2019 - Fellow of the American Academy of Arts and Sciences
2004 - Fellow of the Royal Society, United Kingdom
Richard Durbin mainly investigates Genetics, Genome, Genomics, Computational biology and Human genome. His studies examine the connections between Genetics and genetics, as well as such issues in Evolutionary biology, with regards to Population genetics. His Genome research integrates issues from Sequence analysis and Sequence assembly.
His Genomics research includes themes of Exome sequencing, Exome, Genetic variation and 1000 Genomes Project. He has included themes like Genome resequencing and Variant Call Format in his Exome study. The various areas that Richard Durbin examines in his Hybrid genome assembly study include 2 base encoding and Paired-end tag.
Genetics, Genome, Computational biology, Evolutionary biology and Genomics are his primary areas of study. The study incorporates disciplines such as Sequence analysis, Haplotype and Sequence assembly in addition to Genome. His studies in Computational biology integrate themes in fields like Genome project, Contig, Sequence alignment, Annotation and 1000 Genomes Project.
Richard Durbin interconnects Indel and Graph in the investigation of issues within 1000 Genomes Project. His research investigates the connection between Evolutionary biology and topics such as Denisovan that intersect with problems in Neanderthal. The Genomics study combines topics in areas such as Exome and Caenorhabditis elegans.
Richard Durbin mostly deals with Genome, Evolutionary biology, Computational biology, Sequence assembly and Haplotype. The Genome study which covers Consensus sequence that intersects with Genetic diversity. His research in Computational biology intersects with topics in Proteome, Genetic variants and Ploidy.
Richard Durbin has researched Sequence assembly in several fields, including Comparative genomics and Whole genome sequencing. His Haplotype study combines topics in areas such as Theoretical computer science, Loss of heterozygosity, 1000 Genomes Project, Graph and Search engine indexing. His study in Genomics focuses on Population genomics in particular.
Richard Durbin spends much of his time researching Genome, Evolutionary biology, Neanderthal, Haplotype and Computational biology. His Genome study incorporates themes from Contiguity and DNA. His Evolutionary biology study also includes fields such as
His Haplotype research incorporates themes from Search engine indexing, 1000 Genomes Project, Reference genome, Graph and Focus. His Reference genome research is multidisciplinary, incorporating perspectives in Comparative genomics and Sequence assembly. His Whole genome sequencing study integrates concerns from other disciplines, such as Scalability, Theoretical computer science, Human genome and DNA sequencing.
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Fast and accurate short read alignment with Burrows–Wheeler transform
Heng Li;Richard Durbin.
Bioinformatics (2009)
The Sequence Alignment/Map format and SAMtools
Heng Li;Bob Handsaker;Alec Wysoker;Tim Fennell.
Bioinformatics (2009)
Initial sequencing and analysis of the human genome.
Eric S. Lander;Lauren M. Linton;Bruce Birren;Chad Nusbaum.
Nature (2001)
An integrated map of genetic variation from 1,092 human genomes
Goncalo R Abecasis;Adam Auton;Lisa D Brooks.
Nature (2012)
A global reference for human genetic variation.
Adam Auton;Gonçalo R. Abecasis;David M. Altshuler;Richard M. Durbin.
(2015)
Biological Sequence Analysis: Probabilistic Models of Proteins and Nucleic Acids
Richard Durbin;Sean Eddy;Anders Stærmose Krogh;Graeme Mitchison.
(1998)
The variant call format and VCFtools
Petr Danecek;Adam Auton;Goncalo Abecasis;Cornelis A. Albers.
Bioinformatics (2011)
A Map of Human Genome Variation From Population-Scale Sequencing
Gonçalo R Abecasis;David Altshuler;David Altshuler;Adam Auton.
Nature (2010)
Accurate whole human genome sequencing using reversible terminator chemistry
David R. Bentley;Shankar Balasubramanian;Harold P. Swerdlow;Harold P. Swerdlow;Geoffrey P. Smith.
Nature (2008)
Systematic functional analysis of the Caenorhabditis elegans genome using RNAi
Ravi S. Kamath;Andrew G. Fraser;Andrew G. Fraser;Yan Dong;Gino Poulin.
Nature (2003)
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