Mutations-SNV

Tips: Only data with high sequencing depth can be used for SNV analysis.
Usage: Enter the project accession number (only one at a time) and click "Check" to view the corresponding SNV results.

Examples: SRP029757, SRR20842815, SRR1779078

For questions and suggestions, please contact: heshiyang@seu.edu.cn © HSCGD. State Key Laboratory of Digital Medical Engineering, Southeast University

HSCGD Human Single Cell Genome Database