Clinical genetics and heredity’s Post

New algorithm could improve the search for genetic cause of hereditary diseases. Variations of genetic sequence occur relatively frequently on average, one in a thousand nucleotide of a person's genome is affected. In rare cases, these changes can lead to defective RNAs and hence non functional proteins. This can lead to dysfunction in individual organs. If a rare disease is suspected, computer-assisted diagnosis programs can help in the search for possible genetic causes. Specifically the genome can be analyzed using algorithms to find out whether there is a connection between rare genetic variations and dysfunctions in specific parts of the body. Submissions are open for the upcoming issue. You may submit case reports, case studies, and research or review papers. Submit to: editor.geneticsandheredity@journalmaples.org Follow our page: https://lnkd.in/dd-AwMD8 Visit us: https://lnkd.in/dhyieEcT (Source: internet) #genetic #heredity #research #genes #genomics #algorithm #geneticsequence #diagnosis #submissions #openaccess

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