17b7d3c37be41135afaf8e91e365e3847af96ca5 lrnassar Mon Jun 22 10:56:56 2026 -0700 Add TAD (topologically associating domains) track set on hg19, hg38, mm10, mm39. refs #21599 New "tads" superTrack collecting published TAD calls, alpha-gated via include tad.ra alpha in each assembly's trackDb.ra. hg38 (all five sources): Dixon 2012 domains, Schmitt 2016 boundaries, McArthur & Capra 2021 boundary stability, ENCODE contact domains (faceted composite over 117 biosamples), and 3D Genome Browser 2.0 domains (faceted composite over 464 datasets). hg19: the three sources with hg19-compatible data (Dixon, Schmitt, McArthur). mm10/mm39 (domains only; the boundary sources have no mouse data): Dixon, ENCODE (faceted, 16 biosamples), and 3D Genome Browser (faceted, 30 datasets); mm39 lifted from mm10, lift noted in the long labels. Faceted composites are organ-colored from a TAD-owned organ_colors.json symlinked into /gbdb//bbi/tad/. Build scripts and autoSql are version-controlled under makeDb/scripts/tad/ and symlinked into the per-source build dirs. Provenance and fetch for every dataset are documented in the makedocs (doc/hg38/tad.txt, doc/mm10/tad.txt, doc/mm39/tad.txt, and the hg19 TAD section in doc/hg19.txt). diff --git src/hg/makeDb/trackDb/human/hg38/tadsMcArthur.html src/hg/makeDb/trackDb/human/hg38/tadsMcArthur.html new file mode 100644 index 00000000000..b812a69ba4c --- /dev/null +++ src/hg/makeDb/trackDb/human/hg38/tadsMcArthur.html @@ -0,0 +1,62 @@ +

Description

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+This track shows TAD boundary stability: for each 100 kb genomic window, how many of +37 cell-type contact maps place a TAD boundary there (McArthur & Capra, 2021). +Boundaries shared by many cell types are evolutionarily constrained and enriched for +complex-trait heritability. +

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+This is a derived, cross-study summary, not a primary set of TAD calls. The 37 maps +were uniformly re-processed (via the 3D Genome Browser, using the Dixon directionality +pipeline) from five earlier studies (Rao 2014, Dixon 2015, Leung 2015, Schmitt 2016, and +ENCODE cancer cell lines); 9 of those contexts overlap the Schmitt boundaries track in +this set, so the two are not independent. The input maps were called at heterogeneous +resolution (25 kb for the Rao-lab set, 40 kb for the others). +

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Display Conventions and Configuration

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+Each 100 kb "bookend" boundary bin is shaded by the number of cell-type maps +sharing it (1–37): darker indicates a boundary shared by more cell types. Use the +filter to show only boundaries shared by at least a chosen number of maps. We +describe these as recurrent across N of 37 maps, not "conserved". +

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+Interpreting the score: the score counts how many independent cell-type maps agree on a +boundary, which serves as a confidence measure. High values mark constitutive boundaries +shared across cell types: the most reliable, and enriched for CTCF binding and evolutionary +constraint. Boundaries seen in only one or a few maps are largely cell-type-specific. Raising the +filter yields a smaller, higher-confidence set of boundaries. +

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+Default filter: this track initially shows boundaries shared by at least 4 of the 37 +maps. Boundaries seen in only 1–3 maps are no more CTCF-enriched or evolutionarily +constrained than expected by chance. Lower the filter (minimum maps) to 1 to display all +boundaries. +

+

Methods

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+TAD boundaries from 37 re-processed cell-type maps were each represented as the 100 kb +windows flanking every TAD ("bookend" boundaries); the genome was tiled into +100 kb windows and, for each window, the number of maps with a boundary in it was counted +(McArthur & Capra, 2021). Data were obtained from the authors' repository on assembly +hg19 and lifted to this assembly with the UCSC liftOver tool where needed. +

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Data Access

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+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. +

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References

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+McArthur E, Capra JA. Topologically associating domain boundaries that are stable across +diverse cell types are evolutionarily constrained and enriched for heritability. +Am J Hum Genet. 2021;108(2):269-283. +doi:10.1016/j.ajhg.2021.01.001 +