DNA Sequencing Products & Reviews

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DNA sequencing, such as sanger sequencing, is a biological technique that determines the precise order of nucleotide bases in a fragment or template of DNA. DNA sequencers and genetic analyzers are based on capillary electrophoresis, where labeled DNA fragments are electrophoretically separated by size as they migrate through a polymer. Find the best DNA sequencing products, including DNA sequencing kits, genomic libraries and genetic identity kits in our peer-reviewed product directory: compare products, check customer reviews and receive pricing direct from manufacturers.

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miRNA-29b Forward Primer

Agilent Technologies

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

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miRNA-30c Forward Primer

Agilent Technologies

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

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miRNA-331 Forward Primer

Agilent Technologies

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

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miRNA-92-1 Forward Primer

Agilent Technologies

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

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miRNA-98 Forward Primer

Agilent Technologies

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

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Random 9-mer Primer

Agilent Technologies

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…

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Universal Reverse Primer

Agilent Technologies

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.

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SureCall Software

Agilent Technologies

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. 

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Agilent Solutions for Automated NGS Sample Prep

Agilent Technologies

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…

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GeneSpring NGS Software

Agilent Technologies

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…

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Magnis NGS Prep System

Agilent Technologies

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.

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SureSelect Cancer CGP Assay ​

Agilent Technologies

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).

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Sapio Clinical Diagnostics LIMS

Sapio Sciences

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.

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Microlab® NIMBUS NGS workstation

Hamilton Company

Hamilton’s Microlab® NIMBUS NGS workstation provides a completely automated and affordable solution for emPCR emulsion breaking, enrichment and sequencing primer hybridization for the Roche GS Junior System. The fully tested and validated NIMBUS NGS workstation features an integrated REM e system and provides convenient walk-away automation solution to minimize laborious manual process and reduce human errors.

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KAPA HyperExome

Roche

Efficient, and uniform hybridization-based capture for Whole Exome Sequencing Combining more than a decade of probe-design experience with an improved probe-manufacturing process, the new KAPA HyperExome probe pools enable efficient, uniform hybridization-based capture for Whole Exome Sequencing (WES).

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KAPA HyperPETE

Roche

KAPA HyperPETE (Primer Extension Target Enrichment) is a novel hybridization capture technology designed to employ primer extension reactions to specifically capture and release target library molecules for sequencing.

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KAPA EvoPlus Kit

Roche

KAPA EvoPlus V2 Kits is an enhanced enzymatic DNA library preparation solution that features improved fragmentation performance, insensitivity to inhibitors, increased conversion efficiency & fewer sequencing artifacts.

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KAPA EvoPrep

Roche

Achieve high-performing NGS library preparation from mechanically fragmented DNA or cell-free DNA (cfDNA) in a streamlined, automation-friendly workflow with KAPA EvoPrep Kit. The KAPA EvoPrep workflow reduces pipetting and reagent preparation steps and is validated with challenging sample inputs such as cfDNA and FFPET DNA.

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KAPA HiFi Kits

Roche

KAPA HiFi DNA Polymerase is a novel, single-enzyme system that exhibits industry-leading performance when compared with other high-fidelity polymerases and polymerase blends.

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