OmicSpace
Research in human genetics has produced large amounts of DNA sequence data for relating genetic variation to health and disease. Identifying the genetic variants that are predisposing to complex diseases or traits is one of the most important problems in human genetics. Genome-wide association studies using genotyping are searching for regions of variation in human DNA that underlie particular diseases or effects of medicines. The genetic factors that influence health, disease and response to treatment in these regions need to be examined much more comprehensively by sequencing. The technology for sequencing is advancing rapidly, and will allow the production of sequences in genomic regions and across the genome in many individuals in the near future. Despite the imminent production of large amounts of sequence data, analysis of these data in an appropriate manner is still a problem. New statistical methods and computational tools are necessary to extract useful information from the enormous amount of data, relating the variation to phenotype, assessing the significance of the associations, incorporating population genetic factors such as population history, admixture, and natural selection, and identifying sets of variants that may include functional variants.
OmicSpace provides comprehensive informatics solutions to meet scientists' increasing demand to deal with large and complex genomic, proteomic, and clinomic data in biomedical research for academic and industrial institutes by providing high quality service and technology. We design data model and data warehouse for biomedical studies and medicare. And we also develop statistical methods and computational tools that solve scientific problems in biomedical research.