tailieunhanh - Systematic comparative analysis of singlenucleotide variant detection methods from single-cell RNA sequencing data

While SNV detection from abundant single-cell RNA sequencing (scRNA-seq) data is applicable and cost-effective in identifying expressed variants, inferring sub-clones, and deciphering genotype-phenotype linkages, there is a lack of computational methods specifically developed for SNV calling in scRNA-seq. |

TỪ KHÓA LIÊN QUAN