Cargando…
Effect quantification and value prediction of factors in noninvasive detection for specific fetal copy number variants by semiconductor sequencing
BACKGROUND: The detection limit of noninvasive prenatal testing (NIPT) by next generation sequencing for any given fetal copy number variants (CNV) can be influenced by several factors. In this study, we quantified the effects and predicted the value of parameters for CNVs detection by NIPT. METHODS...
Autores principales: | Zhang, Chunhua, Liang, Bo, Qiao, Longwei, Xuan, Liming, Li, Hong, He, Quanze, Wu, Xiaojuan, Lu, Jiafeng, Yu, Bin, Wang, Ting |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6625335/ https://www.ncbi.nlm.nih.gov/pubmed/31115175 http://dx.doi.org/10.1002/mgg3.718 |
Ejemplares similares
-
Isolation of single circulating trophoblasts from maternal circulation for noninvasive fetal copy number variant profiling
por: Doffini, Anna, et al.
Publicado: (2022) -
Noninvasive prenatal testing for fetal subchromosomal copy number variations and chromosomal aneuploidy by low‐pass whole‐genome sequencing
por: Yu, Dongyi, et al.
Publicado: (2019) -
A fetal fraction enrichment method reduces false negatives and increases test success rate of fetal chromosome aneuploidy detection in early pregnancy loss
por: Qiao, Longwei, et al.
Publicado: (2022) -
Prognostic Value of Germline Copy Number Variants and Environmental Exposures in Non-small Cell Lung Cancer
por: Chen, Shizhen, et al.
Publicado: (2021) -
White blood cell count affects fetal fraction and test failure rates in noninvasive prenatal screening
por: Qiao, Longwei, et al.
Publicado: (2023)