-
1
-
-
65449136284
-
TopHat: Discovering splice junctions with RNA-Seq
-
Trapnell C, Pachter L, Salzberg SL (2009) TopHat: discovering splice junctions with RNA-Seq. Bioinformatics 25(9):1105-11.
-
(2009)
Bioinformatics
, vol.25
, Issue.9
, pp. 1105-1111
-
-
Trapnell, C.1
Pachter, L.2
Salzberg, S.L.3
-
2
-
-
84876996918
-
TopHat2: Accurate alignment of transcriptomes in the presence of insertions, deletions and gene fusions
-
Kim D, Pertea G, Trapnell C, Pimentel H, Kelley R, et al. (2013) TopHat2: accurate alignment of transcriptomes in the presence of insertions, deletions and gene fusions. Genome Biology, 14:R36.
-
(2013)
Genome Biology
, vol.14
-
-
Kim, D.1
Pertea, G.2
Trapnell, C.3
Pimentel, H.4
Kelley, R.5
-
4
-
-
77951820899
-
Fast and SNP-tolerant detection of complex variants and splicing in short reads
-
Wu TD, Nacu S (2010) Fast and SNP-tolerant detection of complex variants and splicing in short reads. Bioinformatics 26 (7): 873-881.
-
(2010)
Bioinformatics
, vol.26
, Issue.7
, pp. 873-881
-
-
Wu, T.D.1
Nacu, S.2
-
5
-
-
78649345104
-
MapSplice: Accurate mapping of RNA-seq reads for splice junction discovery
-
Wang K, Singh D, Zeng Z, Coleman SJ, Huang Y, et al. (2010) MapSplice: accurate mapping of RNA-seq reads for splice junction discovery. Nucleic Acids Res. 38(18).
-
(2010)
Nucleic Acids Res
, vol.38
, Issue.18
-
-
Wang, K.1
Singh, D.2
Zeng, Z.3
Coleman, S.J.4
Huang, Y.5
-
6
-
-
62349130698
-
Ultrafast and memory-efficient alignment of short DNA sequences to the human genome
-
Langmead B, Trapnell C, Pop M, Salzberg SL (2009) Ultrafast and memory-efficient alignment of short DNA sequences to the human genome. Genome Biology. 10:R25.
-
(2009)
Genome Biology
, vol.10
-
-
Langmead, B.1
Trapnell, C.2
Pop, M.3
Salzberg, S.L.4
-
7
-
-
80051507403
-
TopHat-Fusion: An algorithm for discovery of novel fusion transcripts
-
Aug 11
-
Kim D, Salzberg S (2011) TopHat-Fusion: an algorithm for discovery of novel fusion transcripts. Genome Biol 12:R72. Aug 11.
-
(2011)
Genome Biol
, vol.12
-
-
Kim, D.1
Salzberg, S.2
-
8
-
-
77955443472
-
Detection of splice junctions from paired-end RNA-seq data by SpliceMap
-
Au KF, Jiang H, Lin L, Xing Y, Wong WH (2010) Detection of splice junctions from paired-end RNA-seq data by SpliceMap. Nucleic Acids Res. 38(14).
-
(2010)
Nucleic Acids Res
, vol.38
, Issue.14
-
-
Au, K.F.1
Jiang, H.2
Lin, L.3
Xing, Y.4
Wong, W.H.5
-
9
-
-
84876388379
-
TrueSight: A new algorithm for splice junction detection using RNA-seq
-
Li Y, Li-Byarlay H, Burns P, Borodovsky M, Robinson GE, et al. (2012) TrueSight: a new algorithm for splice junction detection using RNA-seq. Nucleic Acids Research. 41(4).
-
(2012)
Nucleic Acids Research
, vol.41
, Issue.4
-
-
Li, Y.1
Li-Byarlay, H.2
Burns, P.3
Borodovsky, M.4
Robinson, G.E.5
-
10
-
-
84878535352
-
OLego: Fast and sensitive mapping of spliced mRNA-Seq reads using small seeds
-
Wu J, Anczuków O, Krainer AR, Zhang MQ, Zhang C (2013) OLego: fast and sensitive mapping of spliced mRNA-Seq reads using small seeds. Nucleic Acids Res. 41(10).
-
(2013)
Nucleic Acids Res
, vol.41
, Issue.10
-
-
Wu, J.1
Anczuków, O.2
Krainer, A.R.3
Zhang, M.Q.4
Zhang, C.5
-
11
-
-
84880708185
-
STAR: Ultrafast universal RNA-seq aligner
-
Oct
-
Dobin A, Davis CA, Schlesinger F, Drenkow J, Zaleski C, et al. (2012) STAR: ultrafast universal RNA-seq aligner. Bioinformatics. Oct 19.
-
(2012)
Bioinformatics
, pp. 19
-
-
Dobin, A.1
Davis, C.A.2
Schlesinger, F.3
Drenkow, J.4
Zaleski, C.5
-
12
-
-
84875689118
-
PASTA: Splice junction identification from RNA-Sequencing data
-
Tang S, Riva A (2013) PASTA: splice junction identification from RNA-Sequencing data. BMC Bioinformatics 14: 116.
-
(2013)
BMC Bioinformatics
, vol.14
, pp. 116
-
-
Tang, S.1
Riva, A.2
-
13
-
-
83755164978
-
SOAPsplice: Genome-wide ab initio detection of splice junctions from RNA-Seq data
-
Huang S1, Zhang J, Li R, Zhang W, He Z, et al. (2011) SOAPsplice: genome-wide ab initio detection of splice junctions from RNA-Seq data. Front. Gene. 2: 46.
-
(2011)
Front. Gene.
, vol.2
, pp. 46
-
-
Huang, S.1
Zhang, J.2
Li, R.3
Zhang, W.4
He, Z.5
-
14
-
-
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: 1754-60.
-
(2009)
Bioinformatics
, vol.25
, pp. 1754-1760
-
-
Li, H.1
Durbin, R.2
-
15
-
-
68549104404
-
The Sequence Alignment/Map format and SAMtools
-
Li H, Handsaker B, Wysoker A, Fennell T, Ruan J, et al. (2009) The Sequence Alignment/Map format and SAMtools. Bioinformatics. 25(16):2078-9.
-
(2009)
Bioinformatics
, vol.25
, Issue.16
, pp. 2078-2079
-
-
Li, H.1
Handsaker, B.2
Wysoker, A.3
Fennell, T.4
Ruan, J.5
-
16
-
-
84858221706
-
Ensembl 2012
-
Flicek P, Amode MR, Barrell D, Beal K, Brent S, et al. (2012) Ensembl 2012 Nucleic Acids Research. 40 Database issue: D84-D90.
-
(2012)
Nucleic Acids Research
, vol.40
, Issue.DATABASE ISSUE
-
-
Flicek, P.1
Amode, M.R.2
Barrell, D.3
Beal, K.4
Brent, S.5
-
17
-
-
78651320424
-
The UCSC Genome Browser database: Update 2011
-
Oct
-
Fujita PA, Rhead B, Zweig AS, Hinrichs AS, Karolchik D, et al. (2011) The UCSC Genome Browser database: update 2011. Nucleic Acids Res. Oct 18.
-
(2011)
Nucleic Acids Res
, pp. 18
-
-
Fujita, P.A.1
Rhead, B.2
Zweig, A.S.3
Hinrichs, A.S.4
Karolchik, D.5
-
18
-
-
84869036699
-
Modelling and simulating generic RNA-Seq experiments with the flux simulator
-
Griebel T, Zacher B, Ribeca P, Raineri E, Lacroix V, et al. (2012). Modelling and simulating generic RNA-Seq experiments with the flux simulator. Nucleic acids research, 40(20):10073-10083.
-
(2012)
Nucleic Acids Research
, vol.40
, Issue.20
, pp. 10073-10083
-
-
Griebel, T.1
Zacher, B.2
Ribeca, P.3
Raineri, E.4
Lacroix, V.5
-
19
-
-
77956295988
-
The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
-
McKenna A, Hanna M, Banks E, Sivachenko A, Cibulskis K, et al. (2010) The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data.Genome Res. 20: 1297-303.
-
(2010)
Genome Res
, vol.20
, pp. 1297-1303
-
-
McKenna, A.1
Hanna, M.2
Banks, E.3
Sivachenko, A.4
Cibulskis, K.5
-
20
-
-
80054123822
-
-
Available: Accessed 2013 Oct (dbSNP Build ID: 137)
-
dbSNP Short Genetic Variations. Available: http://www.ncbi.nlm.nih.gov/ SNP/. Accessed 2013 Oct (dbSNP Build ID: 137). NCBI.
-
dbSNP Short Genetic Variations
-
-
-
21
-
-
84862506964
-
A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff: SNPs in the genome of Drosophila melanogaster strain w1118; iso-2; iso-3
-
AprJun
-
Cingolani P, Platts A, Wang le L, Coon M, Nguyen T, et al. (2012) A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff: SNPs in the genome of Drosophila melanogaster strain w1118; iso-2; iso-3. Fly (Austin). AprJun;6(2):80-92.
-
(2012)
Fly (Austin)
, vol.6
, Issue.2
, pp. 80-92
-
-
Cingolani, P.1
Platts, A.2
Wang Le, L.3
Coon, M.4
Nguyen, T.5
-
22
-
-
84876030710
-
Using Drosophila melanogaster as a model for genotoxic chemical mutational studies with a new program, SnpSift
-
Cingolani P, Patel VM, Coon M, Nguyen T, Land SJ, et al. (2012) Using Drosophila melanogaster as a model for genotoxic chemical mutational studies with a new program, SnpSift. Frontiers in Genetics, 3.
-
(2012)
Frontiers in Genetics
, pp. 3
-
-
Cingolani, P.1
Patel, V.M.2
Coon, M.3
Nguyen, T.4
Land, S.J.5
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