DNA Baser Sequence Assembler
Some of the assembly core features are
Automatic cleaning (trimming) of the bad ends of chromatograms. Details
Synchronized display between chromatograms and contig, which makes the correction of ambiguous bases much faster and easier.
Proprietary algorithm for correction of the ambiguous bases.
A rapid navigation between mismatches. With just one click you can jump to the next mismatch.
Chromatogram viewer and editor (ABI and SCF).
Automatically save the contig to disk.
Automatic primer detection and vector removal.
Fast assembly algorithm
Top accuracy - DNA Baser 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.
Save project to disk and re-load it for later inspection/editing.
Add/remove samples to/from existing projects
Remember base edits made by user!
Embedded biology tools
Batch sequence processing (batch ends trimming, vector removal, metadata integration, FASTA conversion...)
Batch metadata integration tool (RNA Baser only)
State of art GenBank to FASTA converter
One click conversion between several file formats
BEST price on the market and significant discount when several licenses are ordered. Please see the Prices page for more details
Low resource requirement: it can run even on very old systems. Incredibly small size: The size of the whole package is about 2MB.
100% safe. DNA Baser will never alter your input chromatogram files (results are saved in separate files). Details.
Auto updating. The program automatically checks and downloads updates from the Internet. Updates are free.
Minimum system requirements
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