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Hi,
I have an issue with high complexity reads being removed. I am using fasta input because I am only interested in the complexity , not quality.
The files are here:
https://drive.google.com/open?id=1IHfERmzQauE3XNVVzaPU4yLg7dWe5Bmo
command:
InfoTrim.py 69.fasta -o 69_infotrim.fasta --fasta --min_length 100 -p 12
The file 69_trimmed.fasta contains the reads from the original (69.fasta) that were removed in 69_infotrim.fasta.
A quick look at these reads shows that they are not low complexity. I really only want to remove or trim sequence that is'mostly' homopolymer or simple repeat.
Thanks,
Theo
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