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1.

Fast and robust adjustment of cell mixtures in epigenome-wide association studies with SmartSVA
by Chen, Jun

Chen, Jun, Ehsan Behnam, Jinyan Huang, Miriam F. Moffatt, Daniel J. Schaid, Liming Liang, and Xihong Lin. 2017. “Fast and robust adjustment of cell mixtures in epigenome-wide association studies with SmartSVA.” BMC Genomics 18 (1): 413. doi:10.1186/s12864-017-3808-1. http://dx.doi.org/10.1186/s12864-017-3808-1.

2.

A comprehensive survey of genetic variation in 20,691 subjects from four large cohorts
by Lindström, Sara

Lindström, S., S. Loomis, C. Turman, H. Huang, J. Huang, H. Aschard, A. T. Chan, et al. 2017. “A comprehensive survey of genetic variation in 20,691 subjects from four large cohorts.” PLoS ONE 12 (3): e0173997. doi:10.1371/journal.pone.0173997. http://dx.doi.org/10.1371/journal.pone.0173997.

5.

Sequence data and association statistics from 12,940 type 2 diabetes cases and controls
by Jason, Flannick

Jason, F., C. Fuchsberger, A. Mahajan, T. M. Teslovich, V. Agarwala, K. J. Gaulton, L. Caulkins, et al. 2017. “Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.” Scientific Data 4 (1): 170179. doi:10.1038/sdata.2017.179. http://dx.doi.org/10.1038/sdata.2017.179.

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