Easy access to complex data
CUSTOMIZED to your needs
omiics offers high-quality tailored Next Generation Sequencing (NGS) solutions both for complete projects or with partial assistance - from sample to publication-grade figure designed and performed by experienced scientists.
Previous technologies, e.g. microarray and qPCR, requires you to have some preconceivement of what you are looking for, as you need to predefine the RNA to be quantified.
Next Generation Sequencing (NGS) gives you every RNA sequence in your sample. Hence you get a complete, unbiased overview of every difference in RNA between samples. What you did not know to look for, often makes the most significant finding.
Tissues, cells, powder, biofluids (CSF, bile, saliva, exosomes, IVF media ect.)
Map all differences
(e.g. effect of treatment/mutation)
Spot the trend
(e.g. identify biomarkers)
Knowing the changes in RNA levels allows you to pin-point every gene expressions being turned up or down. Through advanced bioinformatics this enables mapping of cellular pathways likely affected.
Catalogue of every difference in RNA levels between samples
Plots for visual presentation of significant trends
Pathway Analysis of protein-networks (mRNA or microRNA targets)
“My lab has recently collaborated with omiics on several different RNAseq projects. Their work is of high quality and their service pleasant and swift. Not only do we always get excellent RNAseq results also the bioinformatics follow-up of omiics is impressive and they are always ready to help with questions”.
- Prof. dr. Jeroen Pasterkamp, Director MIND Facility, the Netherlands -