Are We Ready for Systematic Newborn Genome Sequencing?
Routine sampling and analysis of newborn DNA would enable screening for hundreds of childhood genetic diseases, but also raises concerns about privacy and ethics.
Source: medscape.com
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Newborn genome sequencing project identifies unanticipated disease risks
Genomic sequencing of newborns reveals unanticipated genetic risks, prompting actionable medical interventions and potential life-saving care for infants and their families. This study highlights the value of comprehensive sequencing in newborns for early detection and management of genetic conditions.
Priyom Bose National Institute Of Health American Journal Human Geneticsstudy Image Credit Babyseq Project
Source: news-medical.net
Large-scale comprehensive sequencing helps downstream medical care in newborns
Researchers who lead the world's first comprehensive sequencing program for newborn infants have published the next chapter in the ongoing study of the BabySeq Project, with new findings on infants and families who have been followed for 3-5 years.
Source: news-medical.net