Count Me In (CMI) is a nonprofit research initiative that empowers patients to accelerate cancer research by sharing their samples, their clinical information, and their voices. A key goal of CMI is to enable scientific discoveries and the development of new cancer treatment strategies by widely sharing clinical, genomic, molecular, and patient-reported data.
Program Description
Working together with patients, patient advocates, and caregivers, CMI has launched a number of patient-partnered cancer research projects across different cancer types. Through the utilization of online registration and consent, these projects are open to cancer patients living anywhere in the United States or Canada. Count Me In has been stewarded by four leading organizations: Emerson Collective, a California-based social change organization; the Biden Cancer Initiative, an independent nonprofit organization building on the federal government’s Cancer Moonshot; the Broad Institute of MIT and Harvard; and the Dana-Farber Cancer Institute.
Count Me In projects generate datasets from patient-reported information, abstracted medical records, and sequencing and molecular analyses of biological samples that were acquired remotely. Patients enrolled in CMI projects are geographically dispersed and receive clinical care from different institutions across the United States and Canada. Data from CMI projects are regularly shared as generated, in a pre-publication manner. Researchers anywhere can harness Count Me In data, from repositories like the GDC, to advance cancer research and expand the understanding of cancer.
All CMI projects are currently ongoing. As more patients enroll, more data will be generated and released at the GDC and other scientific data repositories. Please feel free to contact Count Me In for more information about the projects or datasets.
CMI has provided the GDC with genomic data from multiple projects, including in metastatic breast cancer, angiosarcoma, and metastatic prostate cancer. The GDC harmonized DNA sequences from the whole exome sequencing (WES) and RNA sequences using their pipelines. The harmonized genomic data and unprocessed genomic data from CMI projects are available in the GDC Data Portal. Additional data, including expanded clinical information for patients and samples, for Count Me In projects can also be found on The cBioPortal for Cancer Genomics (https://www.cbioportal.org/).
Data Overview
Data Access
Genomic data from CMI projects can be found on the GDC Data Portal. To request access to protected data, please apply to dbGaP for access to the appropriate CMI study (study accessions as follows: phs001931, The Angiosarcoma Project; phs001709, The Metastatic Breast Cancer Project; phs001939, The Metastatic Prostate Cancer Project).
Cancer Types
Disease Type | Primary Site |
---|---|
Adenomas and Adenocarcinomas | Lymph nodes, Prostate gland |
Ductal and Lobular Neoplasms | Breast |
Soft Tissue Tumors and Sarcomas, NOS | Bladder, Breast, Bronchus and lung, Heart, mediastinum, and pleura, Lymph nodes, Other and ill-defined digestive organs, Other and ill-defined sites, Other and ill-defined sites within respiratory system and intrathoracic organs, Skin |
Data Types
Data Type | Data Format | Data Access Level |
---|---|---|
WXS Aligned Reads | BAM | Controlled |
WXS Simple Somatic Mutations | VCF | Controlled |
WXS Annotated Somatic Mutations | VCF, MAF | Controlled |
WXS Aggregated Somatic Mutations | MAF | Controlled |
WXS Masked Somatic Mutations | MAF | Controlled |
RNA-Seq Aligned Reads | BAM | Controlled |
Gene Expression Quantification | TXT | Open |
Splice Junction Quantification | TSV | Controlled |