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11
A Comparison of Whole Genome Gene Expression Profiles of HepaRG Cells and HepG2 Cells to Primary Human Hepatocytes and Human Liver Tissues
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A Comparison of Whole Genome Gene Expression Profiles of HepaRG Cells and HepG2 Cells to Primary Human Hepatocytes and Human Liver Tissues

HART, Steven N ; YE LI ; NAKAMOTO, Kaori ; SUBILEAU, Eva-Anne ; STEEN, David ; ZHONG, Xiao-Bo

Drug metabolism and disposition, 2010-06, Vol.38 (6), p.988-994 [Periódico revisado por pares]

Bethesda, MD: American Society for Pharmacology and Experimental Therapeutics

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12
Mapping molecular subtype specific alterations in breast cancer brain metastases identifies clinically relevant vulnerabilities
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Mapping molecular subtype specific alterations in breast cancer brain metastases identifies clinically relevant vulnerabilities

Cosgrove, Nicola ; Varešlija, Damir ; Keelan, Stephen ; Elangovan, Ashuvinee ; Atkinson, Jennifer M ; Cocchiglia, Sinéad ; Bane, Fiona T ; Singh, Vikrant ; Furney, Simon ; Hu, Chunling ; Carter, Jodi M ; Hart, Steven N ; Yadav, Siddhartha ; Goetz, Matthew P ; Hill, Arnold D K ; Oesterreich, Steffi ; Lee, Adrian V ; Couch, Fergus J ; Young, Leonie S

Nature communications, 2022-01, Vol.13 (1), p.514-514, Article 514 [Periódico revisado por pares]

England: Nature Publishing Group

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13
Strong functional data for pathogenicity or neutrality classify BRCA2 DNA-binding-domain variants of uncertain significance
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Strong functional data for pathogenicity or neutrality classify BRCA2 DNA-binding-domain variants of uncertain significance

Richardson, Marcy E. ; Hu, Chunling ; Lee, Kun Y. ; LaDuca, Holly ; Fulk, Kelly ; Durda, Kate M. ; Deckman, Ashley M. ; Goldgar, David E. ; Monteiro, Alvaro N.A. ; Gnanaolivu, Rohan ; Hart, Steven N. ; Polley, Eric C. ; Chao, Elizabeth ; Pesaran, Tina ; Couch, Fergus J.

American journal of human genetics, 2021-03, Vol.108 (3), p.458-468 [Periódico revisado por pares]

United States: Elsevier Inc

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14
Sentieon DNASeq Variant Calling Workflow Demonstrates Strong Computational Performance and Accuracy
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Sentieon DNASeq Variant Calling Workflow Demonstrates Strong Computational Performance and Accuracy

Kendig, Katherine I ; Baheti, Saurabh ; Bockol, Matthew A ; Drucker, Travis M ; Hart, Steven N ; Heldenbrand, Jacob R ; Hernaez, Mikel ; Hudson, Matthew E ; Kalmbach, Michael T ; Klee, Eric W ; Mattson, Nathan R ; Ross, Christian A ; Taschuk, Morgan ; Wieben, Eric D ; Wiepert, Mathieu ; Wildman, Derek E ; Mainzer, Liudmila S

Frontiers in genetics, 2019-08, Vol.10, p.736-736 [Periódico revisado por pares]

Switzerland: Frontiers Media S.A

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15
Exome sequencing identifies FANCM as a susceptibility gene for triple-negative breast cancer
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Exome sequencing identifies FANCM as a susceptibility gene for triple-negative breast cancer

Kiiski, Johanna I. ; Pelttari, Liisa M. ; Khan, Sofia ; Freysteinsdottir, Edda S. ; Reynisdottir, Inga ; Hart, Steven N. ; Shimelis, Hermela ; Vilske, Sara ; Kallioniemi, Anne ; Schleutker, Johanna ; Leminen, Arto ; Bützow, Ralf ; Blomqvist, Carl ; Barkardottir, Rosa B. ; Couch, Fergus J. ; Aittomäki, Kristiina ; Nevanlinna, Heli

Proceedings of the National Academy of Sciences - PNAS, 2014-10, Vol.111 (42), p.15172-15177 [Periódico revisado por pares]

United States: National Academy of Sciences

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16
Robust hierarchical density estimation and regression for re-stained histological whole slide image co-registration
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Robust hierarchical density estimation and regression for re-stained histological whole slide image co-registration

Jiang, Jun ; Larson, Nicholas B ; Prodduturi, Naresh ; Flotte, Thomas J ; Hart, Steven N Sarder, Pinaki

PloS one, 2019-07, Vol.14 (7), p.e0220074-e0220074 [Periódico revisado por pares]

United States: Public Library of Science

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

Hart, Steven N. ; Hoskin, Tanya ; Shimelis, Hermela ; Moore, Raymond M. ; Feng, Bingjian ; Thomas, Abigail ; Lindor, Noralane M. ; Polley, Eric C. ; Goldgar, David E. ; Iversen, Edwin ; Monteiro, Alvaro N.A. ; Suman, Vera J. ; Couch, Fergus J.

Genetics in medicine, 2019-01, Vol.21 (1), p.71-80 [Periódico revisado por pares]

United States: Elsevier Inc

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18
Recommendations for performance optimizations when using GATK3.8 and GATK4
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Recommendations for performance optimizations when using GATK3.8 and GATK4

Heldenbrand, Jacob R ; Baheti, Saurabh ; Bockol, Matthew A ; Drucker, Travis M ; Hart, Steven N ; Hudson, Matthew E ; Iyer, Ravishankar K ; Kalmbach, Michael T ; Kendig, Katherine I ; Klee, Eric W ; Mattson, Nathan R ; Wieben, Eric D ; Wiepert, Mathieu ; Wildman, Derek E ; Mainzer, Liudmila S

BMC bioinformatics, 2019-11, Vol.20 (1), p.557-557, Article 557 [Periódico revisado por pares]

England: BioMed Central Ltd

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19
SoftSearch: integration of multiple sequence features to identify breakpoints of structural variations
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SoftSearch: integration of multiple sequence features to identify breakpoints of structural variations

Hart, Steven N ; Sarangi, Vivekananda ; Moore, Raymond ; Baheti, Saurabh ; Bhavsar, Jaysheel D ; Couch, Fergus J ; Kocher, Jean-Pierre A Tang, Haixu

PloS one, 2013-12, Vol.8 (12), p.e83356-e83356 [Periódico revisado por pares]

United States: Public Library of Science

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20
The Biological Reference Repository (BioR): a rapid and flexible system for genomics annotation
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The Biological Reference Repository (BioR): a rapid and flexible system for genomics annotation

Kocher, Jean-Pierre A ; Quest, Daniel J ; Duffy, Patrick ; Meiners, Michael A ; Moore, Raymond M ; Rider, David ; Hossain, Asif ; Hart, Steven N ; Dinu, Valentin

Bioinformatics (Oxford, England), 2014-07, Vol.30 (13), p.1920-1922 [Periódico revisado por pares]

England: Oxford University Press

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Deste Autor:

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