Erik P. Garrison
Molecular Biology · 2012–2022
A researcher in the Science corpus: 9 papers; trusts 17 researchers and is trusted by 14 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 162 citations into it; #2,316 of 17,773 by trust here, #1,376 by citations
- Genetics — 126 citations into it
- Artificial Intelligence — 15 citations into it
- Computational Biology & Bioinformatics — 8 citations into it
Whom Erik P. Garrison trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Heng Li
- Richard Maclin
- Bryan N. Howie
- Yun Li
- James Clarke
- Jonathan Marchini
- David W. Opitz
- Mark A. DePristo
- Temple F. Smith
- Gonçalo R. Abecasis
Who trusts Erik P. Garrison overall
- Nicolas C. Rochette
- Heng Li
- Daniel C. Koboldt
- Raquel Dias
- Ryan Poplin
- Arang Rhie
- Julian Catchen
- Todd J. Treangen
- Sergey Koren
- Ali Torkamani
Papers from Erik P. Garrison's perspective
Ordered by how strongly the researchers Erik P. Garrison trusts endorse each paper. Same corpus, a different order for every researcher.
- Exome sequencing as a tool for Mendelian disease gene discovery
- A framework for variation discovery and genotyping using next-generation DNA sequencing data
- The Human Gene Mutation Database: 2008 update
- Identification of common molecular subsequences.
- Genotype Imputation with Thousands of Genomes (G3: Genes, Genomes, Genetics)
- The Diploid Genome Sequence of an Individual Human (PLoS Biology)
- MaCH: Using Sequence and Genotype Data to Estimate Haplotypes and Unobserved Genotypes (Genetic Epidemiology)
- An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people (Science)
- A statistical framework for SNP calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data (Bioinform.)
- SOAP: short oligonucleotide alignment program (Bioinform.)
Their papers
- A global reference for human genetic variation (2015) — 16,925 citations
- Haplotype-based variant detection from short-read sequencing (2012) — 4,999 citations
- SSW Library: An SIMD Smith-Waterman C/C++ Library for Use in Genomic Applications (2012) — 246 citations
- The Human Pangenome Project: a global resource to map genomic diversity (2022) — 392 citations
- Integrative Annotation of Variants from 1092 Humans: Application to Cancer Genomics (2013) — 370 citations
- MOSAIK: A Hash-Based Algorithm for Accurate Next-Generation Sequencing Short-Read Mapping (2013) — 295 citations
- An integrated map of structural variation in 2,504 human genomes (2015) — 2,247 citations
- SpeedSeq: Ultra-fast personal genome analysis and interpretation (2014) — 544 citations
- An integrated map of genetic variation from 1,092 human genomes (2012) — 8,008 citations