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Whole-genome sequencing in newborn screening? A statement on the continued importance of targeted approaches in newborn screening programmes

The advent and refinement of sequencing technologies has resulted in a decrease in both the cost and time needed to generate data on the entire sequence of the human genome. This has increased the accessibility of using whole-genome sequencing and whole-exome sequencing approaches for analysis in bo...

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Detaylı Bibliyografya
Yayımlandı:Eur J Hum Genet
Asıl Yazarlar: Howard, Heidi Carmen, Knoppers, Bartha Maria, Cornel, Martina C, Wright Clayton, Ellen, Sénécal, Karine, Borry, Pascal
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Nature Publishing Group 2015
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4795188/
https://ncbi.nlm.nih.gov/pubmed/25626707
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2014.289
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