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ctDNA analysis across the cancer research continuum

SureSeq: Variant calling best practices

Novogene 10x single cell services

Automated DNA library preparation for PacBio long-read whole genome sequencing with the DreamPrep NGS compact

Advancing polyploid assembly and large-genome assembly in plants through long-read sequencing

Automation of the Agencourt AMPure XP PCR purification system

Fast, inexpensive, sensitive, and high-throughput tool for cytogenetics

Optimization of an Agilent NGS automated workflow for the characterization of NSCLC DNA samples in a molecular diagnostic and anatomic pathology laboratory

Comparison of manual and automated NGS library preparation using the Magnis Dx NGS Prep System with Cancer All-In-One Assay on FFPE samples

Walkaway NGS automation with Magnis NGS Prep System

Magnis SureSelect XT HS2 DNA Reagent Kit data sheet

Magnis SureSelect XT HS2 RNA Reagent Kit data sheet

Identifying monoclonal antibodies with Quantum-Si’s next-generation protein sequencing technology

More insights in sight: Comprehensive genomic profiling with SureSelect Cancer CGP Assay

SureSelect Cancer CGP Assay: Comprehensive genomic profiling (CGP) to maximize tumor insights

6 tips for early-stage MDx companies seeking successful commercialization

Ordering information and troubleshooting tips for NGS

Development of a target-capture NGS assay for use in molecular-based research of myeloid measurable residual disease

Six tips to improve sequencing libraries

Next-generation sequencing sample preparation with the NanoDrop One spectrophotometer

Detection of adapter dimers in NGS libraries with the Agilent Fragment Analyzer and TapeStation Systems

How to choose a microbiome standard

Maximizing the potential of next-generation sequencing through automated liquid-handling technology

Automated NGS solutions for human disease

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