TrialGenomics
exomeSuite: Whole exome sequence variant filtering tool for rapid identification of putative disease causing SNVs/indels.
B Maranhao et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.
14 papers cite it
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TrialGenomics
B Maranhao et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.