Dear all
After setting bowtie and tophat under a path I ran tophat on 20MB fastq reads.
And I found only few aligned reads and junctions in output. When I checked logs the results made me suspicious.
After that
when i ran just default bowtie command, 90% of my reads are failed to align. Does any one know why ?
If I need to change any parameters in bowtie where and how could I change them so that tophat recognizes them every time when i ran tophat?
My reads are 35bp single end illumina-solexa fastq reads (hg18). It would be great if you provide any parameters if I need to change in bowtie especially for these kinda reads.
Thanx in advance
After setting bowtie and tophat under a path I ran tophat on 20MB fastq reads.
And I found only few aligned reads and junctions in output. When I checked logs the results made me suspicious.
After that
when i ran just default bowtie command, 90% of my reads are failed to align. Does any one know why ?
If I need to change any parameters in bowtie where and how could I change them so that tophat recognizes them every time when i ran tophat?
My reads are 35bp single end illumina-solexa fastq reads (hg18). It would be great if you provide any parameters if I need to change in bowtie especially for these kinda reads.
Thanx in advance
Comment