Accel-NGS® 1S Plus DNA Library Kit (24 reactions)
Swift Biosciences, IncDNA library preparation of difficult samples for NGS on Illumina® platforms.
Swift Biosciences opened its doors in February 2010 with a fully equipped laboratory facility in Ann Arbor, MI. The company is backed by experienced private investors. Multiple innovation platforms have been developed “in house” by a growing team of scientists and are covered by multiple patent applications. Swift launched its first retail product in its myT® Primers platform, myT BRAF for detection of BRAF mutations, in February of 2012. The company is also working on additional products for mutation detection and gene sequencing, both internally and with partners.
DNA library preparation of difficult samples for NGS on Illumina® platforms.
Multiplex amplicon panels for Illumina® platform.
Multiplex amplicons for Illumina® platform.
Multiplex amplicon panels for Illumina® platform.
Simply track and manage samples within and between studies.
DNA library preparation of difficult samples for NGS on Illumina® platforms.
Optimal sequencing of your cfDNA, FFPE and ChIP DNA
Optimal sequencing of your cfDNA, FFPE and ChIP DNA
PCR-free NGS prep with highest library diversity, lowest inputs
PCR-free NGS prep with highest library diversity, lowest inputs
NGS library prep for hybridization capture
NGS library prep for hybridization capture
Providing ultimate coverage of methylated DNA.
Providing ultimate coverage of methylated DNA.
DNA library preparation on Ion Torrent platforms
DNA library preparation on Ion Torrent platforms
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…
Customizable Targeting of Key Oncology Variants
Interrogate clinically-relevant colorectal cancer genes
Expansive profiling of BRCA1, BRCA2 and PALB2 genes