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Author Details

Ryan Poplin
2011
19
14
PMIDPaper TitleJournal TitlePublished Year
34739228Evolution of Functionally Enhanced α-l-Threofuranosyl Nucleic Acid Aptamers.ACS Synthetic Biology2021
34283192Challenges of Accuracy in Germline Clinical Sequencing Data.JAMA2021
34084563Identifying viruses from metagenomic data using deep learning.Quantitative Biology2020
30864325CrowdVariant: a crowdsourcing approach to classify copy number variants.Pac Symp Biocomput2019
30916319GenomeWarp: an alignment-based variant coordinate transformation.2019
29360107Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.Sci Data2018
30025129Deep Learning for Predicting Refractive Error From Retinal Fundus Images.Invest Ophthalmol Vis Sci2018
30247488A universal SNP and small-indel variant caller using deep neural networks.Nature Biotechnology2018
29656897In Silico Labeling: Predicting Fluorescent Labels in Unlabeled Images.Cell2018
29257133Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.Sci Data2017
28341696A Low-Frequency Inactivating <i>AKT2</i> Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk.Diabetes2017
27535533Analysis of protein-coding genetic variation in 60,706 humans.Nature2016
27398621The genetic architecture of type 2 diabetes.Nature2016
25954003Human genomics. Effect of predicted protein-truncating genetic variants on the human transcriptome.Science2015
25765891The distribution and mutagenesis of short coding INDELs from 1,128 whole exomes.BMC Genomics2015
23593035Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controls.PLoS Genet2013
25431634From FastQ data to high confidence variant calls: the Genome Analysis Toolkit best practices pipeline.Curr Protoc Bioinformatics2013
22495311Patterns and rates of exonic de novo mutations in autism spectrum disorders.Nature2012
21478889A framework for variation discovery and genotyping using next-generation DNA sequencing data.Nat Genet2011
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