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Scientific Reports
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December 6, 2025
Reproducibility of digital pathology features extracted from deep learning and foundational AI models on sequential tissue slides
Jagadheshwar Balan, Nicholas B Larson
Genetic Epidemiology
|
July 23, 2013
A kernel regression approach to gene-gene interaction detection for case-control studies
Nicholas B Larson, Daniel J Schaid
Genetic Epidemiology
|
January 3, 2014
Regularized rare variant enrichment analysis for case-control exome sequencing data
Nicholas B Larson, Daniel J Schaid
Bioinformatics (Oxford, England)
|
June 11, 2013
PurBayes: estimating tumor cellularity and subclonality in next-generation sequencing data
Nicholas B Larson, Brooke L Fridley
Genetic Epidemiology
|
January 4, 2019
A review of kernel methods for genetic association studies
Nicholas B Larson, Jun Chen, Daniel J Schaid
Nature Reviews. Genetics
|
May 31, 2018
From genome-wide associations to candidate causal variants by statistical fine-mapping
Daniel J Schaid, Wenan Chen, Nicholas B Larson
Frontiers in Genetics
|
October 24, 2022
Recent advances and challenges of rare variant association analysis in the biobank sequencing era
Wenan Chen, Brandon J Coombes, Nicholas B Larson
Cancers
|
June 28, 2023
Deep Learning in Different Ultrasound Methods for Breast Cancer, from Diagnosis to Prognosis: Current Trends, Challenges, and an Analysis
Humayra Afrin, Nicholas B Larson, Mostafa Fatemi, et al.
IEEE Transactions on Bio-Medical Engineering
|
November 22, 2021
Non-Invasive Measurement of the Internal Pressure of a Pressurized Biological Compartment Using Lamb Waves
David P Rosen, Nicholas B Larson, Azra Alizad, et al.
Scientific Reports
|
July 8, 2025
Quantitative microvessel orientation biomarkers derived from contrast free ultrasound imaging for cancer diagnosis
Pradeep Kumar Chaudhary, Nicholas B Larson, Azra Alizad, et al.
Page
of 17
Search research articles
Search
Showing results (1-10 of 166) with videos related to
Sort By:
Page
of 17
Scientific Reports
|
December 6, 2025
Reproducibility of digital pathology features extracted from deep learning and foundational AI models on sequential tissue slides
Jagadheshwar Balan, Nicholas B Larson
Genetic Epidemiology
|
July 23, 2013
A kernel regression approach to gene-gene interaction detection for case-control studies
Nicholas B Larson, Daniel J Schaid
Genetic Epidemiology
|
January 3, 2014
Regularized rare variant enrichment analysis for case-control exome sequencing data
Nicholas B Larson, Daniel J Schaid
Bioinformatics (Oxford, England)
|
June 11, 2013
PurBayes: estimating tumor cellularity and subclonality in next-generation sequencing data
Nicholas B Larson, Brooke L Fridley
Genetic Epidemiology
|
January 4, 2019
A review of kernel methods for genetic association studies
Nicholas B Larson, Jun Chen, Daniel J Schaid
Nature Reviews. Genetics
|
May 31, 2018
From genome-wide associations to candidate causal variants by statistical fine-mapping
Daniel J Schaid, Wenan Chen, Nicholas B Larson
Frontiers in Genetics
|
October 24, 2022
Recent advances and challenges of rare variant association analysis in the biobank sequencing era
Wenan Chen, Brandon J Coombes, Nicholas B Larson
Cancers
|
June 28, 2023
Deep Learning in Different Ultrasound Methods for Breast Cancer, from Diagnosis to Prognosis: Current Trends, Challenges, and an Analysis
Humayra Afrin, Nicholas B Larson, Mostafa Fatemi, et al.
IEEE Transactions on Bio-Medical Engineering
|
November 22, 2021
Non-Invasive Measurement of the Internal Pressure of a Pressurized Biological Compartment Using Lamb Waves
David P Rosen, Nicholas B Larson, Azra Alizad, et al.
Scientific Reports
|
July 8, 2025
Quantitative microvessel orientation biomarkers derived from contrast free ultrasound imaging for cancer diagnosis
Pradeep Kumar Chaudhary, Nicholas B Larson, Azra Alizad, et al.
Page
of 17