Hi

From the human whole-genome sequenced data how can I analyze the gene? I can filter one gene manually, but how about a gene pool??? How do I interpret the annotated data from vcf file? As a whole what will be a general protocol/pipeline to analyze whole human-genome data?

My main aim is to find out the cause of a patient's disease who is not been diagnosed yet but suffering a lot.

Thank you in advance

Dr. Shahina Akter

Email- [email protected]

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