New QIAseq miRNA Library Kit overcomes miRNA-seq challenges

New QIAseq miRNA Library Kit overcomes miRNA-seq challenges

January 04, 2017

microRNA sequencing is the future of gene regulation analysis, providing unmatched specificity for closely related microRNAs as well as the ability to detect novel noncoding transcripts. But challenges in the current workflow can cause up to half of microRNA sequencing data to be missed entirely.

The new QIAseq miRNA Library Kit boosts your miRNA-seq experiments by:

  • Removing contaminants to double your on-target reads from just 1 ng

  • Using Unique Molecular Indices to ensure unbiased data

  • Shortening the workflow by removing the need for gel excision

Want to learn more? Check out the details!

 

New MASTR Facility supports adoption of NGS

New MASTR Facility supports adoption of NGS

Multiplicom is pleased to announce the new MASTR Facility to enable the implementation of massively parallel sequencing capabilities in clinical genetics and pathology laboratories.

September 15, 2015 More +
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 +
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