seqminer (Q31506): Difference between revisions
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Created claim: source code repository (P339): https://github.com/cran/seqminer, #quickstatements; #temporary_batch_1711027662947 |
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point in time: 9 February 2024
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Latest revision as of 18:22, 21 March 2024
Efficiently Read Sequence Data (VCF Format, BCF Format, METAL Format and BGEN Format) into R
Language | Label | Description | Also known as |
---|---|---|---|
English | seqminer |
Efficiently Read Sequence Data (VCF Format, BCF Format, METAL Format and BGEN Format) into R |
Statements
3 February 2024
0 references
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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