Next Generation Sequencing Products & Reviews

The gold standard for NGS library amplification.

KAPA Library Quantification Kits contain all the reagents needed for the accurate, reliable and reproducible qPCR-based quantification of NGS libraries prior to pooling for capture or flow cell amplification. Kits contain KAPA SYBR® FAST qPCR Master Mix, optimized for high-performance SYBR Green I-based qPCR. The engineered KAPA SYBR FAST DNA Polymerase contained in the Master Mix amplifies GC- and AT-rich DNA fragments of…

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.

200 x 20 µl reactions, includes ddPCR Library Quantification Assay and ddPCR Supermix for Probes (No dUTP), for quantification of Illumina TruSeq libraries using the QX200™/QX100™ ddPCR™ Systems

For automated Pyrosequencing with integrated template preparation for advanced methylation, mutation and SNP quantification

Established solid tumour gene panel

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

DNA library preparation on Ion Torrent platforms

DNA library preparation on Ion Torrent platforms

Single base-pair, high-throughput solution for analysis of methylated DNA regions

Comprehensive services for DNA enrichment and profiling of genomic regions marked by DNA methylation or DNA methyl variants

Fastest, most efficient methylated DNA enrichment method on the market

Comprehensive services for DNA enrichment and profiling of genomic regions marked by DNA methylation or DNA methyl variants

Transcriptome profiling by RNA-Seq

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…

The DriverMap™ Human Genome-Wide Targeted Expression Profiling Assay enables researchers to simultaneously measure the expression level of almost 19,000 human protein-coding genes in a single assay. By combining highly multiplexed RT-PCR amplification with the depth and precision of next-generation sequencing (NGS) quantitation, the Driver-Map assay provides convenient, comprehensive, highly sensitive, and quantitative meas…