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- ALFRED
ALFRED online database on allele frequency in human population samples readily available to the scientific community.
- CANCERLIT®
From the National Cancer Institute-contains more than 1.5 million citations and abstracts from over 4,000 different sources including biomedical journals, proceedings, books, reports, and doctoral theses.
- Disease InfoSearchTM
The Genetic Alliance is providing this tool to assist you in finding specific and quality information about genetic conditions, as quickly as possible.
- Entrez-NCBI Databases
Search engine provided by the National Center for Biotechnology Information for obtaining data on DNA sequences, protein sequences and structures, genome/chromosome maps and related bibliographic information.
- Frequency of Inherited Disorders Database
(FIDD)at the Institute of Medical Genetics, University of Wales College of Medicine, Cardiff. Established for use in a clinical context, in medical research, for epidemiological studies and in planning for genetic services.
- GENATLAS
Compiles the information relevant to the mapping efforts of the Human Genome Project. This information is collected from original articles in the literature or from the proceedings of Human Gene Mapping and Single Chromosome Workshop.
- GenBank
National Institute of Health genetic sequence database containing a collection of publicly available DNA sequences maintained by the National Center for Biotechnology Information.
- GeneCards
An electronic encyclopedia integrating information about genes and their products and biomedical applications from the Weizmann Institute of Science Genome and Bioinformatics.
- GeneClinics
Expert-authored resource created to aid healthcare professionals in applying new advances in genetic testing to the diagnosis, management, and counseling of patients and families with inherited disorders.
- GeneMap99
"A new gene map of the human genome" from the National Center for Biotechnology Information.
- GeneSNPs
Web resource integrating gene, sequence and polymorphism data.
- GeneTests
A directory of laboratories providing testing for genetic disorders. Laboratories are listed by disease name. Both research and diagnostic laboratories are included.
- Genes and Disease
New genetic map from the National Center for Biotechnology Information.
- Genetic Analysis Software
This alphabetic list contains computer software on genetic linkage analysis, marker mapping, linkage disequilibrium mapping, and pedigree drawing Genetic Analysis Software.
- Genetic Education Materials (GEM) Database
This is a searchable listing of public health genetics policy documents and clinical genetics educational materials. It is a project of the National Newborn Screening and Genetics Resource Center (NNSGRC).
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Genetic and Rare Diseases Information Center (last accessed
2/2008)
Established by the National Human Genome Research Institute and the Office of Rare Diseases, the Genetic and Rare Diseases Information Center employs experienced information specialists to answer questions from the general public, including patients and their families, health care professionals, and biomedical researchers.
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Genetic Testing and Newborn Screening Information Portal
Provides a user-friendly, easy-to-access resource* to facilitate information search about genetic diseases
detected through newborn screening, currently available genetic tests and testing services, test performance,
and recognized testing algorithms
- Genetics Home Reference
National Library of Medicine's website for consumer information about genetic conditions and the genes responsible for those conditions.
- Genetics Policy Database
This searchable resource aims to be as comprehensive a collection as possible of documents with relevance to public health genetics policy for the UK.
- GENLINK
Provides linkage mapping information and software tools that facilitate the integration of physical and genetic linkage data to produce unified maps of the human genome.
- HGV (the Human Genome Variation Databases)
This
database seeks to provide an accurately and comprehensive catalog of normal human gene and genome variation, useful as a research tool to help define the genetic component of human phenotypic variation.
- HuGE Navigator
An integrated, searchable knowledge base of genetic associations and human genome epidemiology.
- Human Ageing Genomic Resources
The Human Ageing Genomic Resources (HAGR) is a collection of databases and tools designed to help researchers understand the genetics of human ageing through a combination of functional genomics and evolutionary biology.
- Human Gene Mutation Database
Catalog of known gene mutations associated with inherited diseases (developed and maintained at the Institute of Medical Genetics in Cardiff).
- Human Genome Browser Gateway
The
Browser, from the University of California in Santa
Cruz, stacks annotation tracks beneath genome
coordinate positions, allowing rapid visual
correlation of different types of information. The
user can look at a whole chromosome, open a specific cytogenetic band to see a positionally mapped
disease gene candidate, or zoom in to a particular
gene.
- Human SNP Database
From the Whitehead Institute for Biomedical Research/MIT Center for Genome Research.
- LocusLink
Provides a single query interface to information about genetic loci, from the National Center for Biotechnology Information.
- MITOMAP
Human Mitochondrial Genome Database.
- The NHGRI Policy and Legislation Database
The free, searchable database currently focuses on the following subject areas: genetic testing and counseling; insurance and employment discrimination, newborn screening; privacy of genetic information and confidentiality; informed consent; and commercialization and patenting.
- OMIM - Online Mendelian Inheritance in Man
Catalog of human genes and genetic disorders. Its database contains text information, images, reference information, and numerous links to MEDLINE articles and sequence information.
- ORPHANET
A database dedicated to information on rare diseases and orphan drugs. It's access is free of charge.
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PDQ®
PDQ (Physician Data Query) is NCI's comprehensive cancer database with peer-reviewed summaries on cancer treatment, screening, prevention, genetics, and supportive care, and complementary and alternative medicine
- PharmGKB
PharmGKB is an integrated resource about how variation in human genes leads to variation in our response to drugs. Genomic data, molecular and cellular phenotype data, and clinical phenotype data are accepted from the scientific community at large.
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PRoteomics IDEntifications Database
The PRIDE PRoteomics IDEntifications database is a centralized, standards compliant, public data repository for proteomics data. PRIDE has been developed through a collaboration of the EMBL-EBI and Ghent University in Belgium.
- PUBGENE
Online database that provides information on gene and protein relationships from the literature, gene relationships from your gene expression experiments, pointers to pathway information, and other metadata to maximize analysis throughput, and help build sequence homology networks and relate them to literature.
- Ret Net
Cloned and/or mapped genes causing retinal diseases.
- SNP500Cancer Database
SNP500Cancer project seeks to find known or newly discovered single nucleotide polymorphisms (SNPs) which are of immediate importance to molecular epidemiology studies in cancer.
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Provides link to non-governmental sites and does not necessarily represent the views of the Centers for Disease Control and Prevention. |
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