Additional file 14 of SCReadCounts: estimation of cell-level SNVs expression from scRNA-seq data
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Additional file 14: Supplementary Table 8. KRAS output in Discovery mode. 30 distinct SNVs that do not coincide with known germline variants in the coding sequence of KRAS.
附加文件14:补充表8。KRAS在发现模式下的输出结果。共包含30种不同的单核苷酸变异(Single Nucleotide Variants, SNVs),这些变异均未与KRAS编码序列中的已知生殖系变异重合。
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创建时间:
2021-09-23



