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Workflow to decompose scoliosis-related genome and to predict scoliosis-related genotypes. The present workflow was designed for the parsing and cleaning of ClinVar data (A), statistical analysis and screening for scoliosis-related genotypes (B), decomposing scoliosis-related genes (C), unsupervised learning analysis of compositional features of scoliosis-related genes (D), deep learning network structure for predicting scoliosis genotypes (E), and scoliosis genotype prediction (F).
