New and enhanced features for all of your DNA sequence analysis.
Sanger:
- 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.
NGS:
- 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.
RNA-Seq:
- 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.
