|
The tracks listed here contain variants using long-read sequencing technologies.
-
CoLoRSdb small variants: small genetic variants (single nucleotide polymorphisms and
short insertions and deletions) called with DeepVariant and merged with GLnexus/bcftools.
-
CoLoRSdb structural variants: structural variants (insertions, deletions, and
inversions) discovered with pbsv and merged across samples using Jasmine.
To view the full description, click here.
|