Search research articles
Contact Us
Filters
Showing results (1-10 of 20) with videos related to
Page
of 2
Sort By:
JAMA
|
July 20, 2021
Challenges of Accuracy in Germline Clinical Sequencing Data
Ryan Poplin, Justin M Zook, Mark DePristo
Bioinformatics (Oxford, England)
|
March 28, 2019
GenomeWarp: an alignment-based variant coordinate transformation
Cory Y McLean, Yeongwoo Hwang, Ryan Poplin, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing
|
March 14, 2019
CrowdVariant: a crowdsourcing approach to classify copy number variants
Peyton Greenside, Justin Zook, Marc Salit, et al.
Nature Biomedical Engineering
|
April 25, 2019
Prediction of cardiovascular risk factors from retinal fundus photographs via deep learning
Ryan Poplin, Avinash V Varadarajan, Katy Blumer, et al.
Quantitative Biology (Beijing, China)
|
June 4, 2021
Identifying viruses from metagenomic data using deep learning
Jie Ren, Kai Song, Chao Deng, et al.
BMC Genomics
|
March 14, 2015
The distribution and mutagenesis of short coding INDELs from 1,128 whole exomes
Danny Challis, Lilian Antunes, Erik Garrison, et al.
Investigative Ophthalmology & Visual Science
|
July 20, 2018
Deep Learning for Predicting Refractive Error From Retinal Fundus Images
Avinash V Varadarajan, Ryan Poplin, Katy Blumer, et al.
ACS Synthetic Biology
|
November 5, 2021
Evolution of Functionally Enhanced α-l-Threofuranosyl Nucleic Acid Aptamers
Cailen M McCloskey, Qingfeng Li, Eric J Yik, et al.
Nature Biotechnology
|
September 25, 2018
A universal SNP and small-indel variant caller using deep neural networks
Ryan Poplin, Pi-Chuan Chang, David Alexander, et al.
Current Protocols in Bioinformatics
|
November 29, 2014
From FastQ data to high confidence variant calls: the Genome Analysis Toolkit best practices pipeline
Geraldine A Van der Auwera, Mauricio O Carneiro, Christopher Hartl, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 20) with videos related to
Sort By:
Page
of 2
JAMA
|
July 20, 2021
Challenges of Accuracy in Germline Clinical Sequencing Data
Ryan Poplin, Justin M Zook, Mark DePristo
Bioinformatics (Oxford, England)
|
March 28, 2019
GenomeWarp: an alignment-based variant coordinate transformation
Cory Y McLean, Yeongwoo Hwang, Ryan Poplin, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing
|
March 14, 2019
CrowdVariant: a crowdsourcing approach to classify copy number variants
Peyton Greenside, Justin Zook, Marc Salit, et al.
Nature Biomedical Engineering
|
April 25, 2019
Prediction of cardiovascular risk factors from retinal fundus photographs via deep learning
Ryan Poplin, Avinash V Varadarajan, Katy Blumer, et al.
Quantitative Biology (Beijing, China)
|
June 4, 2021
Identifying viruses from metagenomic data using deep learning
Jie Ren, Kai Song, Chao Deng, et al.
BMC Genomics
|
March 14, 2015
The distribution and mutagenesis of short coding INDELs from 1,128 whole exomes
Danny Challis, Lilian Antunes, Erik Garrison, et al.
Investigative Ophthalmology & Visual Science
|
July 20, 2018
Deep Learning for Predicting Refractive Error From Retinal Fundus Images
Avinash V Varadarajan, Ryan Poplin, Katy Blumer, et al.
ACS Synthetic Biology
|
November 5, 2021
Evolution of Functionally Enhanced α-l-Threofuranosyl Nucleic Acid Aptamers
Cailen M McCloskey, Qingfeng Li, Eric J Yik, et al.
Nature Biotechnology
|
September 25, 2018
A universal SNP and small-indel variant caller using deep neural networks
Ryan Poplin, Pi-Chuan Chang, David Alexander, et al.
Current Protocols in Bioinformatics
|
November 29, 2014
From FastQ data to high confidence variant calls: the Genome Analysis Toolkit best practices pipeline
Geraldine A Van der Auwera, Mauricio O Carneiro, Christopher Hartl, et al.
Page
of 2