76eabae1c28bb07c02af6a12fa9222c348b039d9
max
  Sun Sep 6 07:02:29 2026 -0700
DANIO-CODE: open each subtrack description with the sentence saying that the track is part of the DANIO-CODE container, linking to its hgTrackUi page, instead of burying it in a paragraph at the end of the description. refs #38265

diff --git src/hg/makeDb/trackDb/zebrafish/danRer11/dcRNAseqComposite.html src/hg/makeDb/trackDb/zebrafish/danRer11/dcRNAseqComposite.html
index 8745c579795..686b803dc53 100644
--- src/hg/makeDb/trackDb/zebrafish/danRer11/dcRNAseqComposite.html
+++ src/hg/makeDb/trackDb/zebrafish/danRer11/dcRNAseqComposite.html
@@ -1,30 +1,27 @@
 <h2>Description</h2>
 
 <p>
-This track shows RNA-seq read coverage for 361 zebrafish samples collected by the
-DANIO-CODE consortium, covering 31 developmental stages from the 1-cell stage through
+This track is part of the <a href="hgTrackUi?g=danioCode">DANIO-CODE</a> track collection.
+It shows RNA-seq read coverage for 361 zebrafish samples collected by the
+consortium, covering 31 developmental stages from the 1-cell stage through
 epiboly, somitogenesis and organogenesis to the adult fish. The consortium used 139 of
 these samples to build an improved transcript annotation containing 31,458 genes and
 55,596 transcripts, among them 726 long non-coding RNA genes and 167 transcripts of
 uncertain coding potential that Ensembl had not annotated.
 </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>
 Every sample is shown as a coverage graph. For strand-specific libraries there are two
 graphs per sample: coverage on the forward strand in red and coverage on the reverse
 strand in blue. Unstranded libraries have a single graph.
 </p>
 
 <p>
 Nothing is displayed until samples are selected on the track configuration page. There
 are more than 500 individual graphs, so turn on only the ones you need; the display
 becomes very slow otherwise. Samples can be filtered by developmental stage, by
 sequencing sample accession and by strand. Each graph is auto-scaled to the data in
 the window, so the height of a peak can be compared within one sample but not between
 samples.