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    المؤلفون: Ng JK; Department of Genetics, Washington University School of Medicine, St. Louis, Missouri, USA., Vats P; NVIDIA Corporation, Santa Clara, California, USA., Fritz-Waters E; Research Infrastructure Services, Washington University School of Medicine, St. Louis, Missouri, USA., Sarkar S; Department of Genetics, Washington University School of Medicine, St. Louis, Missouri, USA., Sams EI; Department of Genetics, Washington University School of Medicine, St. Louis, Missouri, USA., Padhi EM; Department of Genetics, Washington University School of Medicine, St. Louis, Missouri, USA., Payne ZL; Department of Genetics, Washington University School of Medicine, St. Louis, Missouri, USA., Leonard S; Research Infrastructure Services, Washington University School of Medicine, St. Louis, Missouri, USA., West MA; NVIDIA Corporation, Santa Clara, California, USA., Prince C; Research Infrastructure Services, Washington University School of Medicine, St. Louis, Missouri, USA., Trani L; McDonnell Genome Institute, Washington University School of Medicine, St. Louis, Missouri, USA., Jansen M; Research Infrastructure Services, Washington University School of Medicine, St. Louis, Missouri, USA., Vacek G; NVIDIA Corporation, Santa Clara, California, USA., Samadi M; NVIDIA Corporation, Santa Clara, California, USA., Harkins TT; NVIDIA Corporation, Santa Clara, California, USA., Pohl C; Research Infrastructure Services, Washington University School of Medicine, St. Louis, Missouri, USA., Turner TN; Department of Genetics, Washington University School of Medicine, St. Louis, Missouri, USA.

    المصدر: Human mutation [Hum Mutat] 2022 Dec; Vol. 43 (12), pp. 1979-1993. Date of Electronic Publication: 2022 Sep 10.

    نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

    بيانات الدورية: Publisher: Wiley-Liss Country of Publication: United States NLM ID: 9215429 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1098-1004 (Electronic) Linking ISSN: 10597794 NLM ISO Abbreviation: Hum Mutat Subsets: MEDLINE

    مواضيع طبية MeSH: Neoplasms*/genetics, Humans ; Alleles ; Mutation ; Whole Genome Sequencing