Full description
The data will assist research in population genetic variation in health and disease genomics, cancer genomics and transcriptomics. They include data from the public domain which are frequently used by researchers in the research group, as well as data to be generated and analysis results during the progression of the project. Aim is to enable integration of the data collection to NecTAR which further facilitates genomic and medical research in Australia. Part of the data collection may be shared among researchers nationally, conditioning on ethics clearance.Issued: 2014
Data time period: 06 2014 to 05 2015
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Genetic variation in the SLC8A1 calcium signaling pathway is associated with susceptibility to Kawasaki disease and coronary artery abnormalities
local : UQ:417980
Shimizu, Chisato, Eleftherohorinou, Hariklia, Wright, Victoria J., Kim, Jihoon, Alphonse, Martin P., Perry, James C., Cimaz, Rolando, Burgner, David, Dahdah, Nagib, Hoang, Long T., Khor, Chiea Chuen, Salgado, Andrea, Tremoulet, Adriana H., Davila, Sonia, Kuijpers, Taco W., Hibberd, Martin L., Johnson, Todd A., Takahashi, Atsushi, Tsunoda, Tatsuhiko, Kubo, Michiaki, Tanaka, Toshihiro, Onouchi, Yoshihiro, Yeung, Rae S. M., Coin, Lachlan J. M., Levin, Michael and Burns, Jane C. (2016). Genetic variation in the SLC8A1 calcium signaling pathway is associated with susceptibility to Kawasaki disease and coronary artery abnormalities. Circulation: Cardiovascular Genetics, 9 (6), 559-568. doi: 10.1161/CIRCGENETICS.116.001533
An integrated map of genetic variation from 1,092 human genomes
local : UQ:321461
The 1000 Genomes Project Consortium, Coin, L. J. M. and Li, Yingrui (2012). An integrated map of genetic variation from 1,092 human genomes. Nature, 491 (7422), 56-65. doi: 10.1038/nature11632
cnvHiTSeq: Integrative models for high-resolution copy number variation detection and genotyping using population sequencing data
local : UQ:321502
Bellos, Evangelos, Johnson, Michael R. and Coin, Lachlan J. M. (2012). cnvHiTSeq: Integrative models for high-resolution copy number variation detection and genotyping using population sequencing data. Genome Biology, 13 (12). doi: 10.1186/gb-2012-13-12-r120
Research Data Collections
local : UQ:289097
Institute for Molecular Bioscience - Publications
local : UQ:3858
- DOI : 10.14264/UQL.2016.583
