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Bioaro Calgary is a leading biotechnology company specializing in innovative solutions for the healthcare industry. With a strong focus on research and development, we strive to create cutting-edge products and therapies that improve the lives of patients worldwide. We are committed to pushing the boundaries of medical science and making breakthrough advancements that shape the future of healthcare. Based in Calgary, Canada, Bioaro is proud to contribute to the advancement of medical innovation and provide hope for patients and their families.
BioAro is a leading provider of genetic testing in Calgary. With a focus on cancer, disease, and prenatal Genetics Testing, we strive to provide individuals with valuable insights into their health and well-being. Our advanced genetic analysis technology allows us to deliver accurate and reliable results that can help inform personalized healthcare decisions.
Genetics Home Reference is a comprehensive online resource that offers accessible information about genetic conditions and the genes associated with those conditions. Our platform provides high-school-level language explanations, making it easy for individuals to understand complex genetic concepts.
Telomeres are tiny structures at the ends of our chromosomes that determine how our cells age. They act like protective caps, preventing DNA damage. But every time a cell divides, telomeres shorten. Eventually, they become too short to function, leading to aging and increased disease risk.
Whole exome sequencing is a technique used to sequence all the protein-coding regions of genes in a genome. These regions are known as exons, and they make up about 1% of the human genome. Despite being a small portion, exons are crucial because they contain the instructions for making proteins, which perform most of the functions in our bodies.
Pharmacogenetics refers to a branch of science that researches the implications of genetic makeup in the response to medications in an individual. Ultimately, pharmacogenetics will be able to identify variations in the genes that translate to differences in drug metabolism, efficacy, and safety. At this juncture, pharmacogenetics may enable the customization of medicines with the intent of lessening adverse drug reactions (ADRs). This blog explores the working of pharmacogenetics in preventing adverse drug reactions, improving patient safety, and optimizing the therapeutic efficacy of drugs.
Cancer is one of the leading causes of death worldwide, but the story doesn’t have to end there. The earlier cancer is detected, the higher the chances of successful treatment and survival. This is where cancer screening tests come in. These tests are designed to find cancer in its early stages, often before symptoms appear, allowing doctors to act quickly and prevent the disease from progressing.
Genetic analysis services involve the examination of an individual's DNA to identify genetic variations that may influence their health. These services can range from simple tests that look for specific genetic markers to comprehensive whole-genome sequencing. The information obtained from these analyses can be used to assess the risk of developing certain diseases, understand inherited conditions, and guide personalized treatment plans.
CALGARY, Alberta, Feb. 03, 2025 (GLOBE NEWSWIRE) -- BioAro, a global leader in precision health and genomics, will unveil its groundbreaking AI-powered PanOmiQ platform at the prestigious Precision Medicine World Conference (PMWC) in Silicon Valley. This Whole Genome Sequencing (WGS) solution achieves unparalleled efficiency, reducing analysis time to under two hours and generating Variant Call Format (VCF) files in under five minutes.
Mammography has long been the cornerstone of breast cancer screening, widely used for early detection of tumors, including those that are too small to be felt by physical examination. Despite its effectiveness, mammography has limitations, such as false positives and negatives, especially in dense breast tissue, as well as the inability to detect cancer at the genetic or molecular level.
Genetic testing refers to the analysis of a person’s DNA to identify genetic mutations or variations that could influence their health. These tests can detect changes in genes that might lead to genetic disorders, such as cystic fibrosis or sickle cell anemia, and can also assist in predicting an individual’s susceptibility to diseases, such as cancer, cardiovascular disorders, or diabetes. Genetic testing includes a variety of methods, such as whole genome sequencing, targeted gene testing, and carrier screening.
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