Ryan Poplin
Publications by Year
Research Areas
Genomics and Rare Diseases, Genetic Associations and Epidemiology, Genomics and Phylogenetic Studies, Genomic variations and chromosomal abnormalities, Nutrition, Genetics, and Disease
Most-Cited Works
- → A framework for variation discovery and genotyping using next-generation DNA sequencing data(2011)12,238 cited
- → Analysis of protein-coding genetic variation in 60,706 humans(2016)10,241 cited
- → From FastQ Data to High‐Confidence Variant Calls: The Genome Analysis Toolkit Best Practices Pipeline(2013)7,117 cited
- → Scaling accurate genetic variant discovery to tens of thousands of samples(2017)2,070 cited
- → Patterns and rates of exonic de novo mutations in autism spectrum disorders(2012)1,788 cited
- → A universal SNP and small-indel variant caller using deep neural networks(2018)1,786 cited
- → Prediction of cardiovascular risk factors from retinal fundus photographs via deep learning(2018)1,761 cited
- → In Silico Labeling: Predicting Fluorescent Labels in Unlabeled Images(2018)671 cited
- → Identifying viruses from metagenomic data using deep learning(2020)651 cited
- → Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel(2014)452 cited