R
René L. Warren
Researcher at BC Cancer Agency
Publications - 121
Citations - 10250
René L. Warren is an academic researcher from BC Cancer Agency. The author has contributed to research in topics: Sequence assembly & Genome. The author has an hindex of 35, co-authored 98 publications receiving 8639 citations. Previous affiliations of René L. Warren include BC Cancer Research Centre & McGill University.
Papers
More filters
Journal ArticleDOI
Improved white spruce (Picea glauca) genome assemblies and annotation of large gene families of conifer terpenoid and phenolic defense metabolism.
René L. Warren,Christopher I. Keeling,Macaire M.S. Yuen,Anthony Raymond,Greg Taylor,Benjamin P. Vandervalk,Hamid Mohamadi,Daniel Paulino,Readman Chiu,Shaun D. Jackman,Gordon Robertson,Chen Yang,Brian Boyle,Margarete Hoffmann,Detlef Weigel,David R. Nelson,Carol Ritland,Nathalie Isabel,Barry Jaquish,Alvin D. Yanchuk,Jean Bousquet,Steven J.M. Jones,Steven J.M. Jones,John MacKay,John MacKay,Inanc Birol,Inanc Birol,Joerg Bohlmann +27 more
TL;DR: These analyses highlighted the large extent of gene and pseudogene duplications in a conifer genome, in particular for genes of secondary (i.e. specialized) metabolism, and the potential for gain and loss of function for defense and adaptation.
Journal ArticleDOI
Derivation of HLA types from shotgun sequence datasets
René L. Warren,Gina Choe,Douglas J Freeman,Mauro Castellarin,Sarah Munro,Richard A. Moore,Robert A. Holt,Robert A. Holt +7 more
TL;DR: HLAminer, a computational method for identifying HLA alleles directly from shotgun sequence datasets that circumvents the additional time and cost of generating HLA-specific data and capitalizes on the increasing accessibility and affordability of massively parallel sequencing.
Journal ArticleDOI
NanoSim: nanopore sequence read simulator based on statistical characterization.
TL;DR: NanoSim is introduced, a fast and scalable read simulator that captures the technology-specific features of ONT data and allows for adjustments upon improvement of nanopore sequencing technology and is expected to have an enabling role in the field and benefit the development of scalable next-generation sequencing technologies for the long nanopore reads.
Journal ArticleDOI
ARCS: scaffolding genome drafts with linked reads.
TL;DR: ARCS is presented, an application that utilizes the barcoding information contained in linked reads to further organize draft genomes into highly contiguous assemblies and is expected to have broad utility in harnessing the barCoding informationcontained in linked read data for connecting high‐quality sequences in genome assembly drafts.
Journal ArticleDOI
Sealer: a scalable gap-closing application for finishing draft genomes
Daniel Paulino,René L. Warren,Benjamin P. Vandervalk,Anthony Raymond,Shaun D. Jackman,Inanc Birol,Inanc Birol +6 more
TL;DR: Sealer is an automated finishing application that uses the succinct Bloom filter representation of a de Bruijn graph to close gaps in draft assemblies, including that of very large genomes, to have broad utility for finishing genomes across the tree of life.