The whole genome RNA SNP is used as endogenous markers for lineage study. This package identifies clonal features based on single cell RNA sequencing data solely by integrating mutation type and subspace-subspace cross entropy into consideration.
Package details |
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Author | Jia Song |
Bioconductor views | RNASeq Sequencing SingleCell TranscriptomeVariant |
Maintainer | Jia Song <550238460@qq.com> |
License | GPL-3 |
Version | 0.99.1 |
Package repository | View on GitHub |
Installation |
Install the latest version of this package by entering the following in R:
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