Closed beginner984 closed 5 years ago
Please see the wiki for details of the protocols paper which covers interpretation of results.
Sorry,
This is a few lines of my copynumber.caveman.csv output
1 1 13116 665401 2 1 3 1
2 1 668374 96324627 2 1 2 1
3 1 96326095 96419709 2 1 1 0
4 1 96421112 103508275 2 1 2 1
In protocol paper says
copynumber.caveman.csv Comma-separated values Simple form of copy number segments in format:
Segment number
Chromosome
Start position (origin-1)
End position (origin-1)
Major copy number—normal
Minor copy number—normal
Major copy number—tumor
Minor copy number—tumor
How I can get such information from my file
Chromosome Start End Total_CN Minor_CN
1 10583 1017587 3 1
1 1018144 2466425 5 2
1 2475113 7770901 3 1
People say
If I want to use scatngs output to calculate the seg mean by doing this. 1) Add up the total copy number to get tumor copy number. 2) Segment_Mean = log2(tumor copy number / tumor ploidy). I could use 2 instead of tumor ploidy if I am sure that all of mytumors are diploid and have not gone through genomic doubling.
The number of probes depends on where the data came from.
From whole genome sequencing: Probes are the boundaries of bins used to generate the copy number data and so the number of probes are equal to the number of bins + 1.
But I don't know how to get the boundaries of bins used to generate the copy number data
Any help please?
But my first column does not seem to be total copy number
Because it is not. The protocol paper clearly says (from what you pasted) that the first column is Segment number
.
Thank you for this tool
In copy number analysis from scatngs for each sample I have these outputs
**copynumber.caveman.csv
copynumber.txt
samplestatistics.txt**
Can I use purity and ploidy mentioned in output picture for example from information in this plot, I really need this information
Thank you for any help