-
1
-
-
84975742565
-
A map of human genome variation from population-scale sequencing
-
1000 Genomes Project Consortium
-
1000 Genomes Project Consortium (2010) A map of human genome variation from population-scale sequencing. Nature, 467, 1061-1073.
-
(2010)
Nature
, vol.467
, pp. 1061-1073
-
-
-
2
-
-
55549089660
-
Accurate whole human genome sequencing using reversible terminator chemistry
-
Bentley, D.R. et al. (2008) Accurate whole human genome sequencing using reversible terminator chemistry. Nature, 456, 53-59.
-
(2008)
Nature
, vol.456
, pp. 53-59
-
-
Bentley, D.R.1
-
4
-
-
33846528971
-
Draft genome sequence of the sexually transmitted pathogen. Trichomonas vaginalis
-
Carlton, J.M. et al. (2007) Draft genome sequence of the sexually transmitted pathogen. Trichomonas vaginalis. Science, 315, 207-212.
-
(2007)
Science
, vol.315
, pp. 207-212
-
-
Carlton, J.M.1
-
6
-
-
74949138753
-
Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays
-
Drmanac, R. et al. (2010) Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays. Science (New York, N.Y.), 327, 78-81.
-
(2010)
Science (New York, N.Y.)
, vol.327
, pp. 78-81
-
-
Drmanac, R.1
-
7
-
-
7444260846
-
The ENCODE (ENCyclopedia Of DNA Elements) project
-
Encode Project Consortium
-
ENCODE Project Consortium (2004) The ENCODE (ENCyclopedia Of DNA Elements) project. Science, 306, 636-640.
-
(2004)
Science
, vol.306
, pp. 636-640
-
-
-
8
-
-
79956044149
-
Accuracy and quality assessment of 454 GS-FLX Titanium pyrosequencing
-
Gilles, A. et al. (2011) Accuracy and quality assessment of 454 GS-FLX Titanium pyrosequencing. BMC Genom., 12, 245.
-
(2011)
BMC Genom
, vol.12
, pp. 245
-
-
Gilles, A.1
-
9
-
-
84857411659
-
Genomic epidemiology of the Escherichia coli O104:H4 outbreaks in Europe, 2011
-
Grad, Y.H. et al. (2012) Genomic epidemiology of the Escherichia coli O104:H4 outbreaks in Europe, 2011. Proc. Nat. Acad. Sci., 109, 3065-3070.
-
(2012)
Proc. Nat. Acad. Sci.
, vol.109
, pp. 3065-3070
-
-
Grad, Y.H.1
-
10
-
-
79957460169
-
A novel and well-defined benchmarking method for second generation read mapping
-
Holtgrewe, M. et al. (2011) A novel and well-defined benchmarking method for second generation read mapping. BMC Bioinformatics, 12, 210.
-
(2011)
BMC Bioinformatics
, vol.12
, pp. 210
-
-
Holtgrewe, M.1
-
11
-
-
77951115122
-
International network of cancer genome projects
-
International Cancer Genome Consortium
-
International Cancer Genome Consortium (2010) International network of cancer genome projects. Nature, 464, 993-998.
-
(2010)
Nature
, vol.464
, pp. 993-998
-
-
-
12
-
-
2042437650
-
Initial sequencing and analysis of the human genome
-
International Human Genome Sequencing Consortium
-
International Human Genome Sequencing Consortium (2001) Initial sequencing and analysis of the human genome. Nature, 409, 860-921.
-
(2001)
Nature
, vol.409
, pp. 860-921
-
-
-
13
-
-
78651447845
-
The Uniqueome: a mappability resource for short-tag sequencing
-
Koehler, R. et al. (2010) The Uniqueome: a mappability resource for short-tag sequencing. Bioinformatics, 27, 272-274.
-
(2010)
Bioinformatics
, vol.27
, pp. 272-274
-
-
Koehler, R.1
-
14
-
-
84863651532
-
Hybrid error correction and de novo assembly of single-molecule sequencing reads
-
In Press
-
Koren, S. et al. (2012) Hybrid error correction and de novo assembly of single-molecule sequencing reads. Nat. Biotechnol., In Press.
-
(2012)
Nat. Biotechnol.
-
-
Koren, S.1
-
15
-
-
62349130698
-
Ultrafast and memory-efficient alignment of short DNA sequences to the human genome
-
Langmead, B. et al. (2009) Ultrafast and memory-efficient alignment of short DNA sequences to the human genome. Genome Biol., 10, R25.
-
(2009)
Genome Biol
, vol.10
-
-
Langmead, B.1
-
16
-
-
67649884743
-
Fast and accurate short read alignment with BurrowsWheeler transform
-
Li, H. and Durbin, R. (2009) Fast and accurate short read alignment with BurrowsWheeler transform. Bioinformatics, 25, 1754-1760.
-
(2009)
Bioinformatics
, vol.25
, pp. 1754-1760
-
-
Li, H.1
Durbin, R.2
-
17
-
-
68549104404
-
The sequence alignment/map format and SAMtools
-
Li, H. et al. (2009a) The sequence alignment/map format and SAMtools. Bioinformatics, 25, 2078-2079.
-
(2009)
Bioinformatics
, vol.25
, pp. 2078-2079
-
-
Li, H.1
-
18
-
-
55549097836
-
Mapping short DNA sequencing reads and calling variants using mapping quality scores
-
Li, H. et al. (2008) Mapping short DNA sequencing reads and calling variants using mapping quality scores. Genome Res., 18, 1851-1858.
-
(2008)
Genome Res
, vol.18
, pp. 1851-1858
-
-
Li, H.1
-
19
-
-
67650711615
-
SOAP2: an improved ultrafast tool for short read alignment
-
Li, R. et al. (2009b) SOAP2: an improved ultrafast tool for short read alignment. Bioinformatics (Oxford, England), 25, 1966-1967.
-
(2009)
Bioinformatics (Oxford, England)
, vol.25
, pp. 1966-1967
-
-
Li, R.1
-
20
-
-
78650331647
-
Identification of functional elements and regulatory circuits by Drosophila modENCODE
-
modENCODE Consortium, New York, N.Y
-
modENCODE Consortium (2010) Identification of functional elements and regulatory circuits by Drosophila modENCODE. Science (New York, N.Y.), 330, 1787-1797.
-
(2010)
Science
, vol.330
, pp. 1787-1797
-
-
-
21
-
-
79960597679
-
An integrated semiconductor device enabling non-optical genome sequencing
-
Rothberg, J.M. et al. (2011) An integrated semiconductor device enabling non-optical genome sequencing. Nature, 475, 348-352.
-
(2011)
Nature
, vol.475
, pp. 348-352
-
-
Rothberg, J.M.1
-
22
-
-
77954492012
-
Cloud computing and the DNA data race
-
Schatz, M.C. et al. (2010) Cloud computing and the DNA data race. Nat. Biotechnol., 28, 691-693.
-
(2010)
Nat. Biotechnol.
, vol.28
, pp. 691-693
-
-
Schatz, M.C.1
-
24
-
-
77954526823
-
The case for cloud computing in genome informatics
-
Stein, L.D. (2010) The case for cloud computing in genome informatics. Genome Biol., 11, 207.
-
(2010)
Genome Biol
, vol.11
, pp. 207
-
-
Stein, L.D.1
|