P. Fuentes-Utrilla

Molecular Biology · 2001–2012

A researcher in the Science corpus: 2 papers; trusts 4 researchers and is trusted by 0 researchers here, as inferred from the citation graph.

Subfields

Whom P. Fuentes-Utrilla trusts overall

Their strongest outbound trust, strongest first, inferred from their citations.

  1. Heng Li
  2. J. Davey

Papers from P. Fuentes-Utrilla's perspective

Ordered by how strongly the researchers P. Fuentes-Utrilla trusts endorse each paper. Same corpus, a different order for every researcher.

  1. A framework for variation discovery and genotyping using next-generation DNA sequencing data
  2. A statistical framework for SNP calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data (Bioinform.)
  3. Stacks: Building and Genotyping Loci De Novo From Short-Read Sequences (G3: Genes, Genomes, Genetics)
  4. Rapid SNP Discovery and Genetic Mapping Using Sequenced RAD Markers (PLoS ONE)
  5. A large genome centre’s improvements to the Illumina sequencing system (Nature Methods)
  6. Double Digest RADseq: An Inexpensive Method for De Novo SNP Discovery and Genotyping in Model and Non-Model Species (PLoS ONE)
  7. Genome-wide genetic marker discovery and genotyping using next-generation sequencing (Nature reviews genetics)
  8. SNP DISCOVERY: NEXT GENERATION SEQUENCING Next-generation RAD sequencing identifies thousands of SNPs for assessing hybridization between rainbow and westslope cutthroat trout
  9. Analyzing and minimizing PCR amplification bias in Illumina sequencing libraries (Genome Biology)
  10. De novo assembly of human genomes with massively parallel short read sequencing. (Genome Research)

Their papers