a lot of reads in my data were mapped to rRNA region, how can I filter them in SAM format. is there any command in samtools or other package?
Thanks.
Thanks.
You are currently viewing the SEQanswers forums as a guest, which limits your access. Click here to register now, and join the discussion
Topics | Statistics | Last Post | ||
---|---|---|---|---|
Started by seqadmin, Today, 05:03 AM
|
0 responses
16 views
0 reactions
|
Last Post
by seqadmin
Today, 05:03 AM
|
||
Started by seqadmin, Yesterday, 07:27 AM
|
0 responses
13 views
0 reactions
|
Last Post
by seqadmin
Yesterday, 07:27 AM
|
||
Started by seqadmin, 03-18-2025, 12:50 PM
|
0 responses
15 views
0 reactions
|
Last Post
by seqadmin
03-18-2025, 12:50 PM
|
||
Started by seqadmin, 03-03-2025, 01:15 PM
|
0 responses
185 views
0 reactions
|
Last Post
by seqadmin
03-03-2025, 01:15 PM
|
Comment