메뉴 건너뛰기




Volumn 15, Issue 1, 2014, Pages

Detection of internal exon deletion with exon Del

Author keywords

[No Author keywords available]

Indexed keywords

BREAST CANCER CELLS; COPY NUMBER VARIATIONS; EFFICIENT DETECTION; HUMAN GENOMES; PCR TECHNOLOGY; SOURCE CODES;

EID: 84910156677     PISSN: None     EISSN: 14712105     Source Type: Journal    
DOI: 10.1186/1471-2105-15-332     Document Type: Article
Times cited : (10)

References (18)
  • 1
    • 84882731702 scopus 로고    scopus 로고
    • MitoSeek: extracting mitochondria information and performing high throughput mitochondria sequencing analysis
    • Guo Y, Li J, Li CI, Shyr Y, Samuels DC: MitoSeek: extracting mitochondria information and performing high throughput mitochondria sequencing analysis. Bioinformatics 2013, 29(9):1210-1211.
    • (2013) Bioinformatics , vol.29 , Issue.9 , pp. 1210-1211
    • Guo, Y.1    Li, J.2    Li, C.I.3    Shyr, Y.4    Samuels, D.C.5
  • 3
    • 33845986379 scopus 로고    scopus 로고
    • The influence of antisense oligonucleotide length on dystrophin exon skipping
    • Harding PL, Fall AM, Honeyman K, Fletcher S, Wilton SD: The influence of antisense oligonucleotide length on dystrophin exon skipping. Mol Ther 2007, 15(1):157-166.
    • (2007) Mol Ther , vol.15 , Issue.1 , pp. 157-166
    • Harding, P.L.1    Fall, A.M.2    Honeyman, K.3    Fletcher, S.4    Wilton, S.D.5
  • 4
    • 78650335900 scopus 로고    scopus 로고
    • Deletion-based mechanisms of Notch1 activation in T-ALL: key roles for RAG recombinase and a conserved internal translational start site in Notch1
    • Ashworth TD, Pear WS, Chiang MY, Blacklow SC, Mastio J, Xu L, Kelliher M, Kastner P, Chan S, Aster JC: Deletion-based mechanisms of Notch1 activation in T-ALL: key roles for RAG recombinase and a conserved internal translational start site in Notch1. Blood 2010, 116(25):5455-5464.
    • (2010) Blood , vol.116 , Issue.25 , pp. 5455-5464
    • Ashworth, T.D.1    Pear, W.S.2    Chiang, M.Y.3    Blacklow, S.C.4    Mastio, J.5    Xu, L.6    Kelliher, M.7    Kastner, P.8    Chan, S.9    Aster, J.C.10
  • 8
    • 69749122557 scopus 로고    scopus 로고
    • Sensitive and accurate detection of copy number variants using read depth of coverage
    • Yoon S, Xuan Z, Makarov V, Ye K, Sebat J: Sensitive and accurate detection of copy number variants using read depth of coverage. Genome Res 2009, 19(9):1586-1592.
    • (2009) Genome Res , vol.19 , Issue.9 , pp. 1586-1592
    • Yoon, S.1    Xuan, Z.2    Makarov, V.3    Ye, K.4    Sebat, J.5
  • 9
    • 84859210032 scopus 로고    scopus 로고
    • Fast gapped-read alignment with Bowtie 2
    • Langmead B, Salzberg SL: Fast gapped-read alignment with Bowtie 2. Nat Methods 2012, 9(4):357-359.
    • (2012) Nat Methods , vol.9 , Issue.4 , pp. 357-359
    • Langmead, B.1    Salzberg, S.L.2
  • 10
    • 67649884743 scopus 로고    scopus 로고
    • Fast and accurate short read alignment with Burrows-Wheeler transform
    • Li H, Durbin R: Fast and accurate short read alignment with Burrows-Wheeler transform. Bioinformatics 2009, 25(14):1754-1760.
    • (2009) Bioinformatics , vol.25 , Issue.14 , pp. 1754-1760
    • Li, H.1    Durbin, R.2
  • 12
    • 79951970227 scopus 로고    scopus 로고
    • CNVnator: an approach to discover, genotype, and characterize typical and atypical CNVs from family and population genome sequencing
    • Abyzov A, Urban AE, Snyder M, Gerstein M: CNVnator: an approach to discover, genotype, and characterize typical and atypical CNVs from family and population genome sequencing. Genome Res 2011, 21(6):974-984.
    • (2011) Genome Res , vol.21 , Issue.6 , pp. 974-984
    • Abyzov, A.1    Urban, A.E.2    Snyder, M.3    Gerstein, M.4
  • 16
    • 84861400043 scopus 로고    scopus 로고
    • cn.MOPS: mixture of Poissons for discovering copy number variations in next-generation sequencing data with a low false discovery rate
    • Klambauer G, Schwarzbauer K, Mayr A, Clevert DA, Mitterecker A, Bodenhofer U, Hochreiter S: cn.MOPS: mixture of Poissons for discovering copy number variations in next-generation sequencing data with a low false discovery rate. Nucleic Acids Res 2012, 40(9):e69.
    • (2012) Nucleic Acids Res , vol.40 , Issue.9
    • Klambauer, G.1    Schwarzbauer, K.2    Mayr, A.3    Clevert, D.A.4    Mitterecker, A.5    Bodenhofer, U.6    Hochreiter, S.7
  • 17
    • 84888990872 scopus 로고    scopus 로고
    • Comparative study of exome copy number variation estimation tools using array comparative genomic hybridization as control
    • Guo Y, Sheng Q, Samuels DC, Lehmann B, Bauer JA, Pietenpol J, Shyr Y: Comparative study of exome copy number variation estimation tools using array comparative genomic hybridization as control. Biomed Res Int 2013, 2013:915636.
    • (2013) Biomed Res Int , vol.2013
    • Guo, Y.1    Sheng, Q.2    Samuels, D.C.3    Lehmann, B.4    Bauer, J.A.5    Pietenpol, J.6    Shyr, Y.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.