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Single nucleotide variants passing filters called in each cell line. (XLSX)
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创建时间：
2022-09-13
相关数据集
MOESM4 of Comparison of cytosine base editors and development of the BEable-GPS database for targeting pathogenic SNVs
Additional file 4: Table S5. Calculation of base substitutions of base editing results in Fig. 1 and Additional file 1: Figures S1â S4.
DataCite Commons2024-02-12 更新100
Distribution of SNVs in the exon of NEU1 gene.
Based on NEU1 cDNA sequence NM_000434.3. Numbers in brackets represent the p-value associated to the enrichment of SNVs in the corresponding exon calculated as described in Methods. Classification of
NIAID Data Ecosystem40
Single-nucleotide variants for compound 22-selected clones.
Single-nucleotide variants for compound 22-selected clones.
Figshare2025-02-03 更新30
Patogenic Mutation in 5 Genes
This is a pathogenic mutation profile of colorectal patients specifically in 5 genes, i.e. APC, TP53, PIK3CA, KRAS, and MLH1. Single nucleotide variants identified were synchronized with patients’ cha
NIAID Data Ecosystem80
Additional file 12 of SCReadCounts: estimation of cell-level SNVs expression from scRNA-seq data
Additional file 12: Supplementary Table 6. scVAFRNA estimates. scVAFRNA estimates for positions covered by at least 10 total reads (minR = 10) in 20 and more cells per sample.
NIAID Data Ecosystem30
