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Online Mendelian Inheritance in Man (OMIM): Comprehensive genetic disorder database for inherited phenotypes and genes

<p><strong>ABSTRACT:&nbsp;</strong></p> <p>Online Mendelian Inheritance in Man (OMIM) is a comprehensive and authoritative research resource that provides curated descriptions of human genes and phenotypes, along with their intricate relationships. I have compiled a dataset that specifically focuses on genes from the Online Mendelian Inheritance in Man&nbsp;database. The dataset includes the unique identifiers (MIM IDs) and names of these OMIM genes.</p> <p><strong>Instructions:</strong></p> <p>Dataset was downloaded and uploaded to excel to have unnecessary columns removed. Then dataset was imported to Jupyter Notebook and further cleaned of the nullified values and unrelated gene types such as phenotypes and etc. A new column with the respective links was added to make a total of 4 columns with one type: genes. Dataset was uploaded to the drg-depot cheaha.</p> <p><strong>Inspiration:</strong></p> <p>This dataset uploaded to U-BRITE for&nbsp; &quot;DRG_DEPOT&quot; summer 2023 team project.</p> <p><strong>Acknowledgements:</strong></p> <p>Joanna S. Amberger,&nbsp;Carol A. Bocchini,&nbsp;Fran&ccedil;ois Schiettecatte,&nbsp;Alan F. Scott,&nbsp;Ada Hamosh</p> <p><em>Nucleic Acids Research</em>, Volume 43, Issue D1, 28 January 2015, Pages D789&ndash;D798, DOI:&nbsp;<a href="https://doi.org/10.1093/nar/gku1205">https://doi.org/10.1093/nar/gku1205</a></p> <p><strong>OMIM Access to Gene Information:</strong>&nbsp;https://omim.org/search/advanced/entry</p> <p>U-BRITE Last Updated: July 5, 2023</p>

ShareScore

32/100

Overall dataset sharing score

Score breakdown

These five areas show where the dataset supports — or may limit — practical reuse.

Stewardship
8
Harmonization
8
Access
16
Reuse readiness
0
Engagement
0

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