Colorectal cancer samples WES

Access to NGS data The primary purpose is to accelerate efforts to identify genome sequence variants influencing major causes of human morbidity and mortality, through implementation and analysis of large-scale genome wide association studies. Additional objectives include the development and validation of informatics and analytical solutions appropriate to the scale and nature of the project, as well as use of the data generated to answer important methodological and biological questions relevant to association studies in general, and in Spain in particular. The Consortium anticipates that data generated from the project will be used by others, such as required for developing new analytical methods, in understanding patterns of polymorphism and in guiding selection of markers to map genes involved in specific diseases. Access to summary data and individual-level genotype data is available by application to the Colorectal Cancer samples Data Access Committee. Access to data will be granted to qualified investigators for appropriate use.