OCG Templates and Protocols

The OCG Standard Operating Protocols (SOPs) and templates are guidelines for investigators participating in OCG programs such as CGCI's Burkitt Lymphoma Genome Sequencing Project (BLGSP), and HIV+ Tumor Molecular Characterization Project (HTMCP), the Human Cancer Models Initiative (HCMI), and Therapeutically Applicable Research To Generate Effective Treatments (TARGET). Investigators must follow the protocols in the SOPs when contributing samples and data. The sample and data acquisition process is explained in comprehensive detail to ensure that all materials and data will be of sufficient quality. Depending on the role in the acquisition process, only a certain number of protocols may apply to a particular investigator. Should you require any clarification, please contact the appropriate OCG personnel listed in the SOP.

Burkitt Lymphoma Genome Sequencing Project (BLGSP) Standard Operating Procedures (SOP) Manual

CDE (Common Data Element) Browser User Guide

Characteristics of Successful Standard Operating Procedures (SOPs)

HIV+ Tumor Molecular Characterization Project (HTMCP) Standard Operating Procedures (SOP) Manual

Human Cancer Models Initiative Case Report Forms (CRFs)

Cancer type-specific CRFs have been developed through collaborations with international clinical experts and the clinical data elements have been standardized through the Cancer Data Standards Registry and Repository (caDSR). HCMI Enrollment and Follow-up CRFs are available below for download. As the tumor types modeled through the HCMI are constantly updated, be sure to check back regularly for additional CRFs.

Enrollment CRFs
Follow-up CRFs

Informed Consent Template for Model Development and Distribution

TARGET Project Experimental Methods

On this page researchers can find detailed information describing how TARGET data was generated by genomic platform, including protocols for establishing high-quality nucleic acid samples.