cnvScan: a CNV screening and annotation tool to improve the clinical utility of computational CNV prediction from exome sequencing data

Autor:	Samarakoon, Pubudu S, Sorte, Hanne S, Stray-Pedersen, Asbjørg, Rødningen, Olaug K, Rognes, Torbjørn, Lyle, Robert
Zdroj:	BMC Genomics. 2016 Jan 14;17(1):51
Databáze:	NORA (Norwegian Open Research Archive)
Externí odkaz:	http://hdl.handle.net/10852/48624 https://www.duo.uio.no/bitstream/handle/10852/48624/1/12864_2016_Article_2374.pdf Zobrazit plný text záznamu