This method uses shallow Whole Genome Sequencing (sWGS) and the segmentation of a genomic profile to assess the Homologous Recombination Deficiency of a tumor based on the number of Large-scale Genomic Alterations (LGAs).
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shallowHRD_hg19_1.13_QDNAseq_no_chrX.R zone 21 position inaccuracy #21
Indeed you are right, I mistakenly took the hg38 position instead of the hg19 position. I will push a correction directly in the main directory by this evening (Paris time).
CTTN Position: hg38 chr11:70,398,404-70,436,584