Abstract 7436: DeepSomatic: A SNV and small-indel somatic caller using deep neural networks
Daniel E. Cook(Google (United States)), Kishwar Shafin(Google (United States)), Nicolas Robine(New York Genome Center), Mikhail Kolmogorov(National Institutes of Health), Irina Pushel(Children's Mercy Hospital), Tomi Pastinen(Children's Mercy Hospital), Yongmei Zhao(Leidos (United States)), Karen H. Miga(University of California, Santa Cruz), Pi-Chuan Chang(Google (United States)), Midhat S. Farooqi(Children's Mercy Hospital), Byunggil Yoo(Children's Mercy Hospital), Benedict Paten(University of California, Santa Cruz), Lucas Brambrink(Google (United States)), Alexey Kolesnikov(Google (United States)), Andrew Carroll(Western NSW Local Health District), Joshua Gardner(University of California, Santa Cruz), Ayse Keskus(National Cancer Institute), Samuel Sacco(University of California, Santa Cruz), Jimin Park(University of California, Santa Cruz), Giuseppe Narzisi(Cold Spring Harbor Laboratory), Juan C. Mier(Moog (United States)), Lisa A. Lansdon(Mercy Research), Jyoti Shetty(Leidos (United States)), Margaret Gibson(Children's Mercy Hospital), Tanveer Ahmad(National Cancer Institute), Asher Bryant(National Cancer Institute), Chengpeng Bi(Children's Mercy Hospital), Adam Walter(Children's Mercy Hospital), Bao Tran(Leidos (United States)), Adrienne Hellend(New York Genome Center), Brandy McNulty(University of California, Santa Cruz)
Cited by 0
Related Papers
The complete sequence of a human genome
|Science|2022|3.3k
Genetics and Pathogenesis of Diffuse Large B-Cell Lymphoma
|New England Journal of Medicine|2018|2.3k
Nanopore sequencing and assembly of a human genome with ultra-long reads
|Nature Biotechnology|2018|2.1k
Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genome
|Nature Biotechnology|2019|2k
A universal SNP and small-indel variant caller using deep neural networks
|Nature Biotechnology|2018|2k