The importance of copy numbers in genetic diagnostics and research
Copy number variants play a role in many genetic disorders. The fast, accurate and affordable detection of CNVs is essential for clinical genetic testing and research.
MRC Holland develops tools for the detection of DNA copy numbers and methylation patterns associated with disease. Our MLPA® technique is the gold standard in this field, and is used around the world to study hereditary disorders and tumours.
Latest News
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Sep 21, 2022Wanted: positive DNA samples
MRC Holland is looking for positive samples for Prader-Willi Syndrome (PWS) / Angelman Syndrome (AS), CYP11B1-CYP11B2 fusion gene, Parkinson and MSH2 exon 2 to 6 inversion.
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Sep 21, 2022Last chance to update your Coffalyser.Net software
On May 24 this year, a new version of Coffalyser.Net was released: v.220513.1739. In case you have not yet installed this version, make sure you do so before 30 September in order not to lose access to the software.
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Jul 15, 2022IVDR and MRC Holland products
According to the new extension of the IVDR timelines, MRC Holland’s CE-mark obtained under the IVD Directive is still valid for almost all of MRC Holland’s products until 26 May 2026 or until an IVDR certificate is obtained.
Come and Meet Us
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Oct 25, 2022 - Los Angeles (CA), USA
ASHG
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Nov 01, 2022 - Phoenix (AZ), USA
AMP
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Nov 09, 2022 - Online (starts 17:00 CET; UTC+01:00)
Webinar: Get to Know digitalMLPA
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Nov 17, 2022 - Online (starts 09:00 CET)
Virtual Workshop: MLPA Raw Data Evaluation and Troubleshooting
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Jan 17, 2023 - Online (starts 16:00 CET)
Virtual Workshop: MLPA Raw Data Evaluation and Troubleshooting