The EGSB team has developed bioinformatics capabilities focusing on sequence analysis (e.g., multiple and pair-wise sequence alignment, sequence assembly, open reading frame prediction, phylogenetic tree construction and functional annotation), gene set enrichment analysis, de novo inference of gene regulatory or interactive network by reverse engineering, degenerate primer design, and next-generation sequencing (NGS) data analysis (pre-processing, error correction, SNP and structural variants calling, de novo genome or transcriptome assembly, comparative genomics, and genome-wide gene annotation). A series of bioinformatics tools have been developed.