Biomedical genomics research involves studying the genomes of both human and model organisms. CEN4GEN biomedical genomics services support your research to better understand human biology, and to identify the genetic basis of normal and disease traits. We further help you discover new clinical biomarkers, as well as develop new or more effective therapies for the clinical management of patients. Our genomics research services on model organisms aid in improving your understanding of the biology of living organisms.
As part of biomedical genomics, we also provide molecular epidemiology genome services which involve quality and cost-effective whole human genome re-sequencing as well as genotyping using the most advanced technologies. CEN4GEN molecular epidemiology services assist you to identify genetic factors which may contribute to either biological and/or environmental cues. Moreover, our metagenomic services help you identify with higher sensitivity and accuracy community microbial populations in the native environment, without the need to culture samples. CEN4GEN offers both research based metagenomic services, as well as clinical metagenomic services for the identification of microbial species.
CEN4GEN supports your biomedical and epidemiology genomics research by using quality, efficient, cost-effective and leading-edge technologies with a team of experienced scientists in multidisciplinary genomics research. CEN4GEN biomedical and epidemiology genomics services include:
- single cell genome sequencing services (whole genome, whole exome, targeted exome, RNAseq)
- circulating tumor DNA (ctDNA) genome sequencing services
- human whole genome next generation re-sequencing services
- model organism whole genome next generation re-sequencing services
- new genome discovery or de-novo next generation whole genome sequencing services
- whole exome next generation sequencing services
- targeted exome next generation sequencing services
- ChIP next generation sequencing services
- RNA next generation sequencing services
- whole genome, ITS, 16S, and 18S metagenomic next generation sequencing services
- viral metagenomic next generation sequencing services
- clinical metagenomic services
- whole genome CGH and SNP array services
- custom genotyping services
- methylation detection and quantification services
- next generation library construction services
- re-sequence alignment and variant analysis (bioinformatics) services
- de-novo sequence assembly (bioinformatics) services
- genome data analysis (bioinformatics) services, including:
- comparative genomics
- genome sequence annotation
- customized data analysis
- genotype analysis for specific traits (including disease)
- population based studies of genome data
CEN4GEN biomedical and epidemiology genomics services are for research purposes only.
For more information and a quote, please contact firstname.lastname@example.org and include a description of your service needs.