Paul Flicek
Paul Flicek
EMBL, European Bioinformatics Institute, Wellcome Sanger Institute
ebi.ac.uk üzerinde doğrulanmış e-posta adresine sahip
Başlık
Alıntı yapanlar
Alıntı yapanlar
Yıl
An integrated encyclopedia of DNA elements in the human genome
ENCODE Project Consortium
Nature 489 (7414), 57, 2012
119312012
A global reference for human genetic variation
1000 Genomes Project Consortium
Nature 526 (7571), 68, 2015
7952*2015
Initial sequencing and comparative analysis of the mouse genome
RH Waterston, L Pachter
Nature 420 (6915), 520-562, 2002
74102002
A map of human genome variation from population-scale sequencing
1000 Genomes Project Consortium
Nature 467 (7319), 1061, 2010
73992010
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 2012
69522012
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project
ENCODE Project Consortium
nature 447 (7146), 799, 2007
52912007
The NHGRI GWAS Catalog, a curated resource of SNP-trait associations
D Welter, J MacArthur, J Morales, T Burdett, P Hall, H Junkins, A Klemm, ...
Nucleic acids research 42 (D1), D1001-D1006, 2014
27462014
The ensembl variant effect predictor
W McLaren, L Gil, SE Hunt, HS Riat, GRS Ritchie, A Thormann, P Flicek, ...
Genome biology 17 (1), 1-14, 2016
26042016
Sequence and comparative analysis of the chicken genome provide unique perspectives on vertebrate evolution
LDW Hillier, W Miller, E Birney, W Warren, RC Hardison, CP Ponting, ...
Nature 432 (7018), 695-716, 2004
24382004
Ensembl 2018
DR Zerbino, P Achuthan, W Akanni, MR Amode, D Barrell, J Bhai, K Billis, ...
Nucleic acids research 46 (D1), D754-D761, 2018
21382018
International network of cancer genome projects
International Cancer Genome Consortium
Nature 464 (7291), 993, 2010
17732010
Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor
W McLaren, B Pritchard, D Rios, Y Chen, P Flicek, F Cunningham
Bioinformatics 26 (16), 2069-2070, 2010
15862010
Ensembl 2015
F Cunningham, MR Amode, D Barrell, K Beal, K Billis, S Brent, ...
Nucleic acids research 43 (D1), D662-D669, 2015
15792015
Transcriptome and genome sequencing uncovers functional variation in humans
T Lappalainen, M Sammeth, MR Friedländer, P Ac‘t Hoen, J Monlong, ...
Nature 501 (7468), 506-511, 2013
15572013
The new NHGRI-EBI Catalog of published genome-wide association studies (GWAS Catalog)
J MacArthur, E Bowler, M Cerezo, L Gil, P Hall, E Hastings, H Junkins, ...
Nucleic acids research 45 (D1), D896-D901, 2017
15312017
The IPD and IMGT/HLA database: allele variant databases
J Robinson, JA Halliwell, JD Hayhurst, P Flicek, P Parham, SGE Marsh
Nucleic acids research 43 (D1), D423-D431, 2015
15232015
An integrated map of structural variation in 2,504 human genomes
PH Sudmant, T Rausch, EJ Gardner, RE Handsaker, A Abyzov, ...
Nature 526 (7571), 75-81, 2015
14832015
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
14692014
Ensembl 2016
A Yates, W Akanni, MR Amode, D Barrell, K Billis, D Carvalho-Silva, ...
Nucleic acids research 44 (D1), D710-D716, 2016
14272016
A comparative encyclopedia of DNA elements in the mouse genome
F Yue, Y Cheng, A Breschi, J Vierstra, W Wu, T Ryba, R Sandstrom, Z Ma, ...
Nature 515 (7527), 355-364, 2014
14152014
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Makaleler 1–20