HIGHLIGHTS
- who: Revital Kariv et al. from the Department of Gastroenterology, Sourasky Medical Center, Faculty of Medicine, University, have published the article: Whole Genome Sequencing Applied in Familial Hamartomatous Polyposis Identifies Novel Structural Variations, in the Journal: Genes 2022, 13, 1408. of /2022/
- what: The Analysis platform was used for extraction of raw sequencing data from the sequencing provider, followed by primary and secondary pipelines to generate VCF files with SNVs, SVs, CNVs and repeats.
- how: Briefly the analysis is based on the standard steps of basic variant annotation allele frequency databases and variant . . .
If you want to have access to all the content you need to log in!
Thanks :)
If you don't have an account, you can create one here.