![Chromas Chromas](https://d2.alternativeto.net/dist/s/technelysium_710308_full.png?format=jpg&width=1600&height=1600&mode=min&upscale=false)
Chromas lite can View and edit the output files. Features: * Opens chromatogram files from Applied Biosystems and Amersham MegaBace DNA sequencers. * Opens SCF format chromatogram files created by ALF, Li-Cor, Visible Genetics OpenGene, Beckman CEQ 2000XL and CEQ 8000, and other sequencers.
* Save in SCF or Applied Biosystems format. * Prints chromatogram with options to zoom or fit to one page. * Exports sequences in plaint text or FASTA format.
* Copy the sequence to the clipboard in plain text or FASTA format for pasting into other applications. * Reverse & complement the sequence and chromatogram. * Search for sequences by exact matching or redundant codes.
Chromas is ideal for the most basic of sequencing projects, where assembly of multiple sequences is not required. Also, with this tool you can copy the sequence to the clipboard in plain text or FASTA format for pasting into other applications. Chromas Lite Free Download - Chromas lite can View and edit the output files. Chromas Lite Free Download - Chromas lite can View and edit the output files. Desktop Utilities. Home & Education. Network & Internet. System Utilities.
View chromatogram files from automated sequencers, and Staden SCF file format Chromas is a software that lets you view chromatogram files of automates sequencers manufactured by Amersham MegaBace and Applied biosystems, as well as Staden SCF files. With Chromas you can see the chromosome string, lookup a certain sequence and export the translated frames as a CSV file or copy them to clipboard. You can modify or delete any incorrect basecalls you’ve selected with your mouse. If you hold down backspace or delete keys you will quickly delete successive bases, forwards for delete and backwards if you use backspace. You can move any base in the space between two adjacent bases using click & drag or Ctrl + arrow keys. A colored bar appearing above each base shows the order of magnitude of the probability of error for that base.
Chromas displays a list of the peaks below the chromatogram, for genotyping files that have peak-related information.