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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-8.0-r35hb9bd586_0.tar.bz2  4 years and 9 months ago 1030 main cf202003
conda 2.2 MB | win-64/r-seqminer-8.0-r36hb9bd586_0.tar.bz2  4 years and 9 months ago 1050 main cf202003
conda 2.1 MB | osx-64/r-seqminer-8.0-r36hb8f4850_0.tar.bz2  4 years and 9 months ago 332 main cf202003
conda 2.1 MB | osx-64/r-seqminer-8.0-r35hb8f4850_0.tar.bz2  4 years and 9 months ago 335 main cf202003
conda 2.0 MB | linux-64/r-seqminer-8.0-r36h2b0173a_0.tar.bz2  4 years and 9 months ago 3001 main cf202003
conda 2.0 MB | linux-64/r-seqminer-8.0-r35h2b0173a_0.tar.bz2  4 years and 9 months ago 3039 main cf202003

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