Kenen and Preters designed the Colored Ecological and Genetic Relational Map (CEGRM), a pictoral map used to organize information about client relationships with biological and non-biological kin, for use in genetic counselling research with members of families with suspected risk of cancer or late-onset inherited disorders. Three relationship categories are included in a CEGRM including: 1) "information" or people with whom the client shares genetic and health information, 2) "service" or people who facilitate the client's genetic counseling appointment, and 3) "emotions" or people with whom clients would share their feelings about familial cancer risk or whose feelings they would consider when deciding to go for counseling or testing. Genetic counsellors can direct clients to construct a CEGRM or construct it themselves using information provided by clients.

This physician consent form was approved by the Institutional Review Board for the Baylor College of Medicine and Affiliated Hospitals for use in the Incorporation of Genomic Sequencing into Pediatric Cancer Care Study. The purpose of the study was learn how to report and use clinical exome sequencing test results for childhood cancer patients.

This draft age of majority consent form was designed to be used in the Incorporation of Genomic Sequencing into Pediatric Cancer Care Study. The purpose of the study was learn how to report and use clinical exome sequencing test results for childhood cancer patients.

The purpose of the MedSeq Project was to develop a process for a process for integrating information obtained from whole genome sequencing into clinical practice and to explore how physicians and their patients understand and utilize this information. This consent for primary care physicians provides information on the purpose of the study, study procedures, risks and possible benefits of particpating, payment, contact information for questions or concerns, and privacy protections.

The purpose of the MedSeq Project was to develop a process for a process for integrating information obtained from whole genome sequencing into clinical practice and to explore how physicians and their patients understand and utilize this information. This cardiology patient consent form provides information on the purpose of the study, study procedures, risks and possible benefits of particpating, contact information for questions or concerns, and privacy protections.

The purpose of the MedSeq Project was to develop a process for a process for integrating information obtained from whole genome sequencing into clinical practice and to explore how physicians and their patients understand and utilize this information. This primary care patient consent form provides information on the purpose of the study, study procedures, risks and possible benefits of particpating, contact information for questions or concerns, and privacy protections.

The purpose of PediSeq: The Pediatric Genetic Sequencing Project was to identify best practices for educating patients about exome and genome sequencing, determining the sequencing data relevent to patients, and returning results. This informed consent form and HIPAA authorization is appropriate for use with parents of study participants and children capable to providing assent. It contains consent to future analyses of test results, use of data or specimens for future research, future contact, and photgraphs, in addition to consent to study participation.

This consent form for adult patients or parents of minor patients (with child assent) includes standard consent language and the ability for participants to “opt out” of learning about genome sequencing results, unless a result is of urgent importance to their health.

This consent form for the CanSeq study included permission to perform genetic tests on tissue specimens that had already been collected and stored as part of clinical care or other research studies the person participated in.