Comparison of single cell sequencing data between two whole genome amplification methods on two sequencing platforms

Research based on a strategy of single-cell low-coverage whole genome sequencing (SLWGS) has enabled better reproducibility and accuracy for detection of copy number variations (CNVs). The whole genome amplification (WGA) method and sequencing platform are critical factors for successful SLWGS (<...

Descripción completa

Detalles Bibliográficos
Autores principales: Chen, DaYang, Zhen, HeFu, Qiu, Yong, Liu, Ping, Zeng, Peng, Xia, Jun, Shi, QianYu, Xie, Lin, Zhu, Zhu, Gao, Ya, Huang, GuoDong, Wang, Jian, Yang, HuanMing, Chen, Fang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5862989/
https://www.ncbi.nlm.nih.gov/pubmed/29563514
http://dx.doi.org/10.1038/s41598-018-23325-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5862989/
https://www.ncbi.nlm.nih.gov/pubmed/29563514
http://dx.doi.org/10.1038/s41598-018-23325-2

Ejemplares similares