The invention provides methods for determining aneuploidy and/or fetal fraction in maternal samples comprising fetal and maternal cfDNA by massively parallel sequencing. The method comprises a novel protocol for preparing sequencing libraries that unexpectedly improves the quality of library DNA while expediting the process of analysis of samples for prenatal diagnoses.
申请公布号
EP2366031(B1)
申请公布日期
2015.01.21
申请号
EP20100830938
申请日期
2010.12.01
申请人
VERINATA HEALTH, INC
发明人
RAVA, RICHARD P.;CHINNAPPA, MANJULA;COMSTOCK, DAVID A.;HEILEK, GABRIELLE;RHEES, BRIAN KENT