IntelliSpace Precision Medicine

IntelliSpace Precision Medicine Genomics

Integrative systems. Deeper insights. Precise decisions.

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IntelliSpace Precision Medicine Genomics combines customizable pipelines with deep learning algorithms that turn your evolving data into new insights.

Features
Decode

Decode

Molecular test agnostic processing of raw-omics data using automated pipelines with quality checks and traceability.
Curate

Curate

Create a knowledgebase that transforms previous data into new evidence.
Annotate

Annotate

Variant filtering & annotation of processed genomic data according to functional, biological, pathway and disease indication.
Match

Match

Identification and prioritization of therapies and clinical trials based on patients' genotype and phenotype.
Filter

Filter

Light-up clinically actionable variants.
Reporting

Reporting

Perform cohort analyses on patients and leverage past history for better outcomes.

Reduce IT infrastructure complexity and simplify maintenance

  • Hybrid cloud-based platform
  • Automated data integration, including clinical (EMR. PACS and departmental systems), and molecular (sequencing, pathology) data
  • HL7, FHIR data management capabilities with EMR, PACS, LIS and LIMS, EDW, Registry

Data safety and security

  • Full audit traceability
  • Includes security and privacy features and controls to facilitate compliance with best practices, including HIPAA privacy rules
  • Incorporates backup, recovery and encryption controls to protect confidentiality, integrity and availability
  • Secure authentication and authorization mechanisms

How do you handle the evolving complexity and volume of genomic data?

intellispace genomics tablet

There are many challenges to setting up a precision medicine program. Whether it’s the time and resources to evaluate instruments, assays and software, the continuously evolving test offerings, or the inability to collaborate across departments (i.e communicating with ordering oncologists), there are obstacles that are preventing forward-thinking healthcare organizations from starting and scaling precision medicine operations.
 

To keep pace with the rapid developments in the field of genomics, you need clinical workflow tools that are integrated with the evolving genomic evidence that is being generated everyday both inside your laboratory and in the broader community. Philips IntelliSpace Precision Medicine Genomics combines customizable pipelines with deep learning algorithms that turn your evolving data into new insights.

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Delivering an automated end-to-end workflow

  • Automating pathologists’ workflow from loading sequence file output to customized report generation, including therapy prioritization creating collaboration between oncologists and peer molecular pathologists.
  • Enables discrete data capture and storage of variants, annotations, clinical interpretation and recommended treatments to support adherence and variant-based patient outcomes.
automated workflow chart

Seamless transition between the clinical and curation workflow

Each entry in the knowledgebase is a documented genomic aberration association, which is relevant to understanding genomic drivers of disease and treatment response.
 

Doctors and qualified personnel are allowed to curate this knowledgebase and to continue to enter observations.

Your curated data in a scalable knowledge base

The goal is to provide consistent and transparent clinical interpretation of patient genomic data for:

  1. Improved diagnosis and treatment options
  2. Helps improve selection of treatment options and clinical decision support.
scalable knowledge base graph

Partnering to expand precision care

Philips and Memorial Sloan Kettering Cancer Center announce research agreement to jointly develop advanced genome analytics for precision oncology
Memorial Sloan Kettering Cancer Center will use Philips IntelliSpace Precision Medicine Genomics platform for advanced analytics and research collaboration capabilities
memorial sloan kettering cancer center building

Help reduce the challenges in developing and implementing precision medicine programs.

  • Manage, translate, and securely store genomic data
  • Auto organize relevant data
  • Access cases, anywhere, anytime, and track recommendations
  • Improve communication between Molecular Pathologists and Oncologist via molecular tumor board

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