DATABASES ON MEDICINE AND MOLECULAR BIOLOGY
|Atlas of Genetics" info|
The Atlas of Genetics and Cytogenetics in Oncology and Haematology is a peer reviewed on-line journal and database in free access on internet devoted to genes, cytogenetics, and clinical entities in cancer, and cancer-prone diseases.
|Genome Atlas Database" info|
Database of sequenced bacterial genomes.
|Ensembl Genome Browser" info|
ENSEMBL is a joint project between EMBL-EBI and the Sanger Center to develop a system which automatically tracks all the sequenced pieces of human genome, attempts to assemble them into large single stretches and then analyse the assembled DNA to find genes and other features of interest to biologists and medical researchers.
|Entrez Gene" info|
Gene provides a unified query environment for genes defined by sequence and/or in NCBI's Map Viewer. You can query on names, symbols, accessions, publications, GO terms, chromosome numbers, E.C. numbers, and many other attributes associated with genes and the products they encode.>br>
Entrez integrates the scientific literature, DNA and protein sequence databases, 3D protein structure and protein domain data, population study datasets, expression data, assemblies of complete genomes, and taxonomic information into a tightly interlinked system.
|Gene Location" info|
GeneLoc presents an integrated map for each human chromosome, based on data integrated by the GeneLoc algorithm. GeneLoc includes further links to GeneCards, NCBI's Human Genome Sequencing, UniGene, Genome Database, and mapping resources. GeneLoc is presented by the Weizmann Institute of Science, Rehovot, Israel
|Genome Reviews" info|
The goal of the Genome Reviews project is to provide an up-to-date, standardised and comprehensively annotated view of the genomic sequence of organisms with completely deciphered genomes.
|International HapMap Project" info|
The goal of the International HapMap Project is to develop a haplotype map of the human genome, the HapMap, which will describe the common patterns of human DNA sequence variation. The HapMap is expected to be a key resource for researchers to use to find genes affecting health, disease, and responses to drugs and environmental factors.
|Human Genome Resources (ncbi)" info|
NCBI's Genome Browser.
|Intronless Genes in Eukaryotes" info|
Database about intronless genes.
|MalaCards - Human Disease Database" info|
MalaCards is an integrated database of human maladies and their annotations, modeled on the architecture and richness of the popular GeneCards database of human genes.
The MalaCards disease and disorders database is organized into "disease cards", each integrating prioritized information, and listing numerous known aliases for each disease, along with a variety of annotations, as well as inter-disease connections, empowered by the GeneCards relational database, searches, and GeneAnalytics set-analyses. Annotations include: symptoms, drugs, articles, genes, clinical trials, related diseases/disorders and more. An automatic computational information retrieval engine populates the disease cards, using remote data, as well as information gleaned using the GeneCards platform to compile the disease database. The MalaCards disease database integrates both specialized and general disease lists, including rare diseases, genetic diseases, complex disorders and more.
|NCBI Map View" info|
Graphical view of chromosomes of different organisms, including homo sapiens.
|NCBI Map Viewer (Homo Sapiens Genome)" info|
The NCBI Map Viewer displays genome assemblies using sets of aligned chromosomal maps. A new Map Viewer home page organizes the available organisms by taxonomic group and provides links to both Map Viewer and Genomic BLAST pages.
|OMIM Morbid Map|
The OMIM Morbid Map presents the cytogenetic map location of disease genes described in OMIM.
|The Cancer Genome Atlas|
The Cancer Genome Atlas (TCGA) is a comprehensive and coordinated effort to accelerate our understanding of the molecular basis of cancer through the application of genome analysis technologies, including large-scale genome sequencing. TCGA is a joint effort of the National Cancer Institute (NCI) and the National Human Genome Research Institute (NHGRI), which are both part of the National Institutes of Health, U.S. Department of Health and Human Services.
|TraitMap: Genetic-Map Database|
TraitMap contains curator-checked data records based on published papers of mapping results in Homosapiens, Mus musculus, and Arabidopsis thaliana.