I am trying to find the most significant altered genes and I was thinking of using only 1 tool for significance test which is MutSigCV instead of MutSigCV for mutation data and GISTIC for CNV data. I know that MutSigCV works with short indels but can I merge my CNV segmented data in the MAF file (Divide each long CNV into regions) and input them to MutSigCV or this wouldn't work? Can MutSigCV work with long insertions or deletions? What is the maximum indel length that MutSigCV can operate on?
-
The part about this topic feels surprisingly grounded, and the details on the page is the bit that made me slow down. I’d keep <a href="https://kinpict.com/">ai family photo generator</a> bookmarked for later.Today, 06:37 PM -
NGS has revolutionized clinical microbiology by offering new ways to identify and surveil pathogens without prior knowledge of the target. One popular approach is 16S rRNA and ITS amplicon sequencing, which targets specific microbial markers. But studies are increasingly incorporating shotgun metagenomics, a technique that sequences all DNA from a sample without targeting specific microbial markers. This approach allows more detailed taxonomic classification,...10-30-2026, 06:46 AM
| Topics | Statistics | Last Post | ||
|---|---|---|---|---|
|
0 responses
27 views
0 reactions
|
by SEQadmin2
11-12-2026, 07:59 AM
|
|||
|
0 responses
35 views
0 reactions
|
by SEQadmin2
11-05-2026, 09:25 AM
|
|||
|
2 responses
56 views
0 reactions
|
by kinpict.com
Today, 06:49 PM
|
|||
|
0 responses
175 views
0 reactions
|
by SEQadmin2
10-28-2026, 09:57 AM
|