Welcome to Paragon Genomics - distributed in the UK and Ireland by Caltag Medsystems
Paragon Genomics, headquartered in South San Francisco, develops technology to improve and streamline Next-Generation Sequencing (NGS) targeted library preparation through a proprietary background removal solution.
CleanPlex™ technology was developed by a team of veterans, from leading institutions, who have expertise in genomic research and bioinformatics. This technology alleviates NGS workflow bottlenecks and improves accuracy and speed of sequencing by removing non-specific PCR products during multiplex reactions. This results in the generation of more relevant data, higher on-target rates and greater uniformity, not to mention money and time savings. As a result of the high specificity of library synthesis ultra-low sample input (100 pg to 10 ng) is enabled.
Paragon Genomics offers a custom panel design service which provides the ability to multiplex up to 20,000 amplicons per tube. CleanPlex™ technology provides >98% uniformity and >97% specificity which is paramount to many fast-growing NGS segments such as cancer research, liquid biopsy, biomarker discovery, personalised medicine, non-invasive prenatal testing (NIPT), companion diagnostics, immunotherapy monitoring, genomics-guided breeding, systematic and phylogenetic mapping.
Several key product areas offered by Paragon Genomics are highlighted below:
CleanPlex™ 2.5-hr Multiplex PCR Target Enrichment Workflow for Illumina NGS Platforms
Target Enrichment Library Kits
CleanPlex™ Targeted Library Kit and CleanPlex™ custom panels are used together to amplify target regions of DNA using multiplex PCR for Next-Generation Sequencing (amplicon sequencing) target enrichment and library preparation on Illumina Sequencers.
- Easy integration with liquid handlers and automation devices for high-throughput NGS labs. 2.5-hour and 3-step target enrichment workflow with only 30-minute hands-on time from purified DNA to sequencing-ready library.
- Save time, labour, reagents, and the expense of capital equipment.
- No DNA fragmentation, No overnight hybridisation, No microfluidic device, No ligation, No end repair anymore!
- Save your precious samples. Only 100 pg of input DNA is needed for germline genotype calling and 10 ng for somatic mutation calling with an LOD of 1%.
- Accurate variant calling. High uniformity and on-target rate lead to highly sensitive and specific NGS variant calls.
- Highly scalable multiplex PCR accommodates your expanding panel needs. 7 - 4,000 PCR reactions per tube plus pooling strategy can meet the needs of most applications.
- Enable new applications. Able to amplify difficult or high GC genomic regions such as TERT promoter (involved in many types of human cancers) - this is included the CleanPlex™ OncoZoom Cancer Panel, a 65-gene cancer hotspot panel.
- Save oligo synthesis cost. No chemical modification of primers lowers your oligo synthesis costs by 4-10 fold.
Ready to Use Panels
Ready to use CleanPlex™ panels are available for BRCA1 & BRCA2, OncoZoom, and TP53. The panel kits contain primers, multiplex PCR reagent, digestion reagent and other reagent components necessary for constructing amplicon libraries for Next-Generation Sequencing on Illumina Sequencers.
- 100% coverage of BRCA1, BRCA2, and TP53 with superior uniformity
- Simplified workflow - library preparation in 2.5 hours with 30 minutes hands on time
- Process difficult samples with as little as 200pg of input DNA
Paragon Genomics offers a Custom Panel Design Service in 3 easy steps:
- Submit Design
- Design Review
- 2 weeks - Paragon Genomics provides expert custom panel design fast
- 20,000 amplicons in a single tube - Our team of experienced PhD level bioinformaticians and scientists work collaboratively to design robust panels
- 100% support - Customer care is our utmost priority. We provide from consultation to post purchase support
If you are having difficulty downloading product data or require further information, please contact us.