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]