source cluster code. shortLabels are rebuilt too -- the old ones were raw source strings up to 50 chars with underscores, ArchR filename tails and R-mangled names -- abbreviated through a curated word table to 22 chars, with compact tokens where the longLabel distinction would otherwise be invisible (SEA-AD region + ADNC, CATLAS aging age). All 925/587 longLabels are now unique; no shortLabel exceeds 22 chars or contains an underscore. Also fixed, found while verifying the above: - Correcting source misspellings in the cell types broke the curated lookups, which are keyed on those same misspelled strings, and 16 hg38 tracks silently lost their Cell_class and color. The class map and the hub_config tables now normalize their keys on load, and a cell type with no broad class is reported instead of becoming "unknown". - Nephron progenitor was classed as Neural progenitor: the decode tables give it the bare broad class "Progenitor" and that was blanket-mapped to neural. It is Six2+ kidney cap mesenchyme, so it is now Stromal. The HTML legend had been worded to match the bug. - The plural/case merge picked the most frequent form, which was inconsistent -- singular for 15 of 17 merged groups but plural for Megakaryocytes/Oligodendrocytes. It now prefers the singular. - Removed 42 byte-identical Allen basal-ganglia bigWigs (md5-verified) that were served from four grouping directories and rendered as four indistinguishable mm10 subtracks, freeing 4.4 GB. Where the four copies genuinely differ all are kept and told apart by the grouping-level descriptor. mm10 goes 629 -> 587 subtracks. - Corrected five stale per-dataset subtrack counts in the description pages and spelled out what ADNC means, noting that it grades neuropathology rather than symptoms. - The SEA-AD Dataset facet link used the collection name, which is not a served Cell Browser slug; it now points at sea-ad-mtg+cohort. - Dropped a dead placeholder variable and made the hardcoded hub-build path overridable. refs #37914 Co-Authored-By: Claude Opus 5 (1M context) <noreply@anthropic.com>
• src/hg/makeDb/scripts/singleCellSignalsPeaks/celltype-crosswalks/celltype-palette.tsv
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    d0632693bee08bf61b7990e0c6a1de8c050e337f Sat Aug 1 20:53:09 2026 -0700
    singleCellSignalsPeaks: color by cell class, harmonize labels and facets (hg38) Overhaul of the hg38 track and the shared build scripts it and the mm10 track are generated from: - Color every subtrack by broad cell class from one colorblind-conscious palette (shared with the mm10 track, so a class is the same color on both assemblies); add a color legend to the description page. - Add a "Cell class" facet; the fine cell type becomes a searchable table column. Group subtracks by class via priority; every subtrack is off by default. - Paper-curated cell-type names, redundant-synonym merges, QC-cluster drop, and per-collection tissue/life-stage/condition (including the SEA-AD region and ADNC neuropathology level, from Gabitto 2024 and Hawrylycz 2024). - Rebuild the longLabels from the harmonized cell type + facets, so the cryptic source short labels decode. - Reclassify 10 mislabeled interaction bigBeds out of the signal/peaks composite, retype a narrowPeak-format bigBed, and drop deprecated *.old data (936 -> 925 subtracks). - Archive the curation with the scripts: build_celltype_crosswalks.py and celltype-crosswalks/ (per-collection crosswalks, palette, class map, and the paper-decode source tables). refs #37914 Co-Authored-By: Claude Opus 4.8 (1M context) <noreply@anthropic.com>
• src/hg/makeDb/scripts/singleCellSignalsPeaks/celltype-crosswalks/clean5.tsv
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    d0632693bee08bf61b7990e0c6a1de8c050e337f Sat Aug 1 20:53:09 2026 -0700
    singleCellSignalsPeaks: color by cell class, harmonize labels and facets (hg38) Overhaul of the hg38 track and the shared build scripts it and the mm10 track are generated from: - Color every subtrack by broad cell class from one colorblind-conscious palette (shared with the mm10 track, so a class is the same color on both assemblies); add a color legend to the description page. - Add a "Cell class" facet; the fine cell type becomes a searchable table column. Group subtracks by class via priority; every subtrack is off by default. - Paper-curated cell-type names, redundant-synonym merges, QC-cluster drop, and per-collection tissue/life-stage/condition (including the SEA-AD region and ADNC neuropathology level, from Gabitto 2024 and Hawrylycz 2024). - Rebuild the longLabels from the harmonized cell type + facets, so the cryptic source short labels decode. - Reclassify 10 mislabeled interaction bigBeds out of the signal/peaks composite, retype a narrowPeak-format bigBed, and drop deprecated *.old data (936 -> 925 subtracks). - Archive the curation with the scripts: build_celltype_crosswalks.py and celltype-crosswalks/ (per-collection crosswalks, palette, class map, and the paper-decode source tables). refs #37914 Co-Authored-By: Claude Opus 4.8 (1M context) <noreply@anthropic.com>
  • lines changed 1, context: html, text, full: html, text
    b914d581f876d486caf9404e715e4f61ada38195 Mon Aug 3 16:19:44 2026 -0700
    singleCellSignalsPeaks: make every subtrack label unique, fix cell-class regressions The harmonized labels were not distinguishing tracks. build_long_label composed from cell type + condition + tissue, but the upstream steps discard the discriminators on purpose to keep the facets compact, so hg38 had 925 subtracks sharing only 401 distinct longLabels and mm10 629 sharing 359. Worst case: cortex-atac's MACS, enhancer and cell-type-specific peak sets all read "Astrocytes and oligodendrocytes (Cortex ATAC)", with the peak method surviving only in the raw shortLabel. Labels are now built from the harmonized cell type plus a variant descriptor that recovers what was dropped (peak method, grouping level, cohort, signal vs peaks), and anything still colliding is qualified with its source cluster code. shortLabels are rebuilt too -- the old ones were raw source strings up to 50 chars with underscores, ArchR filename tails and R-mangled names -- abbreviated through a curated word table to 22 chars, with compact tokens where the longLabel distinction would otherwise be invisible (SEA-AD region + ADNC, CATLAS aging age). All 925/587 longLabels are now unique; no shortLabel exceeds 22 chars or contains an underscore. Also fixed, found while verifying the above: - Correcting source misspellings in the cell types broke the curated lookups, which are keyed on those same misspelled strings, and 16 hg38 tracks silently lost their Cell_class and color. The class map and the hub_config tables now normalize their keys on load, and a cell type with no broad class is reported instead of becoming "unknown". - Nephron progenitor was classed as Neural progenitor: the decode tables give it the bare broad class "Progenitor" and that was blanket-mapped to neural. It is Six2+ kidney cap mesenchyme, so it is now Stromal. The HTML legend had been worded to match the bug. - The plural/case merge picked the most frequent form, which was inconsistent -- singular for 15 of 17 merged groups but plural for Megakaryocytes/Oligodendrocytes. It now prefers the singular. - Removed 42 byte-identical Allen basal-ganglia bigWigs (md5-verified) that were served from four grouping directories and rendered as four indistinguishable mm10 subtracks, freeing 4.4 GB. Where the four copies genuinely differ all are kept and told apart by the grouping-level descriptor. mm10 goes 629 -> 587 subtracks. - Corrected five stale per-dataset subtrack counts in the description pages and spelled out what ADNC means, noting that it grades neuropathology rather than symptoms. - The SEA-AD Dataset facet link used the collection name, which is not a served Cell Browser slug; it now points at sea-ad-mtg+cohort. - Dropped a dead placeholder variable and made the hardcoded hub-build path overridable. refs #37914 Co-Authored-By: Claude Opus 5 (1M context) <noreply@anthropic.com>
• src/hg/makeDb/scripts/singleCellSignalsPeaks/celltype-crosswalks/paper-decodes/hg38_ct_class.tsv
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    d0632693bee08bf61b7990e0c6a1de8c050e337f Sat Aug 1 20:53:09 2026 -0700
    singleCellSignalsPeaks: color by cell class, harmonize labels and facets (hg38) Overhaul of the hg38 track and the shared build scripts it and the mm10 track are generated from: - Color every subtrack by broad cell class from one colorblind-conscious palette (shared with the mm10 track, so a class is the same color on both assemblies); add a color legend to the description page. - Add a "Cell class" facet; the fine cell type becomes a searchable table column. Group subtracks by class via priority; every subtrack is off by default. - Paper-curated cell-type names, redundant-synonym merges, QC-cluster drop, and per-collection tissue/life-stage/condition (including the SEA-AD region and ADNC neuropathology level, from Gabitto 2024 and Hawrylycz 2024). - Rebuild the longLabels from the harmonized cell type + facets, so the cryptic source short labels decode. - Reclassify 10 mislabeled interaction bigBeds out of the signal/peaks composite, retype a narrowPeak-format bigBed, and drop deprecated *.old data (936 -> 925 subtracks). - Archive the curation with the scripts: build_celltype_crosswalks.py and celltype-crosswalks/ (per-collection crosswalks, palette, class map, and the paper-decode source tables). refs #37914 Co-Authored-By: Claude Opus 4.8 (1M context) <noreply@anthropic.com>
  • lines changed 5, context: html, text, full: html, text
    b914d581f876d486caf9404e715e4f61ada38195 Mon Aug 3 16:19:44 2026 -0700
    singleCellSignalsPeaks: make every subtrack label unique, fix cell-class regressions The harmonized labels were not distinguishing tracks. build_long_label composed from cell type + condition + tissue, but the upstream steps discard the discriminators on purpose to keep the facets compact, so hg38 had 925 subtracks sharing only 401 distinct longLabels and mm10 629 sharing 359. Worst case: cortex-atac's MACS, enhancer and cell-type-specific peak sets all read "Astrocytes and oligodendrocytes (Cortex ATAC)", with the peak method surviving only in the raw shortLabel. Labels are now built from the harmonized cell type plus a variant descriptor that recovers what was dropped (peak method, grouping level, cohort, signal vs peaks), and anything still colliding is qualified with its source cluster code. shortLabels are rebuilt too -- the old ones were raw source strings up to 50 chars with underscores, ArchR filename tails and R-mangled names -- abbreviated through a curated word table to 22 chars, with compact tokens where the longLabel distinction would otherwise be invisible (SEA-AD region + ADNC, CATLAS aging age). All 925/587 longLabels are now unique; no shortLabel exceeds 22 chars or contains an underscore. Also fixed, found while verifying the above: - Correcting source misspellings in the cell types broke the curated lookups, which are keyed on those same misspelled strings, and 16 hg38 tracks silently lost their Cell_class and color. The class map and the hub_config tables now normalize their keys on load, and a cell type with no broad class is reported instead of becoming "unknown". - Nephron progenitor was classed as Neural progenitor: the decode tables give it the bare broad class "Progenitor" and that was blanket-mapped to neural. It is Six2+ kidney cap mesenchyme, so it is now Stromal. The HTML legend had been worded to match the bug. - The plural/case merge picked the most frequent form, which was inconsistent -- singular for 15 of 17 merged groups but plural for Megakaryocytes/Oligodendrocytes. It now prefers the singular. - Removed 42 byte-identical Allen basal-ganglia bigWigs (md5-verified) that were served from four grouping directories and rendered as four indistinguishable mm10 subtracks, freeing 4.4 GB. Where the four copies genuinely differ all are kept and told apart by the grouping-level descriptor. mm10 goes 629 -> 587 subtracks. - Corrected five stale per-dataset subtrack counts in the description pages and spelled out what ADNC means, noting that it grades neuropathology rather than symptoms. - The SEA-AD Dataset facet link used the collection name, which is not a served Cell Browser slug; it now points at sea-ad-mtg+cohort. - Dropped a dead placeholder variable and made the hardcoded hub-build path overridable. refs #37914 Co-Authored-By: Claude Opus 5 (1M context) <noreply@anthropic.com>
• src/hg/makeDb/scripts/singleCellSignalsPeaks/celltype-crosswalks/paper-decodes/xwalk_allen-basal-ganglia-atac.tsv
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    d0632693bee08bf61b7990e0c6a1de8c050e337f Sat Aug 1 20:53:09 2026 -0700
    singleCellSignalsPeaks: color by cell class, harmonize labels and facets (hg38) Overhaul of the hg38 track and the shared build scripts it and the mm10 track are generated from: - Color every subtrack by broad cell class from one colorblind-conscious palette (shared with the mm10 track, so a class is the same color on both assemblies); add a color legend to the description page. - Add a "Cell class" facet; the fine cell type becomes a searchable table column. Group subtracks by class via priority; every subtrack is off by default. - Paper-curated cell-type names, redundant-synonym merges, QC-cluster drop, and per-collection tissue/life-stage/condition (including the SEA-AD region and ADNC neuropathology level, from Gabitto 2024 and Hawrylycz 2024). - Rebuild the longLabels from the harmonized cell type + facets, so the cryptic source short labels decode. - Reclassify 10 mislabeled interaction bigBeds out of the signal/peaks composite, retype a narrowPeak-format bigBed, and drop deprecated *.old data (936 -> 925 subtracks). - Archive the curation with the scripts: build_celltype_crosswalks.py and celltype-crosswalks/ (per-collection crosswalks, palette, class map, and the paper-decode source tables). refs #37914 Co-Authored-By: Claude Opus 4.8 (1M context) <noreply@anthropic.com>
• src/hg/makeDb/scripts/singleCellSignalsPeaks/celltype-crosswalks/paper-decodes/xwalk_catlas-mouse-aging.tsv
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    d0632693bee08bf61b7990e0c6a1de8c050e337f Sat Aug 1 20:53:09 2026 -0700
    singleCellSignalsPeaks: color by cell class, harmonize labels and facets (hg38) Overhaul of the hg38 track and the shared build scripts it and the mm10 track are generated from: - Color every subtrack by broad cell class from one colorblind-conscious palette (shared with the mm10 track, so a class is the same color on both assemblies); add a color legend to the description page. - Add a "Cell class" facet; the fine cell type becomes a searchable table column. Group subtracks by class via priority; every subtrack is off by default. - Paper-curated cell-type names, redundant-synonym merges, QC-cluster drop, and per-collection tissue/life-stage/condition (including the SEA-AD region and ADNC neuropathology level, from Gabitto 2024 and Hawrylycz 2024). - Rebuild the longLabels from the harmonized cell type + facets, so the cryptic source short labels decode. - Reclassify 10 mislabeled interaction bigBeds out of the signal/peaks composite, retype a narrowPeak-format bigBed, and drop deprecated *.old data (936 -> 925 subtracks). - Archive the curation with the scripts: build_celltype_crosswalks.py and celltype-crosswalks/ (per-collection crosswalks, palette, class map, and the paper-decode source tables). refs #37914 Co-Authored-By: Claude Opus 4.8 (1M context) <noreply@anthropic.com>
• src/hg/makeDb/scripts/singleCellSignalsPeaks/celltype-crosswalks/paper-decodes/xwalk_catlas-mouse-brain.tsv
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    d0632693bee08bf61b7990e0c6a1de8c050e337f Sat Aug 1 20:53:09 2026 -0700
    singleCellSignalsPeaks: color by cell class, harmonize labels and facets (hg38) Overhaul of the hg38 track and the shared build scripts it and the mm10 track are generated from: - Color every subtrack by broad cell class from one colorblind-conscious palette (shared with the mm10 track, so a class is the same color on both assemblies); add a color legend to the description page. - Add a "Cell class" facet; the fine cell type becomes a searchable table column. Group subtracks by class via priority; every subtrack is off by default. - Paper-curated cell-type names, redundant-synonym merges, QC-cluster drop, and per-collection tissue/life-stage/condition (including the SEA-AD region and ADNC neuropathology level, from Gabitto 2024 and Hawrylycz 2024). - Rebuild the longLabels from the harmonized cell type + facets, so the cryptic source short labels decode. - Reclassify 10 mislabeled interaction bigBeds out of the signal/peaks composite, retype a narrowPeak-format bigBed, and drop deprecated *.old data (936 -> 925 subtracks). - Archive the curation with the scripts: build_celltype_crosswalks.py and celltype-crosswalks/ (per-collection crosswalks, palette, class map, and the paper-decode source tables). refs #37914 Co-Authored-By: Claude Opus 4.8 (1M context) <noreply@anthropic.com>
• src/hg/makeDb/scripts/singleCellSignalsPeaks/celltype-crosswalks/paper-decodes/xwalk_catlas-paired-tag.tsv
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    d0632693bee08bf61b7990e0c6a1de8c050e337f Sat Aug 1 20:53:09 2026 -0700
    singleCellSignalsPeaks: color by cell class, harmonize labels and facets (hg38) Overhaul of the hg38 track and the shared build scripts it and the mm10 track are generated from: - Color every subtrack by broad cell class from one colorblind-conscious palette (shared with the mm10 track, so a class is the same color on both assemblies); add a color legend to the description page. - Add a "Cell class" facet; the fine cell type becomes a searchable table column. Group subtracks by class via priority; every subtrack is off by default. - Paper-curated cell-type names, redundant-synonym merges, QC-cluster drop, and per-collection tissue/life-stage/condition (including the SEA-AD region and ADNC neuropathology level, from Gabitto 2024 and Hawrylycz 2024). - Rebuild the longLabels from the harmonized cell type + facets, so the cryptic source short labels decode. - Reclassify 10 mislabeled interaction bigBeds out of the signal/peaks composite, retype a narrowPeak-format bigBed, and drop deprecated *.old data (936 -> 925 subtracks). - Archive the curation with the scripts: build_celltype_crosswalks.py and celltype-crosswalks/ (per-collection crosswalks, palette, class map, and the paper-decode source tables). refs #37914 Co-Authored-By: Claude Opus 4.8 (1M context) <noreply@anthropic.com>
• src/hg/makeDb/scripts/singleCellSignalsPeaks/celltype-crosswalks/paper-decodes/xwalk_clean5.tsv
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    d0632693bee08bf61b7990e0c6a1de8c050e337f Sat Aug 1 20:53:09 2026 -0700
    singleCellSignalsPeaks: color by cell class, harmonize labels and facets (hg38) Overhaul of the hg38 track and the shared build scripts it and the mm10 track are generated from: - Color every subtrack by broad cell class from one colorblind-conscious palette (shared with the mm10 track, so a class is the same color on both assemblies); add a color legend to the description page. - Add a "Cell class" facet; the fine cell type becomes a searchable table column. Group subtracks by class via priority; every subtrack is off by default. - Paper-curated cell-type names, redundant-synonym merges, QC-cluster drop, and per-collection tissue/life-stage/condition (including the SEA-AD region and ADNC neuropathology level, from Gabitto 2024 and Hawrylycz 2024). - Rebuild the longLabels from the harmonized cell type + facets, so the cryptic source short labels decode. - Reclassify 10 mislabeled interaction bigBeds out of the signal/peaks composite, retype a narrowPeak-format bigBed, and drop deprecated *.old data (936 -> 925 subtracks). - Archive the curation with the scripts: build_celltype_crosswalks.py and celltype-crosswalks/ (per-collection crosswalks, palette, class map, and the paper-decode source tables). refs #37914 Co-Authored-By: Claude Opus 4.8 (1M context) <noreply@anthropic.com>
• src/hg/makeDb/scripts/singleCellSignalsPeaks/celltype-crosswalks/sea-ad-celltype-crosswalk.tsv
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    d0632693bee08bf61b7990e0c6a1de8c050e337f Sat Aug 1 20:53:09 2026 -0700
    singleCellSignalsPeaks: color by cell class, harmonize labels and facets (hg38) Overhaul of the hg38 track and the shared build scripts it and the mm10 track are generated from: - Color every subtrack by broad cell class from one colorblind-conscious palette (shared with the mm10 track, so a class is the same color on both assemblies); add a color legend to the description page. - Add a "Cell class" facet; the fine cell type becomes a searchable table column. Group subtracks by class via priority; every subtrack is off by default. - Paper-curated cell-type names, redundant-synonym merges, QC-cluster drop, and per-collection tissue/life-stage/condition (including the SEA-AD region and ADNC neuropathology level, from Gabitto 2024 and Hawrylycz 2024). - Rebuild the longLabels from the harmonized cell type + facets, so the cryptic source short labels decode. - Reclassify 10 mislabeled interaction bigBeds out of the signal/peaks composite, retype a narrowPeak-format bigBed, and drop deprecated *.old data (936 -> 925 subtracks). - Archive the curation with the scripts: build_celltype_crosswalks.py and celltype-crosswalks/ (per-collection crosswalks, palette, class map, and the paper-decode source tables). refs #37914 Co-Authored-By: Claude Opus 4.8 (1M context) <noreply@anthropic.com>
• src/hg/makeDb/scripts/singleCellSignalsPeaks/copySingleCellSignalsPeaksFiles.py
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    d0632693bee08bf61b7990e0c6a1de8c050e337f Sat Aug 1 20:53:09 2026 -0700
    singleCellSignalsPeaks: color by cell class, harmonize labels and facets (hg38) Overhaul of the hg38 track and the shared build scripts it and the mm10 track are generated from: - Color every subtrack by broad cell class from one colorblind-conscious palette (shared with the mm10 track, so a class is the same color on both assemblies); add a color legend to the description page. - Add a "Cell class" facet; the fine cell type becomes a searchable table column. Group subtracks by class via priority; every subtrack is off by default. - Paper-curated cell-type names, redundant-synonym merges, QC-cluster drop, and per-collection tissue/life-stage/condition (including the SEA-AD region and ADNC neuropathology level, from Gabitto 2024 and Hawrylycz 2024). - Rebuild the longLabels from the harmonized cell type + facets, so the cryptic source short labels decode. - Reclassify 10 mislabeled interaction bigBeds out of the signal/peaks composite, retype a narrowPeak-format bigBed, and drop deprecated *.old data (936 -> 925 subtracks). - Archive the curation with the scripts: build_celltype_crosswalks.py and celltype-crosswalks/ (per-collection crosswalks, palette, class map, and the paper-decode source tables). refs #37914 Co-Authored-By: Claude Opus 4.8 (1M context) <noreply@anthropic.com>
  • lines changed 5, context: html, text, full: html, text
    b914d581f876d486caf9404e715e4f61ada38195 Mon Aug 3 16:19:44 2026 -0700
    singleCellSignalsPeaks: make every subtrack label unique, fix cell-class regressions The harmonized labels were not distinguishing tracks. build_long_label composed from cell type + condition + tissue, but the upstream steps discard the discriminators on purpose to keep the facets compact, so hg38 had 925 subtracks sharing only 401 distinct longLabels and mm10 629 sharing 359. Worst case: cortex-atac's MACS, enhancer and cell-type-specific peak sets all read "Astrocytes and oligodendrocytes (Cortex ATAC)", with the peak method surviving only in the raw shortLabel. Labels are now built from the harmonized cell type plus a variant descriptor that recovers what was dropped (peak method, grouping level, cohort, signal vs peaks), and anything still colliding is qualified with its source cluster code. shortLabels are rebuilt too -- the old ones were raw source strings up to 50 chars with underscores, ArchR filename tails and R-mangled names -- abbreviated through a curated word table to 22 chars, with compact tokens where the longLabel distinction would otherwise be invisible (SEA-AD region + ADNC, CATLAS aging age). All 925/587 longLabels are now unique; no shortLabel exceeds 22 chars or contains an underscore. Also fixed, found while verifying the above: - Correcting source misspellings in the cell types broke the curated lookups, which are keyed on those same misspelled strings, and 16 hg38 tracks silently lost their Cell_class and color. The class map and the hub_config tables now normalize their keys on load, and a cell type with no broad class is reported instead of becoming "unknown". - Nephron progenitor was classed as Neural progenitor: the decode tables give it the bare broad class "Progenitor" and that was blanket-mapped to neural. It is Six2+ kidney cap mesenchyme, so it is now Stromal. The HTML legend had been worded to match the bug. - The plural/case merge picked the most frequent form, which was inconsistent -- singular for 15 of 17 merged groups but plural for Megakaryocytes/Oligodendrocytes. It now prefers the singular. - Removed 42 byte-identical Allen basal-ganglia bigWigs (md5-verified) that were served from four grouping directories and rendered as four indistinguishable mm10 subtracks, freeing 4.4 GB. Where the four copies genuinely differ all are kept and told apart by the grouping-level descriptor. mm10 goes 629 -> 587 subtracks. - Corrected five stale per-dataset subtrack counts in the description pages and spelled out what ADNC means, noting that it grades neuropathology rather than symptoms. - The SEA-AD Dataset facet link used the collection name, which is not a served Cell Browser slug; it now points at sea-ad-mtg+cohort. - Dropped a dead placeholder variable and made the hardcoded hub-build path overridable. refs #37914 Co-Authored-By: Claude Opus 5 (1M context) <noreply@anthropic.com>
• src/hg/makeDb/scripts/singleCellSignalsPeaks/makeSingleCellSignalsPeaksRa.py
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    d0632693bee08bf61b7990e0c6a1de8c050e337f Sat Aug 1 20:53:09 2026 -0700
    singleCellSignalsPeaks: color by cell class, harmonize labels and facets (hg38) Overhaul of the hg38 track and the shared build scripts it and the mm10 track are generated from: - Color every subtrack by broad cell class from one colorblind-conscious palette (shared with the mm10 track, so a class is the same color on both assemblies); add a color legend to the description page. - Add a "Cell class" facet; the fine cell type becomes a searchable table column. Group subtracks by class via priority; every subtrack is off by default. - Paper-curated cell-type names, redundant-synonym merges, QC-cluster drop, and per-collection tissue/life-stage/condition (including the SEA-AD region and ADNC neuropathology level, from Gabitto 2024 and Hawrylycz 2024). - Rebuild the longLabels from the harmonized cell type + facets, so the cryptic source short labels decode. - Reclassify 10 mislabeled interaction bigBeds out of the signal/peaks composite, retype a narrowPeak-format bigBed, and drop deprecated *.old data (936 -> 925 subtracks). - Archive the curation with the scripts: build_celltype_crosswalks.py and celltype-crosswalks/ (per-collection crosswalks, palette, class map, and the paper-decode source tables). refs #37914 Co-Authored-By: Claude Opus 4.8 (1M context) <noreply@anthropic.com>
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    b914d581f876d486caf9404e715e4f61ada38195 Mon Aug 3 16:19:44 2026 -0700
    singleCellSignalsPeaks: make every subtrack label unique, fix cell-class regressions The harmonized labels were not distinguishing tracks. build_long_label composed from cell type + condition + tissue, but the upstream steps discard the discriminators on purpose to keep the facets compact, so hg38 had 925 subtracks sharing only 401 distinct longLabels and mm10 629 sharing 359. Worst case: cortex-atac's MACS, enhancer and cell-type-specific peak sets all read "Astrocytes and oligodendrocytes (Cortex ATAC)", with the peak method surviving only in the raw shortLabel. Labels are now built from the harmonized cell type plus a variant descriptor that recovers what was dropped (peak method, grouping level, cohort, signal vs peaks), and anything still colliding is qualified with its source cluster code. shortLabels are rebuilt too -- the old ones were raw source strings up to 50 chars with underscores, ArchR filename tails and R-mangled names -- abbreviated through a curated word table to 22 chars, with compact tokens where the longLabel distinction would otherwise be invisible (SEA-AD region + ADNC, CATLAS aging age). All 925/587 longLabels are now unique; no shortLabel exceeds 22 chars or contains an underscore. Also fixed, found while verifying the above: - Correcting source misspellings in the cell types broke the curated lookups, which are keyed on those same misspelled strings, and 16 hg38 tracks silently lost their Cell_class and color. The class map and the hub_config tables now normalize their keys on load, and a cell type with no broad class is reported instead of becoming "unknown". - Nephron progenitor was classed as Neural progenitor: the decode tables give it the bare broad class "Progenitor" and that was blanket-mapped to neural. It is Six2+ kidney cap mesenchyme, so it is now Stromal. The HTML legend had been worded to match the bug. - The plural/case merge picked the most frequent form, which was inconsistent -- singular for 15 of 17 merged groups but plural for Megakaryocytes/Oligodendrocytes. It now prefers the singular. - Removed 42 byte-identical Allen basal-ganglia bigWigs (md5-verified) that were served from four grouping directories and rendered as four indistinguishable mm10 subtracks, freeing 4.4 GB. Where the four copies genuinely differ all are kept and told apart by the grouping-level descriptor. mm10 goes 629 -> 587 subtracks. - Corrected five stale per-dataset subtrack counts in the description pages and spelled out what ADNC means, noting that it grades neuropathology rather than symptoms. - The SEA-AD Dataset facet link used the collection name, which is not a served Cell Browser slug; it now points at sea-ad-mtg+cohort. - Dropped a dead placeholder variable and made the hardcoded hub-build path overridable. refs #37914 Co-Authored-By: Claude Opus 5 (1M context) <noreply@anthropic.com>
• src/hg/makeDb/trackDb/human/hg38/singleCellSignalsPeaks.html
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    d0632693bee08bf61b7990e0c6a1de8c050e337f Sat Aug 1 20:53:09 2026 -0700
    singleCellSignalsPeaks: color by cell class, harmonize labels and facets (hg38) Overhaul of the hg38 track and the shared build scripts it and the mm10 track are generated from: - Color every subtrack by broad cell class from one colorblind-conscious palette (shared with the mm10 track, so a class is the same color on both assemblies); add a color legend to the description page. - Add a "Cell class" facet; the fine cell type becomes a searchable table column. Group subtracks by class via priority; every subtrack is off by default. - Paper-curated cell-type names, redundant-synonym merges, QC-cluster drop, and per-collection tissue/life-stage/condition (including the SEA-AD region and ADNC neuropathology level, from Gabitto 2024 and Hawrylycz 2024). - Rebuild the longLabels from the harmonized cell type + facets, so the cryptic source short labels decode. - Reclassify 10 mislabeled interaction bigBeds out of the signal/peaks composite, retype a narrowPeak-format bigBed, and drop deprecated *.old data (936 -> 925 subtracks). - Archive the curation with the scripts: build_celltype_crosswalks.py and celltype-crosswalks/ (per-collection crosswalks, palette, class map, and the paper-decode source tables). refs #37914 Co-Authored-By: Claude Opus 4.8 (1M context) <noreply@anthropic.com>
  • lines changed 14, context: html, text, full: html, text
    b914d581f876d486caf9404e715e4f61ada38195 Mon Aug 3 16:19:44 2026 -0700
    singleCellSignalsPeaks: make every subtrack label unique, fix cell-class regressions The harmonized labels were not distinguishing tracks. build_long_label composed from cell type + condition + tissue, but the upstream steps discard the discriminators on purpose to keep the facets compact, so hg38 had 925 subtracks sharing only 401 distinct longLabels and mm10 629 sharing 359. Worst case: cortex-atac's MACS, enhancer and cell-type-specific peak sets all read "Astrocytes and oligodendrocytes (Cortex ATAC)", with the peak method surviving only in the raw shortLabel. Labels are now built from the harmonized cell type plus a variant descriptor that recovers what was dropped (peak method, grouping level, cohort, signal vs peaks), and anything still colliding is qualified with its source cluster code. shortLabels are rebuilt too -- the old ones were raw source strings up to 50 chars with underscores, ArchR filename tails and R-mangled names -- abbreviated through a curated word table to 22 chars, with compact tokens where the longLabel distinction would otherwise be invisible (SEA-AD region + ADNC, CATLAS aging age). All 925/587 longLabels are now unique; no shortLabel exceeds 22 chars or contains an underscore. Also fixed, found while verifying the above: - Correcting source misspellings in the cell types broke the curated lookups, which are keyed on those same misspelled strings, and 16 hg38 tracks silently lost their Cell_class and color. The class map and the hub_config tables now normalize their keys on load, and a cell type with no broad class is reported instead of becoming "unknown". - Nephron progenitor was classed as Neural progenitor: the decode tables give it the bare broad class "Progenitor" and that was blanket-mapped to neural. It is Six2+ kidney cap mesenchyme, so it is now Stromal. The HTML legend had been worded to match the bug. - The plural/case merge picked the most frequent form, which was inconsistent -- singular for 15 of 17 merged groups but plural for Megakaryocytes/Oligodendrocytes. It now prefers the singular. - Removed 42 byte-identical Allen basal-ganglia bigWigs (md5-verified) that were served from four grouping directories and rendered as four indistinguishable mm10 subtracks, freeing 4.4 GB. Where the four copies genuinely differ all are kept and told apart by the grouping-level descriptor. mm10 goes 629 -> 587 subtracks. - Corrected five stale per-dataset subtrack counts in the description pages and spelled out what ADNC means, noting that it grades neuropathology rather than symptoms. - The SEA-AD Dataset facet link used the collection name, which is not a served Cell Browser slug; it now points at sea-ad-mtg+cohort. - Dropped a dead placeholder variable and made the hardcoded hub-build path overridable. refs #37914 Co-Authored-By: Claude Opus 5 (1M context) <noreply@anthropic.com>
• src/hg/makeDb/trackDb/human/hg38/singleCellSignalsPeaks.ra
  • lines changed 3783, context: html, text, full: html, text
    d0632693bee08bf61b7990e0c6a1de8c050e337f Sat Aug 1 20:53:09 2026 -0700
    singleCellSignalsPeaks: color by cell class, harmonize labels and facets (hg38) Overhaul of the hg38 track and the shared build scripts it and the mm10 track are generated from: - Color every subtrack by broad cell class from one colorblind-conscious palette (shared with the mm10 track, so a class is the same color on both assemblies); add a color legend to the description page. - Add a "Cell class" facet; the fine cell type becomes a searchable table column. Group subtracks by class via priority; every subtrack is off by default. - Paper-curated cell-type names, redundant-synonym merges, QC-cluster drop, and per-collection tissue/life-stage/condition (including the SEA-AD region and ADNC neuropathology level, from Gabitto 2024 and Hawrylycz 2024). - Rebuild the longLabels from the harmonized cell type + facets, so the cryptic source short labels decode. - Reclassify 10 mislabeled interaction bigBeds out of the signal/peaks composite, retype a narrowPeak-format bigBed, and drop deprecated *.old data (936 -> 925 subtracks). - Archive the curation with the scripts: build_celltype_crosswalks.py and celltype-crosswalks/ (per-collection crosswalks, palette, class map, and the paper-decode source tables). refs #37914 Co-Authored-By: Claude Opus 4.8 (1M context) <noreply@anthropic.com>
  • lines changed 1473, context: html, text, full: html, text
    b914d581f876d486caf9404e715e4f61ada38195 Mon Aug 3 16:19:44 2026 -0700
    singleCellSignalsPeaks: make every subtrack label unique, fix cell-class regressions The harmonized labels were not distinguishing tracks. build_long_label composed from cell type + condition + tissue, but the upstream steps discard the discriminators on purpose to keep the facets compact, so hg38 had 925 subtracks sharing only 401 distinct longLabels and mm10 629 sharing 359. Worst case: cortex-atac's MACS, enhancer and cell-type-specific peak sets all read "Astrocytes and oligodendrocytes (Cortex ATAC)", with the peak method surviving only in the raw shortLabel. Labels are now built from the harmonized cell type plus a variant descriptor that recovers what was dropped (peak method, grouping level, cohort, signal vs peaks), and anything still colliding is qualified with its source cluster code. shortLabels are rebuilt too -- the old ones were raw source strings up to 50 chars with underscores, ArchR filename tails and R-mangled names -- abbreviated through a curated word table to 22 chars, with compact tokens where the longLabel distinction would otherwise be invisible (SEA-AD region + ADNC, CATLAS aging age). All 925/587 longLabels are now unique; no shortLabel exceeds 22 chars or contains an underscore. Also fixed, found while verifying the above: - Correcting source misspellings in the cell types broke the curated lookups, which are keyed on those same misspelled strings, and 16 hg38 tracks silently lost their Cell_class and color. The class map and the hub_config tables now normalize their keys on load, and a cell type with no broad class is reported instead of becoming "unknown". - Nephron progenitor was classed as Neural progenitor: the decode tables give it the bare broad class "Progenitor" and that was blanket-mapped to neural. It is Six2+ kidney cap mesenchyme, so it is now Stromal. The HTML legend had been worded to match the bug. - The plural/case merge picked the most frequent form, which was inconsistent -- singular for 15 of 17 merged groups but plural for Megakaryocytes/Oligodendrocytes. It now prefers the singular. - Removed 42 byte-identical Allen basal-ganglia bigWigs (md5-verified) that were served from four grouping directories and rendered as four indistinguishable mm10 subtracks, freeing 4.4 GB. Where the four copies genuinely differ all are kept and told apart by the grouping-level descriptor. mm10 goes 629 -> 587 subtracks. - Corrected five stale per-dataset subtrack counts in the description pages and spelled out what ADNC means, noting that it grades neuropathology rather than symptoms. - The SEA-AD Dataset facet link used the collection name, which is not a served Cell Browser slug; it now points at sea-ad-mtg+cohort. - Dropped a dead placeholder variable and made the hardcoded hub-build path overridable. refs #37914 Co-Authored-By: Claude Opus 5 (1M context) <noreply@anthropic.com>
• src/hg/makeDb/trackDb/mouse/mm10/singleCellSignalsPeaks.html
  • lines changed 318, context: html, text, full: html, text
    0abed78024d40b506c2b2e3a49ad483045bc5e1d Sat Aug 1 20:53:25 2026 -0700
    singleCellSignalsPeaks: add native mm10 track mm10 counterpart of the hg38 track: 629 single-cell ATAC signal (bigWig) and peak (bigNarrowPeak) subtracks from 9 Cell Browser datasets, re-parented under one faceted composite in the regulation group. Colored by broad cell class from the same palette as hg38, grouped by class, off by default; cell types are paper-curated and the facets/longLabels are harmonized (see the makeDoc). Data lives in /hive/data/genomes/mm10/bed/singleCellSignalsPeaks and is served via the /gbdb/mm10/bbi symlink; the .ra is regenerated by makeSingleCellSignalsPeaksRa.py from the Cell Browser hub build. Included in mm10 trackDb.ra (alpha). refs #37914 Co-Authored-By: Claude Opus 4.8 (1M context) <noreply@anthropic.com>
  • lines changed 4, context: html, text, full: html, text
    b914d581f876d486caf9404e715e4f61ada38195 Mon Aug 3 16:19:44 2026 -0700
    singleCellSignalsPeaks: make every subtrack label unique, fix cell-class regressions The harmonized labels were not distinguishing tracks. build_long_label composed from cell type + condition + tissue, but the upstream steps discard the discriminators on purpose to keep the facets compact, so hg38 had 925 subtracks sharing only 401 distinct longLabels and mm10 629 sharing 359. Worst case: cortex-atac's MACS, enhancer and cell-type-specific peak sets all read "Astrocytes and oligodendrocytes (Cortex ATAC)", with the peak method surviving only in the raw shortLabel. Labels are now built from the harmonized cell type plus a variant descriptor that recovers what was dropped (peak method, grouping level, cohort, signal vs peaks), and anything still colliding is qualified with its source cluster code. shortLabels are rebuilt too -- the old ones were raw source strings up to 50 chars with underscores, ArchR filename tails and R-mangled names -- abbreviated through a curated word table to 22 chars, with compact tokens where the longLabel distinction would otherwise be invisible (SEA-AD region + ADNC, CATLAS aging age). All 925/587 longLabels are now unique; no shortLabel exceeds 22 chars or contains an underscore. Also fixed, found while verifying the above: - Correcting source misspellings in the cell types broke the curated lookups, which are keyed on those same misspelled strings, and 16 hg38 tracks silently lost their Cell_class and color. The class map and the hub_config tables now normalize their keys on load, and a cell type with no broad class is reported instead of becoming "unknown". - Nephron progenitor was classed as Neural progenitor: the decode tables give it the bare broad class "Progenitor" and that was blanket-mapped to neural. It is Six2+ kidney cap mesenchyme, so it is now Stromal. The HTML legend had been worded to match the bug. - The plural/case merge picked the most frequent form, which was inconsistent -- singular for 15 of 17 merged groups but plural for Megakaryocytes/Oligodendrocytes. It now prefers the singular. - Removed 42 byte-identical Allen basal-ganglia bigWigs (md5-verified) that were served from four grouping directories and rendered as four indistinguishable mm10 subtracks, freeing 4.4 GB. Where the four copies genuinely differ all are kept and told apart by the grouping-level descriptor. mm10 goes 629 -> 587 subtracks. - Corrected five stale per-dataset subtrack counts in the description pages and spelled out what ADNC means, noting that it grades neuropathology rather than symptoms. - The SEA-AD Dataset facet link used the collection name, which is not a served Cell Browser slug; it now points at sea-ad-mtg+cohort. - Dropped a dead placeholder variable and made the hardcoded hub-build path overridable. refs #37914 Co-Authored-By: Claude Opus 5 (1M context) <noreply@anthropic.com>
• src/hg/makeDb/trackDb/mouse/mm10/singleCellSignalsPeaks.ra
  • lines changed 6864, context: html, text, full: html, text
    0abed78024d40b506c2b2e3a49ad483045bc5e1d Sat Aug 1 20:53:25 2026 -0700
    singleCellSignalsPeaks: add native mm10 track mm10 counterpart of the hg38 track: 629 single-cell ATAC signal (bigWig) and peak (bigNarrowPeak) subtracks from 9 Cell Browser datasets, re-parented under one faceted composite in the regulation group. Colored by broad cell class from the same palette as hg38, grouped by class, off by default; cell types are paper-curated and the facets/longLabels are harmonized (see the makeDoc). Data lives in /hive/data/genomes/mm10/bed/singleCellSignalsPeaks and is served via the /gbdb/mm10/bbi symlink; the .ra is regenerated by makeSingleCellSignalsPeaksRa.py from the Cell Browser hub build. Included in mm10 trackDb.ra (alpha). refs #37914 Co-Authored-By: Claude Opus 4.8 (1M context) <noreply@anthropic.com>
  • lines changed 1735, context: html, text, full: html, text
    b914d581f876d486caf9404e715e4f61ada38195 Mon Aug 3 16:19:44 2026 -0700
    singleCellSignalsPeaks: make every subtrack label unique, fix cell-class regressions The harmonized labels were not distinguishing tracks. build_long_label composed from cell type + condition + tissue, but the upstream steps discard the discriminators on purpose to keep the facets compact, so hg38 had 925 subtracks sharing only 401 distinct longLabels and mm10 629 sharing 359. Worst case: cortex-atac's MACS, enhancer and cell-type-specific peak sets all read "Astrocytes and oligodendrocytes (Cortex ATAC)", with the peak method surviving only in the raw shortLabel. Labels are now built from the harmonized cell type plus a variant descriptor that recovers what was dropped (peak method, grouping level, cohort, signal vs peaks), and anything still colliding is qualified with its source cluster code. shortLabels are rebuilt too -- the old ones were raw source strings up to 50 chars with underscores, ArchR filename tails and R-mangled names -- abbreviated through a curated word table to 22 chars, with compact tokens where the longLabel distinction would otherwise be invisible (SEA-AD region + ADNC, CATLAS aging age). All 925/587 longLabels are now unique; no shortLabel exceeds 22 chars or contains an underscore. Also fixed, found while verifying the above: - Correcting source misspellings in the cell types broke the curated lookups, which are keyed on those same misspelled strings, and 16 hg38 tracks silently lost their Cell_class and color. The class map and the hub_config tables now normalize their keys on load, and a cell type with no broad class is reported instead of becoming "unknown". - Nephron progenitor was classed as Neural progenitor: the decode tables give it the bare broad class "Progenitor" and that was blanket-mapped to neural. It is Six2+ kidney cap mesenchyme, so it is now Stromal. The HTML legend had been worded to match the bug. - The plural/case merge picked the most frequent form, which was inconsistent -- singular for 15 of 17 merged groups but plural for Megakaryocytes/Oligodendrocytes. It now prefers the singular. - Removed 42 byte-identical Allen basal-ganglia bigWigs (md5-verified) that were served from four grouping directories and rendered as four indistinguishable mm10 subtracks, freeing 4.4 GB. Where the four copies genuinely differ all are kept and told apart by the grouping-level descriptor. mm10 goes 629 -> 587 subtracks. - Corrected five stale per-dataset subtrack counts in the description pages and spelled out what ADNC means, noting that it grades neuropathology rather than symptoms. - The SEA-AD Dataset facet link used the collection name, which is not a served Cell Browser slug; it now points at sea-ad-mtg+cohort. - Dropped a dead placeholder variable and made the hardcoded hub-build path overridable. refs #37914 Co-Authored-By: Claude Opus 5 (1M context) <noreply@anthropic.com>
• src/hg/makeDb/trackDb/mouse/mm10/trackDb.ra
  • lines changed 1, context: html, text, full: html, text
    0abed78024d40b506c2b2e3a49ad483045bc5e1d Sat Aug 1 20:53:25 2026 -0700
    singleCellSignalsPeaks: add native mm10 track mm10 counterpart of the hg38 track: 629 single-cell ATAC signal (bigWig) and peak (bigNarrowPeak) subtracks from 9 Cell Browser datasets, re-parented under one faceted composite in the regulation group. Colored by broad cell class from the same palette as hg38, grouped by class, off by default; cell types are paper-curated and the facets/longLabels are harmonized (see the makeDoc). Data lives in /hive/data/genomes/mm10/bed/singleCellSignalsPeaks and is served via the /gbdb/mm10/bbi symlink; the .ra is regenerated by makeSingleCellSignalsPeaksRa.py from the Cell Browser hub build. Included in mm10 trackDb.ra (alpha). refs #37914 Co-Authored-By: Claude Opus 4.8 (1M context) <noreply@anthropic.com>