Chromosome files in the 'Fasta' format usually contain large sequences like human genome. Sometimes users have to split these chromosomes into different files according to their chromosome number. The 'chromseq' can help to handle this. So the selected chromosome sequence can be used for downstream analysis like motif finding. Howard Y. Chang(2019) <doi:10.1038/s41587-019-0206-z>.
| Version: | 0.1.3 |
| Depends: | R (≥ 2.10) |
| Imports: | utils, base |
| Published: | 2020-05-11 |
| Author: | Shaoqian Ma [aut, cre] |
| Maintainer: | Shaoqian Ma <897341109 at qq.com> |
| BugReports: | https://github.com/MSQ-123/chromseq/issues |
| License: | Artistic-2.0 |
| URL: | https://github.com/MSQ-123/chromseq |
| NeedsCompilation: | no |
| Materials: | README |
| CRAN checks: | chromseq results |
| Reference manual: | chromseq.pdf |
| Package source: | chromseq_0.1.3.tar.gz |
| Windows binaries: | r-devel: chromseq_0.1.3.zip, r-release: chromseq_0.1.3.zip, r-oldrel: chromseq_0.1.3.zip |
| macOS binaries: | r-release (arm64): chromseq_0.1.3.tgz, r-oldrel (arm64): chromseq_0.1.3.tgz, r-release (x86_64): chromseq_0.1.3.tgz, r-oldrel (x86_64): chromseq_0.1.3.tgz |
Please use the canonical form https://CRAN.R-project.org/package=chromseq to link to this page.