CNVRuler: A copy number variation-based case-control association analysis tool

Bioinformatics

Volumn 28, Issue 13, 2012, Pages 1790-1792

  Kim, Ji Hong ^a   Hu, Hae Jin ^a   Yim, Seon Hee ^a   Bae, Joon Seol ^b   Kim, Seon Young ^c   Chung, Yeun Jun ^a  

^a The Catholic University of Korea   (South Korea)

^b Sogang University   (South Korea)

^c Korea Research Institute of Bioscience and Biotechnology (KRIBB)   (South Korea)

Author keywords

[No Author keywords available]

Indexed keywords

ALGORITHM; ARTICLE; CASE CONTROL STUDY; COMPUTER PROGRAM; COPY NUMBER VARIATION; GENETIC ASSOCIATION;

ALGORITHMS; CASE-CONTROL STUDIES; DNA COPY NUMBER VARIATIONS; GENOME-WIDE ASSOCIATION STUDY; SOFTWARE;

EID: 84864005430     PISSN: 13674803     EISSN: 14602059     Source Type: Journal    
DOI: 10.1093/bioinformatics/bts239     Document Type: Article

References (7)

1. Bae, J.S. et al. (2010) Genome-wide association analysis of copy number variations in subarachnoid aneurysmal hemorrhage. J. Hum. Genet., 55, 726-730.
2. Conrad, D.F. et al. (2010) Origins and functional impact of copy number variation in the human genome. Nature, 464, 704-712.
3. Feuk, L. et al. (2006) Structural variation in the human genome. Nat. Rev Genet., 7, 85-97.
4. Forer, L. et al. (2010) CONAN: copy number variation analysis software for genomewide association studies. BMC Bioinformatics, 11, 318.
5. McCarroll, S.A. and Altshuler, D.M. (2007) Copy-number variation and association studies of human disease. Nat Genet., 39, S37-S42.
6. Redon, R. et al. (2006) Global variation in copy number in the human genome. Nature, 444, 444-454.
7. Yim, S.H. et al. (2010) Copy number variations in East-Asian population and their evolutionary and functional implications. Hum. Mol. Genet., 19, 1001-1008.