NEXT GENERATION SEQUENCING

Next Generation Sequencing(NGS) technologies have become cheaper and easier to use.
Celther can accommodate your sequencing project, whether small sample sizes or a whole genome on hundreds to thousands of samples.

Application

•   All studies can be carried out on the level of DNA and RNA:
  
       – Detection of copy number variation
       – Identification of mutations (insertions, deletions, polymorphisms)
       – de novo sequencing
•  Splice variant characterization
•  Viral and bacterial typing

Research Areas:

•   Cancer driver mutations
•   Inherited disease mutations
•   Quantitative gene expression

Advantages:

•   Minimal sample input (10 ng of DNA or 5 ng of RNA)
•   Fast
•   Quantitative gene expression

We prepare tailored offer for each customer. Ask for an offer: orders@celther.com