Dear colleagues,
how can you tell, just by looking at the read alignment in a genome viewer (IGV or Genome Browse), that there is a small indel in a particular region of interest. Usually, it is needed when checking candidate SNPs manually.
I am working with trios.
Thank you
how can you tell, just by looking at the read alignment in a genome viewer (IGV or Genome Browse), that there is a small indel in a particular region of interest. Usually, it is needed when checking candidate SNPs manually.
I am working with trios.
Thank you