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Analyses in organisms possessing ATGC at the end of chromosomes #107

@toshwatatosh

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@toshwatatosh

We are now working on Nanoseq in a monkey. Human and mouse chromosomes usually start with N. But, in this monkey, some chromosomes start with ATGC. When sequence reads are mapped to the end of such chromosomes, errors happen at the dsa step. To avoid this problem, we remove reads at the ends of the chromosome. Could this removal affect the final mutation burden rate or other results?

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