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In a world where the understanding of genetic variants is expanding, how should changes be communicated to patients who had genetic testing in the past, how often, and who is responsible for this? The authors of this article discuss the topic further in a post on the BMC Series blog.
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This complete software package to analyze single cell gene expression, immune receptor and metadata, allows exploratory and hypothesis-driven analysis of multi-omic datasets.
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BMC Medical Genomics is an open access journal publishing original peer-reviewed research articles in all aspects of functional genomics, genome structure, genome-scale population genetics, epigenomics, proteomics, systems analysis, and pharmacogenomics in relation to human health and disease.
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- Youping Deng, University of Hawaii
- Kun Huang, Ohio State University
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We are recruiting new Editorial Board members
We are now recruiting Associate Editors for our Editorial Board to join our team of academic editors in assessing manuscripts in the field of medical genomics.
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Research Data Support is an optional Springer Nature service available to researchers who have datasets they want to make easier to cite, share and find. Learn more about this service and the many benefits of making your data publicly available.
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COVID-19: The Health Inequity Magnifier
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BMC Series highlights: June 2023
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