-
1
-
-
0034614637
-
The hallmarks of cancer
-
Hanahan D, Weinberg RA (2000) The hallmarks of cancer. Cell 100: 57-70.
-
(2000)
Cell
, vol.100
, pp. 57-70
-
-
Hanahan, D.1
Weinberg, R.A.2
-
2
-
-
0033614998
-
Creation of human tumour cells with defined genetic elements
-
Hahn WC, Counter CM, Lundberg AS, Beijersbergen RL, Brooks MW, et al. (1999) Creation of human tumour cells with defined genetic elements. Nature 400: 464-468.
-
(1999)
Nature
, vol.400
, pp. 464-468
-
-
Hahn, W.C.1
Counter, C.M.2
Lundberg, A.S.3
Beijersbergen, R.L.4
Brooks, M.W.5
-
3
-
-
57749195712
-
RNA-Seq: A revolutionary tool for transcriptomics
-
Wang Z, Gerstein M, Snyder M (2009) RNA-Seq: a revolutionary tool for transcriptomics. Nat Rev Genet 10: 57-63.
-
(2009)
Nat Rev Genet
, vol.10
, pp. 57-63
-
-
Wang, Z.1
Gerstein, M.2
Snyder, M.3
-
4
-
-
0034507456
-
Functions and mechanisms of RNA editing
-
Gott JM, Emeson RB (2000) Functions and mechanisms of RNA editing. Annu Rev Genet 34: 499-531.
-
(2000)
Annu Rev Genet
, vol.34
, pp. 499-531
-
-
Gott, J.M.1
Emeson, R.B.2
-
5
-
-
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: 2078-2079.
-
(2009)
Bioinformatics
, vol.25
, pp. 2078-2079
-
-
Li, H.1
Handsaker, B.2
Wysoker, A.3
Fennell, T.4
Ruan, J.5
-
6
-
-
84863229597
-
VarScan 2: Somatic mutation and copy number alteration discovery in cancer by exome sequencing
-
Koboldt DC, Zhang Q, Larson DE, Shen D, McLellan MD, et al. (2012) VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing. Genome Res 22: 568-576.
-
(2012)
Genome Res
, vol.22
, pp. 568-576
-
-
Koboldt, D.C.1
Zhang, Q.2
Larson, D.E.3
Shen, D.4
McLellan, M.D.5
-
7
-
-
84864153492
-
Strelka: Accurate somatic small-variant calling from sequenced tumor-normal sample pairs
-
Saunders CT, Wong WS, Swamy S, Becq J, Murray LJ, et al. (2012) Strelka: accurate somatic small-variant calling from sequenced tumor-normal sample pairs. Bioinformatics 28: 1811-1817.
-
(2012)
Bioinformatics
, vol.28
, pp. 1811-1817
-
-
Saunders, C.T.1
Wong, W.S.2
Swamy, S.3
Becq, J.4
Murray, L.J.5
-
8
-
-
84856565531
-
SomaticSniper: Identification of somatic point mutations in whole genome sequencing data
-
Larson DE, Harris CC, Chen K, Koboldt DC, Abbott TE, et al. (2012) SomaticSniper: identification of somatic point mutations in whole genome sequencing data. Bioinformatics 28: 311-317.
-
(2012)
Bioinformatics
, vol.28
, pp. 311-317
-
-
Larson, D.E.1
Harris, C.C.2
Chen, K.3
Koboldt, D.C.4
Abbott, T.E.5
-
9
-
-
69949122158
-
VarScan: Variant detection in massively parallel sequencing of individual and pooled samples
-
Koboldt DC, Chen K, Wylie T, Larson DE, McLellan MD, et al. (2009) VarScan: variant detection in massively parallel sequencing of individual and pooled samples. Bioinformatics 25: 2283-2285.
-
(2009)
Bioinformatics
, vol.25
, pp. 2283-2285
-
-
Koboldt, D.C.1
Chen, K.2
Wylie, T.3
Larson, D.E.4
McLellan, M.D.5
-
10
-
-
77951957381
-
SNVMix: Predicting single nucleotide variants from next-generation sequencing of tumors
-
Goya R, Sun MG, Morin RD, Leung G, Ha G, et al. (2010) SNVMix: predicting single nucleotide variants from next-generation sequencing of tumors. Bioinformatics 26: 730-736.
-
(2010)
Bioinformatics
, vol.26
, pp. 730-736
-
-
Goya, R.1
Sun, M.G.2
Morin, R.D.3
Leung, G.4
Ha, G.5
-
11
-
-
84874025843
-
Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples
-
Cibulskis K, Lawrence MS, Carter SL, Sivachenko A, Jaffe D, et al. (2013) Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples. Nat Biotechnol 31: 213-219.
-
(2013)
Nat Biotechnol
, vol.31
, pp. 213-219
-
-
Cibulskis, K.1
Lawrence, M.S.2
Carter, S.L.3
Sivachenko, A.4
Jaffe, D.5
-
12
-
-
84883479141
-
A comparative analysis of algorithms for somatic SNV detection in cancer
-
Roberts ND, Kortschak RD, Parker WT, Schreiber AW, Branford S, et al. (2013) A comparative analysis of algorithms for somatic SNV detection in cancer. Bioinformatics 29: 2223-2230.
-
(2013)
Bioinformatics
, vol.29
, pp. 2223-2230
-
-
Roberts, N.D.1
Kortschak, R.D.2
Parker, W.T.3
Schreiber, A.W.4
Branford, S.5
-
13
-
-
84877254190
-
Integrated genomic characterization of endometrial carcinoma
-
Kandoth C, Schultz N, Cherniack AD, Akbani R, Liu Y, et al. (2013) Integrated genomic characterization of endometrial carcinoma. Nature 497: 67-73.
-
(2013)
Nature
, vol.497
, pp. 67-73
-
-
Kandoth, C.1
Schultz, N.2
Cherniack, A.D.3
Akbani, R.4
Liu, Y.5
-
14
-
-
84905029258
-
Comprehensive molecular profiling of lung adenocarcinoma
-
The Cancer Genome Atlas (2014) Comprehensive molecular profiling of lung adenocarcinoma. Nature 511: 543-550.
-
(2014)
Nature
, vol.511
, pp. 543-550
-
-
-
15
-
-
79954553212
-
Improving SNP discovery by base alignment quality
-
Li H (2011) Improving SNP discovery by base alignment quality. Bioinformatics 27: 1157-1158.
-
(2011)
Bioinformatics
, vol.27
, pp. 1157-1158
-
-
Li, H.1
-
16
-
-
84975742565
-
A map of human genome variation from population-scale sequencing
-
98
-
1000 Genomes Project Consortium (2010) A map of human genome variation from population-scale sequencing. Nature 467: 1061-1073. (98)
-
(2010)
Nature
, vol.467
, pp. 1061-1073
-
-
-
17
-
-
84975795680
-
An integrated map of genetic variation from 1, 092 human genomes
-
99)
-
1000 Genomes Project Consortium (2012) An integrated map of genetic variation from 1, 092 human genomes. Nature 491: 56-65. (99)
-
(2012)
Nature
, vol.491
, pp. 56-65
-
-
-
18
-
-
0035173378
-
DbSNP: The NCBI database of genetic variation
-
Sherry ST, Ward MH, Kholodov M, Baker J, Phan L, et al. (2001) dbSNP: the NCBI database of genetic variation. Nucleic Acids Res 29: 308-311.
-
(2001)
Nucleic Acids Res
, vol.29
, pp. 308-311
-
-
Sherry, S.T.1
Ward, M.H.2
Kholodov, M.3
Baker, J.4
Phan, L.5
-
19
-
-
0036079158
-
The human genome browser at UCSC
-
Kent WJ, Sugnet CW, Furey TS, Roskin KM, Pringle TH, 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
-
20
-
-
84891771466
-
The UCSC Genome Browser database: 2014 update
-
Karolchik D, Barber GP, Casper J, Clawson H, Cline MS, et al. (2014) The UCSC Genome Browser database: 2014 update. Nucleic Acids Res 42: D764-770.
-
(2014)
Nucleic Acids Res
, vol.42
, pp. D764-770
-
-
Karolchik, D.1
Barber, G.P.2
Casper, J.3
Clawson, H.4
Cline, M.S.5
-
21
-
-
74049124308
-
Single nucleotide differences (SNDs) in the dbSNP database may lead to errors in genotyping and haplotyping studies
-
Musumeci L, Arthur JW, Cheung FS, Hoque A, Lippman S, et al. (2010) Single nucleotide differences (SNDs) in the dbSNP database may lead to errors in genotyping and haplotyping studies. Hum Mutat 31: 67-73.
-
(2010)
Hum Mutat
, vol.31
, pp. 67-73
-
-
Musumeci, L.1
Arthur, J.W.2
Cheung, F.S.3
Hoque, A.4
Lippman, S.5
-
22
-
-
84862695743
-
Expressed pseudogenes in the transcriptional landscape of human cancers
-
Kalyana-Sundaram S, Kumar-Sinha C, Shankar S, Robinson DR, Wu YM, et al. (2012) Expressed pseudogenes in the transcriptional landscape of human cancers. Cell 149: 1622-1634.
-
(2012)
Cell
, vol.149
, pp. 1622-1634
-
-
Kalyana-Sundaram, S.1
Kumar-Sinha, C.2
Shankar, S.3
Robinson, D.R.4
Wu, Y.M.5
-
23
-
-
84865760395
-
GENCODE: The reference human genome annotation for the ENCODE Project
-
Harrow J, Frankish A, Gonzalez JM, Tapanari E, Diekhans M, et al. (2012) GENCODE: the reference human genome annotation for The ENCODE Project. Genome Res 22: 1760-1774.
-
(2012)
Genome Res
, vol.22
, pp. 1760-1774
-
-
Harrow, J.1
Frankish, A.2
Gonzalez, J.M.3
Tapanari, E.4
Diekhans, M.5
-
24
-
-
56449118064
-
Retrocopy contributions to the evolution of the human genome
-
Baertsch R, Diekhans M, Kent WJ, Haussler D, Brosius J (2008) Retrocopy contributions to the evolution of the human genome. BMC Genomics 9: 466.
-
(2008)
BMC Genomics
, vol.9
, pp. 466
-
-
Baertsch, R.1
Diekhans, M.2
Kent, W.J.3
Haussler, D.4
Brosius, J.5
-
25
-
-
84875945705
-
ENCODE data in the UCSC Genome Browser: Year 5 update
-
Rosenbloom KR, Sloan CA, Malladi VS, Dreszer TR, Learned K, et al. (2013) ENCODE data in the UCSC Genome Browser: year 5 update. Nucleic Acids Res 41: D56-63.
-
(2013)
Nucleic Acids Res
, vol.41
, pp. D56-63
-
-
Rosenbloom, K.R.1
Sloan, C.A.2
Malladi, V.S.3
Dreszer, T.R.4
Learned, K.5
-
26
-
-
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
-
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) 6: 80-92.
-
(2012)
Fly (Austin)
, vol.6
, pp. 80-92
-
-
Cingolani, P.1
Platts, A.2
Wang Le, L.3
Coon, M.4
Nguyen, T.5
-
27
-
-
0036226603
-
BLAT-the BLAST-like alignment tool
-
Kent WJ (2002) BLAT-the BLAST-like alignment tool. Genome Res 12: 656-664.
-
(2002)
Genome Res
, vol.12
, pp. 656-664
-
-
Kent, W.J.1
-
28
-
-
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.
-
(2009)
Bioinformatics
, vol.25
, pp. 1754-1760
-
-
Li, H.1
Durbin, R.2
-
29
-
-
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: e178.
-
(2010)
Nucleic Acids Res
, vol.38
, pp. e178
-
-
Wang, K.1
Singh, D.2
Zeng, Z.3
Coleman, S.J.4
Huang, Y.5
-
32
-
-
77955660663
-
Diverse somatic mutation patterns and pathway alterations in human cancers
-
Kan Z, Jaiswal BS, Stinson J, Janakiraman V, Bhatt D, et al. (2010) Diverse somatic mutation patterns and pathway alterations in human cancers. Nature 466: 869-873.
-
(2010)
Nature
, vol.466
, pp. 869-873
-
-
Kan, Z.1
Jaiswal, B.S.2
Stinson, J.3
Janakiraman, V.4
Bhatt, D.5
-
33
-
-
84874543751
-
The mitochondrial and autosomal mutation landscapes of prostate cancer
-
Lindberg J, Mills IG, Klevebring D, Liu W, Neiman M, et al. (2013) The mitochondrial and autosomal mutation landscapes of prostate cancer. Eur Urol 63: 702-708.
-
(2013)
Eur Urol
, vol.63
, pp. 702-708
-
-
Lindberg, J.1
Mills, I.G.2
Klevebring, D.3
Liu, W.4
Neiman, M.5
-
34
-
-
84869091997
-
Pancreatic cancer genomes reveal aberrations in axon guidance pathway genes
-
Biankin AV, Waddell N, Kassahn KS, Gingras MC, Muthuswamy LB, et al. (2012) Pancreatic cancer genomes reveal aberrations in axon guidance pathway genes. Nature 491: 399-405.
-
(2012)
Nature
, vol.491
, pp. 399-405
-
-
Biankin, A.V.1
Waddell, N.2
Kassahn, K.S.3
Gingras, M.C.4
Muthuswamy, L.B.5
-
35
-
-
80052266351
-
Frequent mutations of chromatin remodeling genes in transitional cell carcinoma of the bladder
-
Gui Y, Guo G, Huang Y, Hu X, Tang A, et al. (2011) Frequent mutations of chromatin remodeling genes in transitional cell carcinoma of the bladder. Nat Genet 43: 875-878.
-
(2011)
Nat Genet
, vol.43
, pp. 875-878
-
-
Gui, Y.1
Guo, G.2
Huang, Y.3
Hu, X.4
Tang, A.5
-
36
-
-
84880861468
-
The exomes of the NCI-60 panel: A genomic resource for cancer biology and systems pharmacology
-
Abaan OD, Polley EC, Davis SR, Zhu YJ, Bilke S, et al. (2013) The exomes of the NCI-60 panel: a genomic resource for cancer biology and systems pharmacology. Cancer Res 73: 4372-4382.
-
(2013)
Cancer Res
, vol.73
, pp. 4372-4382
-
-
Abaan, O.D.1
Polley, E.C.2
Davis, S.R.3
Zhu, Y.J.4
Bilke, S.5
-
37
-
-
79951934386
-
TP53 mutation is frequently associated with CTNNB1 mutation or MYCN amplification and is compatible with long-term survival in medulloblastoma
-
Pfaff E, Remke M, Sturm D, Benner A, Witt H, et al. (2010) TP53 mutation is frequently associated with CTNNB1 mutation or MYCN amplification and is compatible with long-term survival in medulloblastoma. J Clin Oncol 28: 5188-5196.
-
(2010)
J Clin Oncol
, vol.28
, pp. 5188-5196
-
-
Pfaff, E.1
Remke, M.2
Sturm, D.3
Benner, A.4
Witt, H.5
-
38
-
-
0033766175
-
Heterogeneity in the clinical phenotype of TP53 mutations in breast cancer patients
-
Alsner J, Yilmaz M, Guldberg P, Hansen LL, Overgaard J (2000) Heterogeneity in the clinical phenotype of TP53 mutations in breast cancer patients. Clin Cancer Res 6: 3923-3931.
-
(2000)
Clin Cancer Res
, vol.6
, pp. 3923-3931
-
-
Alsner, J.1
Yilmaz, M.2
Guldberg, P.3
Hansen, L.L.4
Overgaard, J.5
-
39
-
-
84861530773
-
Prognostic and predictive value of TP53 mutations in node-positive breast cancer patients treated with anthracycline-or anthracycline/taxane-based adjuvant therapy: Results from the BIG 02-98 phase III trial
-
Fernandez-Cuesta L, Oakman C, Falagan-Lotsch P, Smoth KS, Quinaux E, et al. (2012) Prognostic and predictive value of TP53 mutations in node-positive breast cancer patients treated with anthracycline-or anthracycline/taxane-based adjuvant therapy: results from the BIG 02-98 phase III trial. Breast Cancer Res 14: R70.
-
(2012)
Breast Cancer Res
, vol.14
, pp. R70
-
-
Fernandez-Cuesta, L.1
Oakman, C.2
Falagan-Lotsch, P.3
Smoth, K.S.4
Quinaux, E.5
-
40
-
-
0038499524
-
A new method for determining the status of p53 in tumor cell lines of different origin
-
Gartel AL, Feliciano C, Tyner AL (2003) A new method for determining the status of p53 in tumor cell lines of different origin. Oncol Res 13: 405-408.
-
(2003)
Oncol Res
, vol.13
, pp. 405-408
-
-
Gartel, A.L.1
Feliciano, C.2
Tyner, A.L.3
-
41
-
-
84877028141
-
Comprehensive molecular portraits of human breast tumours
-
The Cancer Genome Atlas (2012) Comprehensive molecular portraits of human breast tumours. Nature 490: 61-70.
-
(2012)
Nature
, vol.490
, pp. 61-70
-
-
-
42
-
-
77957731999
-
Frequent mutations of chromatin remodeling gene ARID1A in ovarian clear cell carcinoma
-
Jones S, Wang TL, Ie-Shih M, Mao TL, Nakayama K, et al. (2010) Frequent mutations of chromatin remodeling gene ARID1A in ovarian clear cell carcinoma. Science 330: 228-231.
-
(2010)
Science
, vol.330
, pp. 228-231
-
-
Jones, S.1
Wang, T.L.2
Ie-Shih, M.3
Mao, T.L.4
Nakayama, K.5
-
43
-
-
84864444165
-
Novel mutations target distinct subgroups of medulloblastoma
-
Robinson G, Parker M, Kranenburg TA, Lu C, Chen X, et al. (2012) Novel mutations target distinct subgroups of medulloblastoma. Nature 488: 43-48.
-
(2012)
Nature
, vol.488
, pp. 43-48
-
-
Robinson, G.1
Parker, M.2
Kranenburg, T.A.3
Lu, C.4
Chen, X.5
-
44
-
-
72449195871
-
Mutant p53 (G199V) gains antiapoptotic function through signal transducer and activator of transcription 3 in anaplastic thyroid cancer cells
-
Kim TH, Lee SY, Rho JH, Jeong NY, Soung YH, et al. (2009) Mutant p53 (G199V) gains antiapoptotic function through signal transducer and activator of transcription 3 in anaplastic thyroid cancer cells. Mol Cancer Res 7: 1645-1654.
-
(2009)
Mol Cancer Res
, vol.7
, pp. 1645-1654
-
-
Kim, T.H.1
Lee, S.Y.2
Rho, J.H.3
Jeong, N.Y.4
Soung, Y.H.5
-
45
-
-
24744453982
-
Somatic mutations of the protein kinase gene family in human lung cancer
-
Davies H, Hunter C, Smith R, Stephens P, Greenman C, et al. (2005) Somatic mutations of the protein kinase gene family in human lung cancer. Cancer Res 65: 7591-7595.
-
(2005)
Cancer Res
, vol.65
, pp. 7591-7595
-
-
Davies, H.1
Hunter, C.2
Smith, R.3
Stephens, P.4
Greenman, C.5
-
46
-
-
84866410479
-
Mapping the hallmarks of lung adenocarcinoma with massively parallel sequencing
-
Imielinski M, Berger AH, Hammerman PS, Hernandez B, Pugh TJ, et al. (2012) Mapping the hallmarks of lung adenocarcinoma with massively parallel sequencing. Cell 150: 1107-1120.
-
(2012)
Cell
, vol.150
, pp. 1107-1120
-
-
Imielinski, M.1
Berger, A.H.2
Hammerman, P.S.3
Hernandez, B.4
Pugh, T.J.5
-
47
-
-
71849104873
-
P16INK4A inactivation mechanisms in non-small-cell lung cancer patients occupationally exposed to asbestos
-
Andujar P, Wang J, Descatha A, Galateau-Salle F, Abd-Alsamad I, et al. (2010) p16INK4A inactivation mechanisms in non-small-cell lung cancer patients occupationally exposed to asbestos. Lung Cancer 67: 23-30.
-
(2010)
Lung Cancer
, vol.67
, pp. 23-30
-
-
Andujar, P.1
Wang, J.2
Descatha, A.3
Galateau-Salle, F.4
Abd-Alsamad, I.5
-
48
-
-
67650205717
-
Genome wide SNP comparative analysis between EGFR and KRAS mutated NSCLC and characterization of two models of oncogenic cooperation in non-small cell lung carcinoma
-
Blons H, Pallier K, Le Corre D, Danel C, Tremblay-Gravel M, et al. (2008) Genome wide SNP comparative analysis between EGFR and KRAS mutated NSCLC and characterization of two models of oncogenic cooperation in non-small cell lung carcinoma. BMC Med Genomics 1: 25.
-
(2008)
BMC Med Genomics
, vol.1
, pp. 25
-
-
Blons, H.1
Pallier, K.2
Le Corre, D.3
Danel, C.4
Tremblay-Gravel, M.5
-
49
-
-
84863922124
-
Comprehensive molecular characterization of human colon and rectal cancer
-
The Cancer Genome Atlas (2012) Comprehensive molecular characterization of human colon and rectal cancer. Nature 487: 330-337.
-
(2012)
Nature
, vol.487
, pp. 330-337
-
-
-
50
-
-
4544336198
-
Alterations of the p16INK4a/p14ARF pathway in clear cell sarcoma
-
Takahira T, Oda Y, Tamiya S, Yamamoto H, Kawaguchi K, et al. (2004) Alterations of the p16INK4a/p14ARF pathway in clear cell sarcoma. Cancer Sci 95: 651-655.
-
(2004)
Cancer Sci
, vol.95
, pp. 651-655
-
-
Takahira, T.1
Oda, Y.2
Tamiya, S.3
Yamamoto, H.4
Kawaguchi, K.5
-
51
-
-
0141483265
-
Frequent methylation of p16INK4A and p14ARF genes implicated in the evolution of chronic myeloid leukaemia from its chronic to accelerated phase
-
Nagy E, Beck Z, Kiss A, Csoma E, Telek B, et al. (2003) Frequent methylation of p16INK4A and p14ARF genes implicated in the evolution of chronic myeloid leukaemia from its chronic to accelerated phase. Eur J Cancer 39: 2298-2305.
-
(2003)
Eur J Cancer
, vol.39
, pp. 2298-2305
-
-
Nagy, E.1
Beck, Z.2
Kiss, A.3
Csoma, E.4
Telek, B.5
-
52
-
-
1842428729
-
Alterations of p16 and prognosis in biliary tract cancers from a population-based study in China
-
Ueki T, Hsing AW, Gao YT, Wang BS, Shen MC, et al. (2004) Alterations of p16 and prognosis in biliary tract cancers from a population-based study in China. Clin Cancer Res 10: 1717-1725.
-
(2004)
Clin Cancer Res
, vol.10
, pp. 1717-1725
-
-
Ueki, T.1
Hsing, A.W.2
Gao, Y.T.3
Wang, B.S.4
Shen, M.C.5
-
53
-
-
84859413165
-
Exome versus transcriptome sequencing in identifying coding region variants
-
Ku CS, Wu M, Cooper DN, Naidoo N, Pawitan Y, et al. (2012) Exome versus transcriptome sequencing in identifying coding region variants. Expert Rev Mol Diagn 12: 241-251.
-
(2012)
Expert Rev Mol Diagn
, vol.12
, pp. 241-251
-
-
Ku, C.S.1
Wu, M.2
Cooper, D.N.3
Naidoo, N.4
Pawitan, Y.5
-
54
-
-
77952718611
-
Screening the human exome: A comparison of whole genome and whole transcriptome sequencing
-
Cirulli ET, Singh A, Shianna KV, Ge D, Smith JP, et al. (2010) Screening the human exome: a comparison of whole genome and whole transcriptome sequencing. Genome Biol 11: R57.
-
(2010)
Genome Biol
, vol.11
, pp. R57
-
-
Cirulli, E.T.1
Singh, A.2
Shianna, K.V.3
Ge, D.4
Smith, J.P.5
-
55
-
-
63849301203
-
The UCSC cancer genomics browser
-
Zhu J, Sanborn JZ, Benz S, Szeto C, Hsu F, et al. (2009) The UCSC Cancer Genomics Browser. Nat Methods 6: 239-240.
-
(2009)
Nat Methods
, vol.6
, pp. 239-240
-
-
Zhu, J.1
Sanborn, J.Z.2
Benz, S.3
Szeto, C.4
Hsu, F.5
|