NGS Library Preparation Kits Products & Reviews

The NEBNext® Ultra™ Directional RNA Library Prep Kit for Illumina® contains enzymes and buffers that are ideally suited for cDNA library preparation for next-generation sequencing. NEBNext® reagents are a series of highly pure reagents that facilitate sample preparation of DNA or RNA for downstream applications such as next generation sequencing and expression library construction. The reagents included within these master mi…

SMART-Seq v4 Ultra Low Input RNA Kit for Sequencing—Single-Cell Transcriptome Analysis with Ultimate Sensitivity

The SureCell ATAC-Seq Library Prep Kit and ATAC-Seq Analysis Toolkit enable reproducible genome-wide profiling of the epigenomic landscape at the single-cell level with a high number of unique reads per cell so you can better understand the mechanisms that drive how genes are regulated. Features and Benefits Greater than 65% and up to 95% cell capture efficiency Adjustable cell throughput range of as few as…

The NEBNext Ultra II FS DNA PCR-free Library Prep Kit for Illumina offers an amplification-free workflow for DNA-seq based on the streamlined and reliable Ultra II FS workflow. Starting with as little as 50 ng of DNA, get the high-quality, high-yield libraries that you need without PCR bias.

Kit for determining the nucleotide sequence (in extra-long reads, up to 1kb) of an immobilized and clonally amplified DNA library prepared using the GS FLX+ System methods for the preparation of DNA libraries and amplified by the emPCR amplification process, using the appropriate GS FLX Titanium series kit(s). For use in combination with the GS FLX Titanium PicoTiterPlate Kit 70 × 75 and the GS FLX+ Instrument. Contents The GS…

VAHTS ® Universal Plus DNA Library Prep Kit for Illumina is a DNA library construction kit developed for the Illumina ® high-throughput sequencing platform.

Rapidly design your NGS panels for tumor genomic profiling to fit your specific requirements, including incorporation of new and emerging biomarkers. Leverage the curated content of the SureSelect Cancer CGP and Tumor-Specific catalog DNA panels to add or subtract gene content in the SureDesign web portal.

SureSelect Cancer Tumor-Specific assays offer genomic profiling for solid tumors from lung, colon, pancreas, kidney, or bladder tissue, to detect single nucleotide variants (SNVs), copy number variants (CNVs), insertions/deletions (indels), and translocations (TLs). These small cancer panels enable affordable tumor genomic profiling.

Agilent SureSelect All Exon kits are the most widely used target enrichment solution for exome sequencing. SureSelect Human All Exon V5 (targeting coding regions only) and V5+UTRs (targeting coding regions plus UTRs) have been updated to provide the greatest sequencing efficiency and enable samples ready for sequencing the next day. Greater coverage with less sequencing for lower overall costs – up to 60% less sequencing than…

The SureSelect Strand-Specific RNA Library Preparation kit prepares Poly(A) enriched libraries for whole-transcriptome sequencing. Sequence a wide range of RNA to detect gene expression changes and alternative splicing. The kit contains mRNA sequencing library preparation and enrichment materials.

The HaloPlex Cancer Research Panel enables fast, simple, and efficient analysis of genomic regions of interest for cancer research for a large number of sample types, including FFPE. HaloPlex Cancer is uniquely suited to high performance with cancer research samples, which are commonly preserved as formalin fixed and paraffin embedded (FFPE). This FFPE process often results in highly fragmented DNA, resulting in insufficient…

Designed for smaller studies, the SureSelect DNA Capture Arrays complement Agilent's in-solution SureSelect Target Enrichment System, which is designed for medium to large-scale NGS studies of tens through thousands of samples, including automated high-throughput workflows.

Agilent’s market leading SureSelect platform provides a complete portfolio of catalog and custom products, providing the flexibility you need from discovery to follow-up studies. Agilent’s custom solutions offer the only available method for target enrichment of RNA, allowing you to target your regions of interest using our free web portal SureDesign. Custom solutions are available for DNA and RNA target enrichment. • The only…

Transform your laboratory productivity with nanoscale automation delivering substantial cost and operational savings for RNA-Seq library preparation.

Confidently analyze multiple somatic variants with a flexible, automated NGS workflow

Sapio LIMS for clinical diagnostics enables your lab to quickly design, deploy, and automate end-to-end workflows to meet your lab’s exact needs. Including a physician portal; automated accessioning and order processing; multithreaded, out-of-the-box, no/low-code configurable workflows; simple and sophisticated automation rules; and streamlined report generation.

A complete targeted resequencing solution for a wide range of applications, with fast integrated workflow and options for custom and fixed enrichment panels.

A fast, integrated workflow for preparing libraries for use in a wide range of sequencing applications.

The first CE-marked IVD kitted solution for comprehensive genomic profiling (CGP) of DNA and RNA variants, plus MSI and TMB, for multiple solid tumor types.

Fluorescent Annexin V conjugates that are optimized for bright and low background staining of extracellular vesicles for flow cytometry.

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

The Twist FlexPrep™ UHT Library Preparation Kit streamlines ultra-high throughput sequencing by integrating Normalization by Ligation™ technology, enabling efficient sample processing for population studies and agrigenomics.

Twist’s Fast Hybridization and Wash Kit is a revolutionary new system with the flexibility to both save you time and improve the performance of your targeted sequencing efforts. It accommodates your samples, your schedule, and your performance needs: accelerate hybridization to as little as 15 minutes, or adjust the hybridization time to improve coverage for all targeted sequencing applications, including whole exome, custom…

Twist Universal Blockers enhance the specificity of next-generation sequencing (NGS) target enrichment by preventing non-specific hybridization between adapter sequences, thereby improving on-target capture and reducing sequencing costs.

The Twist Universal Adapter System enhances the performance of 'T-A' overhang ligation library preparation workflows in next-generation sequencing (NGS) by reducing adapter dimer formation and increasing library yield.