-
1
-
-
84859436530
-
NCBI Reference Sequences (RefSeq): Current status, new features and genome annotation policy
-
Pruitt KD, Tatusova T, Brown GR, Maglott DR (2012) NCBI Reference Sequences (RefSeq): current status, new features and genome annotation policy. Nucleic Acids Res 40: D130-135. doi: 10.1093/nar/gkr1079
-
(2012)
Nucleic Acids Res
, vol.40
, pp. D130-135
-
-
Pruitt, K.D.1
Tatusova, T.2
Brown, G.R.3
Maglott, D.R.4
-
2
-
-
84866518216
-
An anatomically comprehensive atlas of the adult human brain transcriptome
-
Hawrylycz MJ, Lein ES, Guillozet-Bongaarts AL, Shen EH, Ng L, Miller JA, et al. (2012) An anatomically comprehensive atlas of the adult human brain transcriptome. Nature 489: 391-399. doi: 10.1038/nature11405
-
(2012)
Nature
, vol.489
, pp. 391-399
-
-
Hawrylycz, M.J.1
Lein, E.S.2
Guillozet-Bongaarts, A.L.3
Shen, E.H.4
Ng, L.5
Miller, J.A.6
-
3
-
-
77951221352
-
A reannotation pipeline for Illumina BeadArrays: Improving the interpretation of gene expression data
-
Barbosa-Morais NL, Dunning MJ, Samarajiwa SA, Darot JF, Ritchie ME, Lynch AG, et al. (2010) A reannotation pipeline for Illumina BeadArrays: improving the interpretation of gene expression data. Nucleic Acids Res 38: e17. doi: 10.1093/nar/gkp942
-
(2011)
Nucleic Acids Res
, vol.38
, pp. e17
-
-
Barbosa-Morais, N.L.1
Dunning, M.J.2
Samarajiwa, S.A.3
Darot, J.F.4
Ritchie, M.E.5
Lynch, A.G.6
-
4
-
-
84870895128
-
Analyzing illumina gene expression microarray data from different tissues: Methodological aspects of data analysis in the metaxpress consortium
-
Schurmann C, Heim K, Schillert A, Blankenberg S, Carstensen M, Dörr M, et al. (2012) Analyzing illumina gene expression microarray data from different tissues: methodological aspects of data analysis in the metaxpress consortium. PLoS One 7: e50938. doi: 10.1371/journal.pone.0050938
-
(2012)
PLoS One
, vol.7
, pp. e50938
-
-
Schurmann, C.1
Heim, K.2
Schillert, A.3
Blankenberg, S.4
Carstensen, M.5
Dörr, M.6
-
5
-
-
84864326252
-
Genomic dark matter: The reliability of short read mapping illustrated by the genome mappability score
-
Lee H, Schatz MC (2012) Genomic dark matter: the reliability of short read mapping illustrated by the genome mappability score. Bioinformatics 28: 2097-2105. doi: 10.1093/bioinformatics/bts330
-
(2012)
Bioinformatics
, vol.28
, pp. 2097-2105
-
-
Lee, H.1
Schatz, M.C.2
-
6
-
-
78651447845
-
The uniqueome: A mappability resource for short-tag sequencing
-
Koehler R, Issac H, Cloonan N, Grimmond SM (2011) The uniqueome: a mappability resource for short-tag sequencing. Bioinformatics 27: 272-274. doi: 10.1093/bioinformatics/btq640
-
(2011)
Bioinformatics
, vol.27
, pp. 272-274
-
-
Koehler, R.1
Issac, H.2
Cloonan, N.3
Grimmond, S.M.4
-
7
-
-
84855989774
-
Fast computation and applications of genome mappability
-
Derrien T, Estelle J, Marco Sola S, Knowles DG, Raineri E, Guigo R, et al. (2012) Fast computation and applications of genome mappability. PLoS One 7: e30377. doi: 10.1371/journal.pone.0030377
-
(2012)
PLoS One
, vol.7
, pp. e30377
-
-
Derrien, T.1
Estelle, J.2
Marco Sola, S.3
Knowles, D.G.4
Raineri, E.5
Guigo, R.6
-
8
-
-
67649884743
-
Fast and accurate short read alignment with Burrows-Wheeler transform
-
Li H, Durbin R (2009) Fast and accurate short read alignment with Burrows-Wheeler transform. Bioinformatics 25: 1754-1760. doi: 10.1093/bioinformatics/btp324
-
(2009)
Bioinformatics
, vol.25
, pp. 1754-1760
-
-
Li, H.1
Durbin, R.2
-
9
-
-
68549104404
-
The Sequence Alignment/Map format and SAMtools
-
Li H, Handsaker B, Wysoker A, Fennell T, Ruan J, Homer N, et al. (2009) The Sequence Alignment/Map format and SAMtools. Bioinformatics 25: 2078-2079. doi: 10.1093/bioinformatics/btp352
-
(2009)
Bioinformatics
, vol.25
, pp. 2078-2079
-
-
Li, H.1
Handsaker, B.2
Wysoker, A.3
Fennell, T.4
Ruan, J.5
Homer, N.6
-
10
-
-
77956534324
-
ANNOVAR: Functional annotation of genetic variants from highthroughput sequencing data
-
Wang K, Li M, Hakonarson H (2010) ANNOVAR: functional annotation of genetic variants from highthroughput sequencing data. Nucleic Acids Res 38: e164. doi: 10.1093/nar/gkq603
-
(2011)
Nucleic Acids Res
, vol.38
, pp. e164
-
-
Wang, K.1
Li, M.2
Hakonarson, H.3
-
11
-
-
0036079158
-
The human genome browser at UCSC
-
Kent WJ, Sugnet CW, Furey TS, Roskin KM, Pringle TH, Zahler AM, et al. (2002) The human genome browser at UCSC. Genome Res 12: 996-1006.
-
(2002)
Genome Res
, vol.12
, pp. 996-1006
-
-
Kent, W.J.1
Sugnet, C.W.2
Furey, T.S.3
Roskin, K.M.4
Pringle, T.H.5
Zahler, A.M.6
-
12
-
-
84975795680
-
An integrated map of genetic variation from 1, 092 human genomes
-
The 1000 Genomes Project Consortium
-
The 1000 Genomes Project Consortium (2012) An integrated map of genetic variation from 1, 092 human genomes. Nature 491: 56-65. doi: 10.1038/nature11632
-
(2012)
Nature
, vol.491
, pp. 56-65
-
-
-
13
-
-
39149111937
-
Model-based variance-stabilizing transformation for Illumina microarray data
-
Lin SM, Du P, Huber W, Kibbe WA (2008) Model-based variance-stabilizing transformation for Illumina microarray data. Nucleic Acids Res 36: e11. doi: 10.1093/nar/gkm1075
-
(2008)
Nucleic Acids Res
, vol.36
, pp. e11
-
-
Lin, S.M.1
Du, P.2
Huber, W.3
Kibbe, W.A.4
|