CNVRuler: a copy number variation-based case-control association analysis tool
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Ji-Hong Kim | Hae-Jin Hu | Seon-Hee Yim | Joon Seol Bae | Seon-Young Kim | Yeun-Jun Chung | Seon-Young Kim | Y. Chung | Seon-Hee Yim | J. Bae | Hae-Jin Hu | Ji-Hong Kim | Seon-Young Kim
[1] Tomas W. Fitzgerald,et al. Origins and functional impact of copy number variation in the human genome , 2010, Nature.
[2] Tae-Min Kim,et al. Copy number variations in East-Asian population and their evolutionary and functional implications , 2009, Human molecular genetics.
[3] Ituro Inoue,et al. Genome-wide association analysis of copy number variations in subarachnoid aneurysmal hemorrhage , 2010, Journal of Human Genetics.
[4] S. Mccarroll,et al. Copy-number variation and association studies of human disease , 2007, Nature Genetics.
[5] L. Feuk,et al. Structural variation in the human genome , 2006, Nature Reviews Genetics.
[6] D. Conrad,et al. Global variation in copy number in the human genome , 2006, Nature.
[7] Günther Specht,et al. CONAN: copy number variation analysis software for genome-wide association studies , 2010, BMC Bioinformatics.