Zobrazeno 1 - 7
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pro vyhledávání: '"Wulf, Bryan"'
Autor:
Nie, Allen, Pineda, Arturo L., Wand, Matt W. Wright Hannah, Wulf, Bryan, Costa, Helio A., Patel, Ronak Y., Bustamante, Carlos D., Zou, James
As genetic sequencing costs decrease, the lack of clinical interpretation of variants has become the bottleneck in using genetics data. A major rate limiting step in clinical interpretation is the manual curation of evidence in the genetic literature
Externí odkaz:
http://arxiv.org/abs/1909.10699
Autor:
Wright, Matthew, Preston, Christine, Dalton, Karen, Cheung, Gloria, Mandell, Mark, Wulf, Bryan, Babb, Lawrence, DiStefano, Marina, Harrison, Steven, Klein, Clarissa, Shapira, Rachel, Keseler, Ingrid, Ritter, Deborah, Shah, Neethu, Riehle, Kevin, Milosavljevic, Aleksandar, Plon, Sharon, Klein, Teri
Publikováno v:
In Genetics in Medicine Open 2023 1(1) Supplement
Akademický článek
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Akademický článek
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Autor:
Iacocca, Michael A., Pineda, Arturo Lopez, Wright, Matt W., Wand, Hannah, Zhen, Jimmy, Wulf, Bryan, Patel, Ronak Y, Milosavljevic, Aleksandar, Ritter, Deborah, Snehit Prabhu, Costa, Helio A., Chora, Joana R., Bourbon, Mafalda, Bejerano, Gill, Plon, Sharon E., Bustamante, Carlos D.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dbbd472dfb0ef583d5cb56919fa362d2
Autor:
Wright MW; 1Department of Biomedical Data Science, Stanford University School of Medicine, Stanford, California, USA; email: wrightmw@stanford.edu, teri.klein@stanford.edu., Thaxton CL; 2Department of Genetics, University of North Carolina, Chapel Hill, North Carolina, USA; email: courtney_thaxton@med.unc.edu., Nelson T; 3Geisinger, Danville, Pennsylvania, USA; email: thnelson@geisinger.edu., DiStefano MT; 4Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA., Savatt JM; 3Geisinger, Danville, Pennsylvania, USA; email: thnelson@geisinger.edu., Brush MH; 5Department of Biomedical Informatics, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA., Cheung G; 1Department of Biomedical Data Science, Stanford University School of Medicine, Stanford, California, USA; email: wrightmw@stanford.edu, teri.klein@stanford.edu., Mandell ME; 1Department of Biomedical Data Science, Stanford University School of Medicine, Stanford, California, USA; email: wrightmw@stanford.edu, teri.klein@stanford.edu., Wulf B; 1Department of Biomedical Data Science, Stanford University School of Medicine, Stanford, California, USA; email: wrightmw@stanford.edu, teri.klein@stanford.edu., Ward TJ; 2Department of Genetics, University of North Carolina, Chapel Hill, North Carolina, USA; email: courtney_thaxton@med.unc.edu., Goehringer S; 3Geisinger, Danville, Pennsylvania, USA; email: thnelson@geisinger.edu., O'Neill T; 4Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA., Weller P; 3Geisinger, Danville, Pennsylvania, USA; email: thnelson@geisinger.edu., Preston CG; 1Department of Biomedical Data Science, Stanford University School of Medicine, Stanford, California, USA; email: wrightmw@stanford.edu, teri.klein@stanford.edu., Keseler IM; 1Department of Biomedical Data Science, Stanford University School of Medicine, Stanford, California, USA; email: wrightmw@stanford.edu, teri.klein@stanford.edu., Goldstein JL; 2Department of Genetics, University of North Carolina, Chapel Hill, North Carolina, USA; email: courtney_thaxton@med.unc.edu., Strande NT; 3Geisinger, Danville, Pennsylvania, USA; email: thnelson@geisinger.edu., McGlaughon J; 2Department of Genetics, University of North Carolina, Chapel Hill, North Carolina, USA; email: courtney_thaxton@med.unc.edu., Azzariti DR; 4Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA., Cordova I; 3Geisinger, Danville, Pennsylvania, USA; email: thnelson@geisinger.edu., Dziadzio H; 4Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA., Babb L; 4Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA., Riehle K; 6Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA., Milosavljevic A; 6Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA., Martin CL; 3Geisinger, Danville, Pennsylvania, USA; email: thnelson@geisinger.edu., Rehm HL; 4Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA., Plon SE; 6Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; 7Department of Pediatrics/Hematology-Oncology, Baylor College of Medicine, Houston, Texas, USA., Berg JS; 2Department of Genetics, University of North Carolina, Chapel Hill, North Carolina, USA; email: courtney_thaxton@med.unc.edu., Riggs ER; 3Geisinger, Danville, Pennsylvania, USA; email: thnelson@geisinger.edu., Klein TE; 1Department of Biomedical Data Science, Stanford University School of Medicine, Stanford, California, USA; email: wrightmw@stanford.edu, teri.klein@stanford.edu.; 8Department of Medicine (Biomedical Informatics Research) and Genetics, Stanford University School of Medicine, Stanford, California, USA.
Publikováno v:
Annual review of biomedical data science [Annu Rev Biomed Data Sci] 2024 Apr 25. Date of Electronic Publication: 2024 Apr 25.
Autor:
Nie A; Department of Biomedical Data Science, Stanford University School of Medicine, USA.; Department of Computer Science, Stanford University, USA., Pineda AL, Wright MW, Wand H, Wulf B, Costa HA, Patel RY, Bustamante CD, Zou J
Publikováno v:
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing [Pac Symp Biocomput] 2020; Vol. 25, pp. 67-78.