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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>.
Package details |
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Author | Shaoqian Ma [aut, cre] |
Maintainer | Shaoqian Ma <897341109@qq.com> |
License | Artistic-2.0 |
Version | 0.1.3 |
URL | https://github.com/MSQ-123/chromseq |
Package repository | View on CRAN |
Installation |
Install the latest version of this package by entering the following in R:
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