Our comprehensive enrichment and sequencing services simplify your work. Send your samples and we will return the sequence data with free, basic bioinformatics analysis. Each of our services uses GenCap™ technology to enrich genomic target regions before sequencing. GenCap™ is compatible with any species, FFPE samples, and may capture up to 50 Mb of customized target regions. Please contact us to discuss how our sequencing services can expedite your discovery.

Exome

Our whole exome enrichment kit contains coding exons annotated in CCDS and RefSeq databases and incorporates exonic regions as well as non-coding RNAs. Our enrichment and sequencing service is comprehensive; simply send us your samples and we will return the data, including free basic bioinformatics analysis. Please contact us if you would like more details or if you would like to use customized enrichment and sequencing approaches.

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Disease or Pathway Genes

Our ready-made kits are expertly designed to enrich popular Human target genes involved in cancer, neonatal genetic disease screening, mitochondria deep sequencing, deafness, the kinome and the X-chromosome. Sequencing disease or pathway genes has the potential to empower diagnostic or screening initiatives. Our enrichment and sequencing service is comprehensive; simply send us your samples and we will return the data, including free basic bioinformatics analysis. Please contact us if you would like more details or if you would like to use customized enrichment and sequencing approaches.

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Translocation Breakpoints

Target enrichment and sequencing allows identification of the exact translocation breakpoint for ALK-EML4, TMPRSS2-ERG, VDJ and TCR recombination, Sarcoma fusions and more. Sequencing of breakpoints has the potential to empower diagnostics or prognostic applications and can give much more detailed information than FISH. Use our kits to achieve the highest breakpoint resolution. Our enrichment and sequencing service is comprehensive; simply send us your samples and we will return the data, including free basic bioinformatics analysis. Please contact us if you would like more details or if you would like to use customized enrichment and sequencing approaches.

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SNP Genotyping

Sequencing-based SNP genotyping has considerable advantages over other methods. Our proprietary capture technology can be applied to any species and uniquely allows high-throughput reverse strand confirmation because it captures both strands. Our enrichment and sequencing service is comprehensive; simply send us your samples and we will return the data, including free basic bioinformatics analysis. Please contact us if you would like more details or if you would like to use customized enrichment and sequencing approaches.

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Chromosomal Loci

Quickly bring your GWAS to single base pair resolution by enriching and sequencing large chromosomal regions. Design a custom kit or try our services to narrow down the disease causing SNP. Our enrichment and sequencing service is comprehensive; simply send us your samples and we will return the data, including free basic bioinformatics analysis. Please contact us if you would like more details or if you would like to use customized enrichment and sequencing approaches.

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Gencap™ Custom Enrichment Kits

Design your own enrichment kit and we will use it to process your samples. Capture both strands of your preferred target region with our proprietary technology. Your kits may capture up to 50 Mb. GenCap is compatible with FFPE samples and delivers superior evenness and excellent coverage for any species. Our technology is our major advantage and our data has been looking brilliant: in most cases with 30x to 40x average sequencing coverage, >98% of the target region is represented by 1 or more tags and >95% is represented by 4 or more tags. GenCap kits could translate into significant cost-savings for sequencing projects. Our enrichment and sequencing service is comprehensive; simply send us your samples and we will return the data, including free basic bioinformatics analysis. Please contact us if you would like more details or if you would like to use customized enrichment and sequencing approaches.