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Volumn 32, Issue 4, 2012, Pages 585-599

Clinical Integration of Next-Generation Sequencing Technology

Author keywords

Clinical pathology; Computational pathology; Genomic sequencing; Genomics; Molecular diagnostics; Next generation sequencing; Tumor diagnostics

Indexed keywords

DNA; RNA; VEMURAFENIB;

EID: 84867664513     PISSN: 02722712     EISSN: 15579832     Source Type: Journal    
DOI: 10.1016/j.cll.2012.07.005     Document Type: Review
Times cited : (52)

References (57)
  • 1
    • 44349191457 scopus 로고    scopus 로고
    • Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing
    • Campbell P.J., Stephens P.J., Pleasance E.D., et al. Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing. Nat Genet 2008, 40(6):722-729.
    • (2008) Nat Genet , vol.40 , Issue.6 , pp. 722-729
    • Campbell, P.J.1    Stephens, P.J.2    Pleasance, E.D.3
  • 2
    • 53649106195 scopus 로고    scopus 로고
    • Next-generation DNA sequencing
    • Shendure J., Ji H. Next-generation DNA sequencing. Nat Biotechnol 2008, 26(10):1135-1145.
    • (2008) Nat Biotechnol , vol.26 , Issue.10 , pp. 1135-1145
    • Shendure, J.1    Ji, H.2
  • 3
    • 65449144325 scopus 로고    scopus 로고
    • Evaluation of next generation sequencing platforms for population targeted sequencing studies
    • Harismendy O., Ng P.C., Strausberg R.L., et al. Evaluation of next generation sequencing platforms for population targeted sequencing studies. Genome Biol 2009, 10(3):R32.
    • (2009) Genome Biol , vol.10 , Issue.3
    • Harismendy, O.1    Ng, P.C.2    Strausberg, R.L.3
  • 4
    • 72849144434 scopus 로고    scopus 로고
    • Sequencing technologies - the next generation
    • Metzker M.L. Sequencing technologies - the next generation. Nat Rev Genet 2010, 11(1):31-46.
    • (2010) Nat Rev Genet , vol.11 , Issue.1 , pp. 31-46
    • Metzker, M.L.1
  • 5
    • 80053508491 scopus 로고    scopus 로고
    • Whole cancer genome sequencing by next-generation methods
    • Ross J.S., Cronin M. Whole cancer genome sequencing by next-generation methods. Am J Clin Pathol 2011, 136(4):527-539.
    • (2011) Am J Clin Pathol , vol.136 , Issue.4 , pp. 527-539
    • Ross, J.S.1    Cronin, M.2
  • 6
    • 33745145845 scopus 로고    scopus 로고
    • Embracing the complexity of genomic data for personalized medicine
    • West M., Ginsburg G.S., Huang A.T., et al. Embracing the complexity of genomic data for personalized medicine. Genome Res 2006, 16(5):559-566.
    • (2006) Genome Res , vol.16 , Issue.5 , pp. 559-566
    • West, M.1    Ginsburg, G.S.2    Huang, A.T.3
  • 7
    • 70349969478 scopus 로고    scopus 로고
    • Mutational evolution in a lobular breast tumour profiled at single nucleotide resolution
    • Shah S.P., Morin R.D., Khattra J., et al. Mutational evolution in a lobular breast tumour profiled at single nucleotide resolution. Nature 2009, 461(7265):809-813.
    • (2009) Nature , vol.461 , Issue.7265 , pp. 809-813
    • Shah, S.P.1    Morin, R.D.2    Khattra, J.3
  • 8
    • 84860756398 scopus 로고    scopus 로고
    • Performance comparison of bench top high-throughput sequencing platforms
    • Loman N.J., Misra R.V., Dallman T.J., et al. Performance comparison of bench top high-throughput sequencing platforms. Nat Biotechnol 2012, 30:434-439.
    • (2012) Nat Biotechnol , vol.30 , pp. 434-439
    • Loman, N.J.1    Misra, R.V.2    Dallman, T.J.3
  • 9
    • 84856296578 scopus 로고    scopus 로고
    • Target enrichment via DNA hybridization capture
    • Horn S. Target enrichment via DNA hybridization capture. Methods Mol Biol 2012, 840:177-188.
    • (2012) Methods Mol Biol , vol.840 , pp. 177-188
    • Horn, S.1
  • 10
  • 11
    • 77957968556 scopus 로고    scopus 로고
    • PLX4032, a potent inhibitor of the B-Raf V600E oncogene, selectively inhibits V600E-positive melanomas
    • Lee J.T., Li L., Brafford P.A., et al. PLX4032, a potent inhibitor of the B-Raf V600E oncogene, selectively inhibits V600E-positive melanomas. Pigment Cell Melanoma Res 2010, 23(6):820-827.
    • (2010) Pigment Cell Melanoma Res , vol.23 , Issue.6 , pp. 820-827
    • Lee, J.T.1    Li, L.2    Brafford, P.A.3
  • 12
    • 84860150463 scopus 로고    scopus 로고
    • Agreement in risk prediction between the 21-gene recurrence score assay (Oncotype DX(R)) and the PAM50 breast cancer intrinsic Classifier™ in early-stage estrogen receptor-positive breast cancer
    • Kelly C.M., Bernard P.S., Krishnamurthy S., et al. Agreement in risk prediction between the 21-gene recurrence score assay (Oncotype DX(R)) and the PAM50 breast cancer intrinsic Classifier™ in early-stage estrogen receptor-positive breast cancer. Oncologist 2012, 17(4):492-498.
    • (2012) Oncologist , vol.17 , Issue.4 , pp. 492-498
    • Kelly, C.M.1    Bernard, P.S.2    Krishnamurthy, S.3
  • 13
    • 0037137519 scopus 로고    scopus 로고
    • A gene-expression signature as a predictor of survival in breast cancer
    • van de Vijver M.J., He Y.D., van't Veer L.J., et al. A gene-expression signature as a predictor of survival in breast cancer. N Engl J Med 2002, 347(25):1999-2009.
    • (2002) N Engl J Med , vol.347 , Issue.25 , pp. 1999-2009
    • van de Vijver, M.J.1    He, Y.D.2    van't Veer, L.J.3
  • 14
    • 33947393565 scopus 로고    scopus 로고
    • Mapping the cancer genome. Pinpointing the genes involved in cancer will help chart a new course across the complex landscape of human malignancies
    • Collins F.S., Barker A.D. Mapping the cancer genome. Pinpointing the genes involved in cancer will help chart a new course across the complex landscape of human malignancies. Sci Am 2007, 296(3):50-57.
    • (2007) Sci Am , vol.296 , Issue.3 , pp. 50-57
    • Collins, F.S.1    Barker, A.D.2
  • 15
    • 77951115122 scopus 로고    scopus 로고
    • International network of cancer genome projects
    • International Cancer Genome Consortium
    • International Cancer Genome Consortium International network of cancer genome projects. Nature 2010, 464(7291):993-998.
    • (2010) Nature , vol.464 , Issue.7291 , pp. 993-998
  • 16
    • 55549097836 scopus 로고    scopus 로고
    • Mapping short DNA sequencing reads and calling variants using mapping quality scores
    • Li H., Ruan J., Durbin R. Mapping short DNA sequencing reads and calling variants using mapping quality scores. Genome Res 2008, 18(11):1851-1858.
    • (2008) Genome Res , vol.18 , Issue.11 , pp. 1851-1858
    • Li, H.1    Ruan, J.2    Durbin, R.3
  • 17
    • 25644453578 scopus 로고    scopus 로고
    • A space-efficient construction of the Burrows-Wheeler transform for genomic data
    • [review]
    • Lippert R.A., Mobarry C.M., Walenz B.P. A space-efficient construction of the Burrows-Wheeler transform for genomic data. J Comput Biol 2005, 12(7):943-951. [review].
    • (2005) J Comput Biol , vol.12 , Issue.7 , pp. 943-951
    • Lippert, R.A.1    Mobarry, C.M.2    Walenz, B.P.3
  • 18
    • 39649084637 scopus 로고    scopus 로고
    • Bioinformatics challenges of new sequencing technology
    • [review]
    • Pop M., Salzberg S.L. Bioinformatics challenges of new sequencing technology. Trends Genet 2008, 24(3):142-149. [review].
    • (2008) Trends Genet , vol.24 , Issue.3 , pp. 142-149
    • Pop, M.1    Salzberg, S.L.2
  • 19
    • 40049104732 scopus 로고    scopus 로고
    • SOAP: short oligonucleotide alignment program
    • Li R., Li Y., Kristiansen K., et al. SOAP: short oligonucleotide alignment program. Bioinformatics 2008, 24(5):713-714.
    • (2008) Bioinformatics , vol.24 , Issue.5 , pp. 713-714
    • Li, R.1    Li, Y.2    Kristiansen, K.3
  • 20
    • 54949110994 scopus 로고    scopus 로고
    • ZOOM! Zillions of oligos mapped
    • Lin H., Zhang Z., Zhang M.Q., et al. ZOOM! Zillions of oligos mapped. Bioinformatics 2008, 24(21):2431-2437.
    • (2008) Bioinformatics , vol.24 , Issue.21 , pp. 2431-2437
    • Lin, H.1    Zhang, Z.2    Zhang, M.Q.3
  • 21
    • 67049159825 scopus 로고    scopus 로고
    • SHRiMP: accurate mapping of short color-space reads
    • Rumble S.M., Lacroute P., Dalca A.V., et al. SHRiMP: accurate mapping of short color-space reads. PLoS Comput Biol 2009, 5(5):e1000386.
    • (2009) PLoS Comput Biol , vol.5 , Issue.5
    • Rumble, S.M.1    Lacroute, P.2    Dalca, A.V.3
  • 22
    • 79959640102 scopus 로고    scopus 로고
    • Evaluation of next-generation sequencing software in mapping and assembly
    • Bao S., Jiang R., Kwan W., et al. Evaluation of next-generation sequencing software in mapping and assembly. J Hum Genet 2011, 56(6):406-414.
    • (2011) J Hum Genet , vol.56 , Issue.6 , pp. 406-414
    • Bao, S.1    Jiang, R.2    Kwan, W.3
  • 23
    • 43149115851 scopus 로고    scopus 로고
    • Velvet: algorithms for de novo short read assembly using de Bruijn graphs
    • Zerbino D.R., Birney E. Velvet: algorithms for de novo short read assembly using de Bruijn graphs. Genome Res 2008, 18(5):821-829.
    • (2008) Genome Res , vol.18 , Issue.5 , pp. 821-829
    • Zerbino, D.R.1    Birney, E.2
  • 24
    • 77956967295 scopus 로고    scopus 로고
    • Using the Velvet de novo assembler for short-read sequencing technologies
    • Zerbino D.R. Using the Velvet de novo assembler for short-read sequencing technologies. Curr Protoc Bioinformatics 2010, 11(11):5.
    • (2010) Curr Protoc Bioinformatics , vol.11 , Issue.11 , pp. 5
    • Zerbino, D.R.1
  • 25
    • 39049156065 scopus 로고    scopus 로고
    • Short read fragment assembly of bacterial genomes
    • Chaisson M.J., Pevzner P.A. Short read fragment assembly of bacterial genomes. Genome Res 2008, 18(2):324-330.
    • (2008) Genome Res , vol.18 , Issue.2 , pp. 324-330
    • Chaisson, M.J.1    Pevzner, P.A.2
  • 26
    • 43149085041 scopus 로고    scopus 로고
    • De novo bacterial genome sequencing: millions of very short reads assembled on a desktop computer
    • Hernandez D., François P., Farinelli L., et al. De novo bacterial genome sequencing: millions of very short reads assembled on a desktop computer. Genome Res 2008, 18(5):802-809.
    • (2008) Genome Res , vol.18 , Issue.5 , pp. 802-809
    • Hernandez, D.1    François, P.2    Farinelli, L.3
  • 27
    • 62549098185 scopus 로고    scopus 로고
    • QSRA: a quality-value guided de novo short read assembler
    • Bryant D.W., Wong W.K., Mockler T.C. QSRA: a quality-value guided de novo short read assembler. BMC Bioinformatics 2009, 10:69.
    • (2009) BMC Bioinformatics , vol.10 , pp. 69
    • Bryant, D.W.1    Wong, W.K.2    Mockler, T.C.3
  • 28
    • 66449136667 scopus 로고    scopus 로고
    • ABySS: a parallel assembler for short read sequence data
    • Simpson J.T., Wong K., Jackman S.D., et al. ABySS: a parallel assembler for short read sequence data. Genome Res 2009, 19(6):1117-1123.
    • (2009) Genome Res , vol.19 , Issue.6 , pp. 1117-1123
    • Simpson, J.T.1    Wong, K.2    Jackman, S.D.3
  • 29
    • 2342624080 scopus 로고    scopus 로고
    • EGFR mutations in lung cancer: correlation with clinical response to gefitinib therapy
    • Paez J.G., Jänne P.A., Lee J.C., et al. EGFR mutations in lung cancer: correlation with clinical response to gefitinib therapy. Science 2004, 304(5676):1497-1500.
    • (2004) Science , vol.304 , Issue.5676 , pp. 1497-1500
    • Paez, J.G.1    Jänne, P.A.2    Lee, J.C.3
  • 30
    • 84861550476 scopus 로고    scopus 로고
    • The life history of 21 breast cancers
    • Breast Cancer Working Group of the International Cancer Genome Consortium
    • Nik-Zainal S., Van Loo P., Wedge D.C., Breast Cancer Working Group of the International Cancer Genome Consortium, et al. The life history of 21 breast cancers. Cell 2012, 149(5):994-1007.
    • (2012) Cell , vol.149 , Issue.5 , pp. 994-1007
    • Nik-Zainal, S.1    Van Loo, P.2    Wedge, D.C.3
  • 31
    • 77951957381 scopus 로고    scopus 로고
    • SNVMix: predicting single nucleotide variants from next-generation sequencing of tumors
    • Goya R., Sun M.G., Morin R.D., et al. SNVMix: predicting single nucleotide variants from next-generation sequencing of tumors. Bioinformatics 2010, 26(6):730-736.
    • (2010) Bioinformatics , vol.26 , Issue.6 , pp. 730-736
    • Goya, R.1    Sun, M.G.2    Morin, R.D.3
  • 32
    • 84863229597 scopus 로고    scopus 로고
    • VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing
    • Koboldt D.C., Zhang Q., Larson D.E., et al. VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing. Genome Res 2012, 22(3):568-576.
    • (2012) Genome Res , vol.22 , Issue.3 , pp. 568-576
    • Koboldt, D.C.1    Zhang, Q.2    Larson, D.E.3
  • 33
    • 84856565531 scopus 로고    scopus 로고
    • SomaticSniper: identification of somatic point mutations in whole genome sequencing data
    • Larson D.E., Harris C.C., Chen K., et al. SomaticSniper: identification of somatic point mutations in whole genome sequencing data. Bioinformatics 2012, 28(3):311-317.
    • (2012) Bioinformatics , vol.28 , Issue.3 , pp. 311-317
    • Larson, D.E.1    Harris, C.C.2    Chen, K.3
  • 34
    • 68549104404 scopus 로고    scopus 로고
    • The Sequence Alignment/Map format and SAMtools
    • 1000 Genome Project Data Processing Subgroup
    • Li H., Handsaker B., Wysoker A., 1000 Genome Project Data Processing Subgroup, et al. The Sequence Alignment/Map format and SAMtools. Bioinformatics 2009, 25(16):2078-2079.
    • (2009) Bioinformatics , vol.25 , Issue.16 , pp. 2078-2079
    • Li, H.1    Handsaker, B.2    Wysoker, A.3
  • 35
    • 70350694443 scopus 로고    scopus 로고
    • Pindel: a pattern growth approach to detect break points of large deletions and medium sized insertions from paired-end short reads
    • Ye K., Schulz M.H., Long Q., et al. Pindel: a pattern growth approach to detect break points of large deletions and medium sized insertions from paired-end short reads. Bioinformatics 2009, 25(21):2865-2871.
    • (2009) Bioinformatics , vol.25 , Issue.21 , pp. 2865-2871
    • Ye, K.1    Schulz, M.H.2    Long, Q.3
  • 36
    • 79955483667 scopus 로고    scopus 로고
    • A framework for variation discovery and genotyping using next-generation DNA sequencing data
    • DePristo M.A., Banks E., Poplin R., et al. A framework for variation discovery and genotyping using next-generation DNA sequencing data. Nat Genet 2011, 43(5):491-498.
    • (2011) Nat Genet , vol.43 , Issue.5 , pp. 491-498
    • DePristo, M.A.1    Banks, E.2    Poplin, R.3
  • 37
    • 78049380554 scopus 로고    scopus 로고
    • The patterns and dynamics of genomic instability in metastatic pancreatic cancer
    • Campbell P.J., Yachida S., Mudie L.J., et al. The patterns and dynamics of genomic instability in metastatic pancreatic cancer. Nature 2010, 467(7319):1109-1113.
    • (2010) Nature , vol.467 , Issue.7319 , pp. 1109-1113
    • Campbell, P.J.1    Yachida, S.2    Mudie, L.J.3
  • 38
    • 58149218240 scopus 로고    scopus 로고
    • High-resolution mapping of copy-number alterations with massively parallel sequencing
    • Chiang D.Y., Getz G., Jaffe D.B., et al. High-resolution mapping of copy-number alterations with massively parallel sequencing. Nat Methods 2009, 6(1):99-103.
    • (2009) Nat Methods , vol.6 , Issue.1 , pp. 99-103
    • Chiang, D.Y.1    Getz, G.2    Jaffe, D.B.3
  • 39
    • 69549116107 scopus 로고    scopus 로고
    • BreakDancer: an algorithm for high-resolution mapping of genomic structural variation
    • Chen K., Wallis J.W., McLellan M.D., et al. BreakDancer: an algorithm for high-resolution mapping of genomic structural variation. Nat Methods 2009, 6(9):677-681.
    • (2009) Nat Methods , vol.6 , Issue.9 , pp. 677-681
    • Chen, K.1    Wallis, J.W.2    McLellan, M.D.3
  • 40
    • 80052158097 scopus 로고    scopus 로고
    • The mutational landscape of head and neck squamous cell carcinoma
    • Stransky N., Egloff A.M., Tward A.D., et al. The mutational landscape of head and neck squamous cell carcinoma. Science 2011, 333(6046):1157-1160.
    • (2011) Science , vol.333 , Issue.6046 , pp. 1157-1160
    • Stransky, N.1    Egloff, A.M.2    Tward, A.D.3
  • 41
    • 73649123907 scopus 로고    scopus 로고
    • Integrated genomic analysis identifies clinically relevant subtypes of glioblastoma characterized by abnormalities in PDGFRA, IDH1, EGFR, and NF1
    • Cancer Genome Atlas Research Network
    • Verhaak R.G., Hoadley K.A., Purdom E., Cancer Genome Atlas Research Network, et al. Integrated genomic analysis identifies clinically relevant subtypes of glioblastoma characterized by abnormalities in PDGFRA, IDH1, EGFR, and NF1. Cancer Cell 2010, 17(1):98-110.
    • (2010) Cancer Cell , vol.17 , Issue.1 , pp. 98-110
    • Verhaak, R.G.1    Hoadley, K.A.2    Purdom, E.3
  • 42
    • 77950633122 scopus 로고    scopus 로고
    • Integrative analysis of the melanoma transcriptome
    • Berger M.F., Levin J.Z., Vijayendran K., et al. Integrative analysis of the melanoma transcriptome. Genome Res 2010, 20(4):413-427.
    • (2010) Genome Res , vol.20 , Issue.4 , pp. 413-427
    • Berger, M.F.1    Levin, J.Z.2    Vijayendran, K.3
  • 43
    • 36248980204 scopus 로고    scopus 로고
    • Characterizing the cancer genome in lung adenocarcinoma
    • Weir B.A., Woo M.S., Getz G., et al. Characterizing the cancer genome in lung adenocarcinoma. Nature 2007, 450(7171):893-898.
    • (2007) Nature , vol.450 , Issue.7171 , pp. 893-898
    • Weir, B.A.1    Woo, M.S.2    Getz, G.3
  • 44
    • 65449136284 scopus 로고    scopus 로고
    • TopHat: discovering splice junctions with RNA-Seq
    • Trapnell C., Pachter L., Salzberg S.L. TopHat: discovering splice junctions with RNA-Seq. Bioinformatics 2009, 25(9):1105-1111.
    • (2009) Bioinformatics , vol.25 , Issue.9 , pp. 1105-1111
    • Trapnell, C.1    Pachter, L.2    Salzberg, S.L.3
  • 45
    • 52949088691 scopus 로고    scopus 로고
    • A toolkit for analysing large-scale plant small RNA datasets
    • Moxon S., Schwach F., Dalmay T., et al. A toolkit for analysing large-scale plant small RNA datasets. Bioinformatics 2008, 24(19):2252-2253.
    • (2008) Bioinformatics , vol.24 , Issue.19 , pp. 2252-2253
    • Moxon, S.1    Schwach, F.2    Dalmay, T.3
  • 46
    • 41849084855 scopus 로고    scopus 로고
    • Discovering microRNAs from deep sequencing data using miRDeep
    • Friedländer M.R., Chen W., Adamidi C., et al. Discovering microRNAs from deep sequencing data using miRDeep. Nat Biotechnol 2008, 26(4):407-415.
    • (2008) Nat Biotechnol , vol.26 , Issue.4 , pp. 407-415
    • Friedländer, M.R.1    Chen, W.2    Adamidi, C.3
  • 47
    • 80052701585 scopus 로고    scopus 로고
    • MiRDeep-P: a computational tool for analyzing the microRNA transcriptome in plants
    • Yang X., Li L. miRDeep-P: a computational tool for analyzing the microRNA transcriptome in plants. Bioinformatics 2011, 27(18):2614-2615.
    • (2011) Bioinformatics , vol.27 , Issue.18 , pp. 2614-2615
    • Yang, X.1    Li, L.2
  • 48
    • 84975742565 scopus 로고    scopus 로고
    • A map of human genome variation from population-scale sequencing
    • 1000 Genomes Project Consortium
    • 1000 Genomes Project Consortium A map of human genome variation from population-scale sequencing. Nature 2010, 467(7319):1061-1073.
    • (2010) Nature , vol.467 , Issue.7319 , pp. 1061-1073
  • 49
    • 7244245762 scopus 로고    scopus 로고
    • Finishing the euchromatic sequence of the human genome
    • International Human Genome Sequencing Consortium
    • International Human Genome Sequencing Consortium Finishing the euchromatic sequence of the human genome. Nature 2004, 431(7011):931-945.
    • (2004) Nature , vol.431 , Issue.7011 , pp. 931-945
  • 50
    • 84875367355 scopus 로고    scopus 로고
    • Personal Genome Project. Available at:
    • Accessed May 21
    • Personal Genome Project. Available at: Accessed May 21, 2012. http://www.personalgenomes.org.
    • (2012)
  • 51
    • 77950456427 scopus 로고    scopus 로고
    • Multiple personal genomes await
    • Venter J.C. Multiple personal genomes await. Nature 2010, 464(7289):676-677.
    • (2010) Nature , vol.464 , Issue.7289 , pp. 676-677
    • Venter, J.C.1
  • 52
    • 77956331627 scopus 로고    scopus 로고
    • Integrating common and rare genetic variation in diverse human populations
    • International HapMap 3 Consortium
    • International HapMap 3 Consortium Integrating common and rare genetic variation in diverse human populations. Nature 2010, 467(7311):52-58.
    • (2010) Nature , vol.467 , Issue.7311 , pp. 52-58
  • 53
    • 0031672085 scopus 로고    scopus 로고
    • Population genomics: laying the groundwork for genetic disease modeling and targeting
    • Gulcher J., Stefansson K. Population genomics: laying the groundwork for genetic disease modeling and targeting. Clin Chem Lab Med 1998, 36(8):523-527.
    • (1998) Clin Chem Lab Med , vol.36 , Issue.8 , pp. 523-527
    • Gulcher, J.1    Stefansson, K.2
  • 54
    • 80054122350 scopus 로고    scopus 로고
    • Sequence analysis 101: a newbie's guide to crunching next-generation sequencing data
    • Perkel J.M. Sequence analysis 101: a newbie's guide to crunching next-generation sequencing data. Scientist 2011, 25:60.
    • (2011) Scientist , vol.25 , pp. 60
    • Perkel, J.M.1
  • 55
    • 84867687100 scopus 로고    scopus 로고
    • Harnessing the cloud
    • Maxmen A. Harnessing the cloud. Scientist 2010, 24:71.
    • (2010) Scientist , vol.24 , pp. 71
    • Maxmen, A.1
  • 56
    • 33748491718 scopus 로고    scopus 로고
    • Performance comparison of one-color and two-color platforms within the MicroArray Quality Control (MAQC) project
    • Patterson T.A., Lobenhofer E.K., Fulmer-Smentek S.B., et al. Performance comparison of one-color and two-color platforms within the MicroArray Quality Control (MAQC) project. Nat Biotechnol 2006, 24(9):1140-1150.
    • (2006) Nat Biotechnol , vol.24 , Issue.9 , pp. 1140-1150
    • Patterson, T.A.1    Lobenhofer, E.K.2    Fulmer-Smentek, S.B.3
  • 57
    • 77952968845 scopus 로고    scopus 로고
    • A call to action: training pathology residents in genomics and personalized medicine
    • Haspel R.L., Arnaout R., Briere L., et al. A call to action: training pathology residents in genomics and personalized medicine. Am J Clin Pathol 2010, 133(6):832-834.
    • (2010) Am J Clin Pathol , vol.133 , Issue.6 , pp. 832-834
    • Haspel, R.L.1    Arnaout, R.2    Briere, L.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.