View plasmid maps, automatically annotate vectors, and copy-paste sequences with annotations. View and edit alignments with real-time translation and highlighting.īuild phylogenetic trees using peer-reviewed algorithms, including RAxML and PAUP*. Perform pairwise and multiple alignments using trusted algorithms, including MAFFT and ClustalW. Automatic annotation for gene prediction, motifs, translation, and variant calling. Trim, assemble, and view Sanger sequencing trace files. Students, academics, and government professionals use Geneious Prime in a multitude of research disciplines, due to the comprehensive nature of its operations.ĭe novo assembly or reference mapping of Illumina, PacBio, or Ion Torrent reads, using industry leading algorithms, including TopHat and Velvet.Ĭomprehensive analysis of data, including genome browser, contig visualization, SNP calling, and RNA-Seq expression analysis. New features include improved cloning and plasmid viewing, alignment masking, chimera filtering, and better structural variant mapping and long read assembly.ĭiscover all of the brand new features, improvements and enhancements in Geneious R10. Setup automated workflows to increase efficiency, control business processes and reduce human error in your research. Import and export most industry standard file formats. Centralize and collaborate on data with seamlessly integrated shared repositories. View and edit alignments with real-time translation and highlighting.īuild phylogenetic trees using peer-reviewed algorithms including RAxML and PAUP* and adjust display settings for publication-ready graphics.īatch BLAST against NCBI and directly search GenBank. Perform pairwise and multiple alignments of DNA or protein using trusted algorithms including MAFFT and ClustalW. Genotype microsatellite traces with automated ladder fitting and peak calling and generate tables of alleles. Automatic annotation for gene prediction, motifs, translation and variant calling. Trim, assemble and view Sanger sequencing trace files, correct base calls and create consensus sequences. Geneious is used by all of the top 20 universities globally (Times Higher Education, 2016) and by sixteen of the 20 largest pharmaceutical companies.ĭe novo assembly or reference mapping of Illumina, PacBio or Ion Torrent reads (any length, paired ends, barcodes), using industry leading algorithms including TopHat and Velvet.Ĭomprehensive analysis of data including genome browser, contig visualization, SNP calling and RNA-Seq expression analysis. Discover all of the brand new features, improvements and enhancements.įirst released in 2005, Geneious is the world's leading bioinformatics software platform used by over 3,000 universities, institutes and companies in more than 100 countries.
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