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Hope for Children: Advancing Neurodevelopmental Disease Research
At HudsonAlpha, we are using the power of genomics to uncover answers, accelerate diagnoses, and develop life-changing treatments for children and families facing rare and complex conditions.
"The promise of long-read sequencing for identifying disease-associated genetic variation is exciting. My team and I understand how life-changing a genetic diagnosis can be, and we are motivated every day to come up with ways to uncover new and previously hidden results that might be informative. Through this work, we aim to improve clinical genetics to reduce the uncertainties faced by many families who struggle with rare genetic disorders."
— Greg Cooper, PhD
HudsonAlpha Faculty Investigator
