-
1
-
-
77954242530
-
Molecular circuits of solid tumors: Prognostic and predictive tools for bedside use
-
20551944 1:CAS:528:DC%2BC3cXotFeit7k%3D
-
C. Ferte, F. Andre, J.C. Soria, Molecular circuits of solid tumors: prognostic and predictive tools for bedside use. Nat Rev Clin Oncol 7, 367-380 (2010)
-
(2010)
Nat Rev Clin Oncol
, vol.7
, pp. 367-380
-
-
Ferte, C.1
Andre, F.2
Soria, J.C.3
-
2
-
-
73949159645
-
Does massively parallel DNA resequencing signify the end of histopathology as we know it?
-
19921711 1:CAS:528:DC%2BC3cXht1Ont7w%3D
-
S.A. Aparicio, D.G. Huntsman, Does massively parallel DNA resequencing signify the end of histopathology as we know it? J Pathol 220, 307-315 (2010)
-
(2010)
J Pathol
, vol.220
, pp. 307-315
-
-
Aparicio, S.A.1
Huntsman, D.G.2
-
3
-
-
84882977045
-
Genetics and biomarkers in personalisation of lung cancer treatment
-
23972815 1:CAS:528:DC%2BC3sXhtlClt7fJ
-
R. Rosell, T.G. Bivona, N. Karachaliou, Genetics and biomarkers in personalisation of lung cancer treatment. Lancet 382, 720-731 (2013)
-
(2013)
Lancet
, vol.382
, pp. 720-731
-
-
Rosell, R.1
Bivona, T.G.2
Karachaliou, N.3
-
5
-
-
79959795786
-
Improved survival with vemurafenib in melanoma with BRAF V600E mutation
-
21639808 1:CAS:528:DC%2BC3MXosVeitbs%3D 3549296
-
P.B. Chapman, A. Hauschild, C. Robert, J.B. Haanen, P. Ascierto, J. Larkin, R. Dummer, C. Garbe, A. Testori, M. Maio, D. Hogg, P. Lorigan, C. Lebbe, T. Jouary, D. Schadendorf, A. Ribas, S.J. O'Day, J.A. Sosman, J.M. Kirkwood, A.M. Eggermont, B. Dreno, K. Nolop, J. Li, B. Nelson, J. Hou, R.J. Lee, K.T. Flaherty, G.A. McArthur, Improved survival with vemurafenib in melanoma with BRAF V600E mutation. N Engl J Med 364, 2507-2516 (2011)
-
(2011)
N Engl J Med
, vol.364
, pp. 2507-2516
-
-
Chapman, P.B.1
Hauschild, A.2
Robert, C.3
Haanen, J.B.4
Ascierto, P.5
Larkin, J.6
Dummer, R.7
Garbe, C.8
Testori, A.9
Maio, M.10
Hogg, D.11
Lorigan, P.12
Lebbe, C.13
Jouary, T.14
Schadendorf, D.15
Ribas, A.16
O'Day, S.J.17
Sosman, J.A.18
Kirkwood, J.M.19
Eggermont, A.M.20
Dreno, B.21
Nolop, K.22
Li, J.23
Nelson, B.24
Hou, J.25
Lee, R.J.26
Flaherty, K.T.27
McArthur, G.A.28
more..
-
6
-
-
84883680951
-
Panitumumab-FOLFOX4 treatment and RAS mutations in colorectal cancer
-
24024839 1:CAS:528:DC%2BC3sXhsFGktr3L
-
J.Y. Douillard, K.S. Oliner, S. Siena, J. Tabernero, R. Burkes, M. Barugel, Y. Humblet, G. Bodoky, D. Cunningham, J. Jassem, F. Rivera, I. Kocakova, P. Ruff, M. Blasinska-Morawiec, M. Smakal, J.L. Canon, M. Rother, R. Williams, A. Rong, J. Wiezorek, R. Sidhu, S.D. Patterson, Panitumumab-FOLFOX4 treatment and RAS mutations in colorectal cancer. N Engl J Med 369, 1023-1034 (2013)
-
(2013)
N Engl J Med
, vol.369
, pp. 1023-1034
-
-
Douillard, J.Y.1
Oliner, K.S.2
Siena, S.3
Tabernero, J.4
Burkes, R.5
Barugel, M.6
Humblet, Y.7
Bodoky, G.8
Cunningham, D.9
Jassem, J.10
Rivera, F.11
Kocakova, I.12
Ruff, P.13
Blasinska-Morawiec, M.14
Smakal, M.15
Canon, J.L.16
Rother, M.17
Williams, R.18
Rong, A.19
Wiezorek, J.20
Sidhu, R.21
Patterson, S.D.22
more..
-
7
-
-
84879290901
-
College of American pathologists international association for the study of lung cancer and association for molecular pathology, Molecular testing guideline for selection of lung cancer patients for EGFR and ALK tyrosine kinase inhibitors: Guideline from the college of American pathologists, international association for the study of lung cancer, and association for molecular pathology
-
23562183 1:CAS:528:DC%2BC3sXls1SnsLk%3D
-
N.I. Lindeman, P.T. Cagle, M.B. Beasley, D.A. Chitale, S. Dacic, G. Giaccone, R.B. Jenkins, D.J. Kwiatkowski, J.S. Saldivar, J. Squire, E. Thunnissen, M. Ladanyi, College of American pathologists international association for the study of lung cancer and association for molecular pathology, Molecular testing guideline for selection of lung cancer patients for EGFR and ALK tyrosine kinase inhibitors: guideline from the college of American pathologists, international association for the study of lung cancer, and association for molecular pathology. J Mol Diagn 15, 415-453 (2013)
-
(2013)
J Mol Diagn
, vol.15
, pp. 415-453
-
-
Lindeman, N.I.1
Cagle, P.T.2
Beasley, M.B.3
Chitale, D.A.4
Dacic, S.5
Giaccone, G.6
Jenkins, R.B.7
Kwiatkowski, D.J.8
Saldivar, J.S.9
Squire, J.10
Thunnissen, E.11
Ladanyi, M.12
-
8
-
-
84874144193
-
Personalized cancer medicine: Molecular diagnostics, predictive biomarkers, and drug resistance
-
C.D. de Gonzalez, P.A. Clarke, B. Al-Lazikani, P. Workman, Personalized cancer medicine: molecular diagnostics, predictive biomarkers, and drug resistance. Clin Pharmacol Ther 93, 252-259 (2013)
-
(2013)
Clin Pharmacol Ther
, vol.93
, pp. 252-259
-
-
De Gonzalez, C.D.1
Clarke, P.A.2
Al-Lazikani, B.3
Workman, P.4
-
9
-
-
84875905994
-
Diagnostic applications of high-throughput DNA sequencing
-
23121054 1:CAS:528:DC%2BC3sXltVKqs7s%3D
-
S.D. Boyd, Diagnostic applications of high-throughput DNA sequencing. Annu Rev Pathol 8, 381-410 (2013)
-
(2013)
Annu Rev Pathol
, vol.8
, pp. 381-410
-
-
Boyd, S.D.1
-
10
-
-
84865783136
-
Tackling formalin-fixed, paraffin-embedded tumor tissue with next-generation sequencing
-
22585165 1:CAS:528:DC%2BC38XmtlKgsw%3D%3D
-
C.L. Corless, P.T. Spellman, Tackling formalin-fixed, paraffin-embedded tumor tissue with next-generation sequencing. Cancer Discov 2, 23-24 (2012)
-
(2012)
Cancer Discov
, vol.2
, pp. 23-24
-
-
Corless, C.L.1
Spellman, P.T.2
-
11
-
-
84864917026
-
Identification of high-confidence somatic mutations in whole genome sequence of formalin-fixed breast cancer specimens
-
22492626 1:CAS:528:DC%2BC38XhtF2rsLjM 3413110
-
S.E. Yost, E.N. Smith, R.B. Schwab, L. Bao, H. Jung, X. Wang, E. Voest, J.P. Pierce, K. Messer, B.A. Parker, O. Harismendy, K.A. Frazer, Identification of high-confidence somatic mutations in whole genome sequence of formalin-fixed breast cancer specimens. Nucleic Acids Res 40, e107 (2012)
-
(2012)
Nucleic Acids Res
, vol.40
, pp. 107
-
-
Yost, S.E.1
Smith, E.N.2
Schwab, R.B.3
Bao, L.4
Jung, H.5
Wang, X.6
Voest, E.7
Pierce, J.P.8
Messer, K.9
Parker, B.A.10
Harismendy, O.11
Frazer, K.A.12
-
12
-
-
84860756398
-
Performance comparison of benchtop high-throughput sequencing platforms
-
22522955 1:CAS:528:DC%2BC38XlvVKltrc%3D
-
N.J. Loman, R.V. Misra, T.J. Dallman, C. Constantinidou, S.E. Gharbia, J. Wain, M.J. Pallen, Performance comparison of benchtop high-throughput sequencing platforms. Nat Biotechnol 30, 434-439 (2012)
-
(2012)
Nat Biotechnol
, vol.30
, pp. 434-439
-
-
Loman, N.J.1
Misra, R.V.2
Dallman, T.J.3
Constantinidou, C.4
Gharbia, S.E.5
Wain, J.6
Pallen, M.J.7
-
13
-
-
84865591846
-
A tale of three next generation sequencing platforms: Comparison of Ion Torrent, Pacific Biosciences and Illumina MiSeq sequencers
-
22827831 1:CAS:528:DC%2BC38Xhslaju7zI 3431227
-
M.A. Quail, M. Smith, P. Coupland, T.D. Otto, S.R. Harris, T.R. Connor, A. Bertoni, H.P. Swerdlow, Y. Gu, A tale of three next generation sequencing platforms: comparison of Ion Torrent, Pacific Biosciences and Illumina MiSeq sequencers. BMC Genomics 13, 341 (2012)
-
(2012)
BMC Genomics
, vol.13
, pp. 341
-
-
Quail, M.A.1
Smith, M.2
Coupland, P.3
Otto, T.D.4
Harris, S.R.5
Connor, T.R.6
Bertoni, A.7
Swerdlow, H.P.8
Gu, Y.9
-
14
-
-
84893838300
-
Clinical application of amplicon-based next-generation sequencing in cancer
-
24332266 1:CAS:528:DC%2BC3sXhvFyrurnJ
-
F. Chang, M.M. Li, Clinical application of amplicon-based next-generation sequencing in cancer. Cancer Genet 206, 413-419 (2013)
-
(2013)
Cancer Genet
, vol.206
, pp. 413-419
-
-
Chang, F.1
Li, M.M.2
-
15
-
-
84914162901
-
Next generation diagnostic molecular pathology: Critical appraisal of quality assurance in Europe
-
24704265
-
H.J. Dubbink, Z.C. Deans, B.B. Tops, F.J. van Kemenade, S. Koljenovic, H.J. van Krieken, W.A. Blokx, W.N. Dinjens, P.J. Groenen, Next generation diagnostic molecular pathology: Critical appraisal of quality assurance in Europe. Mol Oncol (2014). doi: 10.1016/j.molonc.2014.03.004
-
(2014)
Mol Oncol
-
-
Dubbink, H.J.1
Deans, Z.C.2
Tops, B.B.3
Van Kemenade, F.J.4
Koljenovic, S.5
Van Krieken, H.J.6
Blokx, W.A.7
Dinjens, W.N.8
Groenen, P.J.9
-
16
-
-
84905858372
-
Next generation sequencing: A change of paradigm in molecular diagnostic validation
-
24756835
-
M. Salto-Tellez, D.G. de Castro, Next generation sequencing: a change of paradigm in molecular diagnostic validation. J Pathol (2014). doi: 10.1002/path.4365
-
(2014)
J Pathol
-
-
Salto-Tellez, M.1
De Castro, D.G.2
-
17
-
-
84894262939
-
FDA-approved Next-Generation sequencing system could expand clinical genomic testing: Experts predict MiSeqDx system will make genetic testing more affordable for smaller labs
-
FDA-approved Next-Generation sequencing system could expand clinical genomic testing: experts predict MiSeqDx system will make genetic testing more affordable for smaller labs. Am. J. Med. Genet. A 164A, x-xi (2014)
-
(2014)
Am. J. Med. Genet
, vol.164 A
, pp. x-xi
-
-
-
18
-
-
84886052163
-
Molecular diagnostic profiling of lung cancer specimens with a semiconductor-based massive parallel sequencing approach: Feasibility, costs, and performance compared with conventional sequencing
-
23973117 1:CAS:528:DC%2BC3sXhs1OqtrrJ
-
V. Endris, R. Penzel, A. Warth, A. Muckenhuber, P. Schirmacher, A. Stenzinger, W. Weichert, Molecular diagnostic profiling of lung cancer specimens with a semiconductor-based massive parallel sequencing approach: feasibility, costs, and performance compared with conventional sequencing. J Mol Diagn 15, 765-775 (2013)
-
(2013)
J Mol Diagn
, vol.15
, pp. 765-775
-
-
Endris, V.1
Penzel, R.2
Warth, A.3
Muckenhuber, A.4
Schirmacher, P.5
Stenzinger, A.6
Weichert, W.7
-
19
-
-
84890421610
-
Validation of a next-generation sequencing assay for clinical molecular oncology
-
24211365 1:CAS:528:DC%2BC3sXhvFyru7nK
-
C.E. Cottrell, H. Al-Kateb, A.J. Bredemeyer, E.J. Duncavage, D.H. Spencer, H.J. Abel, C.M. Lockwood, I.S. Hagemann, S.M. O'Guin, L.C. Burcea, C.S. Sawyer, D.M. Oschwald, J.L. Stratman, D.A. Sher, M.R. Johnson, J.T. Brown, P.F. Cliften, B. George, L.D. McIntosh, S. Shrivastava, T.T. Nguyen, J.E. Payton, M.A. Watson, S.D. Crosby, R.D. Head, R.D. Mitra, R. Nagarajan, S. Kulkarni, K. Seibert, H.W. Virgin, J. Milbrandt, J.D. Pfeifer, Validation of a next-generation sequencing assay for clinical molecular oncology. J Mol Diagn 16, 89-105 (2014)
-
(2014)
J Mol Diagn
, vol.16
, pp. 89-105
-
-
Cottrell, C.E.1
Al-Kateb, H.2
Bredemeyer, A.J.3
Duncavage, E.J.4
Spencer, D.H.5
Abel, H.J.6
Lockwood, C.M.7
Hagemann, I.S.8
O'Guin, S.M.9
Burcea, L.C.10
Sawyer, C.S.11
Oschwald, D.M.12
Stratman, J.L.13
Sher, D.A.14
Johnson, M.R.15
Brown, J.T.16
Cliften, P.F.17
George, B.18
McIntosh, L.D.19
Shrivastava, S.20
Nguyen, T.T.21
Payton, J.E.22
Watson, M.A.23
Crosby, S.D.24
Head, R.D.25
Mitra, R.D.26
Nagarajan, R.27
Kulkarni, S.28
Seibert, K.29
Virgin, H.W.30
Milbrandt, J.31
Pfeifer, J.D.32
more..
-
20
-
-
84880799275
-
Validation of next generation sequencing technologies in comparison to current diagnostic gold standards for BRAF, EGFR and KRAS mutational analysis
-
23922754 1:CAS:528:DC%2BC3sXht1GisLnM 3724913
-
C.M. McCourt, D.G. McArt, K. Mills, M.A. Catherwood, P. Maxwell, D.J. Waugh, P. Hamilton, J.M. O'Sullivan, M. Salto-Tellez, Validation of next generation sequencing technologies in comparison to current diagnostic gold standards for BRAF, EGFR and KRAS mutational analysis. PLoS One 8, e69604 (2013)
-
(2013)
PLoS One
, vol.8
, pp. 69604
-
-
McCourt, C.M.1
McArt, D.G.2
Mills, K.3
Catherwood, M.A.4
Maxwell, P.5
Waugh, D.J.6
Hamilton, P.7
O'Sullivan, J.M.8
Salto-Tellez, M.9
-
21
-
-
84883316129
-
Reducing sequence artifacts in amplicon-based massively parallel sequencing of formalin-fixed paraffin-embedded DNA by enzymatic depletion of uracil-containing templates
-
23649127 1:CAS:528:DC%2BC3sXhsVaiu73P
-
H. Do, S.Q. Wong, J. Li, A. Dobrovic, Reducing sequence artifacts in amplicon-based massively parallel sequencing of formalin-fixed paraffin-embedded DNA by enzymatic depletion of uracil-containing templates. Clin Chem 59, 1376-1383 (2013)
-
(2013)
Clin Chem
, vol.59
, pp. 1376-1383
-
-
Do, H.1
Wong, S.Q.2
Li, J.3
Dobrovic, A.4
-
22
-
-
84896713227
-
Genomes in the clinic: The Gustave Roussy cancer center experience
-
L. Lacroix, A. Boichard, F. Andre, J.C. Soria, Genomes in the clinic: the Gustave Roussy cancer center experience. Curr Opin Genet Dev 24C, 99-106 (2014)
-
(2014)
Curr Opin Genet Dev
, vol.24
, pp. 99-106
-
-
Lacroix, L.1
Boichard, A.2
Andre, F.3
Soria, J.C.4
-
23
-
-
84901604272
-
Sequence artefacts in a prospective series of formalin-fixed tumours tested for mutations in hotspot regions by massively parallel sequencing
-
24885028 4032349
-
S.Q. Wong, J. Li, A.Y. Tan, R. Vedururu, J.M. Pang, H. Do, J. Ellul, K. Doig, A. Bell, G.A. MacArthur, S.B. Fox, D.M. Thomas, A. Fellowes, J.P. Parisot, A. Dobrovic, Sequence artefacts in a prospective series of formalin-fixed tumours tested for mutations in hotspot regions by massively parallel sequencing. BMC Med Genomics 7, 23 (2014)
-
(2014)
BMC Med Genomics
, vol.7
, pp. 23
-
-
Wong, S.Q.1
Li, J.2
Tan, A.Y.3
Vedururu, R.4
Pang, J.M.5
Do, H.6
Ellul, J.7
Doig, K.8
Bell, A.9
Macarthur, G.A.10
Fox, S.B.11
Thomas, D.M.12
Fellowes, A.13
Parisot, J.P.14
Dobrovic, A.15
-
24
-
-
84904383595
-
Next-generation sequencing analysis of lung and colon carcinomas reveals a variety of genetic alterations
-
24990411 1:CAS:528:DC%2BC2cXhsFWhtbjN
-
S. Chevrier, L. Arnould, F. Ghiringhelli, B. Coudert, P. Fumoleau, R. Boidot, Next-generation sequencing analysis of lung and colon carcinomas reveals a variety of genetic alterations. Int J Oncol 45, 1167-1174 (2014)
-
(2014)
Int J Oncol
, vol.45
, pp. 1167-1174
-
-
Chevrier, S.1
Arnould, L.2
Ghiringhelli, F.3
Coudert, B.4
Fumoleau, P.5
Boidot, R.6
-
25
-
-
67650257467
-
A fast, sensitive and accurate high resolution melting (HRM) technology-based assay to screen for common K-ras mutations
-
19478384 1:CAS:528:DC%2BD1MXlsFWgsrs%3D
-
D. Kramer, F.B. Thunnissen, M.I. Gallegos-Ruiz, E.F. Smit, P.E. Postmus, C.J. Meijer, P.J. Snijders, D.A. Heideman, A fast, sensitive and accurate high resolution melting (HRM) technology-based assay to screen for common K-ras mutations. Cell Oncol 31, 161-167 (2009)
-
(2009)
Cell Oncol
, vol.31
, pp. 161-167
-
-
Kramer, D.1
Thunnissen, F.B.2
Gallegos-Ruiz, M.I.3
Smit, E.F.4
Postmus, P.E.5
Meijer, C.J.6
Snijders, P.J.7
Heideman, D.A.8
-
26
-
-
70149091283
-
A panel of high resolution melting (HRM) technology-based assays with direct sequencing possibility for effective mutation screening of EGFR and K-ras genes
-
19759413 1:CAS:528:DC%2BD1MXhtVGju7jI
-
D.A. Heideman, F.B. Thunnissen, M. Doeleman, D. Kramer, H.M. Verheul, E.F. Smit, P.E. Postmus, C.J. Meijer, G.A. Meijer, P.J. Snijders, A panel of high resolution melting (HRM) technology-based assays with direct sequencing possibility for effective mutation screening of EGFR and K-ras genes. Cell Oncol 31, 329-333 (2009)
-
(2009)
Cell Oncol
, vol.31
, pp. 329-333
-
-
Heideman, D.A.1
Thunnissen, F.B.2
Doeleman, M.3
Kramer, D.4
Verheul, H.M.5
Smit, E.F.6
Postmus, P.E.7
Meijer, C.J.8
Meijer, G.A.9
Snijders, P.J.10
-
27
-
-
84859583692
-
KRAS and BRAF mutation analysis in routine molecular diagnostics: Comparison of three testing methods on formalin-fixed, paraffin-embedded tumor-derived DNA
-
22425762 1:CAS:528:DC%2BC38XptVaitbc%3D
-
D.A. Heideman, I. Lurkin, M. Doeleman, E.F. Smit, H.M. Verheul, G.A. Meijer, P.J. Snijders, E. Thunnissen, E.C. Zwarthoff, KRAS and BRAF mutation analysis in routine molecular diagnostics: comparison of three testing methods on formalin-fixed, paraffin-embedded tumor-derived DNA. J Mol Diagn 14, 247-255 (2012)
-
(2012)
J Mol Diagn
, vol.14
, pp. 247-255
-
-
Heideman, D.A.1
Lurkin, I.2
Doeleman, M.3
Smit, E.F.4
Verheul, H.M.5
Meijer, G.A.6
Snijders, P.J.7
Thunnissen, E.8
Zwarthoff, E.C.9
-
29
-
-
84907801375
-
Validation of Illumina TruSeq Amplicon Cancer Panel with concordance testing using Ion AmpliSeq Cancer Panel and other methods
-
Apr 6-10; Washington, DC. Philadelphia (PA): AACR; Cancer Res 73, Abstract nr
-
P.Fang, Z.Yan, W.Liu, A.Darwanto, K.Pelak, K.Anoe, C.Spittle, S.Sankar, C.Galderisi, J.Li, Validation of Illumina TruSeq Amplicon Cancer Panel with concordance testing using Ion AmpliSeq Cancer Panel and other methods. In: Proceedings of the 104th Annual Meeting of the American Association for Cancer Research; 2013 Apr 6-10; Washington, DC. Philadelphia (PA): AACR; Cancer Res 73, Abstract nr 3229 (2013)
-
(2013)
Proceedings of the 104th Annual Meeting of the American Association for Cancer Research
, pp. 3229
-
-
Fang, P.1
Yan, Z.2
Liu, W.3
Darwanto, A.4
Pelak, K.5
Anoe, K.6
Spittle, C.7
Sankar, S.8
Galderisi, C.9
Li, J.10
-
30
-
-
80255127234
-
Cutadapt removes adapter sequences from high-throughput sequencing reads. EMBnet
-
M. Martin, Cutadapt removes adapter sequences from high-throughput sequencing reads. EMBnet. Journal 17, 10-12 (2011)
-
(2011)
Journal
, vol.17
, pp. 10-12
-
-
Martin, M.1
-
31
-
-
79958795493
-
-
Hannon Lab Electronic Citation
-
Hannon Lab, FASTX-Toolkit. http://hannonlab.cshl.edu/fastx-toolkit/. Electronic Citation (2010)
-
(2010)
FASTX-Toolkit
-
-
-
32
-
-
80054913451
-
FLASH: Fast length adjustment of short reads to improve genome assemblies
-
21903629 1:CAS:528:DC%2BC3MXhtlGkur7M 3198573
-
T. Magoc, S.L. Salzberg, FLASH: fast length adjustment of short reads to improve genome assemblies. Bioinformatics 27, 2957-2963 (2011)
-
(2011)
Bioinformatics
, vol.27
, pp. 2957-2963
-
-
Magoc, T.1
Salzberg, S.L.2
-
33
-
-
77949587649
-
Fast and accurate long-read alignment with Burrows-Wheeler transform
-
20080505 2828108
-
H. Li, R. Durbin, Fast and accurate long-read alignment with Burrows-Wheeler transform. Bioinformatics 26, 589-595 (2010)
-
(2010)
Bioinformatics
, vol.26
, pp. 589-595
-
-
Li, H.1
Durbin, R.2
-
34
-
-
84876030710
-
Using Drosophila melanogaster as a model for genotoxic chemical mutational studies with a new program, SnpSift
-
22435069 3304048
-
P. Cingolani, V.M. Patel, M. Coon, T. Nguyen, S.J. Land, D.M. Ruden, X. Lu, Using Drosophila melanogaster as a model for genotoxic chemical mutational studies with a new program, SnpSift. Front Genet 3, 35 (2012)
-
(2012)
Front Genet
, vol.3
, pp. 35
-
-
Cingolani, P.1
Patel, V.M.2
Coon, M.3
Nguyen, T.4
Land, S.J.5
Ruden, D.M.6
Lu, X.7
-
35
-
-
78651271733
-
Integrative genomics viewer
-
21221095 1:CAS:528:DC%2BC3MXjsFWrtg%3D%3D 3346182
-
J.T. Robinson, H. Thorvaldsdottir, W. Winckler, M. Guttman, E.S. Lander, G. Getz, J.P. Mesirov, Integrative genomics viewer. Nat Biotechnol 29, 24-26 (2011)
-
(2011)
Nat Biotechnol
, vol.29
, pp. 24-26
-
-
Robinson, J.T.1
Thorvaldsdottir, H.2
Winckler, W.3
Guttman, M.4
Lander, E.S.5
Getz, G.6
Mesirov, J.P.7
-
36
-
-
84975742565
-
A map of human genome variation from population-scale sequencing
-
20981092
-
G.R. Abecasis, D. Altshuler, A. Auton, L.D. Brooks, R.M. Durbin, R.A. Gibbs, M.E. Hurles, G.A. McVean, A map of human genome variation from population-scale sequencing. Nature 467, 1061-1073 (2010)
-
(2010)
Nature
, vol.467
, pp. 1061-1073
-
-
Abecasis, G.R.1
Altshuler, D.2
Auton, A.3
Brooks, L.D.4
Durbin, R.M.5
Gibbs, R.A.6
Hurles, M.E.7
McVean, G.A.8
-
37
-
-
79960463308
-
Preparing pathology for personalized medicine: Possibilities for improvement of the pre-analytical phase
-
21477258
-
P.J. Groenen, W.A. Blokx, C. Diepenbroek, L. Burgers, F. Visinoni, P. Wesseling, J.H. van Krieken, Preparing pathology for personalized medicine: possibilities for improvement of the pre-analytical phase. Histopathology 59, 1-7 (2011)
-
(2011)
Histopathology
, vol.59
, pp. 1-7
-
-
Groenen, P.J.1
Blokx, W.A.2
Diepenbroek, C.3
Burgers, L.4
Visinoni, F.5
Wesseling, P.6
Van Krieken, J.H.7
|