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PROseq Multimodal Index I SW
The PROseq Multimodal Panel HT (12) includes all necessary reagents (excluding indices) to conduct multimodal HT (DNA and RNA) sequencing on 12 samples. This fixed standard content panel is suitable for a total of 24 reactions.
| Cat. No. | Product Name | Products Type | Tests | Datasheet | Price |
|---|---|---|---|---|---|
| NDCDP-2312-HMS-1 | PROseq Multimodal Panel HT | Standard content/High content/Custom | 12/96 | Datasheet | INQUIRY |
| NDCDP-2312-HMS-2 | PROseq Multimodal Index I SW | Separated enrichment (recommended)/Combined enrichment | 12/96 | Datasheet | INQUIRY |
Features
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A comprehensive system capable of transforming total nucleic acids into a sequencing-ready library within the span of a single day. By using Unique Molecular Indices (UMIs), we implement error correction to increase the sensitivity of the NGS panel. PROseq enrichment technology addresses the shortcomings of traditional amplicon methods by dealing with concerns on primer multiplexing and amplicon size. Unique Dual Indices (UDIs) are utilized in order to decrease the occurrence of sample index hopping. A Sample to Insight solution is ideal for consolidating targeted DNA and RNA sequencing processes. |
Product Details
| PROseq Multimodal HT Panels are designed for unified targeted DNA and RNA enrichment and analysis. These panels offer a unique approach that eliminates the need for two different workflows for DNA and RNA analysis - a feature that saves time and preserves scarce samples. They allow for custom designs that target exonic regions of genes, SNPs or hotspots, as well as intronic and promoter regions. These panels can also locate known gene fusions based on identified breakpoints or identify new fusions. |
Applications
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PROseq Multimodal HT Panels are capable of examining various biomarker types with a unified workflow from total nucleic acids. Specifically designed sample isolation procedures can be used to isolate these nucleic acids for the PROseq Multimodal HT Panels. When examining DNA, these panels can assess: Single nucleotide variants (SNVs) Insertions and Deletions (InDels) Copy number variants (CNVs) While exploring RNA, these panels can evaluate: 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.
