If your .bam file was made by aligning reads to a genome, then it's got the chromosome and position of every read that aligned. So you can filter the bam by position to get only the regions you want. SAMTools view can do this, there are probably ways in other software suits, like Picard and GATK.
After that, you've got to do something with teh .bam, and that depends a lot on what exactly you are trying to do with your data.
Seqanswers Leaderboard Ad
Collapse
Announcement
Collapse
No announcement yet.
X
-
(newbie question) How do you identify a gene from a BAM file?
Hello, I am working with a BAM file which compares a differentiated cell genome to that of a reference sequence genome. To be more specific, I am comparing differentiated T-cell receptor to germ line VDJ regions. Is there any way to output the VDJ region of the differentiated sample as a FASTA file so I can identify it on BLAST? Thanks!Tags: None
Latest Articles
Collapse
-
by seqadmin
Innovations in next-generation sequencing technologies and techniques are driving more precise and comprehensive exploration of complex biological systems. Current advancements include improved accessibility for long-read sequencing and significant progress in single-cell and 3D genomics. This article explores some of the most impactful developments in the field over the past year.
Long-Read Sequencing
Long-read sequencing has seen remarkable advancements,...-
Channel: Articles
12-02-2024, 01:49 PM -
ad_right_rmr
Collapse
News
Collapse
Topics | Statistics | Last Post | ||
---|---|---|---|---|
Started by seqadmin, 12-02-2024, 09:29 AM
|
0 responses
158 views
0 likes
|
Last Post
by seqadmin
12-02-2024, 09:29 AM
|
||
Started by seqadmin, 12-02-2024, 09:06 AM
|
0 responses
56 views
0 likes
|
Last Post
by seqadmin
12-02-2024, 09:06 AM
|
||
Started by seqadmin, 12-02-2024, 08:03 AM
|
0 responses
48 views
0 likes
|
Last Post
by seqadmin
12-02-2024, 08:03 AM
|
||
Started by seqadmin, 11-22-2024, 07:36 AM
|
0 responses
76 views
0 likes
|
Last Post
by seqadmin
11-22-2024, 07:36 AM
|
Leave a comment: