Benedict Paten
Molecular Biology · 2007–2022
A researcher in the Science corpus: 33 papers; trusts 25 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 881 citations into it
- Genetics — 368 citations into it
- Plant Science — 225 citations into it
- Artificial Intelligence — 87 citations into it
- Ecology — 57 citations into it
- Computational Biology & Bioinformatics — 55 citations into it
- Privacy & Security — 10 citations into it
- Safety, Robustness & Interpretability — 9 citations into it
Whom Benedict Paten trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Heng Li
- Richard Durbin
- Pavel A. Pevzner
- Daniel R. Zerbino
- Cynthia Dwork
- W. James Kent
- Na Li
- Stephen F. Altschul
- Alkes L Price
- Cédric Notredame
Who trusts Benedict Paten overall
- Aaron E. Darling
- Paul Flicek
- Jeanne Chèneby
- Martin Kircher
- Miten Jain
- Javier Herrero
- Kathryn M Beal
- Matthieu Muffato
- Bob Mau
- Andrew D. Yates
Papers from Benedict Paten's perspective
Ordered by how strongly the researchers Benedict Paten trusts endorse each paper. Same corpus, a different order for every researcher.
- ImageNet classification with deep convolutional neural networks
- Deep Residual Learning for Image Recognition (Computer Vision and Pattern Recognition)
- GENERATIVE ADVERSARIAL NETS
- Gradient-based learning applied to document recognition
- Adam: A Method for Stochastic Optimization (International Conference on Learning Representations)
- Learning Multiple Layers of Features from Tiny Images
- Long Short-Term Memory
- CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice.
- Delving Deep into Rectifiers: Surpassing Human-Level Performance on ImageNet Classification
- Human-level control through deep reinforcement learning
Their papers
- Enredo and Pecan: genome-wide mammalian consistency-based multiple alignment with paralogs. (2008) — 344 citations
- DP-CGAN: Differentially Private Synthetic Data and Label Generation (2019) — 282 citations
- Nanopore sequencing and assembly of a human genome with ultra-long reads (2017) — 1,714 citations
- Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project (2007) — 5,374 citations
- The UCSC Genome Browser database: 2015 update (2014) — 993 citations
- The UCSC Genome Browser Database: 2008 update (2007) — 560 citations
- Assemblathon 2: evaluating de novo methods of genome assembly in three vertebrate species (2013) — 725 citations
- Assemblathon 1: a competitive assessment of de novo short read assembly methods. (2011) — 544 citations
- Variation graph toolkit improves read mapping by representing genetic variation in the reference (2018) — 681 citations
- Discovery of functional elements in 12 Drosophila genomes using evolutionary signatures (2007) — 657 citations
- Towards complete and error-free genome assemblies of all vertebrate species (2020) — 2,673 citations
- Track data hubs enable visualization of user-defined genome-wide annotations on the UCSC Genome Browser (2013) — 406 citations
- Progressive Cactus is a multiple-genome aligner for the thousand-genome era (2020) — 445 citations
- Toil enables reproducible, open source, big biomedical data analyses (2017) — 1,154 citations
- The Human Pangenome Project: a global resource to map genomic diversity (2022) — 392 citations
- Genome graphs and the evolution of genome inference (2017) — 314 citations
- Pangenomics enables genotyping known structural variants in 5,202 diverse genomes (2021) — 309 citations
- Genetic effects on gene expression across human tissues (2017) — 3,717 citations
- Nanopore sequencing and the Shasta toolkit enable efficient de novo assembly of eleven human genomes (2020) — 428 citations
- The Genome 10K Project: A Way Forward (2015) — 312 citations