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Smaller software changes are not announced here. A summary of the three-weekly release changes can be found here. For the full list of our daily code changes head to our GitHub page. Lastly, see our credits page for acknowledgments of the data we host.
- -We are excited to announce a new Long-read Structural Variants container track on the human assemblies GRCh38/hg38 and T2T-CHM13/hs1. The container track brings together structural variant (SV) callsets from 14 long-read sequencing studies worldwide into a single place where you can compare large genomic rearrangements (deletions, insertions, duplications, inversions, and complex events) across populations, cohorts, and calling strategies. Long-read technologies span repetitive regions and resolve complex loci that are difficult to detect with short reads, giving more precise breakpoints and better sensitivity for large variants.