The raw NGS (Next Generation Sequencing) variants called from GBS (Genotyping by Sequencing) / WES (Whole Exon Sequencing)/ WGS (Whole Genome Sequencing) may include many error sites. The 'binmapr' could fix the potential error sites and generate highly confident markers for downstream analysis, such as QTL (quantitative trait locus) mapping, genetic map construction. Davey, J.W. (2011) <doi:10.1038/nrg3012>.
| Version: | 0.1.3 |
| Depends: | R (≥ 3.5.0) |
| Imports: | vcfR |
| Published: | 2019-10-20 |
| Author: | Zhougeng Xu [aut, cre], Guangwei Li [aut] |
| Maintainer: | Zhougeng Xu <xuzhougeng at 163.com> |
| BugReports: | https://github.com/xuzhougeng/binmapr/issues |
| License: | Artistic-2.0 |
| URL: | https://github.com/xuzhougeng/binmapr |
| NeedsCompilation: | no |
| Materials: | README |
| CRAN checks: | binmapr results |
| Reference manual: | binmapr.pdf |
| Package source: | binmapr_0.1.3.tar.gz |
| Windows binaries: | r-devel: binmapr_0.1.3.zip, r-devel-gcc8: binmapr_0.1.3.zip, r-release: binmapr_0.1.3.zip, r-oldrel: binmapr_0.1.3.zip |
| OS X binaries: | r-release: binmapr_0.1.3.tgz, r-oldrel: binmapr_0.1.3.tgz |
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