Accel-NGS® 2S MID Indexing Kits (48 reactions)
The Accel-NGS 2S MID Indexing Kits have been designed, optimized, and validated for use withAccel-NGS 2S DNA Library Kits on Illumina platforms, and aid in low frequency variant detection, as well as accurate de-duplication of single read sequencing and sequencing from samples with non-random fragmentation. Get the most out of your NGS sequencing data with this powerful tool. Improve detection of low frequency alleles…
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The Accel-NGS 2S MID Indexing Kits have been designed, optimized, and validated for use withAccel-NGS 2S DNA Library Kits on Illumina platforms, and aid in low frequency variant detection, as well as accurate de-duplication of single read sequencing and sequencing from samples with non-random fragmentation. Get the most out of your NGS sequencing data with this powerful tool.
- Improve detection of low frequency alleles
- Identify unique library molecules
- Retain more sequencing data
- Designed for exome sequencing
- Compatible with circulating, cell-free DNA
Supported DNA Sequencing Applications:
- Whole exome sequencing (WES)
- Deep targeted sequencing
- Cell-free DNA sequencing
- Single-end sequencing, such as ChIP-Seq
