Hi all,
I would like to use MiSeq amplicon sequencing to detect the clonal outgrowth of cells harboring small to medium sized deletions (1bp to 160bp) in specific genes generated using CRISPR technology (which makes random sized deletions at specific loci matching a DNA template).
I've used BWA/Varscan in the past to quantify the allele fraction of small (1-3bp) deletions. I've also used pindel to qualitatively identify larger deletions, but I'm unsure if one can quantatively estimate the allele fraction of deletion using pindel or other tools. Has anyone tried this or have any advice?
Thanks!
-Brenton
I would like to use MiSeq amplicon sequencing to detect the clonal outgrowth of cells harboring small to medium sized deletions (1bp to 160bp) in specific genes generated using CRISPR technology (which makes random sized deletions at specific loci matching a DNA template).
I've used BWA/Varscan in the past to quantify the allele fraction of small (1-3bp) deletions. I've also used pindel to qualitatively identify larger deletions, but I'm unsure if one can quantatively estimate the allele fraction of deletion using pindel or other tools. Has anyone tried this or have any advice?
Thanks!
-Brenton
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