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A tool to genotype CYP2D6 with WGS data

Seqarray ⭐ 41

Data management of large-scale whole-genome sequence variant calls (Development version only)

Pyseqarray ⭐ 12

PySeqArray: data manipulation of whole-genome sequencing variants with SeqArray files in Python (pre-release version)

Seave is a web platform that enables genetic variants to be easily filtered and annotated with in silico pathogenicity prediction scores and annotations from popular disease databases. Seave stores genomic variation of all types and sizes, and allows filtering for specific inheritance patterns, quality values, allele frequencies and gene lists. Seave is open source and deployable locally, or on a cloud computing provider, and works readily with gene panel, exome and whole genome data, scaling fr

Multigranular Analysis of Regulatory Variants on the Epigenomic Landscape

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