NGS Library Preparation Kits Products & Reviews

Multiplex amplicon panels for Illumina® platform.

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

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…

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

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

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