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Fig. 1 | BMC Bioinformatics

Fig. 1

From: SoftPanel: a website for grouping diseases and related disorders for generation of customized panels

Fig. 1

Flow chart for this website. Users first define a group of disorders using phenotype keyword searches, disorder phenotype similarity scoring, ICD-10 index specification, or manual editing. After determining a disorder group, known disease-associated genes are extracted from the OMIM database automatically. Users can next perform gene set enrichment analysis (GSEA) on the extracted list of disease-associated genes. Finally, an online supporting vector machine (SVM) is applied to refine the identification of genes that potentially underlie the disorder of interest

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