Simplify your NGS library prep with a fast, streamlined, 3-step protocol from Qiagen

Simplify your NGS library prep with a fast, streamlined, 3-step protocol from Qiagen

March 30, 2017

In any NGS run, library preparation can seriously affect the quality of NGS reads. Constructing a high-quality sequencing library is crucial for every sequencing project.

QIAGEN's enzymatic-based library prep solutions allow you to construct high-quality, whole genome libraries with high conversion rates in just 2.5 hours. Discover how you can maximize per-sample data quality while streamlining your laboratory processes today!

Learn more about the advanced QIAseq FX technology to scale up your WGS research.

 

 

 

Simple new prenatal blood test for early and accurate detection of major chromosomal abnormalities

Simple new prenatal blood test for early and accurate detection of major chromosomal abnormalities

Multiplicom is proud to launch Clarigo™, a new CE-IVD1 non-invasive prenatal test (NIPT). This highly accurate blood test will enable genetic analysis laboratories to detect the presence or absence of major chromosomal abnormalities such as trisomy 21 (Down’s syndrome), 18 (Edwards’ syndrome) and 13 (Patau syndrome), in the fetus, as early as in the first trimester of pregnancy by analysis of the fetus’s DNA in the maternal blood.

October 22, 2015 More +
NEW MilkoScan Mars

NEW MilkoScan Mars

The new MilkoScan Mars is the first FTIR milk analyser tailor made for small dairies, replacing the more than 12 year old filter based MilkoScan Minor.



May 16, 2015 More +
Ready to make an enquiry Call us on: + 961 1 39 66 77
Or email us