DNA Sequencing Products & Reviews

Optimized primers for different human miRNA that were selected based upon their roles in cancer and development.  Detects mature miRNA  Detects human, mouse, rat, worm and other species  Highly-specific sequences assure single nucleotide discrimination

Optimized primers for different human miRNA that were selected based upon their roles in cancer and development.  Detects mature miRNA  Detects human, mouse, rat, worm and other species  Highly-specific sequences assure single nucleotide discrimination

Optimized primers for different human miRNA that were selected based upon their roles in cancer and development.  Detects mature miRNA  Detects human, mouse, rat, worm and other species  Highly-specific sequences assure single nucleotide discrimination

Optimized primers for different human miRNA that were selected based upon their roles in cancer and development.  Detects mature miRNA  Detects human, mouse, rat, worm and other species  Highly-specific sequences assure single nucleotide discrimination

Optimized primers for different human miRNA that were selected based upon their roles in cancer and development.  Detects mature miRNA  Detects human, mouse, rat, worm and other species  Highly-specific sequences assure single nucleotide discrimination

Optimized primers for different human miRNA that were selected based upon their roles in cancer and development.  Detects mature miRNA  Detects human, mouse, rat, worm and other species  Highly-specific sequences assure single nucleotide discrimination

Optimized primers for different human miRNA that were selected based upon their roles in cancer and development.  Detects mature miRNA  Detects human, mouse, rat, worm and other species  Highly-specific sequences assure single nucleotide discrimination

Optimized primers for different human miRNA that were selected based upon their roles in cancer and development.  Detects mature miRNA  Detects human, mouse, rat, worm and other species  Highly-specific sequences assure single nucleotide discrimination

The Prime-It Fluor fluorescence labeling kit generates directly fluoresceinated DNA probes using random 9-mer primers and Exo-Klenow to incorporate fluor-12-dUTP into the probe fragments.  Generates high-specific-activity probes in 2 minutes  Fluorescently labeled probes also available  Produces labeled fragments 400 bp to 10 kb nucleotides in length  Performs equally well with [32P]dATP and [32P]dCTP  Performs well w…

The universal reverse primer is designed for use with the Human U6 forward primer provided in our High-Specificity miRNA QRT-PCR Detection Kit for a complete, validated assay requiring no upfront design work. The Kit delivers sensitive and reproducible detection of miRNA with high specificity.

Agilent's GeneSpring provides powerful, accessible statistical tools for intuitive data analysis and visualization. 

SureCall is a research desktop application combining both novel and widely accepted opensource algorithms for end-to-end NGS data analysis from alignment to categorization and annotation of mutations, supporting Agilent Target Enrichment applications. 

Agilent Solutions for Automated NGS Sample Prep provide: Flexibility to automate virtually any NGS reagent Performance to dramatically increase throughput and walk-away time Optimized SureSelectXT protocols to rapidly automate your NGS Sample Prep Agilent NGS Option A and Option B Both Deliver Higher Throughput with Less Hands-On Time Automating your NGS sample preparation with either Agilent NGS Option A or Option B…

Agilent’s GeneSpring NGS software suite includes data analysis workflows for Methyl-Seq, RNA-Seq, DNA-Seq, Chip-Seq and Small RNA-Seq data. GeneSpring NGS provides SureSelect customers with an easy to use QC, visualization and reporting tool for Methyl-Seq, RNA-Seq and DNA-Seq applications. GeneSpring NGS also allows the detection of transcriptomic changes like splice variants and gene fusions, or identify structural variation…

The Magnis system provides a complete workflow for NGS library preparation that is fully automated and delivers reproducible results. Built on proven Agilent SureSelect XT HS2 chemistry, start from total RNA with integrated cDNA conversion or unfragmented DNA with onboard enzymatic fragmentation for increased workflow efficiency.

Unlock the full potential of molecular diagnostics on a single platform

SureSelect Cancer CGP assay offers comprehensive genomic profiling for solid tumors. This pan-cancer NGS panel enables detection of somatic variants, including single nucleotide variants (SNVs), copy number variants (CNVs), insertions/deletions (indels), translocations (TLs), gene fusions, and the immuno-oncology biomarkers TMB (tumor mutational burden) and MSI (microsatellite instability).

Maximize efficiency with short-read accuracy and long-distance insights

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.

IGT® Adapter & UDI Primers is a series of adapter & unique dual-indexed primer kits used for NGS library construction of dsDNA, ssDNA and methylation DNA. iGeneTech provides 384 combinations of different UDI primers for high-throughput sequencing in a single lane, which reduces the false-positive rate caused by the index contaminations due to index hopping. For MultipSeq® library construction and low-frequency mutation tests,…

Twist also offers Research-Use Only (RUO) target enrichment NGS panels for viral detection and characterization of samples. These panels can be used for environmental monitoring and surveillance testing, while also providing insight into full sequence information for monitoring of viral evolution and strain origin.

The superior performance of Twist Human Core Exome provides the optimal solution for sequencing of protein coding genes. The Twist Human Core Exome however focuses only on the most accurate curated subset—CCDS database. Twist now offers the Twist Human RefSeq Panel, which is designed to expand the content of the Twist Human Core Exome. When combining the two panels, greater than 99% of protein coding genes are covered.

Twist Library Preparation Kit (Mechanical Fragmentation) is designed for use with gDNA that has already been sheared mechanically. It combines the enzymes and reagents for end repair, dA-tailing, and adapter ligation into a single reaction: Accommodates a wide range of DNA input types, enables high-quality sequencing of low-quality samples and minimizes start / stop site artifacts

Twist Library Preparation EF Kit (Enzymatic Fragmentation) incorporates the reagents and enzymes needed for DNA fragmentation with those for end repair, dA-tailing, and adapter ligation into a single reaction:  Ideal for automated, high-throughput library preparation, produces tunable, reproducible fragment sizes and minimizes sequence bias, maximizes coverage depth.