View BAM alignments in the NCBI genome browsers and sequence viewers sorted by haplotype tag

NCBI’s genome browsers and graphical sequence viewers now allow you to view BAM alignments sorted by haplotype tag. This option is useful for analyzing variants within a sequenced sample and can help you detect or validate structural variants.Figure 1. Remote … Continue reading →

Source: NCBI Insights - January 2, 2020 Category: Databases & Libraries Authors: NCBI Staff Tags: What's New Genome Browser genomics Next-gen sequencing variation Source Type: news