Skip to main content
メニュー
Revvity logo
Contact us
JP
Revvity Sites Globally

Select your location.

*e-commerce not available for this region.

australia.webp Australia
austria.webp Austria
belgium.webp Belgium
brazil.webp Brazil *
canada.webp Canada
china.webp China *
denmark.webp Denmark
finland.webp Finland
france.webp France
germany.webp Germany
hong-kong.webp Hong Kong (China) *
india.webp India *
ireland.webp Ireland
italy.webp Italy
japan.webp Japan *
luxembourg.webp Luxembourg
mexico.webp Mexico *
netherlands.webp Netherlands
norway.webp Norway
philippines.webp Philippines *
republic of korea.webp Republic of Korea *
singapore.webp Singapore *
spain.webp Spain
sweden.webp Sweden
switzerland.webp Switzerland
thailand.webp Thailand *
uk.webp United Kingdom
usa.webp United States
Breadcrumb
...
  • ホーム
  • Products
  • 臨床・診断
    • 研究・開発
    • 臨床・診断
    • Reagents
    • プラットフォームと自動化
    • Consumables & Accessories
    • Signals ソフトウエア
    • Revvity Omics Services
  • リプロダクティブ・ヘルス
    • リプロダクティブ・ヘルス
    • 感染症
    • がん
    • 自己免疫(powered by Euroimmun)
    • 内分泌学
    • アレルギー
    • 神経変性
    • ラピッド検査
  • Revvity Genomics Software
    • 出生前検査
    • Revvity Genomics Software
    • 新生児スクリーニング
    • Newborn Sequencing Research
    • Pregnancy-Relevant Infections
    • Endocrine Reproductive
    • cell-free DNA解析
    • Neonatal Research
    • Preimplantation Genetic Testing
    • PlGF Testing Research
    • 分子細胞遺伝学

Revvity Genomics Software

Redefining what's possible in genomic research

Genomic analysis can be complicated, but your software shouldn't be.

Simplify your science with our cloud-based informatics suite – purpose-built for newborn screening and genomic laboratories, trusted throughout Revvity's global laboratory network.

Introducing the Revvity™ Genomics Software. It's time to redefine sequencing research.

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

Contact us Download brochure
Revvity Genomics Software

Modular design for maximum compatibility

Choose all three integrated modules or select only what you need.

Harmonized sample management

Harmonized sample management

With the LIMS module, efficiently manage sample intake with precise accessioning and complete traceability throughout the sample journey. Strategic QC checkpoints ensure quality, allowing immediate exclusion of failed samples to preserve downstream integrity of your results.

Intelligent data processing

Intelligent data processing

The Analyze module combines next-generation sequencing analysis with cloud-based parallel processing to eliminate bottlenecks. Compatible with Element and Illumina sequencers, our user-friendly interface replaces complex bioinformatics environments with an intuitive dashboard. This empowers your team while maintaining compatibility with your current sequencing infrastructure.

Exact genomic interpretations

Exact genomic interpretations

The Interpret module transforms your sequencing data into meaningful, actionable insights with powerful pre-filtering capabilities and pre-classifications. These features are designed to create workflow efficiency - compressing interpretation timelines from several days to less than 2 hours, all while leveraging our continuously curated database of 390+ genes.

Comprehensive gene panel

What’s inside

Comprehensive gene panel

Our targeted gene panel provides thorough coverage for newborn sequencing research, ensuring you have access to all critical genetic markers. Each included gene meets rigorous selection criteria established by our team of genomic experts and bioinformaticians.

About our panel

Take a closer look

Discover the modular and configurable software suite designed to propel your genomic analysis.
Download brochure

Key benefits

Operational excellence
Operational excellence

Reduce complexity and save valuable time with intelligent automation and parallel processing via cloud, designed to covert days of work into hours – allowing your team to focus on what matters most.

Uncompromising accuracy
Uncompromising accuracy

Paring strategic and multi-layered quality control checkpoints alongside a continually curated genomic database ensures reliable results that you can trust.

Seamless adaptation
Seamless adaptation

Configure the platform to your existing workflow and integrate with your preferred sequencing technology, offering true flexibility without forcing you to conform to rigid constraints.

Your partner in genomic excellence

With our reputable software suite and sequencing workflow, Revvity's list of genomic collaborations continues to grow. See what's possible – read about two of our latest projects here.
Discover our collaborations

Stay at the forefront of newborn genomics

Join our community of leading laboratories by subscribing to our newborn sequencing eNewsletter. Packed with the latest insights and developments in newborn genomic research.
Sign up for newsletter


Featured resources

Webinar

The 2025 Newborn Screening and Genomics Roundtable

Learn more
Webinar

The 2024 Newborn Screening and Genomics Roundtable

Learn more
Infographic

Newborn sequencing research with Revvity

Learn more
Brochure

Software suite for NGS research

Learn more
License Agreement

Software as a service license agreement for NGS Software

Learn more
View all resources View all resources
line

It's time to simplify your science.

Request a demo
Request a demo
Download brochure
Download brochure
Revvity Logo

©2025 Revvity - All rights reserved

Revvity is a trademark of Revvity, Inc. All other trademarks are the property of their respective owners.