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. De 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.
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