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,
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,