Hi,
I obtained an old data of RNA-Seq contigs but without raw reads. And my boss wants me to find if those contigs can be comparable with the relative reference genome (which is annotated)
What program or strategy I should use to analyse those contigs? Maybe , I could better annotate them?
Thanks in advance!
I obtained an old data of RNA-Seq contigs but without raw reads. And my boss wants me to find if those contigs can be comparable with the relative reference genome (which is annotated)
What program or strategy I should use to analyse those contigs? Maybe , I could better annotate them?
Thanks in advance!
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