"I love CBR Genomics"

2022-05-20 17:35:20

Our VisionServicesTelemedicineTechnologyGrants & AwardsFeaturedNewsPT|EN.slider-slide > img { width: 100%; display: block; } .slider-slide > img:focus { margin: auto; }Genomics at the service of MedicineWe feel the urgency of putting the latest scientific advances at the service of Medicine, with a positive impact on People's lives, by bringing the genetic information into the clinical practice, to improve clinical outcomes.Our VisionIn the future, checking the DNA sequence will be as ubiquitous and accessible as blood testing or X-ray exams are today.At CBR Genomics, we put Genomics at the service of Medicine, with a positive impact on People's lives - of Patients and their Doctors. We develop clinical tools to support physicians' decisions based on the invaluable information held in the DNA, improving healtcare outcomes as well as people’s quality of life, and extending longevity.With our genetic services, it is possible to experience the Future of Medicine.Predictionof genetic diseases apperancePreventionof disease development, with a proactive and timely approachPersonalizationof clinical decisions and interventionsParticipationand empowerment of individuals on their health managementWith our technology, DNA is a lifelong resource for healthcare management.Confidencein the clinical reports, they are based on highly curated scientific dataProtectionof patients’ identitySecurityin the storage of genetic dataMeet DNA.files ServicesBased on the latest advances in Science and DNA sequencing technology, we have developed genetic analyses (DNA.files) by studying hundreds of genes associated with diseases, from a saliva sample.Early screening for genetic diseases and timely clinical actions allow to significantly reduce the time to diagnosis, prevent or mitigate the diseases’ development, and promote a better and longer life.A postnatal genetic service, as a complement to the heel prick test, for newborns, babies and children. DNA.files BABY screens more than 500 genes associated with over 300 paediatric diseases. If detected early - before the onset of the first symptoms - their development can be prevented or mitigated.Visit WebsiteLearn moreA genetic service for babies, children and young people with some kind of Intellectual Disability, without a conclusive diagnosis. DNA.files INTELLECTUAL DISABILITY analyses over 1 250 genes associated with Intellectual Deficit. Through molecular diagnosis and the most appropriate therapies, it is possible to improve the quality of life of these patients and their families.Learn moreA genetic service to support athletes and their sports physicians on their healthcare management. DNA.files ATHLETE screens for mutations in over 60 genes causing 12 cardiovascular diseases, including hereditary cardiomyopathies and arrhythmias, to prevent or mitigate these conditions or even early deaths.Visit WebsiteLearn moreA genetic screening service to support family planning for future parents, with or without clinical history in the family. DNA.files PARENT identifies whether the parents are carriers of mutations in genes associated with serious diseases that can be passed on to their children, allowing them to consider different conception options to prevent their development.Learn moreLaunching soonA DNA testing for patients with symptoms suggestive of genetic disease, through the analysis of the 20 000 human coding genes. DNA.files CUSTOM can lead to the identification of the molecular cause of the disease, with a positive impact on the patient's clinical follow-up, prescription, diagnosis and prognosis.Learn moreTelemedicine appointments for greater convenienceWe are moving Genetic Medicine to the next level, closer to individuals, with specialised Medical Geneticists.With our Telemedicine services, we offer personalised Genetic Appointments. Terms & ConditionsWith our patented technology, DNA becomes a life-long resource for health managementDNA, the code of life, is unique and holds invaluable information regarding our health. We bring the key to unlock, read and interpret what is written in the genes. Once sequenced and stored by us, it is possible to perform multiple analysis from genes throughout a lifetime. Our technology provides easy-to-read reports containing highly curated genetic information relevant for healthcare management.Controlled data accessFull data anonymitySecure data storageAutomated genetic query & reportGrants & AwardsWe uniquely merge Genetic Medicine at Digital HealthClinical Research GrantIn2GenomeOur DNA analysis methodology was validated by In2Genome, a project promoted by CBR Genomics, in partnership with the Medical Genetics Unit of the Paediatric Hospital of Coimbra and the Advanced Sequencing Unit of Biocant. This project allowed us to develop a new approach for the molecular diagnosis of patients with some type of intellectual deficit, with a diagnosis rate significantly higher than most reported studies.Learn MoreBasic Science Research Grant QuantumMiningThe QuantumMining project aims to develop a new generation of cryptographic technologies, based on the realisation of both high-speed and secure quantum oblivious transfer (QOT) cryptographic primitive.Learn MoreTrademark international development and promotion International Expansion of the ELSIE System (INEXELSys)Project developed to put ELSIE system on a use phase by selected entities in each country, firstly on a demonstration phase and afterwards in a commercial and sales phase.Learn MoreIntelectual PropertyPatented TechnologyOur proprietary Technology, Genome Query Handling, with patents granted in the United States and Europe, as well as deposits in other territories. It provides easy-to-read genomic reports containing relevant information for prescription, diagnosis and prognosis, and allows the storage of users' personal and genetic data in a secure, encrypted, anonymous and confidential way.Load MoreNewsKeep up with our latest articlesTop 10 Emerging Next-Generation Sequencing Company in Europe 2022Participations & PartnershipsApr 29, 2022CBR Genomics launches DNA.files, a unique Genomics-as-a-Service platform to help families thrive through DNA screening. Research & DevelopmentNov 4, 2021CBR Genomics: one of the three Portuguese Start-ups of the Maze X programParticipations & PartnershipsMar 25, 2021View AllAs featured in How can we help you?Get support (during operation hours) from our support team. Click on the WhatsApp button below if you have any questions or want more information. Open [email protected](+351) 231 410 890WhatsAppAddress Biocant Park, Núcleo 04, Lote 3, 3060-197 Cantanhede, PortugalLegalTerms & ConditionsPrivacy PolicyFollow UsFacebook InstagramLinkedinCopyright @ 2021 All Rights Reserved