This category is for listing of human genetic databases and maps. Typically it will include both gene and physical maps, transcription and marker maps, and sequencing data.
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Subcategories 2
Related categories 1
Sites 9
A research community initiative for functional and medical annotation of this chromosome. Toronto Centre for Applied Genomics.
A searchable, integrated database of human genes that provides concise genomic, proteomic, transcriptomic, genetic and functional information on all known and predicted human genes.
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 .
Provides information on the Human Genome Project.
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.
Haplotype Y chromosomes to monitor the male population for forensic science and population analysis, a list of protocols and contacts worldwide, based in Berlin, Germany.
Integrates results from international research projects. Includes data on expression patterns, cellular roles, functions, and evolutionary relationships.
Assists in finding the correct clinical diagnosis by exploiting the semantic structure of the Human Phenotype Ontology.
A database of genes and risk factors (viruses, bacteria and others) in Alzheimer's disease, bipolar disorder and schizophrenia.
Haplotype Y chromosomes to monitor the male population for forensic science and population analysis, a list of protocols and contacts worldwide, based in Berlin, Germany.
Integrates results from international research projects. Includes data on expression patterns, cellular roles, functions, and evolutionary relationships.
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.
A database of genes and risk factors (viruses, bacteria and others) in Alzheimer's disease, bipolar disorder and schizophrenia.
Assists in finding the correct clinical diagnosis by exploiting the semantic structure of the Human Phenotype Ontology.
Provides information on the Human Genome Project.
A searchable, integrated database of human genes that provides concise genomic, proteomic, transcriptomic, genetic and functional information on all known and predicted human genes.
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 .
A research community initiative for functional and medical annotation of this chromosome. Toronto Centre for Applied Genomics.
