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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.

copied from cf-staging / r-seqminer
Type Size Name Uploaded Downloads Labels
conda 2.2 MB | win-64/r-seqminer-9.3-r41h5bfd6cc_0.conda  1 year and 16 days ago 236 main
conda 1.4 MB | osx-64/r-seqminer-9.3-r43h2988cf7_0.conda  1 year and 16 days ago 221 main
conda 1.5 MB | osx-64/r-seqminer-9.3-r42h2988cf7_0.conda  1 year and 16 days ago 204 main
conda 2.1 MB | linux-64/r-seqminer-9.3-r43ha661321_0.conda  1 year and 16 days ago 993 main
conda 2.1 MB | linux-64/r-seqminer-9.3-r42ha661321_0.conda  1 year and 16 days ago 1027 main

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