Efficiently Read Sequence Data (VCF Format, BCF Format, METAL Format and BGEN Format) into R R package seqminer version 9.9 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. Software Suggests: testthat, SKAT Xiaowei Zhan <zhanxw@gmail.com> Comprehensive R Archive Network (CRAN) Xiaowei Zhan [aut, cre], Dajiang Liu [aut], Attractive Chaos [cph] (We have used the following software and made minimal necessary changes: Tabix, Heng Li <lh3@live.co.uk> (MIT license). We removed standard IO related functions, e.g. printf, fprintf ; also changed its un-safe pointer arithmetics.), Broad Institute / Massachusetts Institute of Technology [cph], Genome Research Ltd (GRL) [cph], Facebook, Inc [cph], D. Richard Hipp [cph] GPL file LICENSE (https://CRAN.R-project.org/package=seqminer/LICENSE) 2026-02-24 application/tgz https://CRAN.R-project.org/package=seqminer doi:10.32614/CRAN.package.seqminer