Detecting copy-number variations in whole-exome sequencing data using the eXome Hidden Markov Model: an 'exome-first' approach.

MLA

Miyatake, Satoko, et al. “Detecting Copy-Number Variations in Whole-Exome Sequencing Data Using the EXome Hidden Markov Model: An ‘Exome-First’ Approach.” Journal of Human Genetics, vol. 60, no. 4, Apr. 2015, pp. 175–82. EBSCOhost, https://doi.org/10.1038/jhg.2014.124.

APA

Miyatake, S., Koshimizu, E., Fujita, A., Fukai, R., Imagawa, E., Ohba, C., Kuki, I., Nukui, M., Araki, A., Makita, Y., Ogata, T., Nakashima, M., Tsurusaki, Y., Miyake, N., Saitsu, H., & Matsumoto, N. (2015). Detecting copy-number variations in whole-exome sequencing data using the eXome Hidden Markov Model: an “exome-first” approach. Journal of Human Genetics, 60(4), 175–182. https://doi.org/10.1038/jhg.2014.124

Chicago

Miyatake, Satoko, Eriko Koshimizu, Atsushi Fujita, Ryoko Fukai, Eri Imagawa, Chihiro Ohba, Ichiro Kuki, et al. 2015. “Detecting Copy-Number Variations in Whole-Exome Sequencing Data Using the EXome Hidden Markov Model: An ‘Exome-First’ Approach.” Journal of Human Genetics 60 (4): 175–82. doi:10.1038/jhg.2014.124.