SNV output for CYP2D6 and CYP2C19 and copy number data for CYP2D6 (adjusted where indicated) for 95 samples

The datasets provide the SNV output for CYP2D6 and CYP2C19 and copy number data for CYP2D6 (adjusted where indicated) for 95 samples genotyped in two batches as described in the paper Carvalho Henriques and Buchner et al. <i>Methodology for clinical genotyping of CYP2D6 and CYP2C19. Translational Psychiatry. </i><i><br></i>The material herein are provided on an “as is” basis only and without warranty or representation (whether express or implied) as to its accuracy or reliability. Anyone who uses the material assumes responsibility for the result and its use. Neither the authors nor any funders are responsible for or accepts liability for any direct or indirect loss or damages arising from or connected to the use of this information.<i></i>本数据集包含95份分两批完成基因分型的样本的单核苷酸变异（Single Nucleotide Variant, SNV）检测结果，涉及CYP2D6与CYP2C19两个基因，同时附带CYP2D6的拷贝数数据（如标注所示已完成校正）。相关实验细节详见Carvalho Henriques与Buchner等人发表于《转化精神病学（Translational Psychiatry）》的研究论文《CYP2D6与CYP2C19临床基因分型方法》。 本数据集所提供的材料仅以“现状”（as is）形式交付，不就其准确性或可靠性作出任何明示或默示的担保与声明。任何使用该材料的主体，需自行承担使用该材料所产生的结果及使用行为的全部责任。作者及任何资助方均不对因使用本信息直接或间接引发的任何损失或损害承担责任或接受相关追偿。