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Submission: On September 29 via api from US — Scanned from DE
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* * Home * COVID-19 * Infection Control Program * Environment Control Program * About Us * Leadership * Board of Directors * Consultants * Our Team * Partners * Product * Infectious Diseases – dxn1 * dxn1 BactFast * dxn1 FungiFast * dxn1 Virfast * dxn1 digitalABST * Oncology * gSeek Onco+ * gSeek Bone * gSeek Brain * GSeek Exome * GSeek Breast * GSeek ColoRectal * gSeek Kidney * gSeek Lung * gSeek Liver * gSeek Leukemia * gSeek Pancreas * gSeek Prostate * GSeek Carrier Screening * Transplant * gSeek Transplant High Resolution * gSeek Transplant Low Resolution * Pediatrics * GSeek Newborn Screening * gSeek Rare Diseases * Mother & Baby Wellness * gScan NIPT * gScan NIPT+ * gScan PGD * gScan PGS * Services * Clinical Diagnosis * Research * Technology * NGS * Genetic Consultation * Case Studies * Local * International * Archives * FAQs * Testimonials * Contact Us Toggle navigation * Home * COVID-19 * Infection Control Program * Environment Control Program * About Us * Leadership * Board of Directors * Consultants * Our Team * Partners * Product * Infectious Diseases – dxn1 * dxn1 BactFast * dxn1 FungiFast * dxn1 Virfast * dxn1 digitalABST * Oncology * gSeek Onco+ * gSeek Bone * gSeek Brain * GSeek Exome * GSeek Breast * GSeek ColoRectal * gSeek Kidney * gSeek Lung * gSeek Liver * gSeek Leukemia * gSeek Pancreas * gSeek Prostate * GSeek Carrier Screening * Transplant * gSeek Transplant High Resolution * gSeek Transplant Low Resolution * Pediatrics * GSeek Newborn Screening * gSeek Rare Diseases * Mother & Baby Wellness * gScan NIPT * gScan NIPT+ * gScan PGD * gScan PGS * Services * Clinical Diagnosis * Research * Technology * NGS * Genetic Consultation * Case Studies * Local * International * Archives * FAQs * Testimonials * Contact Us CREDENCE GENOMICS BEYOND THE BOUNDARIES OF HUMAN SCIENCE With the efforts and essence of the right combination of technology and human resources put together, Credence Genomics provides real-time genetic analysis services to their customers. The company’s devotion to molecular biology, genetics and the extensive investment in installation of cutting edge technology tools has placed them at the forefront of medical and genetic research. CLINICAL DIAGNOSIS With a team of experienced scientists and genetic counselors working around the clock to offer high quality services, we have become the industry leader in diagnosis of genetically inherited diseases. Learn More RESEARCH Microorganisms are ubiquitous; some of them are beneficial while others are harmful. Harmful bacteria and fungi can contaminate industrial environments, raw materials and the end products. Therefore, rapid detection methods are needed to identify their presence. Learn More OUR PRODUCTS * ALL * Infectious Diseases * Oncology * Transplant * Pediatrics * Mother & Baby Wellness OUR APPLICATIONS * DIAGNOSTICS * SCREENING * TREATMENT * RESEARCH Culture independent Next Generation Sequencing based diagnostic test for bacteria with 16s rRNA gene and fungi with ITS region amplification (Rapid Infection Detection Test – RID) and sequencing (Bact Fast, Fungi Fast) has revolutionized the modern clinical diagnosis process of infectious diseases. The test can identify over 18,000 bacterial species and 4,500 fungal species with high accuracy and fast turnaround time. Next Generation Sequencing based identification of inherited genetic alterations (within an individual) known as “variants” to predict the likelihood of developing an “inherited” or “complex” genetic disorders (especially for cancers) during an individual’s lifetime. Our vast test scope includes predictive testing (Credence Carrier/ Credence Inherited Disease, Credence New Born, Credence Breast, Credence Colo-rectal, Non-Invasive Prenatal Testing) and ensures fastest delivery of results with an unmatched accuracy of 99.7% Personalized medicine (Credence Tumor Hots pots) – The right medicine at the right time. Identification of responders and non-responders to medications using high end genetic analysis based on Next Generation Sequencing. The process maximizes the therapeutic outcome delivering efficacious, timely, “tailored” treatment to match each individual’s genetic make-up with an unmatched 99.7 % accuracy. Massively parallel sequencing or high-throughput sequencing is the process of sequencing millions of small DNA fragments at once, creating a massive pool of data. NGS technology has been applied in a variety of contexts, including whole-genome sequencing, targeted re sequencing, discovery of transcription factor binding sites etc. This technology has made a huge impact on functional genomics and meta genomics by providing a more descriptive picture of the target site. CASE STUDIES Explore all CASE STUDY ON MASTITIS IN BOVINE MILK Bovine mastitis is probably the most important disease for the dairy industry worldwide, causing economic losses due to reduced milk production, discarded milk, premature culling and excessive antibiotic use. A CASE STUDY ON MICROBIAL QUALITY TESTING OF COSMETIC AND PERSONAL CARE PRODUCTS The microbial safety of cosmetic and personal care products is an important consideration. About 30% of cosmetics currently sold in supermarkets… A CASE STUDY ON ASSESSING STERILITY OF PHARMACEUTICAL PRODUCTS Sri Lanka produces about 1035 million of medical drugs annually through the State Pharmaceutical Manufacturing Corporation (SPMC) [1], and another large quantity of pharmaceuticals are being imported to the country to cover the medical needs of about 20 million people. Explore all CUSTOMERS, SUPPLIERS & SERVICE PROVIDERS TESTIMONIALS GSeek Exome Rare Disease Identification NGS NGS offers an ideal platform for comprehensive mutation analysis of constitutional disorders (germline variations) and cancer diagnostics (somatic variations). With the rapid growth of this ground breaking technology, Clinical laboratories have become able to facilitate comprehensive gene panels for several complex inherited disorders. Explore More GENETIC CONSULTATION A service that provides information and support to people who have or who is in a risk of getting genetic disorders. During a consultation, the geneticist will discuss the genetic risks of a person or a family and diagnose the disorder, confirm it or exclude from the disorder. Explore More FOR AN INDIVIDUAL? Explore Genomic Research & Diagnosis Browse our Resource Hub Request a Screening FOR A MEDICAL PROFESSIONAL? Sign up to offer Credence Learn about Credence for your institution Manage your Credence patients OUR TEAM DR. VAZ S GNANAM Chairman / CEO MRS. PRADEEPA GNANAM Director RAVEEN WICKREMASINGHE Director JANITH K. LIYANAGE Director Hotline +94 705551990 011 2890687 / 011 2818370 info@credencegenomics.com 12-3/2 Sunethra Devi Road, Kohuwala, Sri Lanka. CALL ME BACK Please fill out this form if you would want us to call you back. LATEST NEWS FEED APOLLO INDIA LAUNCHES DNA BASED DIAGNOSTICS WITH SRI LANKA’S CREDENCE GENOMICS December 3, 2017 Chennai – The Apollo Hospitals Group, India’s largest integrated... Read More EYE LIVE INTERVIEW DR. VAZ SANTOSH GNANAM – CEO / DIRECTOR – CREDENCE GENOMICS December 2, 2017 Eye Live morning TV show interviewing Dr. Vaz Santosh... Read More BMC INFECTIOUS DISEASES PUBLISHES CREDENCE RID, BACTFAST & FUNGIFAST December 2, 2017 Credence Genomics Ltd., Sri Lanka’s premier specialised DNA diagnostics... Read More VIEW ALL © Credence Genomics 2022. BenWorldwide | Feedback THANK YOU Your inquiry has been received. Contact us