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Plos One
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March 29, 2019
Machine learning for patient risk stratification for acute respiratory distress syndrome
Daniel Zeiberg, Tejas Prahlad, Brahmajee K Nallamothu, et al.
Bioinformatics (Oxford, England)
|
September 5, 2020
Classification in biological networks with hypergraphlet kernels
Jose Lugo-Martinez, Daniel Zeiberg, Thomas Gaudelet, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing
|
December 21, 2022
Multi-objective prioritization of genes for high-throughput functional assays towards improved clinical variant classification
Yile Chen, Shantanu Jain, Daniel Zeiberg, et al.
Biorxiv : the Preprint Server for Biology
|
February 27, 2026
Ancestry-specific performance of variant effect predictors in clinical variant classification
Rachel Hoffing, Daniel Zeiberg, Sarah L Stenton, et al.
Biorxiv : the Preprint Server for Biology
|
July 14, 2025
Gene-based calibration of high-throughput functional assays for clinical variant classification
Daniel Zeiberg, Malvika Tejura, Abbye E McEwen, et al.
Biorxiv : the Preprint Server for Biology
|
February 6, 2026
An integrated, scaled approach to resolve TSC2 variants of uncertain significance
Carina G Biar, Ziyu R Wang, Nathan D Camp, et al.
Nucleic Acids Research
|
December 8, 2025
The IGVF catalog-from genetic variation to function
Daofeng Li, Shane Liu, Pedro R Assis, et al.
Human Genetics
|
March 7, 2025
Evaluation of enzyme activity predictions for variants of unknown significance in Arylsulfatase A
Shantanu Jain, Marena Trinidad, Thanh Binh Nguyen, et al.
Biorxiv : the Preprint Server for Biology
|
May 27, 2024
Evaluation of enzyme activity predictions for variants of unknown significance in Arylsulfatase A
Shantanu Jain, Marena Trinidad, Thanh Binh Nguyen, et al.
Medrxiv : the Preprint Server for Health Sciences
|
August 14, 2023
Critical assessment of variant prioritization methods for rare disease diagnosis within the Rare Genomes Project
Sarah L Stenton, Melanie O'Leary, Gabrielle Lemire, et al.
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of 2
Search research articles
Search
Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 2
Plos One
|
March 29, 2019
Machine learning for patient risk stratification for acute respiratory distress syndrome
Daniel Zeiberg, Tejas Prahlad, Brahmajee K Nallamothu, et al.
Bioinformatics (Oxford, England)
|
September 5, 2020
Classification in biological networks with hypergraphlet kernels
Jose Lugo-Martinez, Daniel Zeiberg, Thomas Gaudelet, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing
|
December 21, 2022
Multi-objective prioritization of genes for high-throughput functional assays towards improved clinical variant classification
Yile Chen, Shantanu Jain, Daniel Zeiberg, et al.
Biorxiv : the Preprint Server for Biology
|
February 27, 2026
Ancestry-specific performance of variant effect predictors in clinical variant classification
Rachel Hoffing, Daniel Zeiberg, Sarah L Stenton, et al.
Biorxiv : the Preprint Server for Biology
|
July 14, 2025
Gene-based calibration of high-throughput functional assays for clinical variant classification
Daniel Zeiberg, Malvika Tejura, Abbye E McEwen, et al.
Biorxiv : the Preprint Server for Biology
|
February 6, 2026
An integrated, scaled approach to resolve TSC2 variants of uncertain significance
Carina G Biar, Ziyu R Wang, Nathan D Camp, et al.
Nucleic Acids Research
|
December 8, 2025
The IGVF catalog-from genetic variation to function
Daofeng Li, Shane Liu, Pedro R Assis, et al.
Human Genetics
|
March 7, 2025
Evaluation of enzyme activity predictions for variants of unknown significance in Arylsulfatase A
Shantanu Jain, Marena Trinidad, Thanh Binh Nguyen, et al.
Biorxiv : the Preprint Server for Biology
|
May 27, 2024
Evaluation of enzyme activity predictions for variants of unknown significance in Arylsulfatase A
Shantanu Jain, Marena Trinidad, Thanh Binh Nguyen, et al.
Medrxiv : the Preprint Server for Health Sciences
|
August 14, 2023
Critical assessment of variant prioritization methods for rare disease diagnosis within the Rare Genomes Project
Sarah L Stenton, Melanie O'Leary, Gabrielle Lemire, et al.
Page
of 2