numbat
cranv1.5.2Haplotype-Aware CNV Analysis from scRNA-Seq. A computational method that infers copy number variations (CNVs) in cancer scRNA-seq data and reconstructs the tumor phylogeny. 'numbat' integrates signals from gene expression, allelic ratio, and population haplotype structures to accurately infer allele-specific CNVs in single cells and reconstruc
License MIT + file LICENSE0 versions1 maintainers34 deps128 weekly dl
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curl https://depscope.dev/api/check/cran/numbatFirst published · 2026-02-04 09:25:39
Last updated · 2026-02-04T07:20:15+00:00