da9a225ac1d17c6c6659209c0dfb4534e6ab51d7 jnavarr5 Tue Sep 30 16:16:07 2025 -0700 Fixing a typo in CoLoRSdb (missing S). Bolding the track names. Using lowercase s in 'small' and 'structural', refs #34120 diff --git src/hg/makeDb/trackDb/human/longReadVariants.html src/hg/makeDb/trackDb/human/longReadVariants.html index 703efc0c8a4..630ead4fa43 100644 --- src/hg/makeDb/trackDb/human/longReadVariants.html +++ src/hg/makeDb/trackDb/human/longReadVariants.html @@ -1,19 +1,21 @@ <h2>Description</h2> <p> The tracks listed here contain variants using long-read sequencing technologies.</p> <ul> - <li>CoLoRSdb Small variants: small genetic variants (single nucleotide polymorphisms and short - insertions and deletions) called with DeepVariant and merged with GLnexus/bcftools.</li> - <li>CoLoRdb Structural variants: structural variants (insertions, deletions, and inversions) - discovered with pbsv and merged across samples using Jasmine.</li> + <li> + <b>CoLoRSdb small variants:</b> small genetic variants (single nucleotide polymorphisms and + short insertions and deletions) called with DeepVariant and merged with GLnexus/bcftools.</li> + <li> + <b>CoLoRSdb structural variants:</b> structural variants (insertions, deletions, and + inversions) discovered with pbsv and merged across samples using Jasmine.</li> </ul> <h2>Display conventions</h2> <p> Hover over the feature to see more information, explained on teh track details page of the particular track or when clicking onto the feature.</p> <h2>Credits</h2> <p> For data provenance, access and descriptions, please click the documentation via the link above. </p>