Hi all,
I am starting my PhD and am new in genome assembly. I started assembling 42 large contigs from 454 sequencing technology and I reduced the number to 7 but it is impossible to join the rest unless I use short-reads against the draft genome or something like this. Could anyone recomend any final step to close the genome? I am near...and a little bit desperated
Thank you in advance
Inma
I am starting my PhD and am new in genome assembly. I started assembling 42 large contigs from 454 sequencing technology and I reduced the number to 7 but it is impossible to join the rest unless I use short-reads against the draft genome or something like this. Could anyone recomend any final step to close the genome? I am near...and a little bit desperated
Thank you in advance
Inma
Comment