Supporting data for "The Genetic and Molecular Basis of Congenital Scoliosis"

Supporting data for "The Genetic and Molecular Basis of Congenital Scoliosis". Our project is a thorough identification of both single nucleotide variants and copy number variants based on the exome sequencing data of patients and their close family members. This dataset includes all the references used, the codes, the experiment results, and the lab notebook. The README.txt explains all the information needed for this dataset.《先天性脊柱侧凸的遗传与分子基础》研究配套支撑数据。本项目基于患者及其直系亲属的外显子组测序（exome sequencing）数据，对单核苷酸变异（single nucleotide variants, SNV）与拷贝数变异（copy number variants, CNV）开展了全面鉴定。本数据集涵盖了本研究使用的全部参考文献、代码、实验结果以及实验记录本。README.txt文件已对本数据集的所有必要信息进行了详细说明。