Filter
Reset all

Subjects

Content Types

Countries

API

Data access

Data access restrictions

Database access

Database access restrictions

Database licenses

Data licenses

Data upload

Data upload restrictions

Enhanced publication

Institution responsibility type

Institution type

Keywords

PID systems

Provider types

Quality management

Repository languages

Software

Syndications

Repository types

Versioning

  • * at the end of a keyword allows wildcard searches
  • " quotes can be used for searching phrases
  • + represents an AND search (default)
  • | represents an OR search
  • - represents a NOT operation
  • ( and ) implies priority
  • ~N after a word specifies the desired edit distance (fuzziness)
  • ~N after a phrase specifies the desired slop amount
  • 1 (current)
Found 14 result(s)
The Breast Cancer Surveillance Consortium (BCSC) is a research resource for studies designed to assess the delivery and quality of breast cancer screening and related patient outcomes in the United States. The BCSC is a collaborative network of seven mammography registries with linkages to tumor and/or pathology registries. The network is supported by a central Statistical Coordinating Center.
THIN has created a medical research database of anonymised patient records from information entered by general practices in their ViSion systems. THIN will supply anonymised data (with the identities of patients and practices fully protected) to approved researchers for drug safety and epidemiological studies. Such research will be approved by the appropriate ethics/scientific committee. The anonymised patient data will be collected from the practice's Vision clinical system, with the help of In Practice Systems, on a regular basis without interruption to the running of the system. CSD Medical Research UK can supply non-interventional, anonymised, longitudinal patient data for UK, France, Italy, Germany, Spain, Belgium and Australia. Data for the USA will be available in the near future.
Country
The SHIP study┬┤s main aims include the investigation of health in all its aspects and complexity involving the collection and assessment of data relevant to the prevalence and incidence of common, population-relevant diseases and their risk factors.
Country
Oral Cancer Gene Database is an initiative of the Advanced Centre for Treatment, Research and Education in Cancer, Navi Mumbai. The present database, version II, consists of 374 genes. It is developed as a user friendly site that would provide the scientist, information and external links from one place. The database is accessed through a list of all genes, and Keyword Search using gene name or gene symbol, chromosomal location, CGH (in %), and molecular weight. Interaction Network shows the interaction between genes for particular biological processes and molecular functions.
Content type(s)
Country
A small genotype data repository containing data used in recent papers from the Estonian Biocentre. Most of the data pertains to human population genetics. PDF files of the papers are also freely available.
Content type(s)
!! see caMOD Retirement Announcement https://wiki.nci.nih.gov/display/caMOD/caMOD+Retirement+Announcement !! Query the Cancer Models database for models submitted by fellow researchers. Retrieve information about the making of models, their genetic description, histopathology, derived cell lines, associated images, carcinogenic agents, and therapeutic trials. Links to associated publications and other resources are provided.
NURSA began in 2002 with the objective to accrue, develop and communicate information about the nuclear receptor superfamily. Over the last ten years, NURSA has developed a website that has developed into a comprehensive source of information about nuclear receptors, and their co-regulators, ligands, and downstream targets. Through a series of integrated 'omics-scale and informatic approaches projects, NURSA has fostered a systems biology understanding of nuclear receptor function, physiology and regulation of target gene networks in vivo.
Recode2 is a database of genes that utilize non-standard translation for gene expression purposes. Recoding events described in the database include programmed ribosomal frameshifting, translational bypassing (aka hopping) and mRNA specific codon redefinition. Frameshifting at a particular site often yields two protein products from one coding sequence and sometimes serves a regulatory purpose by acting as a sensor of the level of product protein or of some external ligand. Bypassing (hopping) allows the coupling of two ORFs separated on an mRNA by a coding gap. Codon redefinition occurs when a stop codon is decoded as a standard amino acid (often glutamine or tryptophan), or the 21st amino acid selenocysteine. These recoding events are in competition with standard decoding and are site specific. The efficiency of recoding is often modulated by cis-stimulators and sometimes by trans-factors. The sequences of the genes that use recoding for their expression are in the database. The recoding sites and the known stimulatory signals are annotated in the database together with notes on factors that are known to affect recoding efficiencies.
The Behavioral Risk Factor Surveillance System (BRFSS) is the world's largest, on-going telephone health survey system. As a result, surveys were developed and conducted to monitor state-level prevalence of the major behavioral risks among adults associated with premature morbidity and mortality. The basic philosophy was to collect data on actual behaviors, rather than on attitudes or knowledge, that would be especially useful for planning, initiating, supporting, and evaluating health promotion and disease prevention programs. Currently data are collected monthly in all 50 states.
HumanCyc provides an encyclopedic reference on human metabolic pathways. It provides a zoomable human metabolic map diagram, and it has been used to generate a steady-state quantitative model of human metabolism.
The Medical Expenditure Panel Survey (MEPS) is a set of large-scale surveys of families and individuals, their medical providers, and employers across the United States. MEPS is the most complete source of data on the cost and use of health care and health insurance coverage.