How to combine HiSeq and MiSeq reads?
Hello, I am trying to use Spades for genome assembly of paired HiSeq and MiSeq reads but I am not getting better coverage when I combine those reads compare to the separate HiSeq assembly. Do you please know what could be the problem?
• 808 views
•
link
0 answers
No answers yet.
Log in to answer this question.
What kind of coverage? Not recovering all expected regions of genome?
Is the same library sequenced on both HiSeq and MiSeq? Perhaps it is the library characteristic.