I have 3 human genomes short sequencing reads of Illumina. I want to assemble these data, Can anybody suggest me a standard pipeline for this??
i would suggest abyss if you want to do denova, and bowtie2 for reference based
Suheel Yousuf Wani Thank you for the suggestion..
Dose anybody Know how to get a Branch Specific Ka/Ks value? And, any good tool available for that? Thank you in advance.
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