NDBL / HECIL

Hybrid Error Correction of Long Reads using Iterative Learning
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distinguish allelic variation from sequencing error #10

Open ghandschin opened 5 years ago

ghandschin commented 5 years ago

Hi, I am working with a highly heterozygote genome and I wanted to ask if the software is able to tell apart real allelic variation form a sequencing error? I have illumina reads 2 by 260 bp reads and an average size of fragments of 470 bp. (so I have 50 bp double coverage per readpair). Thanks,

ghandschin commented 5 years ago

Sorry I just saw that you have already answered this question in another thread...