W. Cresko
Genetics · 2007–2013
A researcher in the Science corpus: 5 papers; trusts 9 researchers and is trusted by 19 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 54 citations into it; #678 of 6,854 by trust here, #759 by citations
- Molecular Biology — 46 citations into it; #3,059 of 17,773 by trust here, #4,543 by citations
Whom W. Cresko trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts W. Cresko overall
- Deren A. R. Eaton
- Julian Catchen
- Nicolas C. Rochette
- J. Davey
- Paul A Hohenlohe
- M. Thomson
- J. Paris
- B. E. Rubin
- Adam D. Leaché
Papers from W. Cresko's perspective
Ordered by how strongly the researchers W. Cresko trusts endorse each paper. Same corpus, a different order for every researcher.
- The Sequence Alignment/Map format and SAMtools (Bioinform.)
- Mapping and quantifying mammalian transcriptomes by RNA-Seq (Nature Methods)
- Velvet: algorithms for de novo short read assembly using de Bruijn graphs.
- The power and promise of population genomics: from genotyping to genome typing (Nature reviews genetics)
- Inference of population structure using multilocus genotype data: linked loci and correlated allele frequencies. (Genetics)
- Gapped BLAST and PSI-BLAST: a new generation of protein database search programs.
- The impact of next-generation sequencing technology on genetics. (Trends in Genetics)
- Ultrafast and memory-efficient alignment of short DNA sequences to the human genome (Genome Biology)
- Identifying adaptive genetic divergence among populations from genome scans (Molecular Ecology)
- Next-generation DNA sequencing (Nature Biotechnology)
Their papers
- Rapid SNP Discovery and Genetic Mapping Using Sequenced RAD Markers (2008) — 3,361 citations
- Stacks: Building and Genotyping Loci De Novo From Short-Read Sequences (2011) — 1,963 citations
- Stacks: an analysis tool set for population genomics (2013) — 3,778 citations
- Population Genomics of Parallel Adaptation in Threespine Stickleback using Sequenced RAD Tags (2010) — 1,454 citations
- Rapid and cost-effective polymorphism identification and genotyping using restriction site associated DNA (RAD) markers. (2007) — 979 citations