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

• Main 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., King C.R., 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., 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.
• Other Authors: DEPT OF MEDICINE
• Format: Article
• Published: BioMed Central Ltd. 2018
• Online Access: http://scholarbank.nus.edu.sg/handle/10635/143209
• Institution: National University of Singapore

10.1186/s12864-015-2192-y