Next Generation Sequencing Products & Reviews

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

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

Sequence key genes implicated in Lynch Syndrome

Interrogate NSCLC and SCLC genes

Interrogate hematological malignancy genes

All-exon sequencing of TP53

All-exon profiling of BRCA1 and BRCA2 genes

Expansive profiling of BRCA1, BRCA2 and PALB2 genes