Search Results - Steven N. Hart

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  1. 1
    Bioinformatics for Clinical Next Generation Sequencing

    Bioinformatics for Clinical Next Generation Sequencing by Gavin R. Oliver, Steven N. Hart, Eric W. Klee

    Published 2014
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  2. 2
    Three Patterns of Cytochrome P450 Gene Expression during Liver Maturation in Mice

    Three Patterns of Cytochrome P450 Gene Expression during Liver Maturation in Mice by Steven N. Hart, Yue Cui, Curtis D. Klaassen, Xiao-bo Zhong

    Published 2008
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  3. 3
    Dynamic Patterns of Histone Methylation Are Associated with Ontogenic Expression of the <i>Cyp3a</i> Genes during Mouse Liver Maturation

    Dynamic Patterns of Histone Methylation Are Associated with Ontogenic Expression of the <i>Cyp3a</i> Genes during Mouse Liver Maturation by Ye Li, Yue Cui, Steven N. Hart, Curtis D. Klaassen, Xiao Zhong

    Published 2009
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  4. 4
    Calculating Sample Size Estimates for RNA Sequencing Data

    Calculating Sample Size Estimates for RNA Sequencing Data by Steven N. Hart, Terry M. Therneau, Yuji Zhang, Gregory A. Poland, Jean‐Pierre Kocher

    Published 2013
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  5. 5
    Genome-wide tissue-specific farnesoid X receptor binding in mouse liver and intestine

    Genome-wide tissue-specific farnesoid X receptor binding in mouse liver and intestine by Ann Thomas, Steven N. Hart, Bo Kong, Jianwen Fang, Xiao‐bo Zhong, Grace L. Guo

    Published 2009
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  6. 6
    A Comparison of Whole Genome Gene Expression Profiles of HepaRG Cells and HepG2 Cells to Primary Human Hepatocytes and Human Liver Tissues

    A Comparison of Whole Genome Gene Expression Profiles of HepaRG Cells and HepG2 Cells to Primary Human Hepatocytes and Human Liver Tissues by Steven N. Hart, Ye Li, Kaori Nakamoto, Eva-Anne Subileau, David Steen, Xiao-bo Zhong

    Published 2010
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  7. 7
    VCF-Miner: GUI-based application for mining variants and annotations stored in VCF files

    VCF-Miner: GUI-based application for mining variants and annotations stored in VCF files by Steven N. Hart, Patrick Duffy, Daniel Quest, Asif Hossain, Mike A Meiners, Jean‐Pierre Kocher

    Published 2015
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  8. 8
    SoftSearch: Integration of Multiple Sequence Features to Identify Breakpoints of Structural Variations

    SoftSearch: Integration of Multiple Sequence Features to Identify Breakpoints of Structural Variations by Steven N. Hart, Vivekananda Sarangi, Raymond M. Moore, Saurabh Baheti, Jaysheel Bhavsar, Fergus J. Couch, Jean-Pierre A. Kocher

    Published 2013
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  9. 9
    Cybersecurity and Information Assurance for the Clinical Laboratory

    Cybersecurity and Information Assurance for the Clinical Laboratory by Ankush Patel, Christopher L. Williams, Steven N. Hart, Christopher A. Garcia, Thomas J S Durant, Toby C. Cornish, David S. McClintock

    Published 2023
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  10. 10
    The Biological Reference Repository (BioR): a rapid and flexible system for genomics annotation

    The Biological Reference Repository (BioR): a rapid and flexible system for genomics annotation by Jean-Pierre A. Kocher, Daniel Quest, Patrick E. Duffy, Michael A. Meiners, Raymond M. Moore, David A. Rider, Asif Hossain, Steven N. Hart, Valentin Dinu

    Published 2014
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  11. 11
    Organizational preparedness for the use of large language models in pathology informatics

    Organizational preparedness for the use of large language models in pathology informatics by Steven N. Hart, Noah G. Hoffman, Peter Gershkovich, Chancey Christenson, David S. McClintock, Lauren J. Miller, Ronald Jackups, Vahid Azimi, Nicholas C. Spies, Victor Brodsky

    Published 2023
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  12. 12
    Frequency of mutations in a large series of clinically ascertained ovarian cancer cases tested on multi-gene panels compared to reference controls

    Frequency of mutations in a large series of clinically ascertained ovarian cancer cases tested on multi-gene panels compared to reference controls by Jenna Lilyquist, Holly LaDuca, Eric C. Polley, Brigette Tippin Davis, Hermela Shimelis, Chunling Hu, Steven N. Hart, Jill S. Dolinsky, Fergus J. Couch, David E. Goldgar

    Published 2017
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  13. 13
    Prevalence of Pathogenic Mutations in Cancer Predisposition Genes among Pancreatic Cancer Patients

    Prevalence of Pathogenic Mutations in Cancer Predisposition Genes among Pancreatic Cancer Patients by Chunling Hu, Steven N. Hart, William R. Bamlet, Raymond M. Moore, Kannabiran Nandakumar, Bruce W. Eckloff, Yean Kee Lee, Gloria M. Petersen, Robert R. McWilliams, Fergus J. Couch

    Published 2015
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  14. 14
    Cancer susceptibility gene mutations in type I and II endometrial cancer

    Cancer susceptibility gene mutations in type I and II endometrial cancer by Beverly Long, Jenna Lilyquist, Amy L. Weaver, Chunling Hu, Rohan Gnanaolivu, Kun Y. Lee, Steven N. Hart, Eric C. Polley, Jamie N. Bakkum‐Gamez, Fergus J. Couch, Sean C. Dowdy

    Published 2018
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  15. 15
    The Contribution of Germline Predisposition Gene Mutations to Clinical Subtypes of Invasive Breast Cancer From a Clinical Genetic Testing Cohort

    The Contribution of Germline Predisposition Gene Mutations to Clinical Subtypes of Invasive Breast Cancer From a Clinical Genetic Testing Cohort by Chunling Hu, Eric C. Polley, Siddhartha Yadav, Jenna Lilyquist, Hermela Shimelis, Jie Na, Steven N. Hart, David E. Goldgar, Swati Shah, Tina Pesaran, Jill S. Dolinsky, Holly LaDuca, Fergus J. Couch

    Published 2020
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  16. 16
    Comparison of the Prevalence of Pathogenic Variants in Cancer Susceptibility Genes in Black Women and Non-Hispanic White Women With Breast Cancer in the United States

    Comparison of the Prevalence of Pathogenic Variants in Cancer Susceptibility Genes in Black Women and Non-Hispanic White Women With Breast Cancer in the United States by Susan M. Domchek, Song Yao, Fei Chen, Chunling Hu, Steven N. Hart, David E. Goldgar, Katherine L. Nathanson, Christine B. Ambrosone, Christopher A. Haiman, Fergus J. Couch, Eric C. Polley, Julie R. Palmer

    Published 2021
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  17. 17
    Comprehensive annotation of BRCA1 and BRCA2 missense variants by functionally validated sequence-based computational prediction models

    Comprehensive annotation of BRCA1 and BRCA2 missense variants by functionally validated sequence-based computational prediction models by Steven N. Hart, Tanya L. Hoskin, Hermela Shimelis, Raymond M. Moore, Bing Feng, Abigail Thomas, Noralane M. Lindor, Eric C. Polley, David E. Goldgar, Edwin S. Iversen, Álvaro N.A. Monteiro, Vera J. Suman, Fergus J. Couch

    Published 2018
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  18. 18
    Multigene Hereditary Cancer Panels Reveal High-Risk Pancreatic Cancer Susceptibility Genes

    Multigene Hereditary Cancer Panels Reveal High-Risk Pancreatic Cancer Susceptibility Genes by Chunling Hu, Holly LaDuca, Hermela Shimelis, Eric C. Polley, Jenna Lilyquist, Steven N. Hart, Jie Na, Abigail Thomas, Kun Y. Lee, Brigette Tippin Davis, Mary Helen Black, Tina Pesaran, David E. Goldgar, Jill S. Dolinsky, Fergus J. Couch

    Published 2018
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  19. 19
    Strong functional data for pathogenicity or neutrality classify BRCA2 DNA-binding-domain variants of uncertain significance

    Strong functional data for pathogenicity or neutrality classify BRCA2 DNA-binding-domain variants of uncertain significance by Marcy E. Richardson, Chunling Hu, Kun Y. Lee, Holly LaDuca, Kelly Fulk, Kate Durda, Ashley Deckman, David E. Goldgar, Álvaro N.A. Monteiro, Rohan Gnanaolivu, Steven N. Hart, Eric C. Polley, Elizabeth Chao, Tina Pesaran, Fergus J. Couch

    Published 2021
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  20. 20
    PatternCNV: a versatile tool for detecting copy number changes from exome sequencing data

    PatternCNV: a versatile tool for detecting copy number changes from exome sequencing data by Chen Wang, Jared M. Evans, Aditya Bhagwate, Naresh Prodduturi, Vivekananda Sarangi, Mridu Middha, Hugues Sicotte, Peter T. Vedell, Steven N. Hart, Gavin R. Oliver, Jean‐Pierre Kocher, Matthew J. Maurer, Anne J. Novak, Susan L. Slager, James R. Cerhan, Yan W. Asmann

    Published 2014
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