I have some RNASeq fastq files (>6 G/each) and using the first create soap files (>20 G, each). Then I need SAM format files then.
I use the soap2sam.pl by the author of soap, but it goes very very slow.
How can I do this more quick?!
I use the soap2sam.pl by the author of soap, but it goes very very slow.
Code:
$ soap2sam.pl in.soap >in.sam
How can I do this more quick?!