G/JISTIC is good one..
Hi, I am looking for a method/algorithm for the identification of focal amplification ( agilent CGH data or Affymetrix SNP6) in a set of tumors. Any suggestions are welcome. Thanks,
2 answers
Hi @Rm and @Chris Miller,
I am trying to use JISTIC to analyze CNV across large cohort. I am stuck with making probe_location_file, that is used to make input matrix file. I had posted the question here: JISTIC. Make Probe location file to compare copy number among samples
Alternatively, can I just make matrix for gene based, by interesting gene coordinates with CNV coordinates, and assign the CNV(amplification/deletion) value. But not samples will have some value to assign in the output file from DNACopy. So what do I insert in those missing values.
Thank you!
Try Agilent's Genomic Workbench: (you can get a trial version of it from their website)
and try Affy's Genotyping console to handle SNP6 data. ( I think this too freely available for academic use)
For focal (you can define the size) regions write a simple script to extract the information required.
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