Next Generation Sequencing Products & Reviews

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

Ion AmpliSeq HD technology is a new amplicon-based library preparation technology for Ion Torrent next-generation sequencing (NGS) that gives you the power to design your own panels and find variants with a low limit of detection—down to 0.1% for cell-free DNA samples. This revolutionary technology enables researchers to routinely get answers when ultrahigh sensitivity is required, such as when detecting low-frequency alleles…

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

Sequence hotspots in EGFR, KRAS, NRAS and BRAF

Build Your Own Custom Targeted NGS Panel

Interrogate Key Oncology Mutations

Targeted Sequencing for Cystic Fibrosis

Fingerprint and Track Samples  

A Reliable Long-Read Sequencing Solution  

DNA library preparation for damaged samples