CLC RNA Workbench

Bioinformatics program for advanced RNA sequence analysis.
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CLC RNA Workbench Ranking & Summary

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  • Rating:
  • License:
  • Trial
  • Price:
  • USD 1975.00 | BUY the full version
  • Publisher Name:
  • CLC bio
  • Publisher web site:
  • http://www.clcbio.com
  • Operating Systems:
  • Mac OS X 10.4 or later
  • File Size:
  • 34.8 MB

CLC RNA Workbench Tags


CLC RNA Workbench Description

Bioinformatics program for advanced RNA sequence analysis. The CLC RNA Workbench gives the user easy access to a range of complex algorithms and options. RNA secondary structures can be predicted using state-of-the-art free energy minimization algorithms.CLC RNA Workbench is a bioinformatics program for advanced RNA sequence analysis. All analyzes are fully integrated in one single, intuitive and user-friendly software application. Here are some key features of "CLC RNA Workbench": · Secondary structure prediction. · Graphical view and editing of secondary structure. · Tabular view of structures and energy contributions. · Symbolic representation in sequence view. · Pattern search. · BLAST searches. · General sequence analyses. · Nucleotide analyses. · Sequence alignment. · Dot plots. · Virtual gel viewer. Requirements: · 256 MB RAM required. · 512 MB RAM recommended. · 1024 x 768 display recommended. Limitations: · 4 weeks fully functional trial. What's New in This Release: Deployment: · You can set a path to the default data location used when the Workbench starts for the first time. This is a feature to help system administrators control where new installations per default save their data. Read more... · Support for removing tools accessing the internet (NCBI BLAST, update notifications etc). Read more... General import and export: · Support for import of complex regions from GFF files · Export tables and reports in Excel format. · Import section of user manual re-structured to provide better overview. Read more.... Expression data importers are now described in technical details in a separate section. Read more.... · You can now export multiple sequence lists in fasta format · Forced import of zip files is now supported (it will force import the contents of the zip file) · The standard import now accepts gzip and tar files as well as zip · If a forced import fails, there will be more technical information about what went wrong, allowing you to identify bad formatting of the import files · Both Genbank and gff importer now makes several attempts at naming genes that do not have a gene name. It will iteratively try the following qualifiers: "product", "locus_tag", "protein_id" and "transcript_id" · When importing genbank files where the length stated does not match the actual sequence, a warning is shown but the sequence is accepted. · When exporting in csv format, the Locale settings are used to determine whether comma or semi-colons should be used as delimiter (comma used for US locales) · GFF plug-in has been updated to accept complex annotations Miscellaneous: · Advanced retyping of annotations using the annotation table. Read more... · Improved reporting of situations when a full disk prevents saving of data · Downloading sequences using drag and drop from the search table no longer creates a "Downloading..." node in the folder. The download process can be monitored in the Processes tab. · Extract Sequences moved from File menu to Toolbox-> General Sequence Analysis. Read more... · Better progress feedback on various dialogs Bug-fixes: · Fixed problem displaying the "Copying..." label when copying data and then updating the folder · Fixed problem with naming of tabs. The fix means that on Windows and Linux unsaved data now gets a * rather than make the tab name bold and italics. (This has always been the behavior on Mac OS X).


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