I got multiple genomes for different gram-negative bacteria. What program could I use to identify specific core genes under negative selection but with smaller regions that exhibit positive selection? Is there any limitations/problems I might encounter along the way?
Seqanswers Leaderboard Ad
Collapse
Announcement
Collapse
No announcement yet.
X
-
Do you have annotated genomes? Or just the assemblies?
If you have annotations, your project is quite similar to one project I'm working on right now...
My strategy is:
blast all genes vs each other
use R to look for gene clusters (then, you can apply the thresholds you want to decide whether a cluster has to be reported or not...)
If you don't have annotations, I would do more or less the same, instead that I would first try to make annotations using a software like glimmer...
Latest Articles
Collapse
-
by seqadmin
In recent years, precision medicine has become a major focus for researchers and healthcare professionals. This approach offers personalized treatment and wellness plans by utilizing insights from each person's unique biology and lifestyle to deliver more effective care. Its advancement relies on innovative technologies that enable a deeper understanding of individual variability. In a joint documentary with our colleagues at Biocompare, we examined the foundational principles of precision...-
Channel: Articles
01-27-2025, 07:46 AM -
ad_right_rmr
Collapse
News
Collapse
Topics | Statistics | Last Post | ||
---|---|---|---|---|
Started by seqadmin, 02-05-2025, 10:34 AM
|
0 responses
16 views
0 likes
|
Last Post
by seqadmin
02-05-2025, 10:34 AM
|
||
Started by seqadmin, 02-03-2025, 09:07 AM
|
0 responses
19 views
0 likes
|
Last Post
by seqadmin
02-03-2025, 09:07 AM
|
||
Started by seqadmin, 01-31-2025, 08:31 AM
|
0 responses
33 views
0 likes
|
Last Post
by seqadmin
01-31-2025, 08:31 AM
|
||
Started by seqadmin, 01-24-2025, 07:35 AM
|
0 responses
81 views
0 likes
|
Last Post
by seqadmin
01-24-2025, 07:35 AM
|
Comment