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Additional file 1 of Clinical efficiency of simultaneous CNV-seq and whole-exome sequencing for testing fetal structural anomalies

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posted on 2022-01-04, 05:09 authored by Xinlin Chen, Yulin Jiang, Ruiguo Chen, Qingwei Qi, Xiujuan Zhang, Sheng Zhao, Chaoshi Liu, Weiyun Wang, Yuezhen Li, Guoqiang Sun, Jieping Song, Hui Huang, Chen Cheng, Jianguang Zhang, Longxian Cheng, Juntao Liu
Additional file 1: Figure S1. Sequencing and bioinformatics analysis pipeline of CNV-seq and WES combined analysis to detect alteration related to congenital structural anomalies. QC quality control; WES whole-exome sequencing; CNV copy number variation; XHMM eXome Hidden Markov model.

Funding

CAMS Innovation Fund for Medical Sciences (CIFMS) National Key R&D Program of China Hubei Province health and family planning scientific research project Hubei Province Natural Science Foundation Key R&D Program of Hubei Science and Technology Department Key Program of Hubei Science and Technology Department aiding Xinjiang and Tibet Province

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    Journal of Translational Medicine

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    Whole-exome sequencingPrenatal diagnosisCNV-seqStructural anomaly

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