May someone help me to knkw how to detect copy number variation from Illumina 50k Snp chip, i am using genome studio i input all the files but it is showing error in sample sheet...sample sheet from Illumina downloads, idat file from NCBI repositories and bpm file from Illumina downloads, please help me with this issue or any other way of cnv detection from Snp genotyping.i have SNP genotyping data.
Question: Cnv analysis through Snp genotyping
2.1 years ago by
Bhavya • 0
Bhavya • 0 wrote:
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