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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. A powerful and comprehensive suite of molecular biology and NGS analysis toolsĭe 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.