Ryan Poplin
Molecular Biology · 2011–2025
A researcher in the Science corpus: 15 papers; trusts 16 researchers and is trusted by 1 researcher here, as inferred from the citation graph.
Subfields
- Molecular Biology — 172 citations into it; #17,325 of 17,773 by trust here, #627 by citations
- Artificial Intelligence — 76 citations into it
- Computer Vision and Pattern Recognition — 48 citations into it; #21,415 of 21,575 by trust here, #8,205 by citations
- Computational Biology & Bioinformatics — 26 citations into it
- Ecology — 22 citations into it
- Model Architectures — 18 citations into it
- Safety, Robustness & Interpretability — 17 citations into it; #2,234 of 2,251 by trust here, #1,205 by citations
Whom Ryan Poplin trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Heng Li
- Erik P. Garrison
- Richard Durbin
- Christian Szegedy
- Alex Krizhevsky
- Geoffrey E. Hinton
- Diederik P. Kingma
- Gabor T. Marth
- Mark A. DePristo
- Temple F. Smith
Who trusts Ryan Poplin overall
- Raquel Dias
- Arvid Lundervold
- Sara Beery
- Nicolas C. Rochette
- Eric J. Topol
- Wan Zhu
- Joe G. Greener
- Ursula Schmidt-Erfurth
- Ali Torkamani
- Heng Li
Papers from Ryan Poplin's perspective
Ordered by how strongly the researchers Ryan Poplin trusts endorse each paper. Same corpus, a different order for every researcher.
- Deep Residual Learning for Image Recognition (Computer Vision and Pattern Recognition)
- Adam: A Method for Stochastic Optimization (International Conference on Learning Representations)
- ImageNet classification with deep convolutional neural networks
- Long Short-Term Memory
- Gradient-based learning applied to document recognition
- Going deeper with convolutions
- Attention is All you Need (Neural Information Processing Systems)
- ImageNet: A large-scale hierarchical image database
- Dropout: a simple way to prevent neural networks from overfitting
- Learning Multiple Layers of Features from Tiny Images
Their papers
- Likelihood Ratios for Out-of-Distribution Detection (2019) — 840 citations
- A framework for variation discovery and genotyping using next-generation DNA sequencing data (2011) — 11,249 citations
- A global reference for human genetic variation (2015) — 16,925 citations
- From FastQ data to high confidence variant calls: the Genome Analysis Toolkit best practices pipeline (2013) — 6,636 citations
- Creating a universal SNP and small indel variant caller with deep neural networks (2016) — 103 citations
- The genetic architecture of type 2 diabetes (2016) — 1,066 citations
- Scaling accurate genetic variant discovery to tens of thousands of samples (2017) — 1,758 citations
- A deep learning approach to pattern recognition for short DNA sequences (2018) — 59 citations
- Gemini 2.5: Pushing the Frontier with Advanced Reasoning, Multimodality, Long Context, and Next Generation Agentic Capabilities (2025) — 3,609 citations
- Identifying viruses from metagenomic data using deep learning (2020) — 553 citations
- A universal SNP and small-indel variant caller using deep neural networks (2018) — 1,463 citations
- In silico labeling: Predicting fluorescent labels in unlabeled images (2018) — 587 citations
- Predicting Cardiovascular Risk Factors from Retinal Fundus Photographs using Deep Learning (2017) — 1,503 citations
- Patterns and rates of exonic de novo mutations in autism spectrum disorders (2012) — 1,772 citations
- An integrated map of genetic variation from 1,092 human genomes (2012) — 8,008 citations