M. Chaffin
Genetics · Nature · 2017–2023
A researcher in the Science corpus: 7 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 94 citations into it
Whom M. Chaffin trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Papers from M. Chaffin's perspective
Ordered by how strongly the researchers M. Chaffin trusts endorse each paper. Same corpus, a different order for every researcher.
- Automatic differentiation in PyTorch
- Massively parallel digital transcriptional profiling of single cells
- Large-scale simultaneous measurement of epitopes and transcriptomes in single cells
- Integrating single-cell transcriptomic data across different conditions, technologies, and species
- Comprehensive integration of single-cell data (bioRxiv)
- AUTO-ENCODING VARIATIONAL BAYES
- Bayesian Inference for a Generative Model of Transcriptome Profiles from Single-cell RNA Sequencing
- Single-cell RNA-seq denoising using a deep count autoencoder (Nature Communications)
- SCANPY: large-scale single-cell gene expression data analysis
- PyTorch: An Imperative Style, High-Performance Deep Learning Library
Their papers
- Transfer learning enables predictions in network biology (2023) — 1,094 citations
- Genome-wide polygenic score to identify a monogenic risk-equivalent for coronary disease (2017) — 34 citations
- Polygenic prediction of weight and obesity trajectories from birth to adulthood (2019) — 657 citations
- Unsupervised removal of systematic background noise from droplet-based single-cell experiments using CellBender (2019) — 712 citations
- Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations (2018) — 2,683 citations
- Multi-Ethnic Genome-wide Association Study for Atrial Fibrillation (2018) — 699 citations
- Analysis of predicted loss-of-function variants in UK Biobank identifies variants protective for disease (2018) — 80 citations