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Indel frequency analysis from CRISPR modification using sequencing data.

Hello,

I could use some help/direction with finding the right pipeline/package to analyze sequencing data in order to quantify indel variants and their respective amounts created by CRISPR modification.

In particular I would like to recreate a figure similar to this:

enter image description here

Any help is greatly appreciated.

Thanks.

crispr indel cas9 frequency site cut

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