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Pharmacogenomics

Unlocking the Genome for Precision Medicine

Next Generation Sequence Pharmacogenomics (PGx) Pipeline

 

With our NGS PGx pipeline, healthcare providers can tailor specific treatment and prescribe the correct drug dosage based on their patients’ genetic profiles.

Key Features

pgx-key-features-1

Comprehensive Genomic Analysis

 

Performs SNPs detection, infer haplotypes and diplotypes, and genotype/phenotype of PGx genes, including complex genes, e.g., CYP2D6.

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Curated Guideline Recommendations

 

Established guidelines from Clinical Pharmacogenetics Implementation Consortium (CPIC) and Dutch Pharmacogenetics Working Group (PharmGKB-DPWG)

pgx-key-features-3

Customisable Report

 

Customisable PGx report that best aligns with individual requirements. Reports available in HTML, PDF and JSON formats.

How It Works

Our PGx pipeline manages the interpretation of raw genomic data to the predictions of star alleles to expected phenotype and it defines the rules which associate a phenotype with recommended changes to clinical care.

pgx-how-it-works

Comprehensive Analysis

Precision Genetic Analysis

SNPs Detection

Identify single nucleotide polymorphisms (SNPs), which can affect how individuals respond to medications.

Haplotype and Diplotype Inference

By analyzing combinations of SNPs, our PGx pipeline infers haplotypes and diplotypes, providing deeper insight into genetic variations and their potential impact on drug response.

Genotyping and Phenotyping

Perform both genotyping and phenotyping to predict how these variants manifest in drug response of PGx genes.

Complex Gene Analysis

Precisely analyse complex genes such as CYP2D6, which play a critical role in drug metabolism, for accurate treatment recommendations.

pgx-guidelines

Curated guideline recommendations

Expert-Driven Guidelines

Our PGx pipeline leverages established guidelines from the Clinical Pharmacogenetics Implementation Consortium (CPIC) and the Dutch Pharmacogenetics Working Group (PharmGKB-DPWG) to provide curated, evidence-based recommendations. By integrating these authoritative resources, we ensure that our guidance on drug selection and dosing is both precise and reliable, aligning with the latest standards in pharmacogenomics. This approach empowers healthcare providers to make informed, confident decisions tailored to each patient’s genetic profile, enhancing treatment effectiveness and safety.

pgx-report

Customisable PGx report

Personalised Reporting

  • Designed to meet individual requirements
  • Enable users to select specific gene and drug combinations
  • Tailor report to address particular medical conditions
  • Relevant and actionable information from established guidelines
  • Customisable report template

 

Available in:

pgx-report-format

Integration Capabilities

Seamless Integration with Clinical Pipeline

 

Our PGx pipeline seamlessly integrates with our clinical pipeline powered by novoClinic, enhancing efficiency and enabling streamlined data exchange. Whether it’s data ingestion, interoperability, or real-time updates, our solution harmonises with novoClinic, ensuring a cohesive and powerful clinical experience.

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Across Diverse Medical Fields

pgx-field-cardiology
Cardiology
pgx-field-brain
Neurology
pgx-field-oncology
Oncology
pgx-field-psychiatry
Psychiatry
pgx-field-lung
Pulmonary
pgx-field-dental

Dental

pgx-field-rheumatology
Rheumatology
pgx-field-gastroentrology
Gastroenterology
pgx-field-infectious-disease
Infectious Disease
pgx-field-urology
Urology
pgx-field-lung
Hematology
pgx-field-gynecology
Gynecology

And many more…

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