Table 2.
Useful Internet Resources for Array Data Interpretation
| Name | URL | Main objective |
|---|---|---|
| COREMINE | www.coremine.com | COREMINE Medical is a product of the PubGene Company designed to be used by anyone seeking information on health, medicine, and biology. |
| ENDEAVOUR | www.esat.kuleuven.be/endeavour | ENDEAVOUR is a Web resource for the prioritization of candidate genes that uses a training set of genes known to be involved in a biological process of interest. |
| GECCO | http://sourceforge.net/projects/genomegecco/ | GeCCO (Genomic CNV Classification Objectively) is a bioinformatics tool for classifying copy number variants as either benign or pathogenic. |
| GeneImprint | www.geneimprint.com | GeneImprint is a portal into the burgeoning field of genomic imprinting, collecting relevant articles and reviews, press reports, video and audio lectures, and genetic information. |
| Genomic Oligoarray and SNP array evaluation tool v1.0 | www.ccs.miami.edu/cgi-bin/ROH/ROH_analysis_tool.cgi | This tool is designed to assist in the evaluation of genes, and subselections, including OMIM genes, OMIM genes annotated as associated with autosomal and/or autosomal recessive inherited phenotypes in runs of homozygosity (ROH), and chromosomal regions involved in microdeletions and microduplications. |
| GeneTests | www.ncbi.nlm.nih.gov/sites/GeneTests | Medical genetics information resource developed for physicians, other healthcare providers, and researchers. |
| Chromosomal Mosaicism | http://mosaicism.cfri.ca | A Website to provide information to patients, families, health care providers, students, and the general public on the unique conditions of chromosomal mosaicism. |
| Orphanet | www.orpha.net | Orphanet is the reference portal for information on rare diseases and orphan drugs, for all audiences. Orphanet’s aim is to help improve the diagnosis, care, and treatment of patients with rare diseases. |
| Small Supernumerary Marker Chromosomes Database | www.med.uni-jena.de/fish/sSMC/00START.htm | To collect all available case reports on small supernumerary marker chromosomes (sSMC) and provide detailed information for patients and medical professionals. |
| Unique | www.rarechromo.org | Unique is a source of information and support to families and individuals affected by any rare chromosome disorder and to the professionals who work with them. |