What’s new in genetics?

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Dark side of precision medicine:

A report from the Mayo Clinic highlights one fear as precision medicine continues to expand, that the quality of databases used to interpret genetic information are not up to date. The report includes several cases in which patients were treated based on a genetic mutation that was believed to be disease causing. A later reanalysis revealed the mutation did not cause the heart condition the patients were concerned about. How will we prevent misdiagnoses and potentially harmful treatment via precision medicine?

Should we sequence the genes of our newborns?

The BabySeq project funded by the NIH aims to understand how sequencing newborns will affect the children and families involved. Researchers hope to investigate whether having more information about what lies in a baby’s genes will lead to higher health care costs. You can read how some families responded to the option and results of sequencing, here.    

Onward to a synthetic genome:

The scientists behind Genome Project-Write, the project to create an entire genome from scratch, have released a draft timeline of how they expect the research to progress. The team of researchers has yet to decide which genomes to focus their efforts on and are currently seeking proposals for pilot projects to begin this effort.

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CooperGenomics

Together as part of the CooperSurgical family, we are the pioneers and global leaders of comprehensive reproductive genetic testing. Through expanded carrier screening, PGD, PGS, NIPS and beyond, our team is committed to advancing the field of reproductive genetics, improving outcomes, and empowering families worldwide.

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