In Partnership with AOL
See also:
  • Bruns Laboratory - Database of novel human ancient sequence genes that define new protein families.
    [!]
  • Centre d'Etude du Polymorphisme Humain (CEPH) - Maintains a database of genotypes for genetic markers in the reference families for linkage mapping of the human chromosomes. Includes project scope, marker submission, and data dumps.
    [!]
  • Chromosome 7 Annotation Project - A research community initiative for functional and medical annotation of this chromosome. Toronto Centre for Applied Genomics.
    [!]
  • Cooperative Human Linkage Center - Genetic maps showing the positions of genetic markers. The maps are searchable by name. Includes project information and publications.
    [!]
  • Earth Human Short Tandem Repeat Allele Frequencies Database - EHSTRAFD is a non-profit organization undertaking promotion, operation and development of a database with STR genetic markers allele frequencies specific for human species, representative at the planetary level.
    [!]
  • GeneCards - Offers information about human genes and their mouse homologs, with a focus on cellular functions and involvement in diseases. Features a what's new section and data sources.
    [!]
  • The GeneCards Database of Human Genes - A searchable, integrated database of human genes that provides concise genomic, proteomic, transcriptomic, genetic and functional information on all known and predicted human genes.
    [!]
  • GeneMap'99 - Searchable map for human gene loci. Indexed by chromosome. Includes identification and isolation of genes that either directly cause human ailments or increase susceptibility to disease .
    [!]
  • The Genome Database - Provides information on the Human Genome Project.
    [!]
  • GenomeNet - Japanese network of database and computational services for genomic and related research in molecular and cellular biology. Includes a range of databases and an encyclopedia of genes and genomes.
    [!]
  • Moroccan Human Mutation Database - The first catalog of human genetic disorders and mutations found in Moroccan population. This website has been created to provide clinicians and scientists access to a central genetic database for the local population.
    [!]
  • The Phenomizer - Assists in finding the correct clinical diagnosis by exploiting the semantic structure of the Human Phenotype Ontology.
    [!]
  • Polygenic Signaling Pathways - A database of genes and risk factors (viruses, bacteria and others) in Alzheimer's disease, bipolar disorder and schizophrenia.
    [!]
  • TIGR Human Gene Index (HGI) - Integrates results from international research projects. Includes data on expression patterns, cellular roles, functions, and evolutionary relationships.
    [!]
Volunteer to edit this category.
Copyright © 1998-2014 AOL Inc. Terms of Use
Visit our sister sites  mozilla.org | MusicMoz | Wikipedia

Last update: May 31, 2013 at 8:05:05 UTC - edit