Next Generation Sequencing Products & Reviews

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

The new Sequel System is based on Pacific Bioscience’s proven Single Molecule, Real-Time (SMRT) technology and delivers about 7X more reads with 1 million zero-mode waveguides (ZMWs) per SMRT Cell. The Sequel System is ideal for projects such as rapidly and cost-effectively generating high-quality whole genome de novo assemblies. This innovative sequencing system features automated reagent and SMRT Cell handling and an inte…

Established solid tumour gene panel

DNA library preparation of difficult samples for NGS on Illumina® platforms.

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

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…

Cellecta’s LINE-1 Assay Kit provides a convenient, efficient, and targeted Next-Generation Sequencing (NGS) based approach to identify polymorphic insertion sites of LINE-1 in the human genome. The LINE-1 Assay Kit includes all the components needed to detect and identify novel LINE-1-induced genomic variations in genomic DNA isolated from tumors, blood, cells or other samples. Only a few hundred nanograms of DNA are requir…

Exceptional flexibility in next-generation sequencing

Insights into the diversity of microbial communities

Reliable detection of cancer-associated mutations in 597 genes from liquid biopsy samples

Simple, reproducible automated sequencing