Will Digital Pathology be as Disruptive as Genomics?

por Hart, Steven N.
Publicado 2018

Succinate dehydrogenase variants in paraganglioma: why are B subunit variants ‘bad’?

por Gruber, Lucinda M, Hart, Steven N, Maher III, Louis James
Publicado 2023

Empowering Mayo Clinic Individualized Medicine with Genomic Data Warehousing

por Horton, Iain, Lin, Yaxiong, Reed, Gay, Wiepert, Mathieu, Hart, Steven
Publicado 2017

From Days to Hours: Reporting Clinically Actionable Variants from Whole Genome Sequencing

por Middha, Sumit, Baheti, Saurabh, Hart, Steven N., Kocher, Jean-Pierre A.
Publicado 2014

Using an anomaly detection approach for the segmentation of colorectal cancer tumors in whole slide images

por Gu, Qiangqiang, Meroueh, Chady, Levernier, Jacob, Kroneman, Trynda, Flotte, Thomas, Hart, Steven
Publicado 2023

Dicom_wsi: A Python Implementation for Converting Whole-Slide Images to Digital Imaging and Communications in Medicine Compliant Files

por Gu, Qiangqiang, Prodduturi, Naresh, Jiang, Jun, Flotte, Thomas J., Hart, Steven N.
Publicado 2021

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

por Jiang, Jun, Larson, Nicholas B., Prodduturi, Naresh, Flotte, Thomas J., Hart, Steven N.
Publicado 2019

Prediction of the functional impact of missense variants in BRCA1 and BRCA2 with BRCA-ML

por Hart, Steven N., Polley, Eric C., Shimelis, Hermella, Yadav, Siddhartha, Couch, Fergus J.
Publicado 2020

Geobacter Dominates the Inner Layers of a Stratified Biofilm on a Fluidized Anode During Brewery Wastewater Treatment

por Tejedor-Sanz, Sara, Fernández-Labrador, Patricia, Hart, Steven, Torres, Cesar I., Esteve-Núñez, Abraham
Publicado 2018

A high-throughput-sequence analysis infrastructure technology investigation framework for the evaluation of next-generation sequencing software

por Liu, Xiaoyu, Middha, Sumit, Hart, Steven, Nair, Asha, Hadad, Ahmed, Duffy, Patrick, Kocher, Jean-Pierre
Publicado 2011

VCF-Miner: GUI-based application for mining variants and annotations stored in VCF files

por Hart, Steven N., Duffy, Patrick, Quest, Daniel J., Hossain, Asif, Meiners, Mike A, Kocher, Jean-Pierre
Publicado 2016

SoftSearch: Integration of Multiple Sequence Features to Identify Breakpoints of Structural Variations

por Hart, Steven N., Sarangi, Vivekananda, Moore, Raymond, Baheti, Saurabh, Bhavsar, Jaysheel D., Couch, Fergus J., Kocher, Jean-Pierre A.
Publicado 2013

Classification of Melanocytic Lesions in Selected and Whole-Slide Images via Convolutional Neural Networks

por Hart, Steven N., Flotte, William, Norgan, Andrew P., Shah, Kabeer K., Buchan, Zachary R., Mounajjed, Taofic, Flotte, Thomas J.
Publicado 2019

Genetic Selection for Resistance to Gastrointestinal Parasitism in Meat Goats and Hair Sheep through a Performance Test with Artificial Infection of Haemonchus contortus

por Tsukahara, Yoko, Gipson, Terry A., Hart, Steven P., Dawson, Lionel, Wang, Zaisen, Puchala, Ryszard, Sahlu, Tilahun, Goetsch, Arthur L.
Publicado 2021

PANDA: pathway and annotation explorer for visualizing and interpreting gene-centric data

por Hart, Steven N., Moore, Raymond M., Zimmermann, Michael T., Oliver, Gavin R., Egan, Jan B., Bryce, Alan H., Kocher, Jean-Pierre A.
Publicado 2015

Microarray analysis of the in vivo sequence preferences of a minor groove binding drug

por Eckdahl, Todd T, Brown, Adam D, Hart, Steven N, Malloy, Kelly J, Shott, Martha, Yiu, Gloria, Hoopes, Laura L Mays, Heyer, Laurie J
Publicado 2008

Organizational preparedness for the use of large language models in pathology informatics

por Hart, Steven N., Hoffman, Noah G., Gershkovich, Peter, Christenson, Chancey, McClintock, David S., Miller, Lauren J., Jackups, Ronald, Azimi, Vahid, Spies, Nicholas, Brodsky, Victor
Publicado 2023

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

por Kocher, Jean-Pierre A., Quest, Daniel J., Duffy, Patrick, Meiners, Michael A., Moore, Raymond M., Rider, David, Hossain, Asif, Hart, Steven N., Dinu, Valentin
Publicado 2014

Mutation prevalence tables for hereditary cancer derived from multigene panel testing

por Hart, Steven N., Polley, Eric C., Yussuf, Amal, Yadav, Siddhartha, Goldgar, David E., Hu, Chunling, LaDuca, Holly, Smith, Laura P., Fujimoto, June, Li, Shuwei, Couch, Fergus J., Dolinsky, Jill S.
Publicado 2020

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

por Hu, Chunling, Polley, Eric C, Yadav, Siddhartha, Lilyquist, Jenna, Shimelis, Hermela, Na, Jie, Hart, Steven N, Goldgar, David E, Shah, Swati, Pesaran, Tina, Dolinsky, Jill S, LaDuca, Holly, Couch, Fergus J
Publicado 2020