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Inferring fetal fractions from read heterozygosity empowers the noninvasive prenatal screening
PURPOSE: Fetal fraction (FF) is the percent of cell-free DNA (cfDNA) in the mother’s peripheral blood that is of fetal origin, which plays a pivotal role in noninvasive prenatal screening (NIPS). We present a method that can reliably estimate FFs by examining autosome single-nucleotide polymorphisms...
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| 出版年: | Genet Med |
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| 主要な著者: | , , , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Nature Publishing Group US
2019
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7000331/ https://ncbi.nlm.nih.gov/pubmed/31467446 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41436-019-0636-5 |
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