b7b9978c92a2376d6d9ef4f0a4974cb8167295f8 gperez2 Wed Sep 30 14:17:50 2026 -0700 Updating the TAD tracks from the qa-track SKILL.md pass (hg19, hg38, mm10, mm39): shortLabel fixes for cut-off and duplicate ENCODE and 3DGB subtracks, lowercase biosamples in ENCODE longLabels, " bnd" dropped from Schmitt shortLabels, 3DGB subtracks set to pack with three mm10/mm39 defaults turned on, allButtonPair removed so the Schmitt matrix shows, and McArthur item labels hidden. Merged identical description pages into human/ and mouse/, plus description page cleanups (regenerated References, removed the "How to use these tracks" section, ENCODE pages now say 112 of 117 biosamples use Arrowhead). Also updated the ENCODE metadata columns and organ example in the hg38 makedoc. refs #21599 diff --git src/hg/makeDb/trackDb/human/hg38/tadsEncode.html src/hg/makeDb/trackDb/human/hg38/tadsEncode.html index c3c86012a19..fef9dd725b6 100644 --- src/hg/makeDb/trackDb/human/hg38/tadsEncode.html +++ src/hg/makeDb/trackDb/human/hg38/tadsEncode.html @@ -1,80 +1,97 @@

Description

-This composite shows TAD domains ("contact domains") called by the ENCODE -uniform Hi-C pipeline across 117 human biosamples on hg38. Contact domains are -regions that preferentially self-interact, called by the Arrowhead algorithm (Juicer). -Each subtrack is one biosample, browsable with a faceted selector (filter by organ, -biosample type, assay, life stage, and call type). +This composite shows TAD domains ("contact domains") from ENCODE for +117 human biosamples on hg38. For 112 biosamples, the domains were called by the +ENCODE uniform Hi-C pipeline with the Arrowhead algorithm (Juicer). The other 5 come from a +different ENCODE pipeline (see Calls below). Contact domains are regions that +preferentially self-interact. Each subtrack is one biosample, browsable with a +faceted selector (filter by organ, biosample type, assay, life stage, and call type).

ENCODE provides contact domains for many human biosamples across hundreds of files. This track shows one representative experiment per biosample; by default a set of 14 reference biosamples is displayed (GM12878, K562, HepG2, HCT116, IMR-90, A549, HL-60/S4, heart left/right ventricle, dorsolateral prefrontal cortex, ovary, pancreas, transverse colon, and motor neuron), and the remaining biosamples are turned off and reached through the faceted selector. The complete set is available at the ENCODE portal.

Display Conventions and Configuration

-Each domain is drawn as a box, and subtracks are colored by organ. Mousing over a -domain shows the biosample and the Arrowhead corner score (the likelihood that the spot is -a contact-domain corner); the details page also reports Arrowhead's upper/lower variance -and sign scores. These calls use a different algorithm and a finer resolution (5 kb, calling -sub-TAD contact domains) than the other TAD tracks, and are not directly comparable to them. +Subtracks are colored by organ. Mousing over a domain shows the biosample and the +Arrowhead corner score (the likelihood that the spot is a contact-domain corner). The +details page also reports Arrowhead's upper/lower variance and sign scores. The Arrowhead +calls use a different algorithm and a finer resolution (5 kb) than the other TAD tracks, +produce smaller domains, and are not directly comparable to them.

Use the faceted selector on the track configuration page to choose biosamples by Organ, Biosample type (cell line, tissue, primary cell, in vitro -differentiated), Assay (intact or in situ Hi-C), Life stage, and -Calls. Where a biosample had both an untreated baseline and a perturbed (treated or -genetically modified) experiment, the baseline was chosen; a handful of biosamples that -exist only in a stimulated state (e.g. activated immune cells) are named accordingly. The -Calls facet distinguishes the 112 biosamples with native hg38 Arrowhead calls +differentiated), Assay (intact or in situ Hi-C), Life stage, and Calls. +Where a biosample had both an untreated baseline and a perturbed (treated or genetically +modified) experiment, the baseline was chosen; a handful of biosamples that exist only in a +stimulated state (e.g. activated immune cells) are named accordingly. The Calls facet +distinguishes the 112 biosamples with native hg38 Arrowhead calls ("Arrowhead (hg38)") from 5 biosamples (LNCaP clone FGC, NCI-H460, RPMI7951, SJCRH30, SK-N-MC) for which ENCODE provides only domains lifted from hg19 -("Lifted from hg19"); the lifted domains carry no Arrowhead scores. +("Lifted from hg19"). These 5 were produced by a different ENCODE pipeline (Dekker +lab, on hg19) and lifted to hg38. Their domains do not overlap each other, are much larger +(median about 760 kb), and carry no Arrowhead scores.

Methods

-Contact domains were produced by the ENCODE uniform Hi-C processing pipeline (developed by -the Aiden lab, built on Juicer), which calls domains with Arrowhead on GRCh38. For each -biosample, one representative experiment was selected (preferring native hg38 Arrowhead -calls, then an untreated baseline experiment over a perturbed one where both were available, -then the deepest experiment by assay type and data volume), and that -experiment's contact-domain files were pooled: each Juicer/Arrowhead paired-anchor BEDPE -record (in which both anchors describe the same domain interval) was reduced to a single -domain interval, the five Arrowhead scores were retained, and replicate calls whose +For 112 biosamples, contact domains were produced by the ENCODE uniform Hi-C processing +pipeline (developed by the Aiden lab, built on Juicer), which calls domains with Arrowhead +on hg38. For the other 5, ENCODE provides domains produced by the Dekker lab on hg19 and +lifted to hg38. For each biosample, one representative experiment was selected (preferring +native hg38 Arrowhead calls, then an untreated baseline experiment over a perturbed one +where both were available, then the deepest experiment by assay type and data volume), and +that experiment's contact-domain files were pooled: each Juicer/Arrowhead paired-anchor +BEDPE record (in which both anchors describe the same domain interval) was reduced to a +single domain interval, the five Arrowhead scores were retained, and replicate calls whose endpoints fell within one 5 kb bin were merged, keeping the call with the higher corner score. The chosen ENCODE experiment accession is given in each subtrack's long label.

Data Access

The raw data can be explored interactively with the Table Browser or the Data Integrator. For programmatic access, the track can be accessed using the Genome Browser's REST API. The underlying bigBed files can be downloaded from our download server.

References

-ENCODE Project Consortium. An integrated encyclopedia of DNA elements in the human genome. -Nature. 2012;489(7414):57-74. -doi:10.1038/nature11247 +Durand NC, Shamim MS, Machol I, Rao SS, Huntley MH, Lander ES, Aiden EL. + +Juicer Provides a One-Click System for Analyzing Loop-Resolution Hi-C Experiments. +Cell Syst. 2016 Jul;3(1):95-8. +DOI: 10.1016/j.cels.2016.07.002; PMID: 27467249; PMC: PMC5846465

-Rao SS, Huntley MH, Durand NC, Stamenova EK, et al. -A 3D map of the human genome at kilobase resolution reveals principles of chromatin -looping. Cell. 2014;159(7):1665-80. -doi:10.1016/j.cell.2014.11.021 +ENCODE Project Consortium. + +An integrated encyclopedia of DNA elements in the human genome. +Nature. 2012 Sep 6;489(7414):57-74. +DOI: 10.1038/nature11247; PMID: 22955616; PMC: PMC3439153

-Durand NC, Shamim MS, Machol I, Rao SS, Huntley MH, Lander ES, Aiden EL. -Juicer Provides a One-Click System for Analyzing Loop-Resolution Hi-C Experiments. -Cell Syst. 2016;3(1):95-8. -doi:10.1016/j.cels.2016.07.002 +Rao SS, Huntley MH, Durand NC, Stamenova EK, Bochkov ID, Robinson JT, Sanborn AL, Machol I, Omer AD, +Lander ES et al. + +A 3D map of the human genome at kilobase resolution reveals principles of chromatin looping. +Cell. 2014 Dec 18;159(7):1665-80. +DOI: 10.1016/j.cell.2014.11.021; PMID: 25497547; PMC: PMC5635824