Data analysis for disease association research, cancer genomics, personalised medicine, agriculture biotechnology, and life sciences using Next Generation Sequencing (NGS).
Bioinformatics assistance and extensive workflows for RNA-Seq, DNA-Seq, ChIP-Seq, small RNA-Seq, and Methyl-Seq analysis are provided for preclinical and clinical data.
Extend support for genome-wide association studies (GWAS), whole genome sequencing (WGS) analysis, SNP detection, and haplotype analysis to make it easier to find and type disease-linked SNPs.
Provide personalised analysis, interpretation, and visualisation of genome-wide data through computer analysis.