exomeSuite: Whole exome sequence variant filtering tool for rapid identification of putative disease causing SNVs/indels
exomeSuite:用于快速识别潜在致病性SNV/indel的全外显子组序列变异过滤工具
期刊:Genomics
影响因子:3
doi:10.1016/j.ygeno.2014.02.006
Maranhao, B; Biswas, P; Duncan, J L; Branham, K E; Silva, G A; Naeem, M A; Khan, S N; Riazuddin, S; Hejtmancik, J F; Heckenlively, J R; Riazuddin, S A; Lee, P L; Ayyagari, R