exomeSuite: Whole exome sequence variant filtering tool for rapid identification of putative disease causing SNVs/indels
Titel:
exomeSuite: Whole exome sequence variant filtering tool for rapid identification of putative disease causing SNVs/indels
Auteur:
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.