PerkinElmer

Genomics

PerkinElmer’s optimized, automated solutions are designed to improve the efficiency of your genomic workflows. These solutions are designed to eliminate the challenges associated with genomic analysis by providing labs with complete, single source solutions encompassing everything from sample to solution.

Automated workflow solutions have been developed for a range of applications including nucleic acid isolation and PCR setup, NGS sample prep, long-read sequencing, CRISPR fragment analysis, molecular cytogenetics and protein characterization. By enabling complete application-based solutions PerkinElmer increases your throughput while simplifying the generation of accurate, reproducible analysis. These solutions offer the flexibility to automate of automating a single protocol within your workflow or obtaining a complete single source solution that has been optimized to meet specific application requirements.

Explore the areas below to learn how you can increase the efficiency of your applications.

For research use only. Not for use in diagnostic procedures.

Applications

Nucleic Acid Isolation and PCR Setup

We offer automated solutions for nucleic acid isolation and PCR setup to increase the throughput and reproducibility of PCR workflows for virtually any applicat ...

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AG NGS Workflow Solutions

With our optimized nucleic acid extraction, DNA/RNA quantitation, automated library preparation, NGS library QC prep kits and technical expertise, you have an a ...

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Long-Read Sequencing

The predominant method for large-scale population research analysis of whole-genomes has historically involved sequencing an individual genome using short-reads ...

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Solutions

Integrated Laboratory Automation

From cellular screening and imaging applications to high-throughput screening and genomics-based applications, custom explorer™ G3 integrated workstations provi ...

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Molecular Cytogenetics

Fast, precise, and cost-effective targeted molecular karyotyping Molecular cytogenetics plays an important role in the characterization of chromosome anomalies ...

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