Target Enrichment | Gene Sequencing | Kailos Genetics

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With growing interest in the ability to sequence samples from a wide variety of diseases, coupled with the desire for targeted panels to more efficiently utilize sequencer capacity, Kailos Genetics now offers a custom design direct amplicon solution.

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Our Products

TargetRich Custom

TargetRich custom designs enable you to target the regions you desire, while delivering the results you need. Trust your research to TargetRich.

Contact usfor your next design, and let Kailos Genetics show you why TargetRich Custom is setting new expectations in targeted enrichment.

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TargetRich CRX DA

TargetRich™ CRX DA - new direct amplicon version

Complete coverage of the coding regions in 10 commonly mutated genes associated with cancer research: BRAF, EGFR, FLT3, JAK2, KIT, KRAS, PIK3CA, PTEN, TP53 and VEGFA. Captures known and novel mutations.

Available for Illumina® (MiSeq®, GAIIx®, HiSeq®) and Life Technologies™ Ion Torrent™.

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Coming Soon: Kailos Blue

KailosBlue is a highly secure, easily accessible cloud environment, for investigators to manage their NGS workflow, analyze sequences post-target enrichment and actively utilize their stored data. In combining the Amazon® cloud (secure & scalable), the industry leading alignment and genotyping systems (BWA & GATK), statistical resources and an intuitive user interface, investigators from any size lab can perform complex analysis of samples within a run and across multiple runs over time, independent of the sequencing equipment utilized.

KailosBlue provides an end-to-end informatics solution for targeted next-generation sequencing. The system can be used to plan and organize flowcells and configure sequencing runs. This feature is especially important for targeted sequencing approaches, such as Kailos Genetics’ TargetRich™ system, where dozens of samples are barcoded and pooled to efficiently and optimally utilize sequencer capacity. Raw data can be uploaded from sequencing instruments to the cloud for fast and secure alignment and analysis. Analysis, including variant identification, can be performed on DNA samples and compared against a reference sample (1000 Genomes, HapMap, User Defined) or across multiple samples run over any period of time, enabling entire studies to be compiled and analyzed in one system. KailosBlue cloud-based bioinformatics solution is compatible with data generated on the Illumina MiSeq®, GAIIx® and the Ion Torrent PGM®.

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News

Got Coverage?

September 12, 2012

University of Miami Considers PGM, MiSeq for New CLIA Sequencing Services

July 26, 2012

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Kailos Genetics

601 Genome Way

Suite 2005

Huntsville, AL 35806

(866) 833-6865

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