Biobank Lifespan

This website gives access to information about, and documents referring to, the classification of drugs.
This website was initiated to address the impact of specific specimen handling variables on molecular testing of human tissues. The BRN database can be surveyed by biospecimen type or by experimental factor.
This website aims to contribute to the integration of genetics and epidemiologic research.
This website lists studies investigating the interaction of genotype and phenotype. Open access data includes a study description, phenotypic variables of interest, study documents (questionnaire, standard operating procedures, consent forms, etc), and genotype-phenotype analyses.
The ESPRESSO project and the DataSHIELD project develop statistical methods for meta-analysis of large scale studies.
This website aims to unify human- and model-organism genetic variation databases towards increasingly holistic views into Genotype-To-Phenotype (G2P) data, and to link this system into other biomedical knowledge sources via genome browser functionality.
This website presents the last version of the ICD-10, a detailed description of known diseases and injuries. Every disease (or group of related diseases) is described together with its diagnosis and its unique code. A World Health Organization classification.
This website details a standardized system for classifying of health and health related domains that describe body functions and structures, activities and participation. The domains are classified from body, individual and societal perspectives.
This website presents the classification structure for organizing jobs into a defined set of groups according to the tasks and duties undertaken in the job. Developed by the International Labour Organization.
This website provides a complete listing of all the categories under which Canadian jobs are classified and their description. A Statistics Canada-maintained website.
This website aims to solve the author/contributor name ambiguity problem in scholarly communications by creating a central registry of unique identifiers for individual researchers and an open and transparent linking mechanism between ORCID and other current author ID schemes.
This section of the website is a collection of research questionnaires intended to serve only as models and be adapted by researchers to suit their particular needs. This tool is provided by the National Cancer Institute's Division of Cancer Epidemiology and Genetics.
This website presents a database of international, regional and national laws and policies and literature addressing human genetic population research.
This website displays an archive of the results of genetic association studies of complex human diseases and disorders.
This website includes various research tools and presents social, ethical and legal aspects of human genetics.
This website discusses three main issues. First, it helps in locating tumor specimens and related data of interest. Legal and ethical issues are addressed and a model informed consent and patient information sheet are available.