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.

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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.

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Our Products

Our Applications

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

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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.

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Customers, Suppliers & Service Providers

Testimonials

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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.

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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.

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