Just Released
21 March 2013
SignalMap available for download SignalMap User's Guide20 March 2013
SeqCap EZ Developer Flyer
Discover more variants and reduce the sequencing output needed to verify mutations potentially responsible for disease.
Designs for focused research areas, developed in collaboration with researchers like you.
Discover variants in the exome and UTRs with our 96 Mb capture tool.
Enhance your exome research by adding up to 50 Mb custom target regions to our comprehensive Exome.
Capture YOUR regions of interest regardless of size with capture capabilities from 100 kb up to 50 Mb.
Design your genome specific capture experiment with the same target enrichment technology used in our SeqCap EZ Exome products.Research
Apr 2013 | Nat. Genet.
SMIM1 underlies the Vel blood group and influences red blood cell traits.Mar 2013 | Cell
Endogenous retrotransposition activates oncogenic pathways in hepatocellular carcinoma.Apr 2013 | Am. J. Hum. Genet.
WNT1 Mutations in Families Affected by Moderately Severe and Progressive Recessive Osteogenesis Imperfecta.Apr 2013 | Am. J. Hum. Genet.
Hypomorphic Mutations in PGAP2, Encoding a GPI-Anchor-Remodeling Protein, Cause Autosomal-Recessive Intellectual Disability.Apr 2013 | Am. J. Hum. Genet.
Mutations in LARS2, Encoding Mitochondrial Leucyl-tRNA Synthetase, Lead to Premature Ovarian Failure and Hearing Loss in Perrault Syndrome.For life science research only. Not for use in diagnostic procedures. This website contains information on products which is targeted to a wide range of audiences and could contain product details or information otherwise not accessible or valid in your country. Please be aware that we do not take any responsibility for accessing such information which may not comply with any valid legal process, regulation, registration or usage in the country of your origin.