Improving the Identification of Missing People Using NGS
News Sep 30, 2016
QIAGEN and the International Commission on Missing Persons (ICMP) have announced a collaboration on a project to enhance ICMP's ability to identify missing persons using next-generation sequencing (NGS) technologies. QIAGEN and ICMP will work together at the ICMP's laboratory in The Hague to develop and validate a complete NGS solution, including QIAGEN’s “Sample to Insight” GeneReader NGS System* and other QIAGEN workflow solutions, as well as innovative forensic panels designed for identification of missing persons using single nucleotide polymorphisms (SNPs).
The joint efforts integrate QIAGEN’s “Sample to Insight” integrated GeneReader NGS workflow with ICMP’s on-going efforts to advance the science of human identification through a consultative process that includes the world’s leading forensic geneticists.
“The tragedy of missing persons, often due to armed conflicts or natural disasters, impacts families and whole societies. We are pleased to partner with ICMP to bring efficient, actionable next-generation sequencing to ICMP, which maintains the world’s leading laboratory for human identification,” said Peer Schatz, Chief Executive Officer of QIAGEN. “Working with ICMP we will create Sample to Insight NGS workflows, including technologies to prepare even the most difficult samples and to conduct highly sensitive DNA analysis for successful identification.”
Scientists report a novel gene therapy that halts vision loss in a canine model of a blinding condition called autosomal dominant retinitis pigmentosa (adRP). The strategy could one day be used to slow or prevent vision loss in people with the disease. NEI is part of the National Institutes of Health.