Customer testimonials
Here's what some of our customers say about working with Congenica...
"Congenica has been able to process a huge number of samples for the 100,000 Genomes Project and routinely process thousands of samples for Genomics England every month. Working with Congenica we’ve been able to provide high quality variant interpretation of genome sequences to the NHS, helping deliver benefits to patients at scale."
Dr Augusto Rendon, Director of Bioinformatics of Genomics England
"Using Congenica we significantly increased our diagnostic yield and lab efficiency."
Gianpiero Cavalleri Ph.D.Professor of Human Genetics at Royal College of Surgeons Ireland (RCSI), Deputy Director of the SFI FutureNeuro Research Centre and Director of the Human Genetic Variation Research Group
"By utilising Congenica we increased our diagnostic yield and delivered a molecular diagnosis to patients who would not have received one using our standard bioinformatic pipeline."
Dr Katherine Benson, Postdoctoral Researcher, Royal College of Surgeons Ireland (RCSI)
"Achieving a rapid prenatal exome result with Congenica allowed us to consider potentially life-saving interventions in pregnancy that would not otherwise have been possible. This result allows us to tailor monitoring of the baby and mother both before and after birth and provide personalised care as appropriate."
Dr Tessa Homfray, Consultant in Medical Genetics, NHS
"Congenica represents an outstanding technology for the interpretation of genetic variants. This helps us to make a genetic diagnosis in a very short time for targeted and therapy-relevant questions. Especially in prenatal genetic diagnostics as well as in unclear syndromal cases, Congenica supports us in the evaluation in a unique way. Thanks to Congenica, we can now achieve incredibly short turnaround times, which will be of great benefit to our patients."
Dr Anne-Karin Kahlert, Institute of Immunology and Genetics in Kaiserslautern
"In the past a baby with neurological problems would first see a paediatrician, then a neurologist, and if there’s ophthalmic problems they’ll see the ophthalmologist. Now on day one we can look at a panel of genes that cause cataracts and not worry about all the other biochemical tests that take a long time and cost the NHS a lot of money. It has radically changed the experience for patients."
Dr Simon Ramsden, BSC MSc PhD FRCPath, Consultant Clinical Scientist, Manchester Centre for Genomic Medicine
"Congenica’s clinical team is a unique differentiator. As practicing genomic interpretation scientists they understand the clinical questions we are trying to address and work with us to develop flexible solutions. Their knowledge and experience has been key in making our variant interpretation services a success."
Dr Gholson Lyon, M.D., Ph.D.Principal Investigator and Clinician, Institute for Basic Research in Developmental Disabilities, New York
"I have been using Congenica for the last two years, as a biomedical scientist. I found tremendous support in Congenica’s team, from the very beginning. All our questions were answered in a very detailed manner, all our inquiries were carefully listened to, and help - when needed - was provided promptly, thus making our journey of setting and developing our NGS data analysis protocols an exciting learning experience. The assistance provided has been not only scientifically and logistically impeccable, but also has had a precious, yet rarely found, sense of human connection beyond borders and screens."
Andreea Tutulan-Cunita, PhD Cytogenomic Medical Laboratory, Romania
“We have utilised the knowledge and skills of Congenica and their Clinical team to implement new innovative genetics services in the NHS. Using Congenica software and working collaboratively with their experienced Clinical team has significantly improved the services we provide to patients. We cannot recommend Congenica highly enough.”
Dr Sahar Mansour Professor in Clinical Genetics, St George's University Hospitals NHS