A new strategy for enhancing imputation quality of rare variants from next-generation sequencing data via combining SNP and exome chip data

Kim, Y. J.; Park, T.; Pollin, T. I.; Prokopenko, I.; Reich, D.; Rivas,; Scott, L. J.; Seielstad, M.; Sim, X.; Sladek, R.; Smith, P.; Tachmazidou, I.; Tai, E. S.; Teo, Y. Y.; Teslovich, T. M.; Torres, J.; Trubetskoy,; Willems, S. M.; Williams, A. L.; Wilson, J. G.; Wiltshire, S.; Won, S.; Wood, A. R.; Xu, W.; Yoon, J.; Zawistowski, M.; Zeggini, E.; Zhang, W.; Zöllner, S.; Abecasis, G.; Almeida, M.; Altshuler, D.; Asimit, J. L.; Atzmon, G.; Barber, M.; Barzilai, N.; Beer, N. L.; Bell, G. I.; Below, J.; Blackwell, T.; Blangero, J.; Boehnke, M.; Bowden, D. W.; Burtt, N.; Chambers, J.; Chen, H.; Chen, P.; Chines, P. S.; Choi, S.; Churchhouse, C.; Cingolani, P.; Cornes, B. K.; Cox, N.; Day-Williams, A. G.; Duggirala, R.; Kim, Young Jin; Dupuis, J.; Lee, Juyoung; Dyer, T.; Feng, S.; Fernandez-Tajes, J.; Ferreira, T.; Fingerlin, T. E.; Flannick, J.; Florez, J.; Fontanillas, P.; Frayling, T. M.; Fuchsberger, C.; Gamazon, E. R.; Gaulton, K.; Ghosh, S.; Glaser, B.; Gloyn, A.; Grossman, R. L.; Kim, Bong-Jo; Grundstad, J.; Hanis, C.; Heath, A.; Highland, H.; Horikoshi, M.; Huh, I.-S.; Huyghe,; Ikram, K.; Jablonski, K. A.; Jun, G.; Kato, N.; Kim, J.; Kim, B.-J.; Lee, J.; King, C. R.; Park, Taesung; Kooner, J.; Kwon, M.-S.; Im, H. K.; Laakso, M.; Lam, K. K.-Y.; Lee, S.; Lehman, D. M.; Li, H.; Lindgren, C. M.; Liu, X.; Livne, O. E.; Locke, A. E.; Mahajan, A.; Maller, J. B.; Manning, A. K.; Maxwell, T. J.; Mazoure, A.; McCarthy, M. I.; Meigs, J. B.; Min, B.; Mohlke, K. L.; Morris, A. P.; Musani, S.; Nagai, Y.; Ng, M. C. Y.; Nicolae, D.; Oh, S.; Palmer, N.; Cho, Y. S.

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BioMed Central, BMC Genomics, 1(16), 2015

DOI: 10.1186/s12864-015-2192-y

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A new strategy for enhancing imputation quality of rare variants from next-generation sequencing data via combining SNP and exome chip data

Journal article published in 2015 by Y. J. Kim, T. Park, T. I. Pollin, I. Prokopenko, D. Reich, Rivas, L. J. Scott, M. Seielstad, X. Sim, R. Sladek, P. Smith, I. Tachmazidou, E. S. Tai, Y. Y. Teo, T. M. Teslovich and other authors.

This paper is made freely available by the publisher.

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A new strategy for enhancing imputation quality of rare variants from next-generation sequencing data via combining SNP and exome chip data