Single nucleotide variants - filtered data for publication: " Evolution in the landscape of single nucleotide variants at diagnosis and relapse in patients with B-acute lymphoblastic leukaemia (ALL)
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
Variants from NL1I reads on the BCMVS2 genome assembly. Variant-call-format file, showing single-nucleotide variants between the NL1I genomic reads and the BCMVS2 genome assembly. (ZIP 12Â kb)
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
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.
