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PROseq Multimodal HC Panel HT
The PROseq Multimodal HC Panel HT (12) has all the necessary reagents (excluding indices) to process 12 samples for multimodal HT (DNA and RNA) sequencing. It is a fixed high content panel for a total of 24 reactions.
Cat. No. | Product Name | Products Type | Tests | Datasheet | Price |
---|---|---|---|---|---|
NDCDP-2312-HMS-3 | PROseq Multimodal HC Panel HT | 12/96 | Datasheet | INQUIRY | |
NDCDP-2312-HMS-4 | PROseq Multimodal Index I SW | 12/96 | Datasheet | INQUIRY |
Features
The PROseq enrichment technology serves as the foundation for Multimodal's comprehensive and uniform coverage of objectives, which includes intricate genes like CEPBA and also offers dependable recognition of existing and new fusions. A pre-optimized procedure is available, which allows transition from total nucleic acid extraction to the creation of unique, dual-indexed, NGS-ready libraries that contain UMI. This is done as part of a single-day workflow to help amplify sensitivity, enhance error rectification, and decrease index hopping. A pre-set, automation-compatible workflow solution that includes secondary analysis and variant interpretation is offered for quick integration, accelerated processing period, and better expandability. |
Product Details
The development of PROseq Multimodal HT Panels aims to streamline targeted DNA and RNA enrichment and analyses. These panels differentiate themselves from other methods on the market by negating the need for two separate workflows for DNA and RNA analysis, thereby saving time and preserving scarce sample resources. |
Applications
PROseq Multimodal HT Panels have the ability to examine various types of biomarkers through a unified workflow derived from total nucleic acids. The total nucleic acids can be obtained using specialized sample isolation protocols specifically designed for the PROseq Multimodal HT Panels. From DNA, PROseq Multimodal HT Panels can identify various characteristics such as: Single Nucleotide Variants (SNVs) Insertions and Deletions (InDels) Copy Number Variants (CNVs) Tumor Mutational Burden (TMB) score Microsatellite Instability (MSI) status From RNA, the panels can recognize: Fusions Exon skipping events Gene expression levels |
All of our services and products are intended for preclinical research use only and cannot be used to diagnose, treat or manage patients.