Thurnherr, T., Singer, F., Stekhoven, D. J., & Beerenwinkel, N. (2016). Genomic variant annotation workflow for clinical applications. F1000Res.
シカゴスタイル引用形Thurnherr, Thomas, Franziska Singer, Daniel J. Stekhoven, , Niko Beerenwinkel. "Genomic Variant Annotation Workflow for Clinical Applications." F1000Res 2016.
MLA引用形式Thurnherr, Thomas, Franziska Singer, Daniel J. Stekhoven, , Niko Beerenwinkel. "Genomic Variant Annotation Workflow for Clinical Applications." F1000Res 2016.
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