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Richard Durbin
Názov
Citované v
Citované v
Rok
The sequence alignment/map format and SAMtools
H Li, B Handsaker, A Wysoker, T Fennell, J Ruan, N Homer, G Marth, ...
bioinformatics 25 (16), 2078-2079, 2009
600232009
Fast and accurate short read alignment with Burrows–Wheeler transform
H Li, R Durbin
bioinformatics 25 (14), 1754-1760, 2009
491552009
Initial sequencing and analysis of the human genome
US DOE Joint Genome Institute: Hawkins Trevor 4 Branscomb Elbert 4 Predki ...
nature 409 (6822), 860-921, 2001
314972001
A global reference for human genetic variation
1000 Genomes Project Consortium
Nature 526 (7571), 68, 2015
165322015
The variant call format and VCFtools
P Danecek, A Auton, G Abecasis, CA Albers, E Banks, MA DePristo, ...
Bioinformatics 27 (15), 2156-2158, 2011
146022011
Fast and accurate long-read alignment with Burrows–Wheeler transform
H Li, R Durbin
Bioinformatics 26 (5), 589-595, 2010
126392010
A map of human genome variation from population scale sequencing
1000 Genomes Project Consortium
Nature 467 (7319), 1061, 2010
90452010
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 2012
86342012
The Pfam protein families database
A Bateman, E Birney, L Cerruti, R Durbin, L Etwiller, SR Eddy, ...
Nucleic acids research 30 (1), 276-280, 2002
84172002
Biological sequence analysis: probabilistic models of proteins and nucleic acids
R Durbin, SR Eddy, A Krogh, G Mitchison
Cambridge university press, 1998
82831998
Accurate whole human genome sequencing using reversible terminator chemistry
DR Bentley, S Balasubramanian, HP Swerdlow, GP Smith, J Milton, ...
nature 456 (7218), 53-59, 2008
52352008
Ensembl 2014
P Flicek, MR Amode, D Barrell, K Beal, K Billis, S Brent, D Carvalho-Silva, ...
Nucleic acids research 42 (D1), D749-D755, 2014
4737*2014
Systematic functional analysis of the Caenorhabditis elegans genome using RNAi
RS Kamath, AG Fraser, Y Dong, G Poulin, R Durbin, M Gotta, A Kanapin, ...
Nature 421 (6920), 231-237, 2003
43132003
Mapping short DNA sequencing reads and calling variants using mapping quality scores
H Li, J Ruan, R Durbin
Genome research 18 (11), 1851-1858, 2008
35452008
A reference panel of 64,976 haplotypes for genotype imputation
Nature genetics 48 (10), 1279-1283, 2016
31652016
Pfam: clans, web tools and services
RD Finn, J Mistry, B Schuster-Böckler, S Griffiths-Jones, V Hollich, ...
Nucleic acids research 34 (suppl_1), D247-D251, 2006
27002006
GeneWise and genomewise
E Birney, M Clamp, R Durbin
Genome research 14 (5), 988-995, 2004
26952004
The complete sequence of a human genome
S Nurk, S Koren, A Rhie, M Rautiainen, AV Bzikadze, A Mikheenko, ...
Science 376 (6588), 44-53, 2022
26112022
Genome sequence of the Brown Norway rat yields insights into mammalian evolution
University of Utah Weiss Robert B. 14 Dunn Diane M. 14, ...
Nature 428 (6982), 493-521, 2004
25642004
Inference of human population history from individual whole-genome sequences
H Li, R Durbin
Nature 475 (7357), 493-496, 2011
25402011
Systém momentálne nemôže vykonať operáciu. Skúste to neskôr.
Články 1–20