Gather, process, and organize data, perform bioinformatics analyses, view generated graphics, and export the result in various formats. Work with different alignments of RNA, DNA, proteins, and consensus sequences, create reverse complements, shuffle sequences, and check genetic translations.
CLC Sequence Viewer includes a number of features for doing basic bioinformatics analysis. You can create and edit alignments, work with interactive restriction site analysis, phylogenetics, or advanced DNA to protein translation, or you can use the integrated GenBank search options and many other features.
Bioinformatics features: Multiple alignment of DNA, RNA, and proteins , consensus sequence determination and management, conservation score along alignments, etc.
v6.8 [Jan 13, 2013]
Improvements
For alignments, sequence lists and other sequence views, the right-click options to Open Copy of Sequence and Open This Sequence have been merged to Open Sequence. If a copy should be created, use Save As with the new sequence, or drag it into a folder in the Navigation Area.
Bug fixes
Errors related to managing Workspaces have been fixed.
Annotations were added by the Find Open Reading Frames tool, even though the option to add annotations was not selected. This is now fixed.
Fixed an out-of-memory problem in the Create Alignment tool.
Mall Creeps
