11/18/2012 |
| Company Information:
Fast and cheaper next generation sequencing (NGS) technologies will generate unprecedentedly massive (thousands or even ten thousands of individuals) and highly-dimensional (ten or even dozens of millions ) genomic and epigenomic variation data that allow nearly complete evaluation of genomic and epigenomic variation including common and rare variants, insertion/deletion, CNVs, mRNA by sequencing (RNA-seq), microRNA by sequencing (mRNA-seq), methylation by sequencing (methylation-seq) and Chip-seq. Analysis of these extremely big and diverse types of data sets provide powerful tools to comprehensively understand the genome and epigenomes, but also pose great conceptual, analytical and computational challenges. A deluge of genomic and epigenomic data generated by NGS and enormous amounts of personal phenotype data demand the paradigm shift in genomic and epigenomic data analysis from standard multivariate data analysis to functional data analysis, from low dimensional data analysis to high dimensional data analysis, from independent sampling to dependent sampling, from single type data analysis to integrated multiple types of data analysis, and from individual PC to parallel computing.
Position Title:
Postdoctoral Training in Biostatistics, Statistical Genetics, Bioinformatics and Computational Systems Biology. |