A. Amores
Genetics · 2007–2013
A researcher in the Science corpus: 3 papers; trusts 6 researchers and is trusted by 9 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 33 citations into it; #1,271 of 6,854 by trust here, #1,692 by citations
- Molecular Biology — 33 citations into it; #4,583 of 17,773 by trust here, #9,367 by citations
Whom A. Amores trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Paul A Hohenlohe
- Daniel R. Zerbino
- Daniel Falush
- Susana Vinga
- Heng Li
- J. K. Pritchard
- David R. Kelley
- Matthew Stephens
- François Rousset
- Karl W. Broman
Who trusts A. Amores overall
- Deren A. R. Eaton
- Nicolas C. Rochette
- Julian Catchen
- M. Thomson
- J. Paris
- J. Davey
- Paul A Hohenlohe
- Adam D. Leaché
Papers from A. Amores's perspective
Ordered by how strongly the researchers A. Amores 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)
- Gapped BLAST and PSI-BLAST: a new generation of protein database search programs.
- Velvet: algorithms for de novo short read assembly using de Bruijn graphs.
- Ultrafast and memory-efficient alignment of short DNA sequences to the human genome (Genome Biology)
- The impact of next-generation sequencing technology on genetics. (Trends in Genetics)
- Next-generation DNA sequencing (Nature Biotechnology)
- Inference of population structure using multilocus genotype data: linked loci and correlated allele frequencies. (Genetics)
- Inference of population structure using multilocus genotype data: dominant markers and null alleles (Molecular Ecology Notes)
- The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. (Genome Research)
Their papers
- 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
- Rapid and cost-effective polymorphism identification and genotyping using restriction site associated DNA (RAD) markers. (2007) — 979 citations