How to Analyze CNV with Autism
I am starting a bioinformatics projects (to which the field I am completely new) and I want to analyze CNV regarding autism. After a lot of looking around I still don't know what tools to use or what data to use, so I was looking for some guidance. Anything would be appreciated. Thanks!
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We just published this paper Frequency and Complexity of De Novo Structural Mutation in Autism.
If you have whole genome data please use my CNV genotyper! gtCNV: genotype Copy Number Variation with machine learning
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What data do you have available? SNP array, array CGH, DNA sequencing, qPCR? Or are you looking to reuse any public data?