Results 151 to 160 of about 790,983 (253)

A Comprehensive Workflow for Read Depth-Based Identification of Copy-Number Variation from Whole-Genome Sequence Data.

American Journal of Human Genetics, 2018
B. Trost, S. Walker, Zhuozhi Wang, B. Thiruvahindrapuram, J. MacDonald, W. Sung, S. Pereira, J. Whitney, A. Chan, G. Pellecchia, M. Reuter, S. Lok, R. Yuen, C. Marshall, D. Merico, S. Scherer   +15 more
semanticscholar   +1 more source

A copy number variation detection method based on OCSVM algorithm using multi strategies integration. [PDF]

Sci Rep
Zhou M, Dong J, Jiang H, Zhao Z, Yuan T.
europepmc   +1 more source

A Microhomology-Mediated Break-Induced Replication Model for the Origin of Human Copy Number Variation

, 2009
P. J. Hastings, Grzegorz Ira, James R. Lupski   +2 more
openalex   +2 more sources

Establishing a prognostic threshold for total copy number variation within adult IDH-mutant grade II/III astrocytomas

Acta Neuropathologica Communications, 2019
Kanish Mirchia, Matija Snuderl, Kristyn Galbraith, Kimmo J. Hatanpaa, Jamie M. Walker, Timothy E. Richardson   +5 more
doaj   +1 more source

Copy Number Variation Shapes Genome Diversity in Arabidopsis Over Immediate Family Generational Scales [PDF]

, 2010
Seth DeBolt
openalex   +1 more source

Application of copy number variation sequencing combined with whole exome sequencing in prenatal left-right asymmetry disorders. [PDF]

BMC Genomics
Qin Y, Senglong M, Touch K, Xiao J, Fang R, Kang Q, Fan L, Li S, Liu J, Wu J, Wu Y, Shi X, Liu H, Gong X, Lin X, Feng L, Chen S, Li W.   +17 more
europepmc   +1 more source

Genomic microarrays in mental retardation: from copy number variation to gene, from research to diagnosis

, 2009
Lisenka E.L.M. Vissers, Bert B.A. de Vries, Joris A. Veltman   +2 more
openalex   +1 more source

Optimal Sparse Segment Identification With Application in Copy Number Variation Analysis [PDF]

, 2010
X. Jessie Jeng, Tommaso Cai, Hongzhe Li
openalex   +1 more source

Comparative Analyses of Copy-Number Variation in Autism Spectrum Disorder and Schizophrenia Reveal Etiological Overlap and Biological Insights.

Cell Reports, 2018
I. Kushima, B. Aleksic, M. Nakatochi, Teppei Shimamura, T. Okada, Y. Uno, M. Morikawa, K. Ishizuka, Tomoko Shiino, H. Kimura, Yuko Arioka, A. Yoshimi, Yuto Takasaki, Yanjie Yu, Yukako Nakamura, Maeri Yamamoto, T. Iidaka, S. Iritani, T. Inada, Nanayo Ogawa, Emiko Shishido, Youta Torii, N. Kawano, Yutaka Omura, T. Yoshikawa, T. Uchiyama, Toshimichi Yamamoto, M. Ikeda, R. Hashimoto, H. Yamamori, Y. Yasuda, T. Someya, Yuichiro Watanabe, J. Egawa, A. Nunokawa, M. Itokawa, Makoto Arai, M. Miyashita, A. Kobori, Michio Suzuki, Tsutomu Takahashi, M. Usami, M. Kodaira, Kyota Watanabe, Tsukasa Sasaki, Hitoshi Kuwabara, Mamoru Tochigi, Fumichika Nishimura, H. Yamasue, Yosuke Eriguchi, Seico Benner, Masaki Kojima, Walid Yassin, T. Munesue, S. Yokoyama, Ryo Kimura, Yasuko Funabiki, H. Kosaka, M. Ishitobi, T. Ohmori, Shusuke Numata, T. Yoshikawa, T. Toyota, K. Yamakawa, Toshimitsu Suzuki, Y. Inoue, Kentaro Nakaoka, Y. Goto, M. Inagaki, N. Hashimoto, I. Kusumi, Shuraku Son, T. Murai, Tempei Ikegame, N. Okada, K. Kasai, Shohko Kunimoto, D. Mori, N. Iwata, N. Ozaki   +79 more
semanticscholar   +1 more source

Genome-wide copy number variation association study in anorexia nervosa. [PDF]

Mol Psychiatry
Walker A, Karlsson R, Szatkiewicz JP, Thornton LM, Yilmaz Z, Leppä VM, Savva A, Lin T, Sidorenko J, McRae A, Kirov G, Davies HL, Fundín BT, Chawner SJRA, Song J, Borg S, Wen J, Watson HJ, Munn-Chernoff MA, Baker JH, Gordon S, Berrettini WH, Brandt H, Crawford S, Halmi KA, Kaplan AS, Kaye WH, Mitchell J, Strober M, Woodside DB, Pedersen NL, Parker R, Jordan J, Kennedy MA, Birgegård A, Landén M, Martin NG, Sullivan PF, Bulik CM, Wray NR.   +39 more
europepmc   +1 more source