Next Generation Sequencing Products & Reviews

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…

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…

Insights into the diversity of microbial communities

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

Automated Purification of High-Quality Total RNA with an Enhanced miRNA Enrichment

For low-to-medium throughput NGS needs, the Zephyr™ G3 NGS workstation is a compact, semi-automated solution designed to construct up to 96 NGS libraries per day. This compact workstation is equipped with a highly precise, 96-channel pipetting head and includes an integrated gripper. For Research Use Only. Not for use in diagnostic procedures.

High-throughput, low-volume automated platform for NGS library preparation.

Comprehensive profile of all mutations present in the exome

The NEXTflex® Dual-Indexed DNA Barcodes are two kits that each contain 96 combinatorial dual indexed barcoded adapters for Illumina® library prep which enable deep multiplexing of NGS sequencing samples compatible with high-throughput automation.They significantly increase scale, while reducing costs by allowing the user to pool up to 192 samples in a single flow cell.

SMARTer smRNA-Seq Kit for Illumina—Sequence Small RNAs with High Sensitivity and Minimal Bias

SMARTer Human TCR a/b Profiling Kit—Obtain Full-Length Sequences of TCR-alpha and TCR-beta V(D)J Variable Regions

Targeted RNA-Seq for Capture of Full-Length Transcript Information—SMARTer Target RNA Capture for Illumina

SMARTer Apollo NGS library prep system

ThruPLEX DNA-seq Kit—General Purpose Library Preparation for Illumina NGS Platforms

SMARTer PicoPLEX DNA-seq Kit—Single-Cell Library Preparation for Illumina NGS Platforms

Customizable Targeting of Key Oncology Variants  

Interrogate clinically-relevant colorectal cancer genes