€4,326.00
Delivery time: 2 to 3 weeks
Product number:
NGS_GAL_HCP_FR_16
Product information "GALEAS HereditaryPlus Kit Frag "
GALEAS™ HereditaryPlus Kit is a Next-Generation Sequencing (NGS) library preparation and targeted enrichment kit designed to detect germline mutations in 146 genes associated with increased hereditary cancer risk, including breast cancer, prostate cancer, Lynch syndrome, and Wilms tumor. It profiles diagnostically meaningful SNVs, INDELs, and a wide range of CNVs across targeted regions. The kit is optimized for genomic DNA (gDNA) from blood or saliva samples, with an input range of 10–100 ng. This provides flexibility in sample collection. The protocol uses enzymatic fragmentation reagents for gDNA library preparation, eliminating the need for physical shearing by sonication. GALEAS™ HereditaryPlus Kit includes Illumina adapters with Unique Dual Indexes (UDI) to identify and prevent sample index skipping, plus 9 bp Unique Molecular Identifiers (UMI) for PCR and sequencing error removal and single molecule counting in bioinformatic analysis. GALEAS Analysis Software is a cloud-based set of optimized bioinformatics pipelines that provides accurate calling of SNVs, INDELs, and a wide range of CNVs from single exons to whole genes. The software offers an easy-to-use method for uploading batches of FASTQ files and downloading results with just a few clicks.
| Product type: | NGS Assay |
|---|---|
| Regulatory status: | RUO |
| Platform: | Illumina |
| Content: | 16 Samples |
| Storage temperature: | -20 °C |
| Shipping method: | Dry ice |
| Country of distribution: | Germany |