Focus on deep sequencing to detect activating point mutations, amplifications, and structural rearrangements (fusions) in known and novel oncogenes.
Learn More →Creative Biolabs provides high-resolution molecular intelligence essential for advanced oncology research and pre-clinical development. We provide deep multi-omics data (genomics, transcriptomics, TME analysis) to identify and validate novel therapeutic targets and resistance mechanisms. Clients gain a complete, actionable molecular blueprint that enhances the efficacy signals in their discovery programs, significantly accelerating the path from bench science to translational breakthroughs.
Cancer progression is fundamentally driven by the dual dysfunction of activating oncogenes (e.g., MYC) and deactivating tumor suppressor genes (TSGs, e.g., TP53). Our profiling service provides the deep genomic and transcriptomic analysis required to map the complex interplay of these drivers, which govern critical signaling pathways like PI3K/AKT/mTOR and Wnt/β-catenin. This comprehensive view is essential for understanding tumor heterogeneity, predicting drug response, and validating molecular mechanisms against the latest scientific findings.
Reach out to our team to discuss the specific sensitivity metrics for your research, request a consultation.
Fig.1 The interplay between oncogenes and tumor-suppressor genes.1
Creative Biolabs offers specialized modules tailored to distinct research needs, all built upon our foundational multi-omics platform:
Focus on deep sequencing to detect activating point mutations, amplifications, and structural rearrangements (fusions) in known and novel oncogenes.
Learn More →Specialized analysis for identifying loss-of-function events, including deep deletions, large insertions/deletions, loss of heterozygosity (LOH), and epigenetic silencing markers.
Learn More →Investigates the regulatory role of non-coding RNA, mapping crucial miRNA-mRNA interactions that impact the expression and function of key oncogenes and TSGs.
Learn More →Utilizes AI/ML to combine multiple genomic and transcriptomic inputs into a unified predictive signature for prognosis, survival, or drug response risk stratification.
Learn More →Provides detailed, interactive network maps illustrating the functional relationships and co-dependencies between altered oncogenes and TSGs within a specific tumor cohort.
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We provide the necessary contextual genomic background—including co-mutations in TSGs like STK11 and oncogenes like KRAS - to predict compound efficacy and define polygenic drug dependencies before committing to costly research stages.
By quantifying global gene expression changes (transcriptomics), we can dynamically monitor a therapeutic agent's effect, for example, validating the curcumin-mediated reactivation of tumor suppressor genes like ARHGEF12 in colon cancer inhibition.
Through longitudinal profiling of tissue and liquid biopsy samples, we pinpoint secondary driver mutations and bypass mechanisms that lead to acquired resistance, facilitating the rapid design of rational combination therapies.
Our multi-variant reports allow for the precise stratification of research groups, linking specific genomic signatures (e.g., alterations in CDKN2A/B and TP53) to predictable biomarker response rates under various treatments, thereby optimizing late-stage research design.
We encourage you to contact us to review your specific project requirements.
Basic research panels are typically limited to a few hundred "hotspot" genes, often missing critical non-coding regions, complex structural variants, and the necessary depth for detecting subclonal mutations or MRD markers in liquid biopsies. Our service uses whole-exome sequencing and integrates comprehensive TSG analysis, offering a dramatically more complete molecular picture.
Yes, the liquid biopsy module within our profiling service is specifically optimized for high sensitivity. We utilize high-depth sequencing and proprietary bioinformatics algorithms to accurately detect low-frequency circulating analytes, such as ctDNA and cell-free RNA, which are essential for the identification of early molecular markers and monitoring resistance evolution.
This advanced service provides unprecedented insight into the functional landscape of the Tumor Microenvironment (TME) by assessing the spatial distribution of both metabolites and proteins.
Learn More →This specialized service utilizes advanced stable isotope tracing and flux analysis to quantify the dynamic consumption and production of key metabolites within the TME.
Learn More →At Creative Biolabs, we understand that precision is paramount. Our lead generation commitment is simple: We provide the deepest, most accurate genomic intelligence available, enabling you to make breakthroughs faster. Contact our lead scientist today for a complimentary consultation and tailored proposal.
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