You can make use of batch processing in order to convert various files (e.g.
There’s support for several post processing options that you can take advantage of, namely sequence dereplicator (if duplicate files are found, you can copy or move them to a custom folder) and reverse complement. If you opt for the mutation detection process, you are given the freedom to apply this particular task in a single chromatogram or through sequence assembly/alignment from a single organism (multiploid with cloning or diploid without cloning) or from different organisms (two or more), such as haploids, multiploids with cloning or diploids without cloning.
A rich suite of tasks that you can work withĭNA Baser lists all tasks in the main panel, so you can easily proceed with working with sequence processing, namely sequence assembly (single contig assembly or batch assembly based on name pattern or subfolders) or editing and cleaning options (single sequence editing and cleaning or batch sequence cleaning). When it comes to importing data into your projects, you are allowed to add information from ABI, SCF, FAST, TXT, SEQ, GBK, or CSV file format. The tool displays a user-friendly layout, embeds tutorials for helping you learn more about its features, gives you quick access to an online help manual, and provides several samples that can be imported in your projects. However, this is clearly not the case with DNA Baser.
FREE CHROMATOGRAM VIEWER AND ALIGNMENT TOOL SOFTWARE
When you think about molecular biology programs you automatically link them with a comprehensive and sometimes a crowded interface where you need to dedicate your time in order to get an idea about how the software can be tweaked. Clean feature lineup and importing options DNA Baser is an advanced bioinformatics software application specialized in DNA sequence assembly, sequence analysis, contig editing and mutation detection.
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