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exomeSuite: Whole exome sequence variant filtering tool for rapid identification of putative disease causing SNVs/indels
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.Volume:
103
Language:
english
Journal:
Genomics
DOI:
10.1016/j.ygeno.2014.02.006
Date:
February, 2014
File:
PDF, 1.01 MB
english, 2014