What does CCGL mean in CLINICAL MEDICINE
The Clinical Cancer Genomics Laboratory (CCGL) is a dedicated facility that provides comprehensive services for clinical oncology, personalized medicine and cancer genomics research. It provides the tools, technologies and expertise necessary to bring clinical cancer genomic research from concept to real world application. The CCGL strives to improve patient outcomes by providing reliable, high-quality results.
CCGL meaning in Clinical Medicine in Medical
CCGL mostly used in an acronym Clinical Medicine in Category Medical that means Clinical Cancer Genomics Laboratory
Shorthand: CCGL,
Full Form: Clinical Cancer Genomics Laboratory
For more information of "Clinical Cancer Genomics Laboratory", see the section below.
What We Do
At the CCGL, our team of highly experienced professionals use cutting-edge sequencing and computationally intensive analysis techniques to help oncologists and researchers develop novel diagnostic tests and therapeutic strategies tailored to individual patients. Our work involves the application of advanced bioinformatics tools for the analysis of nucleic acid sequence data generated from tumor samples, including whole genome sequencing, targeted resequencing panels and single cell tools. We also offer customized technical support for bioinformatics pipelines development and deployment in clinical settings. Our focus is on utilizing next-generation sequencing (NGS) technologies to accurately identify actionable genetic alterations across multiple cancer types aiding in both early disease detection as well as monitoring therapeutic response in an effort to further personalize care for patients with cancer. Through this work we aim to improve diagnosis accuracy and discrimination between tumors that respond differently to available therapies which will ultimately lead to improved healthcare outcomes.
Essential Questions and Answers on Clinical Cancer Genomics Laboratory in "MEDICAL»CLINICAL"
What services does the Clinical Cancer Genomics Laboratory provide?
The Clinical Cancer Genomics Laboratory specializes in providing advanced genomic testing and interpretation services for cancer patients. We provide targeted sequencing of cancer-related genes, constitutional testing and molecular diagnostics, which can aid physicians in understanding the cause of their patient's cancer and guide treatment decisions.
How long does it take to get results from a Clinical Cancer Genomics Laboratory test?
Once the specimen is received at the laboratory, the turnaround time for most tests is approximately 2-4 weeks. However, if additional testing or analysis is required, this may increase the time frame for obtaining results.
What type of specimens does Clinical Cancer Genomics Laboratory accept?
The CCGL accepts both archival and fresh tumor specimens as well as peripheral blood (PBMC) specimens for certain tests. Please contact us directly for details about specimen requirements and sample submission guidelines.
Does Clinical Cancer Genomics Laboratory accept international samples?
Yes, we do accept international samples; however additional documentation must be supplied before an order can be placed with our laboratory. Please direct all enquiries related to international orders to our customer service department by email or telephone.
Does the CCGL offer consultations on my results?
Yes, we do offer consultations with a board-certified genetic counselor regarding any results that are generated by our laboratory through interpretation services. Please note that a consultation fee will be charged for these services; please contact us directly for more information about fees and scheduling.
Is there any way to view my reports online?
Yes! The CCGL offers secure online access to all reports generated by our laboratory through a secure patient portal on our website. You can log in using your unique username and password to view your report from anywhere at any time!
Final Words:
The Clinical Cancer Genomics Laboratory (CCGL) offers a range of services that enable clinical oncologists and researchers alike to utilize the latest advances in cancer genomics technology to identify actionable genetic alterations leading to improved medical treatment plans and better healthcare outcomes for those with cancer diagnoses. By providing access to state-of-the-art sequencing technologies combined with cutting edge analysis techniques, we are committed to revolutionizing how medicine is practiced through personalized approaches tailored specifically towards individuals' needs.
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