I remember reading a paper talking about how denovo sequencing is useful even on known reference. Because each people's genome is slightly different. I am trying to find that paper again but couldn't anymore.
I have some exome sequencing illumina data, I am wondering if it is worth it to do denovo sequencing in this case.
What is your take on this subject?
Thanks
I have some exome sequencing illumina data, I am wondering if it is worth it to do denovo sequencing in this case.
What is your take on this subject?
Thanks
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