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Pathology Genomics Workspace From molecular data to clinical impact

Pathology Genomics Workspace

From molecular data to clinical impact

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Creating a complete biomarker-informed diagnostic and therapeutic picture of your patients through comprehensive molecular patient data, disease histology, and patient phenotype.

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Features
Genomic analysis

Genomic analysis

Offers a controlled bioinformatics environment for processing pipelines, built to medical device QMS standards. It offers traceability, reproducibility, QC, storage, and a versatile pipeline builder for cancer genomic data. The data may include .fastq, .bcl formats, as well as .vcf , .json and .xml.
Automated end-to-end workflow

Automated end-to-end workflow

Automating pathologists’ workflow from loading sequencing output files to customized report generation, including therapy options and trial matching with expert curated clinical knowledgebase.
Secure, sustainable, and scalable infrastructure

Secure, sustainable, and scalable infrastructure

Dependable mechanism for automatic, secure, quality assured acquisition of clinical and genomic data. Distributed software system with microservices.
Comprehensive variant review and filter

Comprehensive variant review and filter

Automated and streamlined variant calling and prioritization using leading variant annotation databases and clinical evidence.
Clinical data integration

Clinical data integration

Automated clinical data inbound/outbound integration per specification with our IntelliBridge Enterpise integration engine from/to EHR or other clinical IT systems.
Multiple knowledgebases

Multiple knowledgebases

Comprehensive clinical knowledgebases of most up-to-date literature, therapies and clinical trials from Qiagen N-of-One, Jackson Laboratory, and MD Anderson.
  • Genomic analysis
  • Automated end-to-end workflow
  • Secure, sustainable, and scalable infrastructure
  • Comprehensive variant review and filter
See all features
Genomic analysis

Genomic analysis

Offers a controlled bioinformatics environment for processing pipelines, built to medical device QMS standards. It offers traceability, reproducibility, QC, storage, and a versatile pipeline builder for cancer genomic data. The data may include .fastq, .bcl formats, as well as .vcf , .json and .xml.
Automated end-to-end workflow

Automated end-to-end workflow

Automating pathologists’ workflow from loading sequencing output files to customized report generation, including therapy options and trial matching with expert curated clinical knowledgebase.
Secure, sustainable, and scalable infrastructure

Secure, sustainable, and scalable infrastructure

Dependable mechanism for automatic, secure, quality assured acquisition of clinical and genomic data. Distributed software system with microservices.
Comprehensive variant review and filter

Comprehensive variant review and filter

Automated and streamlined variant calling and prioritization using leading variant annotation databases and clinical evidence.
Clinical data integration

Clinical data integration

Automated clinical data inbound/outbound integration per specification with our IntelliBridge Enterpise integration engine from/to EHR or other clinical IT systems.
Multiple knowledgebases

Multiple knowledgebases

Comprehensive clinical knowledgebases of most up-to-date literature, therapies and clinical trials from Qiagen N-of-One, Jackson Laboratory, and MD Anderson.
  • -Some products are only available in selected countries. Please consult your Philips representative for further details.

Napsauttamalla linkkiä poistut viralliselta Philips Electronics Ltd:n ("Philips") verkkosivustolta. Kaikki tällä sivustolla mahdollisesti olevat linkit kolmansien osapuolten verkkosivustoille tarjotaan vain avuksesi, eivätkä ne millään tavalla edusta minkäänlaista yhteyttä tai tukea näillä linkitetyillä verkkosivustoilla annettuihin tietoihin. Philips ei anna minkäänlaisia väitteitä tai takuita kolmansien osapuolien verkkosivustoista tai niiden sisältämistä tiedoista.

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