![]() |
|
![]() |
||||
Thread | Thread Starter | Forum | Replies | Last Post |
Extract unaligned reads (Tophat) from FastQ | Uwe Appelt | Bioinformatics | 5 | 08-07-2012 05:33 AM |
how to extract raw unaligned reads? | joseph | Bioinformatics | 2 | 12-20-2011 06:24 PM |
how to filter unaligned duplicate reads | HESmith | Bioinformatics | 4 | 11-30-2011 03:13 AM |
Tophat options to report unaligned reads and controlling Bowtie options | Siva | Bioinformatics | 0 | 10-15-2010 08:38 PM |
Seqman Leaves most of the reads unaligned | Mansequencer | Bioinformatics | 5 | 07-28-2010 03:05 PM |
![]() |
|
Thread Tools |
![]() |
#1 |
Member
Location: los angeles, ca Join Date: Aug 2010
Posts: 11
|
![]()
Does anyone know a way to see which reads from tophat are unaligned? I figured out how to do this in bowtie with the --un and --max options, but does someone have a way to do this in tophat?
|
![]() |
![]() |
![]() |
#2 | |
Senior Member
Location: Rochester, MN Join Date: Mar 2009
Posts: 191
|
![]() Quote:
|
|
![]() |
![]() |
![]() |
Thread Tools | |
|
|