Table 7. Genetic Research Information

ResourceDescription
Chromosomal Variation in Man Searchable database of literature citations on chromosomal variants and anomalies.
Ensembl (Joint software project between the European Bioinformatics Institute and the Wellcome Sanger Institute) Data sets resulting from an automated genome analysis and annotation process.
Leiden Open Variation Database A flexible, free tool for gene-centered collection, curation, and display of DNA variation.
KMcancerDB Human pathogenic variant database with graphical display of molecular information for cancer-related genes.
National Center for Biotechnology Information: Genome Views of chromosomes, maps, and loci; links to other NCBI resources.
Online Mendelian Inheritance in Man (OMIM) Catalog of human genes and genetic disorders.
UCSC Genome Browser Reference sequence for the human and C. elegans genomes and working drafts for the mouse, rat, Fugu, Drosophila, C. briggsae, yeast, and SARS genomes.
Human Subjects Research in Genomics (National Human Genome Research Institute [NHGRI]) Discusses many issues that continue to challenge institutional review boards, investigators, and policy makers today.

UCSC = University of California, Santa Cruz.

From: Cancer Genetics Overview (PDQ®)

Cover of PDQ Cancer Information Summaries
PDQ Cancer Information Summaries [Internet].
Bethesda (MD): National Cancer Institute (US); 2002-.

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