第11章

参考文献：第11章 深度测序的数据可视化软件


Arner, E., et al. 2010. NGSView: an extensible open source editor for next-generation sequencing data. Bioinformatics. 26(1): 125-126. [PubMed]

Carver, T., et al. 2012. Artemis: an integrated platform for visualization and analysis of high-throughput sequence-based experimental data. Bioinformatics. 28(4): 464-469. [PubMed]

Coordinators, N. R. 2016. Database resources of the National Center for Biotechnology Information. Nucleic Acids Res. 44(D1): D7-19. [PubMed]

Fiume, M., et al. 2010. Savant: genome browser for high-throughput sequencing data. Bioinformatics. 26(16): 1938-1944. [PubMed]

Kent, W. J., et al. 2002. The human genome browser at UCSC. Genome Res. 12(6): 996-1006. [PubMed]

Milne, I., et al. 2010. Tablet--next generation sequence assembly visualization. Bioinformatics. 26(3): 401-402. [PubMed]

Milne, I., et al. 2013. Using Tablet for visual exploration of second-generation sequencing data. Brief Bioinform. 14(2): 193-202. [PubMed]

Rutherford, K., et al. 2000. Artemis: sequence visualization and annotation. Bioinformatics. 16(10): 944-945. [PubMed]

Speir, M. L., et al. 2016. The UCSC Genome Browser database: 2016 update. Nucleic Acids Res. 44(D1): D717-725. [PubMed]

Thorvaldsdottir, H., et al. 2013. Integrative Genomics Viewer (IGV): high-performance genomics data visualization and exploration. Brief Bioinform. 14(2): 178-192. [PubMed]

Yates, A., et al. 2016. Ensembl 2016. Nucleic Acids Res. 44(D1): D710-716. [PubMed]