Nicolas C. Rochette
Molecular Biology · 2017–2019
A researcher in the Science corpus: 2 papers; trusts 25 researchers and is trusted by 2 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 41 citations into it; #12,501 of 17,773 by trust here, #17,476 by citations
- Genetics — 37 citations into it; #4,477 of 6,854 by trust here, #6,768 by citations
- Plant Science — 13 citations into it
Whom Nicolas C. Rochette trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- J. Ross-Ibarra
- Julian Catchen
- Heng Li
- Erik P. Garrison
- P. Meirmans
- Paul A Hohenlohe
- Thorfinn Sand Korneliussen
- Gabor T. Marth
- Sharon R. Browning
- J. Paris
Who trusts Nicolas C. Rochette overall
Papers from Nicolas C. Rochette's perspective
Ordered by how strongly the researchers Nicolas C. Rochette trusts endorse each paper. Same corpus, a different order for every researcher.
- The Sequence Alignment/Map format and SAMtools (Bioinform.)
- A framework for variation discovery and genotyping using next-generation DNA sequencing data
- The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. (Genome Research)
- Velvet: algorithms for de novo short read assembly using de Bruijn graphs.
- Population Genomics of Parallel Adaptation in Threespine Stickleback using Sequenced RAD Tags (PLoS Genetics)
- Stacks: Building and Genotyping Loci De Novo From Short-Read Sequences (G3: Genes, Genomes, Genetics)
- Genome-wide genetic marker discovery and genotyping using next-generation sequencing (Nature reviews genetics)
- A statistical framework for SNP calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data (Bioinform.)
- Double Digest RADseq: An Inexpensive Method for De Novo SNP Discovery and Genotyping in Model and Non-Model Species (PLoS ONE)
- Fast gapped-read alignment with Bowtie 2
Their papers
- Deriving genotypes from RAD-seq short-read data using Stacks (2017) — 439 citations
- Stacks 2: Analytical Methods for Paired-end Sequencing Improve RADseq-based Population Genomics (2019) — 1,064 citations