989d891c0c0a500e584d55f2f368b52f2abe5f1d
max
  Tue Apr 21 06:25:48 2026 -0700
kwanhoSv: flag as preliminary, ask users to contact authors

Mark the Kim et al. 2026 PD brain long-read SV subtrack as
preliminary in its shortLabel and longLabel, and add a prominent
warning banner at the top of the description page telling users to
contact the authors (ASAP / Kim lab) before using the data, since
the callset will be updated before publication.

refs #36258

diff --git src/hg/makeDb/trackDb/human/kwanhoSv.html src/hg/makeDb/trackDb/human/kwanhoSv.html
index d888c3a6f52..4c641c20175 100644
--- src/hg/makeDb/trackDb/human/kwanhoSv.html
+++ src/hg/makeDb/trackDb/human/kwanhoSv.html
@@ -1,16 +1,25 @@
 <h2>Description</h2>
+
+<p style="background-color:#fff3cd; border-left:4px solid #856404; padding:10px 14px; margin-bottom:18px;">
+<b>Preliminary data.</b> This callset is a pre-publication release that will be
+updated before the final publication. Before using these data for analysis or
+in a paper, please contact the authors at the Aligning Science Across
+Parkinson's (ASAP) consortium / the Kim lab to check for the latest version
+and for guidance on appropriate use.
+</p>
+
 <p>
 This track shows structural variants (SVs) identified by PacBio HiFi long-read
 whole-genome sequencing of 100 post-mortem human brain samples, split across
 three diagnostic groups: Parkinson's disease (PD), incidental Lewy body
 disease (ILBD) and healthy controls (HC). The high-confidence catalog
 contains 74,552 SVs: 34,056 insertions, 29,545 deletions, 9,707 duplications
 and 1,244 inversions.
 </p>
 <p>
 The dataset accompanies Kim et al. (2026), which combines the long-read SV
 catalog with single-nucleus RNA-seq from the same donors to identify SVs
 associated with cell-type-specific gene expression, including variants
 near genes nominated as causal targets of PD GWAS loci.
 </p>