Bulked Segregant Analysis platform consists of one-step standard analysis and advanced analysis with customized parameter setting. BSA is a technique employed to quickly identify phenotype associated genetic markers. Main workflow of BSA contains: 1. selecting two groups of individuals with extremely opposing phenotypes; 2. pooling the DNA, RNA or SLAF-seq(Developed by Biomarker) of all individuals to form two bulk of DNA; 3. identifying differential sequences against reference genome or in between, 4. predicting candidate linked regions by ED and SNP-index algorithm; 5. Functional analysis and enrichment on genes in candidate regions, etc. More advanced mining in data including genetic marker screening and primer design are also available.