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Job Vacancies Vacancy: Scientist Key Responsibilities Conducting and reporting molecular diagnostics for infectious and genetic diseases. Delivering lectures and practical sessions at the Genetech School. Supervising undergraduate students on research projects. Ensuring compliance with ISO 15189:2022 Quality Management System requirements. Representing Genetech at conferences, forums, and other professional engagements. Qualifications and Experience A Master’s degree (or higher) in biological sciences or a related field, inclusive of a research component. A minimum of two years’ experience in a medical laboratory and/or teaching experience at a university. How to Apply To apply, please email your detailed CV along with the contact details of two non-related referees to info@genetechsrilanka.com .

Internships Internship with Industry Based Training Programme Our internships consist of shadow learning and hands-on training with individual attention, and self-learning is facilitated through the provision of appropriate reading materials. This will be supervised by the experts in the relevant fields. These internships are ideal for: • Graduates aiming to pursue careers or postgraduate studies in molecular biology, either in Sri Lanka or abroad. • Undergraduate and postgraduate students seeking practical experience in molecular biology applications. • Local and International A/L students looking to gain early exposure to molecular biology techniques. We provide the following 4 types of internships: Two-Week Industry Based Training Programme with an Optional Four-Week Internship involving an Individual Research Assignment Students can participate in the Two-Week Industry Based Training Programme to receive the required two weeks of training before being eligible to enrol in the four week internship involving an individual research assignment. The total fee for this Six-Week Internship will vary depending on the type of individual research assignment and equipment used. However, the fee for the first two weeks of this six-week internship is Rs. 64,500. Internship Programme in DNA Fingerprinting and Genetic Testing (Two Weeks, Four Weeks, and Six Weeks) Learn more 3. Internship Programme on Molecular Disease Diagnostics (Two Weeks and Six Weeks) Learn more Customised Internships Customised Internship Programmes to Meet Specific Requirements We offer tailor-made internship programmes designed to meet the specific needs of students and researchers. This includes the long-term internships required by the undergraduate degree programmes. The cost of these customised internships will vary based on the length of the programme and the specific requirements. 4. View FAQs Contact us If you are interested in doing an internship at Genetech, please submit the Inquiry Form below or email us at info@genetechsrilanka.com to receive further details. View Inquiry Form

Laboratory Practical Courses for A/L Students and Teachers One day workshop on gene technology Laboratory safety and handling of micropipettes Polymerase Chain Reaction (PCR) Extraction of DNA from human blood and plants Preparation of agarose gels and agarose gel electrophoresis Basics in DNA profiling, DNA fingerprinting and DNA typing Basics in applications of PCR in disease diagnosis Fee: Rs. 6,000 per person (Minimum 10 students per session) Three day course on gene technology qPCR (Real time PCR) - Theory and Practicals Laboratory safety and handling of micropipettes Extraction of DNA from human blood and plants Preparation of agarose gels and agarose gel electrophoresis Polymerase Chain Reaction (PCR) and gel electrophoresis of PCR products Basics in DNA profiling, DNA fingerprinting and DNA typing Basics in applications of PCR in disease diagnosis Fee: Rs. 18 ,000 per person (Minimum 10 students per session) View FAQs Contact us If you are interested in doing this course at Genetech, please submit the Inquiry Form below or email us at info@genetechsrilanka.com to receive further details. View Inquiry Form

Bird DNA Sexing Why DNA Sexing Matters Accurate sex determination is essential for breeding, conservation, and pet ownership, particularly in monomorphic species where males and females appear identical. Even in species with visible differences between males and females, gender traits often develop only in adulthood. Knowing a bird’s sex is crucial for forming proper breeding pairs, helping breeders, and providing important information to pet owners and buyers before selling birds. Sample Collection Process To submit a sample for Bird DNA Sexing, follow these steps: Pluck 5-6 feathers from the bird’s chest area. Place the feathers in an envelope or a plastic zip-lock bag. Label the envelope or zip-lock bag with your bird ID (such as the bird’s name, ring number, or cage number). Complete the sample acceptance form and submit it along with the samples (available at the Genetech Reception or downloadable here ). You can submit the samples in person or by courier to: Genetech 54 Kitulwatte Road, Colombo 00800 For mail or courier submissions, place the sealed samples and completed sample acceptance form inside an envelope. We will notify you once the samples have been received. What we offer We provide 99.9% accurate molecular sexing for a wide range of bird species. Our method is non-invasive, typically using feathers, though blood and other tissues are also accepted. The process is quick, efficient, and cost-effective, delivering reliable results for bird owners, breeders, and conservationists. Contact us View Price List Sample Acceptance Sheet

Dhammika Gunasekera Owner of Genetech and Managing Trustee of Genetech Research Institute (GRI) Dhammika Gunasekera is the Owner of Genetech after the demise of his beloved wife Dr. Maya Gunasekera, the Founder of Genetech. He is also the owner of Dienge purveyors of handcrafted silver, fine art, gems and jewellery. Dhammika greatly values generosity and helps a large number of people and institutions financially. For example, he has given donations to the Sri Lanka Cancer Society, sponsored the Devapathiraja College (a school founded by his grandfather Sir Ernest De Silva) Rugby team in Rathgama, a rural area in Sri Lanka and met university tuition fees of students. He was a partner at Messrs. U. N. Gunasekera, a construction firm in Sri Lanka established by his father. The first two five-star hotels in Sri Lanka, namely, Lanka Oberoi (Cinnamon Grand) and Ceylon Inter-Continental (Kingsbury) were built by this company. He graduated from Imperial College London in 1989 with first class honours in civil engineering (BEng). Broadening his horizons to the field of accountancy, he became a passed finalist of the Institute of Chartered Accountants of Sri Lanka in 1986. Furthermore, he topped his batch in the Bachelor of Science degree that he completed at University of Colombo in 1984. He was also the head prefect of Royal College, Colombo in 1980.

DNA Typing Our passion to improve We pioneered the use of DNA typing for human identification for forensic casework and analysis of family relationships including parentage testing. We are a major supplier of this technology to the medico-legal community and the judicial system in Sri Lanka. Our reputation for integrity and reliability has made us the main provider of forensic DNA testing in the country. Over 4000 cases of disputed parentage and another 4000 criminal cases have had the advantage of DNA evidence through Genetech. What is DNA typing? DNA typing is a method of identifying individuals from the differences in their DNA. It is used for forensic casework as well as for determining familial relationships between individuals including paternity, maternity and siblingship. Advantages of DNA typing The science of DNA typing relies on technology that allows an individual's DNA to be examined and analysed. A person's DNA is unique: no two individuals (with the exception of identical twins) have the same DNA. Every cell in a person's body has the same DNA. Hence, DNA taken from any part of the body from the same individual will always be the same. DNA typing can be performed from many types of biological specimens including blood, saliva, sperm cells, muscle, teeth and bones. Thus, a person's DNA can be typed from very little tissue or body fluid. DNA typing is used for two major purposes: Identification of individuals from biological samples: This is mainly done in forensic casework, where it is possible to determine the identity of a criminal by typing the DNA left behind at the scene of the crime. Determination of familial relationships: This includes paternity testing, maternity testing, sibling testing, grand-parent testing, and even the identification of mutilated bodies. DNA typing is the best method of identifying individuals and determining familial relationships due to many reasons. It is extremely sensitive: with even a very small amount of tissue, the test can be performed successfully. It is also very accurate: it can give a test result with a very high degree of certainty. It is very reliable: the likelihood of obtaining a false result can be minimised, and the likelihood of making an error in the conclusion can be calculated. How does DNA typing work? In the DNA typing process, a DNA banding pattern or profile of an individual is first obtained from a tissue sample. The DNA profile is observed in the form of a set of DNA bands known as alleles. Each person has a maximum of two specific alleles for a given genetic location. This DNA profile is compared with the profile obtained from a sample taken from the scene of a crime. If the alleles in the two profiles match, then it can be said that the sample taken from the scene of the crime is from the individual that was tested. DNA typing services Child custody and maintenance: In cases where one parent is claiming the custody and maintenance of a child and the other parent is refusing to accept parentage. Proof of adultery: Especially in divorce cases where the paternity of the child is suspect, and the wife is being accused of adultery, DNA typing can be used to determine whether the husband is the father of the child. View all Cost We are happy to announce that after much research and optimisation, we have streamlined our DNA typing methods, and we are therefore able to provide DNA typing services at a reasonable cost. We perform the same DNA typing tests which are used by internationally recognised laboratories, and maintain the same standards of quality so that the conclusions made by us can be verified by any accredited forensic DNA typing laboratory in the world. Contact us View Price List Quality control DNA typing is a highly specialised procedure which requires knowledge and skill. Furthermore, for DNA typing evidence to be acceptable in a Court of Law, it has to meet certain quality standards, which have been well documented and followed by forensic DNA laboratories worldwide. Accordingly in 2010, we became the first DNA typing laboratory in Sri Lanka to achieve ISO 15189:2007 (now 15189:2012) accreditation from Sri Lanka Accreditation Board (SLAB). Read more Accuracy of evidence DNA testing is the most accurate and reliable means of identity verification and parentage testing. The degree of accuracy of the test will depend on the genetic diversity of the Sri Lankan population as well as the number of genetic locations (STR loci) which are tested. There is no mandatory number of STR loci required for a test, but the testing of nine STR loci or more is generally considered to be sufficiently accurate. We test up to 15 STR loci. Read more Ethical Guidelines DNA typing is performed ethically only with the informed consent of the individual whose DNA is being typed. The persons concerned will be informed about the consequences of the test. Where such consent cannot be given such as in the case of minors, the consent of the guardian has to be obtained. We will not undertake samples for parentage testing without written consent from all living parties who will be tested. Read more Please contact us for personalised support on parentage and testing of other family relationships.

5 Day Practical Training Programme for A Level Students Why choose this programme? The programme will consist of lectures, practicals, and demonstrations covering various topics in molecular biology, biotechnology, and gene technology. It will also provide exposure to the applications of these subjects in the fields of Molecular Diagnostics and DNA Fingerprinting as an introducti on. Who can register for this programme? This programme is specifically designed for Edexcel, Cambridge, and Local A/L Students (AS, A2 and post-A/Ls) to fulfill the basic practical experience requirements in molecular biology and gene technology applications. It is intended for students who will be applying to and awaiting entry into tertiary programmes, particularly those planning to join universities in the US, UK and other countries in the near future. Email now If you are interested in participating in this training programme, send us an email with your details to info@genetechsrilanka.com View FAQs Contact us View Inquiry Form

​ Weiskopf, D., Bangs, D. J., Sidney, J., Kolla, R. V., De Silva, A. D., de Silva, A. M., Crotty, S., Peters, B. & Sette, A. (2015) Dengue virus infection elicits highly polarized CX3CR1+ cytotoxic CD4+ T cells associated with protective immunity. Proc Natl Acad Sci USA. 112(31), E4256-E4263. Available from: doi: 10.1073/pnas.1505956112 Krishnananthasivam, S., Fernando, A. N., Tippalagama, R., Tennekoon, R., De Man, J., Seneviratne, D., Premawansa, S., Premawansa, G. & De Silva, A. D. (2015) Evaluation of a commercial rapid test kit for detection of acute dengue infection. Southeast Asian Journal of Tropical Medicine and Public Health. 46(4), 602-610. Available from: https://www.researchgate.net/publication/280836227_Evaluation_of_a_commercial_rapid_test_kit_for_detection_of_acute_dengue_infection Sathkumara, H. D., De Silva, N. R., Handunnetti, S. & De Silva, A. D. (2015) Genetics of common variable immunodeficiency: role of transmembrane activator and calcium modulator and cyclophilin ligand interactor. Int J Immunogenet. 42(4), 239-253. Available from: doi: 10.1111/iji.12217 Tillekeratne, L., Bodinayake, C., Nagahawatte, A., Vidanagama, D., Devasiri, V., Kodikara Arachchi, W., Kurukulasooriya, R., De Silva, A. D., Østybe, T., Reller, M. E. & Woods, C. W. (2015) An Under-Recognized Influenza Epidemic Identified by Rapid Influenza Testing, Southern Sri Lanka, 2013. American journal of tropical medicine and hygiene . 92(5), 1023-1029. Available from: doi: 10.4269/ajtmh.14-0708 Jayawardana, W. A. D., Jayasekera, G. A. U., Wijesundara, R. L. C., Dissanayake, D. M. N., Sooriyapathirana, S. D. S. S., Webadde, C. K., Perera, K. L. N. S., Gunapala, K. R. D. & Hettige, P. (2014). “Evaluation of DNA markers Linked to Blast Resistance Genes Pikh, Pitp and Pita for parental selection in Sri Lankan Rice Breeding”. Tropical Agricultural Research. 26(1), 82-95. Available from: doi: 10.4038/tar.v26i1.8074 Kamaral, L. C. J., Perera, S. A. C. N., Perera, K. L. N. S. & Dasanayake, P. N. (2014). Genetic Diversity of the Sri Lanka Yellow Dwarf Coconut Form as Revealed by Microsatellite Markers. Tropical Agriculture Research. Vol. 26 (1): 131-139. Available from: doi: 10.4038/tar.v26i1.8078 Weiskopf, D., Angelo, M. A., Bangs, D. J., Sidney, J., Paul, S., Peters, B., De Silva, A. D., Lindow, J. C., Diehl, S. A., Whitehead, S., Durbin, A., Kirkpatrick, B. & Sette, A. (2014) The Human CD8+ T Cell Responses Induced by a Live Attenuated Tetravalent Dengue Vaccine Are Directed against Highly Conserved Epitopes. J Virol. 89(1), 120-8. Available from: doi: 10.1128/JVI.02129-14 Corbett, K. S., Katzelnick, L., Tissera, H., Amerasinghe, A., de Silva, A. D. & de Silva A. M. (2014) Preexisting Neutralising Antibody Responses Distinguish Clinically Inapparent and Apparent Dengue Virus Infections in a Sri Lankan Pediatric Cohort. J Infect Dis. 211(4), 590-599. Available from: doi: 10.1093/infdis/jiu481 Tissera, H., Amarasinghe, A., De Silva, A. D., Kariyawasam, P., Corbett, K. S., Katzelnick, L., Tam, C., Letson, G. W., Margolis, H. S. & de Silva, A. M. (2014) Burden of Dengue Infection and Disease in a Pediatric Cohort in Urban Sri Lanka. American Journal of Tropical Medicine & Hygiene . 91(1), 132-137. Available from: doi: 10.4269/ajtmh.13-0540 Ocwieja, K. E., Fernando, A. N., Sherrill-Mix, S., Sundararaman, S. A., Tennekoon, R. N., Tippalagama, R., Krishnananthasivam, S., Premawansa, G., Premawansa, S. & De Silva, A. D. (2014) Phylogeography and Molecular Epidemiology of an epidemic strain of Dengue Virus Type 1 in Sri Lanka. American Journal of Tropical Medicine & Hygiene . 91(2), 225-234. Available from: doi: 10.4269/ajtmh.13-0523 Calis, J. J. A., Maybeno, M., Greenbaum, J. A., Weiskopf, D., De Silva, A. D., Sette, A., Kesmir, C. & Peters, B. (2013) Properties of MHC Class I Presented Peptides That Enhance Immunogenicity. PLoSComputBiol 9(10): e1003266. Available from: doi: 10.1371/journal.pcbi.1003266 Tissera, H. A., Amarasinghe, A., de Silva, A. M., Tam, C. C., De Silva, A. D., Letson, G. W. & Margolis, H. S. (2013) Surveillance of dengue in a community cohort in Metropolitan Colombo, Sri Lanka: part I methods and study population. Dengue Bulletin. 37, 141-159. Available from: https://www.researchgate.net/profile/Anun_Chaikoolvatana/publication/266919317_GIS_Based_Surveillance_to_Support_DHF_Control_in_Thailand_from_2009_to_2011/links/543f70430cf21c84f23cd2d0.pdf#page=149 Tissera, H. A., Amarasinghe, A., de Silva, A. M., De Man, J. & De Silva, A. D. (2013) A comparison of an in-house IgM and IgG assay with a commercial Panbio kit, in a paediatric cohort in Colombo, Sri Lanka. Dengue Bulletin . 37, 101-106. Available from: http://apps.who.int/iris/bitstream/handle/10665/204944/B5077.pdf;jsessionid=020BC61ACDC2C27C6A59AA5E97637C71?sequence=1 Tam, C. C., Tissera, H., de Silva, A. M., De Silva, A. D., Margolis, H. S. & Amarasinge, A. (2013) Estimates of dengue force of infection in children in Colombo, Sri Lanka. PLoSNegl Trop Dis. 7(6):e2259. Available from: doi: 10.1371/journal.pntd.0002259 Weiskopf, D., Angelo, M. A., de Azeredoa, E. L., Sidney, J., Greenbaum, J. A., Fernando, A. N., Broadwater, A., Kolla, R. V., De Silva, A. D., de Silva, A. M., Mattia, K. A., Doranz, B. J., Grey, H. M., Shresta, S., Peters, B. & Sette, A. (2013) Comprehensive analysis of dengue virus-specific responses supports an HLA-linked protective role for CD8+ T cells. Proc Natl Acad Sci USA . Available from: doi: 10.1073/pnas.1305227110 Rathnayake, N. R. M. K. N. D., Bentota, A. P., Dissanayake, D. M. N., Perera, K. L. N. S., Sooriyapathirana, S. D. S. S. & Jayasekera, G. A. U. (2012) DNA Markers RM 464A and RM 219 Haplotypes are Effective in Selecting Sub-1 locus for the Introgression of Submergence Tolerance into New Rice Varieties. Ceylon Journal of Science (Bio. Sci.) 41 (2): 125-136. Available from: doi: 10.4038/cjsbs.v41i2.5382 Tissera, H. A., Ooi, E. E., Gubler, D. J., Tan, Y., Logendra, B., Wahala, M. P. B. W., de Silva, A. M., Abeysinghe, M. R. N., Palihawadana, P., Gunasena, S., Tam, C. C., Amarasinghe, A., Letson, G. W., Margolis, H. S. & De Silva, A. D. (2011) New dengue virus type 1 genotype in Colombo, Sri Lanka. Emerging Infectious Diseases. 17(11), 2053-2055. Available from: doi: 10.3201/eid1711.101893 Weiskopf, D., Yauch, L. E., Angelo, M. A., John, D. V., Greenbaum, J. A., Sidney, J., Kolla, R. V., De Silva, A. D., de Silva, A. M., Grey, H., Peters, B., Shresta, S. & Sette, A. (2011) Insights into HLA-Restricted T Cell Responses in a Novel Mouse Model of Dengue Virus Infection Point toward New Implications for Vaccine Design. J. Immunol. Available from: doi: 10.4049/jimmunol.1101970 Malavige, G. N., Rostron, T., Rohanachandra, L. T., Jayaratne, S. D., Fernando, N., De Silva, A. D., Liyanage, M. & Ogg, G. (2011) HLA Class I and Class II Associations in Dengue Viral Infections in a Sri Lankan Population. PLoS ONE 6(6): e20581. Available from: doi: 10.1371/journal.pone.0020581 Seneviratne, D. B., Amuduwage, S., Weerasingam, S. & Fernandopulle, N. D. (2010) Hepatitis C virus in healthy blood donors in Sri Lanka. Asian Journal of Transfusion Science. Available from: doi: 10.4103/0973-6247.75976 Tissera, H. A., De Silva, A. D., Abeysinghe, M. R. N., De Silva, A. M., Palihawadana, P., Gunasena, S., Tam, C. C., Gamage, T. M., De Silva, T., Rajapaksa, L. C., Amarasinghe, A., Letson, G. W. & Margolis, H. S. (2010) Dengue Surveillance in Colombo, Sri Lanka: Baseline seroprevalence among children. Procedures in Vaccinology 2: 2010) 109-112. Available from: doi: 10.1016/j.provac.2010.03.020 Illeperuma, R. J., Markalanda, D., Fernanadopulle, N. D. & Ratnasooriya, W. D. (2010). Genetic variation at 11 autosomal STR loci in the aboriginal people, the Veddahs of Sri Lanka. Forensic Science international: Genetics 4 (2010) 142. Available from: doi: 10.1016/j.fsigen.2009.05.007 Illeperuma, R. J., Markalanda, D., Mountain, J. L., Ratnasooriaya, W. D., Fernandopullae, N. D. & Bamshad, M. J. (2010) Haplotype data for 12 Y-chromosome STR loci of Sri Lankans. Forensic Science international: Genetics 4 (2010) e119e120. Available from: doi: 10.1016/j.fsigen.2009.10.003 Kanakaratne, N., Wahala, W. M. P. B., Messer, W. B., Tissera, H. A., Shahani, A., Abeysinghe, N., Thevanesam, V., de Silva, A. M. & Gunasekera, M. (2009) Severe dengue epidemics in Sri Lanka: 2003-2006. Journal of CDC-Emerging Infectious Diseases. 15 (2). Available from: doi: 10.3201/eid1502.080926 Illeperuma, R. J., Mohotti, S. N. K., De Silva, M. T., Fernandopulle, N. D. & Ratnasooriya, W. D. (2008) Genetic Profile of 11 Autosomal STR Loci Among the Four Major Ethnic Groups in Sri Lanka, Forensic Science International: Genetics 3 (3): 105-106. Available from: doi: 10.1016/j.fsigen.2008.10.002 Senevirathna, D., Ranaweera, D., Abeysekera, D., Kanakarathana, N., De Silva, D., Abeysundara, S., Samaraweera, P., Jayasinghe, S. & Fernandopulle, N. (2008) Genotypes of hepatitis C virus (HCV) in liver disease patients in Sri Lanka. Southeast Asian J Trop Med Public Health. 2008 Nov;39(6):1054-6. Available from: https://pubmed.ncbi.nlm.nih.gov/19062694/ ​ ​ Page 3 of 3 Journal Publications 1 2 3

Animal Testing What is Parvovirus and why is early diagnosis essential? Canine Parvovirus (CPV) is a highly contagious pathogen primarily affecting dogs. This virus can also infect other mammals including cats. If untreated, the risk of death may be high. Thus, a rapid and early diagnosis could save their lives. ​ Detection of the virus can help you select an appropriate treatment regimen for your animals, prevent the spread of the virus and save them from secondary infections. Why we recommend a PCR test over an ELISA test The sensitivity of an ELISA test depends on the Ag/Ab concentration and the availability. Thus, it could lead to false positive or negative results. In contrast, our PCR (Polymerase Chain Reaction) test detects the viral genome and produces no false positive or negative results. This is because it is dependent on the availability of the virus but not its products or Abs. The positive result of an ELISA test can be caused by organisms other than the target. On the other hand, our PCR test detects genetic sequences unique to the target pathogen. Therefore, its specificity is much higher than an ELISA test. The accuracy of the ELISA test varies, and it depends on the Ag/Ab availability. Our PCR test offers a consistent accuracy of 99%. What is tick fever and why may early detection be crucial? Tick fever is a common canine disease in Sri Lanka which is caused through the bite of an infected tick carrying an insidious and deadly organism. Scientifically, it is known as Canine Ehrlichiosis and Canine Babesiosis. ​ Early detection may prevent the dog from experiencing severe anemic conditions caused by the disease due to the highly pathogenic nature of it. Furthermore, the specific detection will help choose a suitable treatment regimen for your dog. Why microscopy and antibody tests are not ideal Some stages of the parasite life cycle cannot be observed through the microscope. Therefore, the probability of obtaining false results is high. It takes several days to develop antibodies against a certain infection in the body. Hence, it is difficult to diagnose the infection early. Antibodies may be present in the body even after the disease is cured. Thus, if the test is done after the infection is cured, the result may be false positive. What we offer We are the first firm to provide a PCR based animal disease testing service in Sri Lanka. We offer tests which detect Canine Parvovirus, Canine Distemper, Canine Babesiosis and Canine Ehrlichiosis. In addition to animal disease testing, we provide a cattle parentage testing service through the use of DNA typing. Contact us View price list

Product Development Our research projects often aim for a final product which can range from developing a new diagnostic test to a commercial nucleic acid extraction or amplification kit. Research and development projects have given rise to Genetech's new product line. DNA and RNA extraction kits We have developed a wide range of DNA/RNA extraction kits such as viral RNA/DNA extraction kits, Bacterial genomic and plasmid DNA extraction kits, plant DNA extraction kits, human and other animal genomic DNA extraction kits. The kits are starting from 25 prep size and are scaled up to 100s to meet the wide array of requirements found in the research community. For optimum results, we also provide customised extraction kits for low yielding starting materials like insect and bone samples. PCR amplification kits We offer customised conventional and real time PCR amplification kits (Ready mix PCR kits) for both DNA and RNA. This can be integrated with primer designing and PCR optimisation as required for the best results. Industrially important kits We offer to develop industrially important test kits to meet specific needs. For example, White Spot Syndrome Virus Detection Kit for shrimps was developed for the shrimp farm industry, based on customer requirements. You can contact us to discuss your specific requirement. We are able to design and develop customised kits for a wide variety of industrial needs. Contact us

Our Leadership Dr. Maya Gunasekera Founder of Genetech 1961 - 2006 Dr. Maya Gunasekera founded Genetech in 2002 to develop the field of biotechnology in Sri Lanka. She pioneered the use of DNA testing in forensic casework in Sri Lanka, and was involved in almost all DNA typing tests done in Sri Lanka until the time of her death. Research teams led by Maya developed the first DNA probe for the malaria vector, Anopheles culicifacies, introduced a new molecular test for the early diagnosis of dengue, pioneered genetic work on the Sri Lankan elephant and resolved the taxonomic status of a fruit bat species complex. In 1999, Maya gave expert evidence on DNA typing for the Hokandara murder trial making history as the first court case to accept DNA evidence in Sri Lanka. READ MORE Dhammika Gunasekera Owner of Genetech and Managing Trustee of Genetech Research Institute (GRI) Dhammika Gunasekera is the Owner of Genetech after the demise of his beloved wife Dr. Maya Gunasekera, the Founder of Genetech. He is also the owner of Dienge purveyors of handcrafted silver, fine art, gems and jewellery. Dhammika greatly values generosity and helps a large number of people and institutions financially. For example, he has given donations to the Sri Lanka Cancer Society, sponsored the Devapathiraja College (a school founded by his grandfather Sir Ernest De Silva) Rugby team in Rathgama, a rural area in Sri Lanka and met university tuition fees of students. READ MORE Dr. Nandika Perera Head of Forensic DNA Typing and Parentage Testing Dr. Nandika Perera joined Genetech in early 2004 soon after its inception and was part of the pioneering team led by late Dr. Maya Gunasekera, who introduced molecular diagnostics and DNA typing services to Sri Lanka. In subsequent years, he was promoted to the post of Senior Scientist and in 2010, he became the Head of the Parentage Testing Section. Currently, he is also the Head of Forensic DNA typing and has provided more than 2500 DNA typing reports to the Sri Lankan Judiciary. ​ He together with his team has established several in-house molecular diagnostic tests including a test for prenatal diagnosis of thalassemia disease. READ MORE Samudi Mohotti Senior Scientist Samudi Mohotti commenced her professional career at Genetech as a Scientific Officer at the division of parentage testing in 2004. In subsequent years, she was promoted to the post of Senior Scientist and currently oversees the entire process of parentage testing. She is one of the most experienced scientists in the field of DNA typing and has contributed to submit over 3,000 DNA test reports for civil and criminal cases to the Sri Lankan Judiciary. She took part in the development of an allele frequency databases of autosomal STR markers for Sri Lankans ethnicities and co-authored a journal paper in a high-impact journal, Forensic Science International: Genetics. READ MORE

Ethical Guidelines DNA typing is performed ethically only with the informed consent of the individual whose DNA is being typed. The persons concerned will be informed about the consequences of the test. Where such consent cannot be given such as in the case of minors, the consent of the guardian has to be obtained. We will not undertake samples for parentage testing without written consent from all living parties who will be tested. In the instance of criminal casework, we adhere to provisions in the Law, with respect to taking samples from suspects, victims and other living individuals involved in the case. Strict confidentiality will be maintained at all times with respect to individuals being tested. The results of DNA typing tests and the conclusions drawn from them will be divulged only to the persons being tested, and Courts of Law which order such tests. The test result will be given in a numerical format; a Scientist from Genetech will interpret the results, drawing a clear, unambiguous conclusion, and express it in simple terms. DNA typing is performed by analysing non-coding regions of an individual's DNA. It does not give the analyst any information about the ethnicity, race, social background, physical or mental make up of that person. Therefore, no other genetic information will be retrieved from an individual's DNA.