Package: seqminer 9.9
seqminer: Efficiently Read Sequence Data (VCF Format, BCF Format, METAL Format and BGEN Format) into R
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.
Authors:
seqminer_9.9.tar.gz
seqminer_9.9.zip(r-4.7)seqminer_9.9.zip(r-4.6)seqminer_9.9.zip(r-4.5)
seqminer_9.9.tgz(r-4.6-x86_64)seqminer_9.9.tgz(r-4.6-arm64)seqminer_9.9.tgz(r-4.5-x86_64)seqminer_9.9.tgz(r-4.5-arm64)
seqminer_9.9.tar.gz(r-4.7-arm64)seqminer_9.9.tar.gz(r-4.7-x86_64)seqminer_9.9.tar.gz(r-4.6-arm64)seqminer_9.9.tar.gz(r-4.6-x86_64)
manual.pdf |manual.html✨
card.svg |card.png
seqminer/json (API)
| # Install 'seqminer' in R: |
| install.packages('seqminer', repos = c('https://zhanxw.r-universe.dev', 'https://cloud.r-project.org')) |
Bug tracker:https://github.com/zhanxw/seqminer/issues
annotationbcfbgenmeta-analysisnext-generation-sequencingplinksequencingtabixvcfworkflowzlibbzip2libzstdsqlite3cpp
Last updated from:46e3c9ab06. Checks:10 OK, 2 WARNING, 1 FAIL. Indexed: yes.
| Target | Result | Time | Files | Syslog |
|---|---|---|---|---|
| linux-devel-arm64 | OK | 185 | ||
| linux-devel-x86_64 | OK | 148 | ||
| source / vignettes | OK | 203 | ||
| linux-release-arm64 | OK | 184 | ||
| linux-release-x86_64 | OK | 183 | ||
| macos-release-arm64 | OK | 208 | ||
| macos-release-x86_64 | WARNING | 286 | ||
| macos-oldrel-arm64 | OK | 206 | ||
| macos-oldrel-x86_64 | WARNING | 433 | ||
| windows-devel | OK | 266 | ||
| windows-release | OK | 283 | ||
| windows-oldrel | OK | 276 | ||
| wasm-release | FAIL | 109 |
Exports:addJobannotateGeneannotatePlainannotateVcfcreateSingleChromosomeBCFIndexcreateSingleChromosomeVCFIndexdownload.annotation.resourcegetRefBaseisInRangeisTabixRangemakeAnnotationParameternewJobnewWorkflowopenPlinkreadBGENToListByGenereadBGENToListByRangereadBGENToMatrixByGenereadBGENToMatrixByRangereadPlinkToMatrixByIndexreadSingleChromosomeBCFToMatrixByRangereadSingleChromosomeVCFToMatrixByRangereadVCFToListByGenereadVCFToListByRangereadVCFToMatrixByGenereadVCFToMatrixByRangervmeta.readCovByRangervmeta.readDataByGenervmeta.readDataByRangervmeta.readNullModelrvmeta.readScoreByRangervmeta.readSkewByRangervmeta.writeCovDatarvmeta.writeScoreDatatabix.createIndextabix.createIndex.metatabix.createIndex.vcftabix.readtabix.read.headertabix.read.tablevalidateAnnotationParameterwriteWorkflow
Dependencies:
