The Cystic Fibrosis Foundation’s Whole Genome Sequencing (WGS) project contains WGS data from over 5,000 people with cystic fibrosis in the United States that is linked with data from the CF Foundation Patient Registry.
This program is intended to introduce students to cystic fibrosis research and encourage them to remain engaged in the field.
The Cystic Fibrosis Foundation's Research Development Programs are a network of basic science research centers around the country that brings together leading scientists to pool their talents and advance understanding of the basic science of CF and the complex ways the disease affects different parts of the body.
The Cystic Fibrosis Foundation can help you engage people with cystic fibrosis so that you can incorporate their voices into the decision-making process throughout the development lifecycle of your
A diverse group of talented academic investigators leads the cystic fibrosis research community. The Cystic Fibrosis Foundation is pleased to support these investigators through a variety of opportunities.
The Cystic Fibrosis Foundation is aware that many labs and clinical studies have been impacted by the recent response to COVID-19. It is the CF Foundation's intention to work with funding applicants and CF Foundation-funded investigators to minimize the effects of the pandemic on research that is critical to advancing the mission of the Foundation.
Awards for the Infection Research Initiative will support proposals for basic or
The primary purpose of the K-Boost Award is to provide supplemental funding to qualified and promising scientists early in their faculty careers who have obtained K funding from the National Institutes of Health in areas that reflect the Cystic Fibrosis Foundation's research priorities.
The objective of this award is to support excellent cystic fibrosis-related research projects that have been approved by the National Institutes of Health (or governmental funding agencies in other countries) but cannot be supported by available funds.