SeqVersa™ UMI Index Multiplex Oligomers

Price range: $607.00 through $2,189.00

SeqVersa™ UMI Index Multiplex Oligomers offer comprehensive, unique dual index UMI adapters for precise and high-throughput multiplex DNA sequencing, enhancing data accuracy and reducing sequencing errors.

Purchase this item and get 60-218 Points
Purchase this item and get 60-218 Points
Product Description

SeqVersa™ UMI Index Multiplex Oligomers are designed to provide unparalleled accuracy and efficiency in next-generation sequencing (NGS) workflows. These oligomers incorporate unique molecular identifiers (UMIs) and dual index adapters, specifically engineered for high-throughput multiplex DNA sequencing. By integrating UMIs, the SeqVersa™ oligomers allow for the correction of sequencing errors and the elimination of PCR duplicates, ensuring high-fidelity data.

Each set includes a comprehensive collection of adapters with unique dual indices, which significantly reduces the risk of index hopping and cross-contamination, thus maintaining the integrity of multiplex sequencing projects. The SeqVersa™ UMI Index Multiplex Oligomers are compatible with Illumina sequencing platforms and are ideal for a wide range of applications, including genomic studies, cancer research, and complex sample analysis.

Key features of the SeqVersa™ UMI Index Multiplex Oligomers include: Unique Molecular Identifiers (UMIs): UMIs tag each DNA molecule, allowing for the identification and removal of PCR duplicates and correction of sequencing errors, leading to more accurate data. Dual Index Adapters: The dual indexing system minimizes the risk of cross-contamination and index hopping, ensuring the reliability of multiplexed sequencing.

High Throughput: Suitable for high-throughput sequencing projects, enabling the processing of multiple samples simultaneously and efficiently. Versatility: Compatible with Illumina sequencing platforms, these oligomers can be integrated into a variety of NGS workflows.

The SeqVersa™ UMI Index Multiplex Oligomers are essential for researchers aiming to achieve high-precision sequencing results, particularly in fields requiring accurate genomic analysis and the study of genetic variations.

Kit Contents

● UMI Index Adapter Pairs
● Index Adapters

Technical Parameters​

● Indexing: Unique dual indices to prevent index hopping
● UMIs: Incorporated for error correction and duplicate removal
● Compatibility: Optimized for Illumina sequencing platforms
● Throughput: Suitable for high-throughput sequencing applications
● Storage Conditions: -20°C for all reagents

Applications

● Genomic studies
● Cancer research
● Complex sample analysis
● High-throughput sequencing projects

Product FAQs
What are SeqVersa™ UMI Index Multiplex Oligomers used for?

These oligomers are used for high-precision multiplex DNA sequencing. incorporating unique molecular identifiers (UMIs) and dual index adaptors to enhance data accuracy and throughput.

How do UMIs in the SeqVersa™ Oligomers improve sequencing accuracy?

UMIs tag each DNA molecule, allowing for the identification and removal of PCR duplicates and correction of sequencing errors, resulting in more accurate sequencing data.

Are SeqVersa™ UMI Index Multiplex Oligomers compatible with Illumina sequencing platforms?

Yes, these oligomers are specifically designed for compatibility with Illumina sequencing platforms, ensuring seamless integration into existing workflows.

What are the benefits of using SeqVersa™ UMI Index Multiplex Oligomers for multiplex sequencing?

Benefits include high data accuracy through UMI incorporation, reduced cross-contamination via dual indexing, and increased efficiency and cost savings in high-throughput sequencing projects.

What are the storage requirements for the SeqVersa™ UMI Index Multiplex Oligomers?

All components should be stored at -20°C to maintain their stability and performance, as recommended in the user manual.

Can SeqVersa™ UMI Index Multiplex Oligomers be used in cancer research?

Yes, these oligomers are ideal for applications in cancer research, where precise genomic analysis and the study of genetic variations are crucial.

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