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 Liquid-based cytology is a new generation cytosmear used in prevention of cervical cancer.  HPV genotyping is the earliest prognostic marker for cervical cancer. The test detects 12 oncogenic types.

Sofia - Medical University Office - 31 Pencho Slaveykov Str.

Genetic panel Healthy Diet and Sport includes an analysis of genetic variants related to the proper absorption of fats and carbohydrates, as well as a person's tendency to benefit from exercising. 

PCR method  allows up to 21 different viruses to be detected in one test, distinguishing between emerging viruses, such as SARS-CoV-2 (COVID-19), influenza and cold.

Genomic diagnostics offers a wide range of tests using molecular, cytogenetic, and genomic methods to assist in the diagnosis and treatment of hematological diseases. Using genetic technology, we can provide treating clinicians with key information and personalize patient care.

CINtec® PLUS Cytology is a triage test for cervical cancer screening and the only one using dual biomarker technology to detect p16 and Ki-67 simultaneously. Thus, it provides a powerful cytological indicator of the presence of oncotransforming HPV infections.

The Mental Health Pharmacogenetic Test is a modern diagnostic tool to help determine drug therapy. The test results are a factor in optimizing the dose or in choosing an alternative drug to avoid side effects and to optimize the efficacy of the prescribed therapy. 

The only method for diagnosing HPV is to perform PCR assay, where DNA fragments of the virus are isolated and amplified. The HPV 16/18 test has extremely high specificity and sensitivity. It is the earliest prognostic marker for cervical cancer. 

The DNA Sport Plus is an extended version of the DNA Sport Panel and includes analysis of genetic markers providing information for preparing a highly effective personalized training program.

Cervical cancer is the second most common cancer globally among women between the ages of 20 and 55. It is caused by the human papillomavirus (HPV). Up to 93% of cervical cancers are preventable with GENICA’s diagnostic solutions.

Diamine oxidase (DAO) is an intestinal enzyme that normally destroys histamine contained in food. In carriers of genetic variants, DAO deficiency is observed, and undigested histamine is unnecessarily absorbed, exhibiting various symptoms.

The GENICA’s Mental Health Genetic Test analyzes how patients’ genes can affect their response to certain medicines. The test result provides the doctor with information about which drugs are most effective and least toxic for the patient, as well the dose needed.

The MyHappySkin Panel is a full package of genetic markers, divided into 5 categories, which can be analyzed separately. The test result assists the dermatologist in creating a personalized approach to proper care of your skin.

Modern genetic methods (PCR; RT-PCR; sequencing; hybridization techniques) are the gold standard for detecting viral and bacterial genomes. These tests are faster, more sensitive, and more specific than any other diagnostic approach.

Chlamydia is a common STD that can infect both men and women. It can cause serious, permanent damage to a woman's reproductive system. Currently, PCR assay is the gold standard for the diagnosis of chlamydial infections.

The test is an analysis of a genetic variant affecting the production of the enzyme lactase, encoded by the LCT gene. This enzyme is responsible for the lactose breakdown and its reduced function leads to impaired breakdown and absorption of the lactose in milk. 

 Pazardzhik - Office -  74 Hristo Botev Str.

Genetic testing in pediatric patients is used to solve several clinical problems. These problems can range from acute respiratory infections to syndromic features such as developmental delay, mental retardation, autism spectrum disorders, neurodevelopmental disorders, short stature and delayed puberty to more specific diseases, such as cystic fibrosis.

The Microbiome MIDI genetic panel is an extension of Microbiome MINI panel and additional types of parasites (Giardia lamblia, Entamoeba histolytica, etc.) are included.

Celiac disease is an autoimmune disease occurring in genetically predisposed people of different ages. The test is prescribed when celiac disease is suspected and positive immunological markers for this disease exist. Genetic analysis makes it possible to detect patients at risk without performing an invasive small bowel biopsy.

The test is used to study paternal lineage by analyzing the Y chromosome. The analysis can only be performed on males, determining paternal lineage.

An accurate diagnosis based on genetic tests is at the start for an effective treatment and management of many neurological disorders. As an invaluable tool, genetic testing allows the identification of inherited neurological conditions, such as mental retardation, neurodegeneration, learning disabilities, movement disorders and muscle control.

Trichomoniasis is a very common sexually transmitted disease caused by infection with a protozoan parasite called Trichomonas vaginalis. It is not possible to diagnose trichomoniasis based on symptoms alone. For both men and women, the care provider should prescribe a laboratory test to diagnose trichomoniasis.

This test is prescribed when positive results from NIFTY Pro® and / or fetal morphology are registered. It is used for final conclusion regarding Down syndrome, Edwards syndrome, Patau syndrome, Klinefelter syndrome, monosomy X, syndrome XXX, triplodia.

The test is used to determine maternal lineage by analysis of mitochondrial DNA (mtDNA). Regardless of their sex, children inherit this haplogroup from their mother, so the analysis is applicable to both men and women.

Allergy tests are used to detect if the blood contains antibodies to a particular substance, such as peanuts or pollen, for example. These antibodies are called immunoglobulin E or IgE antibodies.

Premature ovarian failure (POF)— also called Primary ovarian insufficiency (POI) - occurs when the ovaries stop functioning normally before age 40. POF is one of the main causes of infertility in women.

Testing of Genetic Variants in the Genes HLA-G, IL1A, IL1B, TNFα.

The genetic factors analyzed identify the levels and degree of glycation, as well as the need to avoid sugar intake.

Early detection and diagnosis of cardiovascular disease can help prevent sudden cardiac death and improve the prognosis and treatment of affected patients. Genetic tests provide important diagnostic and prognostic information for myocardial infarction, deep vein thrombosis, arrhythmias, familial hypercholesterolemia, and others. 

Pharmacogenetics in cardiology allows the identification of patients at risk of severe toxicity or those who are likely to benefit from a particular treatment. Thus, it helps to design individualized cancer therapy. 

This test detects mutations in the RET gene associated with MEN2 multiple endocrine neoplasia.

This test detects mutations in 12 genes associated with pancreatic cancer.

Find out if you need iron or if you are overloaded with iron. Iron deficiency is observed when the amount of iron after depletion of reserves is not sufficient to cover functional needs, or when there is insufficient release of iron from reserves as a result of genetic modification.

COVID-19 Antibodies (for green certificate)

Our diagnostic solutions are much more than a laboratory and medical interpretation. GENICA’s leading-edge lab equipment guarantees a high level of competence, combined with the application of the most modern diagnostic practices. I

Prof. Albena Todorova is the head of Department of Molecular Genetics.

The test detects mutations in 74 genes associated with hereditary cancer in women. Genetic testing for hereditary and somatic cancers is the basis for proper diagnosis and treatment in affected patients.

Founded in 2006 GENICA is the only specialized laboratory in Bulgaria for performing molecular genetic tests. The lab provides a full spectrum of modern genetic methods and technologies for analysis of human, viral and bacterial genomes (PCR; RT-PCR; sequencing; hybridization techniques).

The DNASportFit panels analyze genetic markers, based on which an individual and effective diet and training program, in accordance with the specifics of your genome, is prepared.

The DNA Nutri panel includes genetic markers known to be most important for the metabolism of essential macronutrients. 

Femoflor plus® is a modern PCR-based test and the only diagnostic method that allows complex evaluation of vaginal microbiome composition, diagnosis of dysbiosis and detection of sexually transmitted infections. 

Allergy tests are used to detect if the blood contains antibodies to a particular substance, such as peanuts or pollen, for example. These antibodies are called immunoglobulin E or IgE antibodies. 

DNA testing is currently the latest and the most accurate technology for determining origin. The standard DNA paternity test generates convincing results to prove the father-child relationship.

Vitamin B12 Genetic Panel includes analysis of genetic variants associated with disorders in the absorption of the vitamin in the small intestine, reduced transport to the liver and faster depletion of its active form.

The DNA Pro panel includes analysis of genetic markers that determine differences in metabolism, lipolysis, and fat absorption. The results are useful in providing an appropriate nutrition and sport plan.

The test detects all 14 oncogenic types of HPV associated with a high risk of developing cervical cancer. The test does NOT detect a specific virus type and the result represents a total value - positive or negative.

Pharmacogenetics aims to determine the most appropriate drug treatment for a person. It examines how the DNA affects the way one responds to drugs.

Blood tests for allergies measure the quantity of antibodies that cause allergies, known as antibodies to immunoglobulin E (IgE). 

The pharmacogenetics of cancer identifies patients at risk of severe toxicity or those who are likely to benefit from a particular treatment. Thus, it helps to design individualized cancer therapy

A group of DNA tests associated with gynecologic cancers, including cervical cancer (SEE MORE), endometrial cancer, ovarian cancer, breast cancer.

The DNA Nutri Plus panel is an extended version of the DNA Nutri panel and includes genetic markers known to be most important for the metabolism of essential macronutrients as well as those involved in the absorption of important for the body vitamins. The test will also provide information about the need to take additional antioxidants to cleanse the body.

The rendering fee is a fee for the disposal of biological waste. 

 The HPV genotyping test is the earliest prognostic marker for cervical cancer. It detects 12 oncogenic types associated with a high risk of developing cervical cancer. 

GENICA Lab - address, contacts and business hours.

Vitamin A is a fat-soluble vitamin extremely important for vision, skin, teeth, bones, and tissues. The most common symptom of vitamin A deficiency is associated with changes in vision, as well as various diseases such as asthma and cardiovascular disorders.

PCR test for simultaneous detection of 18 pathogens associated with acute respiratory viral infections. It includes testing for the new coronavirus, the two influenza and 15 non-influenza viruses. 

In man, genital mycoplasmas are responsible for approximately 15%–20% of nongonococcal urethritis (NGU) cases, 20%–25% of nonchlamydial NGU, and approximately 30% of persistent or recurrent urethritis. In women, genital mycoplasmas are associated with the development of bacterial vaginosis and can be detected in 10%–30% of women with clinical cervicitis. 

The genetic panel for predisposition to overweight and obesity in early childhood is based on individual genetic differences in fat and carbohydrate metabolism, fat absorption, regulation of insulin and leptin, and regulation of appetite. The analysis involves study of genetic variations, marked as the most important in the genetic map of this pathology in childhood.

 Chromosome analysis or karyotyping is a genetic test that evaluates the number and structure of a person's chromosomes in order to detect abnormalities.  

Varna - Medical Complex Mladost Office - 15 Republika Blvd, 6th fl., units 601 and 602

The HPV 16/18 test has extremely high specificity and sensitivity. It is the earliest prognostic marker for cervical cancer (the second most common cancer after breast cancer among women). 

WES® detects pathological genetic variants in the whole protein coding sequence in the human genome. 

The anti-SARS-CoV-2 VNT (Neutralizing Antibody Virus) test can show if a person has developed immunity to the infection after recovering from it or after vaccination.

Genetic testing for hereditary and somatic cancers is the basis for proper diagnosis and treatment of affected patients. It can help families better understand their risk of cancer and to decide if they should get tested or learn about how to lower their risk of cancer. 

Kremena Mesechkova is the CEO of GMDL GENICA Ltd.

The preparation of the sample before the analytical phase includes registration, labeling, acceptance in the laboratory department and pre-processing of the sample in analytical form.

Next-Generation sequencing (NGS)/ Whole Exome Sequencing (WES)

GENICA Lab has the most comprehensive range of genetic tests to cover the needs of each patient. A definitive diagnosis can bring great relief to patients and their families, especially when they seek answers for a long time.

Medical lab technicians collect venous blood samples using closed blood collection systems.

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