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Personalizing Whole Genome Sequencing Doubles Diagnosis of Rare Diseases

Tailoring the analysis of whole genome sequencing to individual patients could double the diagnostic rates of rare diseases.

Posted by Andy Lundin | Nov 7, 2022 | Breast |

MicroRNA (miRNA) can be used as a biomarker to predict which patients are likely to face breast cancer recurrence and mortality.

The organizations have established an exclusive license agreement to any diagnostic techniques utilizing imprintome control regions.

Sema4 presented research to debunk the belief that exome and genome sequencing deliver more inconclusive results than multi-gene panels.

Cystic fibrosis is often missed in newborn screenings for non-white babies, creating higher risk for other races.