650b51533a44058e6e9129448dc33eb947105a43
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  Sun Sep 6 06:55:18 2026 -0700
DANIO-CODE: remove leftover getTrackReferences error message from the References section of 10 track description pages. refs #38265

diff --git src/hg/makeDb/trackDb/zebrafish/danRer11/dcHiC_Composite.html src/hg/makeDb/trackDb/zebrafish/danRer11/dcHiC_Composite.html
index 70c4558f6c2..a80cec298de 100644
--- src/hg/makeDb/trackDb/zebrafish/danRer11/dcHiC_Composite.html
+++ src/hg/makeDb/trackDb/zebrafish/danRer11/dcHiC_Composite.html
@@ -1,126 +1,125 @@
 <h2>Description</h2>
 
 <p>
 A chromosome is not a straight line in the nucleus. It is folded so that some parts
 touch each other far more often than others, and the regions of preferential contact
 are called topologically associating domains. Domain boundaries matter for gene
 regulation, because an enhancer usually acts on genes inside its own domain and rarely
 across a boundary. Hi-C measures which parts of the genome are in contact by
 crosslinking, cutting and religating chromatin, then sequencing the resulting pairs.
 </p>
 
 <p>
 This track does not show the contact matrix itself but two summary scores computed
 from it along the genome. The <b>insulation index</b> is low where few contacts cross a
 position, so its local minima mark domain boundaries. The <b>directionality index</b>
 measures whether the contacts at a position point mostly upstream or mostly downstream,
 and it flips sign at a boundary. Both are shown for 4 samples at 4 developmental stages
 (256-cell, Dome, 75% epiboly and Prim-5) and at three window sizes, 50 kb, 500 kb and
 1 Mb.
 </p>
 
 <p>
 This track is part of the <a href="hgTrackUi?g=danioCode">DANIO-CODE</a> collection.
 </p>
 
 <h2>Display Conventions and Configuration</h2>
 
 <p>
 Each combination of sample, index type and window size is a separate auto-scaled graph.
 Positive values are drawn in red and negative values in blue. The window size sets the
 scale at which the index is computed, so the 50 kb tracks respond to local boundaries
 and the 1 Mb tracks to large-scale compartments.
 </p>
 
 <p>
 Nothing is displayed until tracks are selected on the configuration page, where they
 can be filtered by developmental stage, window size, index type and sample.
 </p>
 
 <h2>Methods</h2>
 
 <p>
 The DANIO-CODE consortium assembled 1,802 zebrafish developmental genomics datasets,
 1,438 of them already published and 366 generated by consortium members, and
 reprocessed all of them from the raw sequencing reads so that samples from different
 laboratories and different protocols can be compared with each other. ChIP-seq and
 ATAC-seq were run through the ENCODE pipelines, CAGE-seq through the FANTOM pipeline,
 and Hi-C and 4C-seq through the pipelines of the groups that produced them. The
 pipelines are published at
 <a href="https://gitlab.com/danio-code" target="_blank">gitlab.com/danio-code</a>, and
 samples were assigned to developmental stages using ZFIN and ENCODE nomenclature. See
 Baranasic <em>et al</em>. 2022 for details.
 </p>
 
 <p>
 The Hi-C data were processed by the group that produced them, and the insulation and
 directionality indices were computed from the resulting contact matrices at 50 kb,
 500 kb and 1 Mb windows. The samples come from the de Wit laboratory and were
 originally deposited under GSE105015.
 </p>
 
 <p>
 At UCSC the tracks were converted from the consortium's public track hub at
 <a href="https://trackhub2.genereg.net/DANIO-CODE/DANIO-CODE.hub.txt" target="_blank">
 trackhub2.genereg.net/DANIO-CODE</a> with the script
 <a href="https://github.com/ucscGenomeBrowser/kent/tree/master/src/hg/makeDb/scripts/danioCode"
 target="_blank">danioCodeHubToRa.py</a>, and the data files were copied from the same
 server. The data themselves were not modified. The steps are documented in
 <a href="https://github.com/ucscGenomeBrowser/kent/blob/master/src/hg/makeDb/doc/danRer11/danioCode.txt"
 target="_blank">our makeDoc</a>.
 </p>
 
 <h2>Data Access</h2>
 
 <p>
 The data can be explored interactively in table format with the
 <a href="../cgi-bin/hgTables">Table Browser</a> or the
 <a href="../cgi-bin/hgIntegrator">Data Integrator</a> and exported from there to
 spreadsheet or tab-separated tables. From scripts, the data can be accessed through
 our <a href="https://api.genome.ucsc.edu">API</a>, track=<i>dcHiC_Composite</i>.
 </p>
 
 <p>
 For automated download and analysis, the annotations are stored in bigWig files that
 can be downloaded from
 <a href="http://hgdownload.soe.ucsc.edu/gbdb/danRer11/danioCode/" target="_blank">our
 download server</a>. Files are named after the sample, the window size and the index type, for example <tt>DCD003008SQ_DCD017502DT_50000_di.bigWig</tt> for the directionality index at 50 kb and <tt>..._ii.bigWig</tt> for the insulation index. Individual regions or the whole genome annotation can be
 obtained using our tool <tt>bigWigToBedGraph</tt>, which can be compiled from the source code
 or downloaded as a precompiled binary for your system. Instructions for downloading
 source code and binaries can be found
 <a href="http://hgdownload.soe.ucsc.edu/downloads.html#utilities_downloads">here</a>.
 The tool can also be used to obtain features within a given range, for example
 </p>
 <pre>bigWigToBedGraph http://hgdownload.soe.ucsc.edu/gbdb/danRer11/danioCode/DCD003008SQ_DCD017502DT_50000_di.bigWig \
     -chrom=chr1 -start=20000000 -end=21000000 stdout</pre>
 
 <p>
 The original data files, and the sample and protocol metadata behind them, are
 available from the DANIO-CODE data coordination center at
 <a href="https://danio-code.zfin.org" target="_blank">danio-code.zfin.org</a> and from
 the consortium's track hub at
 <a href="https://trackhub2.genereg.net/DANIO-CODE/DANIO-CODE.hub.txt" target="_blank">
 trackhub2.genereg.net/DANIO-CODE</a>.
 </p>
 
 <h2>Credits</h2>
 
 <p>
 Thanks to the DANIO-CODE consortium for collecting, reprocessing and publishing these
 data, and to the laboratories that produced the original datasets.
 </p>
 
 <h2>References</h2>
-Failed to fetch complete links from NCBI after 10 tries.  Try again later or just use the PubMed paper link.
 
 <p>
 Baranasic D, Hörtenhuber M, Balwierz PJ, Zehnder T, Mukarram AK, Nepal C, Várnai C, Hadzhiev Y,
 Jimenez-Gonzalez A, Li N <em>et al</em>.
 <a href="https://www.ncbi.nlm.nih.gov/pubmed/35789323" target="_blank">
 Multiomic atlas with functional stratification and developmental dynamics of zebrafish cis-
 regulatory elements</a>.
 <em>Nat Genet</em>. 2022 Jul;54(7):1037-1050.
 PMID: <a href="https://www.ncbi.nlm.nih.gov/pubmed/35789323" target="_blank">35789323</a>; PMC: <a
 href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9279159/" target="_blank">PMC9279159</a>
 </p>