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| Title: | A new strategy for enhancing imputation quality of rare variants from next-generation sequencing data via combining SNP and exome chip data | Authors: | Kim Y.J. Lee J. Kim B.-J. Park T. 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. Dupuis J. 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. Grundstad J. Hanis C. Heath A. Highland H. Horikoshi M. Huh I.-S. Huyghe J.R. Ikram K. Jablonski K.A. Jun G. Kato N. Kim J. Kim Y.J. Kim B.-J. Lee J. King C.R. Kooner J. Kwon M.-S. Im H.K. Laakso M. Lam K.K.-Y. Lee J. Lee S. 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. Park T. Pollin T.I. Prokopenko I. Reich D. Rivas M.A. Scott L.J. Seielstad M. Cho Y.S. Sim X. Sladek R. Smith P. Tachmazidou I. Tai E.S. Teo Y.Y. Teslovich T.M. Torres J. Trubetskoy V. 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. |
Issue Date: | 2015 | Publisher: | BioMed Central Ltd. | Citation: | Kim Y.J., Lee J., Kim B.-J., Park T., 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., Dupuis J., 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., Grundstad J., Hanis C., Heath A., Highland H., Horikoshi M., Huh I.-S., Huyghe J.R., Ikram K., Jablonski K.A., Jun G., Kato N., Kim J., Kim Y.J., Kim B.-J., Lee J., King C.R., Kooner J., Kwon M.-S., Im H.K., Laakso M., Lam K.K.-Y., Lee J., Lee S., 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., Park T., Pollin T.I., Prokopenko I., Reich D., Rivas M.A., Scott L.J., Seielstad M., Cho Y.S., Sim X., Sladek R., Smith P., Tachmazidou I., Tai E.S., Teo Y.Y., Teslovich T.M., Torres J., Trubetskoy V., 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. (2015). A new strategy for enhancing imputation quality of rare variants from next-generation sequencing data via combining SNP and exome chip data. BMC Genomics 16 (1) : 1109. ScholarBank@NUS Repository. https://doi.org/10.1186/s12864-015-2192-y | Source Title: | BMC Genomics | URI: | http://scholarbank.nus.edu.sg/handle/10635/143209 | ISSN: | 14712164 | DOI: | 10.1186/s12864-015-2192-y |
| Appears in Collections: | Staff Publications |
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