Andrew G. Clark
Molecular Biology · Nature · 2001–2020
A researcher in the Science corpus: 23 papers; trusts 10 researchers and is trusted by 6 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 312 citations into it; #11,105 of 17,773 by trust here, #395 by citations
- Genetics — 201 citations into it; #2,560 of 6,854 by trust here, #53 by citations
- Plant Science — 63 citations into it
- Computational Biology & Bioinformatics — 15 citations into it
Whom Andrew G. Clark trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Andrew G. Clark overall
- Huaiyu Mi
- James R. Brown
- Paul D. Thomas
- Steven Pinker
- Dapeng Wang
- H. Hoekstra
- Matthieu Foll
- Rasmus Nielsen
- Anushya Muruganujan
- Simon Gravel
Papers from Andrew G. Clark's perspective
Ordered by how strongly the researchers Andrew G. Clark trusts endorse each paper. Same corpus, a different order for every researcher.
- Automated de novo identification of repeat sequence families in sequenced genomes. (Genome Research)
- CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice.
- The Human Gene Mutation Database: 2008 update
- Removing near-neighbour redundancy from large protein sequence collections
- Exome sequencing as a tool for Mendelian disease gene discovery
- Repbase Update, a database of repetitive elements in eukaryotic genomes (Mobile DNA)
- Genotype Imputation with Thousands of Genomes (G3: Genes, Genomes, Genetics)
- Generating samples under a Wright-Fisher neutral model of genetic variation (Bioinform.)
- Inaugural Article: Bayesian Markov chain Monte Carlo sequence analysis reveals varying neutral substitution patterns in mammalian evolution
- MAFFT: a novel method for rapid multiple sequence alignment based on fast Fourier transform.
Their papers
- A global reference for human genetic variation (2015) — 16,925 citations
- The Sequence of the Human Genome (2001) — 6,774 citations
- Human genetics shape the gut microbiome. (2014) — 2,776 citations
- Discovery of functional elements in 12 Drosophila genomes using evolutionary signatures (2007) — 657 citations
- The Genome Sequence of the Malaria Mosquito Anopheles gambiae (2002) — 2,077 citations
- Inferring Nonneutral Evolution from Human-Chimp-Mouse Orthologous Gene Trios (2003) — 648 citations
- A Scan for Positively Selected Genes in the Genomes of Humans and Chimpanzees (2005) — 972 citations
- Natural selection on protein-coding genes in the human genome (2005) — 803 citations
- Genomic scans for selective sweeps using SNP data. (2005) — 1,022 citations
- Assessing the Evolutionary Impact of Amino Acid Mutations in the Human Genome (2008) — 675 citations
- Natural selection shaped regional mtDNA variation in humans (2002) — 1,017 citations
- RepeatModeler2: automated genomic discovery of transposable element families (2019) — 1,040 citations
- Evolutionary changes in cis and trans gene regulation (2004) — 892 citations
- Host genetic variation impacts microbiome composition across human body sites (2015) — 700 citations
- Genetic determinants of the gut microbiome in UK Twins (2016) — 960 citations
- RepeatModeler2 for automated genomic discovery of transposable element families (2020) — 2,373 citations
- Estimating Mutation Load in Human Genomes (2015) — 256 citations
- Recent Explosive Human Population Growth Has Resulted in an Excess of Rare Genetic Variants (2012) — 583 citations
- An integrated map of genetic variation from 1,092 human genomes (2012) — 8,008 citations
- Demographic history and rare allele sharing among human populations (2011) — 660 citations