New and enhanced features for all of your DNA sequence analysis.
Send primer pair sequences from Primer-BLAST runs in Sequencher Connections to your Sequencher project.
Easily use consensus sequences from the Project Window as a reference sequence for NGS alignments for hybrid sequencing projects.
New Batch Revert Trim Ends command.
Ability to adjust the font size in the Project Window.
Faster GSNAP and BWA-MEM workflows.
Build GSNAP Databases and BWA Indexes that can be re-used for aligning to whole genomes.
View and save quality scores and metadata of your NGS raw data files with FastQC reports.
Generate Variant Calling Files (VCF) to flag variants in your NGS alignments using SAMtools.
Expanded Cufflinks suite with the addition of Cuffquant and Cuffnorm.
A unique Conditions and Replicates Editor for Cuffdiff and Cuffnorm.
Enhanced RNA-Seq visualizations with custom sorting and filtering options.
Easily manage all of your DNA-Seq and RNA-Seq projects with an enhanced External Data Browser.