Some of the assembly core features are:
Automatic cleaning (trimming) of the bad ends of chromatograms, based on the confidence scores (confidence score). The resolution of the trimming engine can be fully adjusted by the user; this operation saves significant time, as manual ‘cleaning’ of the trace sequences is not needed any more.
Synchronized display between chromatograms and contig, which makes the correction of ambiguous bases much faster and easier.
A rapid navigation between mismatches. With just one click you can jump to the next mismatch.
Chromatogram viewer and editor (ABI and SCF).
Easy to use interface: the user can make a contig with only 3 mouse clicks.
Automatically save the contig to disk.
Automatic primer detection and vector removal.
Top accuracy - DNA Sequence Assembler is not using a "partial solution" algorithm like other programs. The precision of ambiguity correction recorded during testing was better than 96%. The user must only have to confirm program's suggestions instead of editing the contig.
Fast assembly algorithm
Intelligent, ergonomic, easy to use interface. Just drag and drop your files, then press the 'Start' button and the contig is done. The user has full control over the graphic user interface (GUI) and the sounds.
Low resource requirement: it can run even on very old systems. Incredibly small size: The full package has about 2MB and it includes few SCF samples, sounds, skins.
100% safe. DNA Baser will never alter your chromatogram files (results are saved in separate files) and it will never harm your computer by installing files in your operating system / registry. It does not use abusing/dangerous technologies like DCOM, Dot Net, DLL's, Java, ActiveX, MFC, VBR, scripts.
Auto updating. The program automatically checks and download the updates from the Internet. Updates are free.