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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Jul 13, 2021SALSA MC002 SMA Newborn Screen implemented in Poland
Poland has implemented spinal muscular atrophy (SMA) newborn screening using MRC Holland's CE-IVD marked SALSA MC002 SMA Newborn Screen.
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Jul 13, 2021New version of Coffalyser.Net available
Coffalyser.Net, our MLPA analysis software, has received a major upgrade.
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Mar 09, 2021Wanted: samples with aberrations in the AIP, LDLR, MEN1, or PKD1 genes
We are currently looking for DNA samples (1–5 µg) with copy number changes in the AIP, LDLR, MEN1, or PKD1 genes.
Come and Meet Us
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Aug 28, 2021 - Online
ESHG
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Sep 09, 2021 - Online (starts 09:00 CEST; 12:30 PM IST)
Virtual Workshop: MLPA Raw Data Evaluation and Troubleshooting
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Oct 26, 2021 - Online (starts 16:00 CEST; UTC+02:00)
Webinar: Get to Know digitalMLPA
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Oct 28, 2021 - Online (starts 12:00 CEST; 3:30 PM IST)
Virtual Workshop: MLPA Raw Data Evaluation and Troubleshooting
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Nov 18, 2021 - Berlin, Germany
Workshop: "MLPA – Expert in a Day" – Germany