Integrate sequencing data (Variant call format, e.g. VCF or BCF) or meta-analysis results in R. This package can help you (1) read VCF/BCF/BGEN files by chromosomal ranges (e.g. 1:100-200); (2) read RareMETAL summary statistics files; (3) read tables from a tabix-indexed files; (4) annotate VCF/BCF files; (5) create customized workflow based on Makefile.
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curl https://depscope.dev/api/check/conda/r-seqminerFirst published · 2021-06-04 15:05:09.262000+00:00
Last updated · 2025-09-28 09:37:59.103000+00:00