A Complete Pedigree-Based Graph Workflow for Rare Candidate Variant Analysis
Charles Markello(University of California, Santa Cruz), Benedict Paten(University of California, Santa Cruz), Pi-Chuan Chang(Google (United States)), Andrew Carroll(Western NSW Local Health District), Charles Huang, Álex Rodríguez(National Institutes of Health), Thomas C. Markello(National Human Genome Research Institute), David Haussler(Santa Cruz County Office of Education), Jordan M. Eizenga(University of California, Santa Cruz)
Cited by 2
Related Papers
Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes
|Genome Research|2005|4.4k
Molecular Profiling Reveals Biologically Discrete Subsets and Pathways of Progression in Diffuse Glioma
|Cell|2016|2.4k
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