Eric Banks

bioRxiv · 2010–2023

A researcher in the Science corpus: 23 papers; trusts 1 researcher and is trusted by 3 researchers here, as inferred from the citation graph.

Whom Eric Banks trusts overall

Their strongest outbound trust, strongest first, inferred from their citations.

1. Muthu Dayalan
2. Gerd Kempermann

Who trusts Eric Banks overall

1. Heng Li
2. B. Knaus
3. Daniel C. Koboldt
4. Anton Nekrutenko
5. Todd J. Treangen
6. B. Feng
7. Nicolas C. Rochette
8. Ryan Poplin
9. Hannah Carter
10. Julian Catchen

Papers from Eric Banks's perspective

Ordered by how strongly the researchers Eric Banks trusts endorse each paper. Same corpus, a different order for every researcher.

1. Exome sequencing as a tool for Mendelian disease gene discovery
2. A framework for variation discovery and genotyping using next-generation DNA sequencing data
3. The Human Gene Mutation Database: 2008 update
4. The diploid genome sequence of an Asian individual (Nature)
5. SOAP: short oligonucleotide alignment program (Bioinform.)
6. Identification of common molecular subsequences.
7. An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people (Science)
8. Genotype Imputation with Thousands of Genomes (G3: Genes, Genomes, Genetics)
9. dbSNP: the NCBI database of genetic variation
10. A method and server for predicting damaging missense mutations

Their papers

• A framework for variation discovery and genotyping using next-generation DNA sequencing data (2011) — 11,249 citations
• The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. (2010) — 25,882 citations
• A systematic survey of loss-of-function variants in human protein-coding genes (2012) — 1,227 citations
• The mutational constraint spectrum quantified from variation in 141,456 humans (2020) — 8,441 citations
• From FastQ data to high confidence variant calls: the Genome Analysis Toolkit best practices pipeline (2013) — 6,636 citations
• Tools and best practices for data processing in allelic expression analysis (2015) — 359 citations
• De novo mutations in schizophrenia implicate synaptic networks (2014) — 1,622 citations
• A polygenic burden of rare disruptive mutations in schizophrenia (2014) — 1,469 citations
• The genetic architecture of type 2 diabetes (2016) — 1,066 citations
• Variation across 141,456 human exomes and genomes reveals the spectrum of loss-of-function intolerance across human protein-coding genes (2019) — 1,088 citations
• Scaling accurate genetic variant discovery to tens of thousands of samples (2017) — 1,758 citations
• Discovery and statistical genotyping of copy-number variation from whole-exome sequencing depth. (2012) — 577 citations
• Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals (2019) — 162 citations
• A genomic mutational constraint map using variation in 76,156 human genomes (2023) — 1,228 citations
• A genome-wide mutational constraint map quantified from variation in 76,156 human genomes (2022) — 258 citations
• Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes (2020) — 126 citations
• A structural variation reference for medical and population genetics (2020) — 876 citations
• Evaluating drug targets through human loss-of-function genetic variation (2019) — 168 citations
• An open resource of structural variation for medical and population genetics (2019) — 76 citations
• Unsupervised removal of systematic background noise from droplet-based single-cell experiments using CellBender (2019) — 712 citations