5e4ca58df1b5bfe554fe5cc3309a39736ca256ee max Tue Apr 21 08:08:52 2026 -0700 cpc1Sv: restrict to the 58 CPC samples, drop HPRC-specific SVs Rewrite lrSvCpc1VcfToBed.py to identify the 58 CPC sample columns by name prefix (HIFI032* or RY*), recompute AC/AN/NS from those GT columns only, and skip any snarl that no CPC sample carries. The HPRC portion is already represented elsewhere in lrSv, so this keeps the track population-consistent with its label. Rebuild results: 46,092 snarl sites on hs1 (down from 97,205 when combined with HPRC), 36,030 lifted to hg38 (down from 81,261; 10,062 unmapped). Updates cpc1Sv.html, lrSv.ra labels, and the makeDoc. refs #36258 diff --git src/hg/makeDb/trackDb/human/cpc1Sv.html src/hg/makeDb/trackDb/human/cpc1Sv.html index e3f5e3f01a7..470d401eb9d 100644 --- src/hg/makeDb/trackDb/human/cpc1Sv.html +++ src/hg/makeDb/trackDb/human/cpc1Sv.html @@ -1,64 +1,71 @@ <h2>Description</h2> <p> -This track displays structural variants (SVs) — deletions, insertions, and -complex substitutions of at least 50 bp — identified by the Chinese -Pangenome Consortium (CPC) from a pangenome graph built from 58 core samples -representing 36 Chinese minority ethnic groups, jointly with 47 samples from -Phase 1 of the Human Pangenome Reference Consortium (HPRC). After -decomposition of the graph bubbles, each distinct graph site (snarl) is -displayed as one variant record, with genotypes aggregated across 105 -samples.</p> +This track displays structural variants (SVs) — deletions, insertions, +and complex substitutions of at least 50 bp — identified by the +Chinese Pangenome Consortium (CPC) in 58 samples representing 36 Chinese +minority ethnic groups.</p> + +<p> +The upstream release combined the 58 CPC samples with 47 samples from +Phase 1 of the Human Pangenome Reference Consortium (HPRC) into a single +pangenome graph built on the T2T-CHM13v2 assembly with Minigraph-Cactus. +For this track we recomputed allele counts (AC), allele numbers (AN) and +sample counts (NS) using only the 58 CPC sample columns (those with +<tt>HIFI032*</tt> or <tt>RY*</tt> prefixes in the source VCF) and dropped +all snarls that no CPC sample carries (HPRC-specific SVs). To see the +HPRC data on its own, use the HPRC SV tracks elsewhere in this collection.</p> <p> A pangenome is a graph that represents many genomes simultaneously, letting variants that are missing from a single linear reference be captured and -typed directly. Because the CPC pangenome was built on the T2T-CHM13v2 -assembly, variants are shown natively on the hs1 browser and lifted to hg38 -using the UCSC <tt>hs1ToHg38.over.chain.gz</tt> chain. About 16% of the -97,205 hs1 sites did not lift over cleanly (usually in highly repetitive -regions added to T2T-CHM13).</p> +typed directly. Variants are shown natively on the hs1 browser and lifted +to hg38 using the UCSC <tt>hs1ToHg38.over.chain.gz</tt> chain. The track +contains 46,092 snarl sites on hs1 and 36,030 lifted to hg38 (10,062 did +not lift, typically in T2T-added repetitive regions).</p> <h2>Display conventions</h2> <p>Items are colored by SV type:</p> <ul> <li><span style="background-color:rgb(0,0,200);color:white;padding:1px 6px">INS</span> insertion (net ALT longer by ≥50 bp)</li> <li><span style="background-color:rgb(200,0,0);color:white;padding:1px 6px">DEL</span> deletion (net REF longer by ≥50 bp)</li> <li><span style="background-color:rgb(230,140,0);color:white;padding:1px 6px">CPX</span> complex substitution (similar-length REF and ALT but at least one ≥50 bp)</li> <li><span style="background-color:rgb(120,120,120);color:white;padding:1px 6px">MIXED</span> snarl whose collapsed alt alleles belong to different classes</li> </ul> <p> Each bed item spans from the start of the REF allele to its end on the reference. Pure insertions (where REF is a single base) therefore appear as narrow single-base marks; DELs and CPX items span the affected reference interval.</p> <p> The <i>name</i> field is the graph snarl ID (two node identifiers separated by strand arrows, e.g. <tt>>2541>2547</tt>). It is stable across the graph but has no meaning outside the CPC pangenome graph file.</p> <h2>Collapsing of multi-allelic sites</h2> <p> The source VCF was decomposed with <tt>bcftools norm -m -any</tt>, so each graph snarl appears as one VCF row per alternative allele (a single -bubble in the graph may have 2-20+ alt paths). For display, all alternative -alleles sharing the same snarl ID are collapsed into one track item:</p> +bubble in the graph may have 2-20+ alt paths). For this track we first +compute the CPC-only allele count per alt, drop any alt that no CPC sample +carries, then collapse all remaining alts sharing the same snarl ID into +one track item:</p> <ul> <li><b>SV type</b> is the common class of all alts, or <tt>MIXED</tt> if they disagree (for example one alt is a DEL and another is an INS).</li> <li><b>SV length</b> is the maximum |len(ALT) − len(REF)| across alts.</li> <li><b>Allele count</b> is the sum of the per-alt allele counts.</li> <li><b>Number of alts</b> records how many alternative alleles were merged.</li> </ul> <h2>Filters</h2> <p>Available filters:</p> <ul> <li><b>SV type</b> — any combination of INS, DEL, CPX, MIXED.</li> <li><b>SV length</b> — maximum allele-length difference.</li> <li><b>Allele frequency</b> and <b>allele count</b> across the combined