Expanding the Scope of Non-invasive Prenatal Testing to Detect Fetal Chromosomal Copy Number Variations

Non-invasive prenatal testing (NIPT) for common fetal trisomies is effective. However, the usefulness of cell-free DNA testing to detect other chromosomal abnormalities is poorly understood. We analyzed the positive rate at different read depths in next-generation sequencing (NGS) and identified a s...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Front Mol Biosci
Päätekijät: Chen, Songchang, Zhang, Lanlan, Gao, Jiong, Li, Shuyuan, Chang, Chunxin, Chen, Yiyao, Fei, Hongjun, Zhang, Junyu, Wang, Yanlin, Huang, Hefeng, Xu, Chenming, Lu, Daru
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Frontiers Media S.A. 2021
Aiheet:
Molecular Biosciences
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC8149898/
https://ncbi.nlm.nih.gov/pubmed/34055879
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fmolb.2021.649169
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