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\ Graphic Apps
\ CAD \ Geneious Basic
Geneious Basic6.0.4 by Biomatters Ltd |
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Software Description:
... for the retrieval, organization and analysis of biomolecular data that allows any molecular biologist do core bioinformatics tasks in a flash by removing painful data-administration. ...
type: Freeware
Download Geneious Basiccategories: molecular biology, biochemistry research, molecular research, bioinformatics, biology, research Add to Download Basket Report virus or spyware |
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Best Vista Download periodically updates pricing and software information of Geneious Basic full version from the publisher,
but some information may be out-of-date. You should confirm all information. Software piracy is theft, using crack, warez passwords, patches, serial numbers, registration codes, key generator, keymaker or keygen for Geneious Basic license key is illegal and prevent future development of Geneious Basic. Download links are directly from our mirrors or publisher's website, Geneious Basic torrent files or shared files from rapidshare, yousendit or megaupload are not allowed! |
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| Released: | December 03, 2012 |
| Filesize: | 53.80 MB |
| Platform: | Windows XP, Windows Vista, Windows 7 |
| Install | Instal And Uninstall |
| Add Your Review or Windows Vista Compatibility Report |
Geneious Basic- Releases History |
| Software: | Geneious Basic 6.0.4 |
| Date Released: | Dec 3, 2012 |
| Status: | New Release |
| Release Notes: | · Sequence Viewer: Fixed hang working with annotation types in tracks that contain '_' or '.' in their type name · Sequence Viewer: Fixed crash in rare situations when clicking on annotations in contigs · Sequence Viewer: Fixed crash and/or loss of newly added annotations on consensus sometimes when saving contigs · Sequence Viewer: Fixed poor performance/hangs viewing large contigs with non-trim annotations on the reads · Sequence Viewer: Fixed statistics that are too small to read sometimes · Reference assembly: Fixed crash and/or incorrect results when choosing to map paired reads to all matching locations. · Reference assembly: Fixed poor sensitivity mapping to genomes of several hundred MB (larger genome sizes (e.g. human genomes) were fine). The increased sensitivity will also slightly improve small genome results. · Reference assembly: Fixed poor sensitivity mapping reads spanning the origin of circular reference sequences |
| Software: | Geneious Basic 6.0.3 |
| Date Released: | Nov 12, 2012 |
| Status: | New Release |
| Release Notes: | · Added fastq export option to export paired reads to parallel files Bugs fixed: · Read mapping: Fixed incorrect read mapping results and/or poor performance sometimes with circular reference sequences · 3D Structure Viewer: Fixed a bug where the selection in the tree was being calculated incorrectly, causing the tree and selections to behave incorrectly · Fixed bug where extraction of multi-interval annotations from long sequences with many annotations could result in extra annotations · Made PMID show up correctly on PubMed documents · Fixed extraction of primers from regions of alignments containing gaps · Fixed crash when concatenating sequence lists or alignments such that that total number of bases was greater than around 2,000,000,000 · Fixed issue where tree viewer options didn't update when saving document · Fixed issue where jmol viewer selection misbehaved when a PDB document contains HETATM records prior to the last ATOM record |
| Software: | Geneious Basic 5.6.6 |
| Date Released: | Oct 22, 2012 |
| Status: | New Release |
| Release Notes: | Features: · Restored the old annotation table view Bugs fixed: · Fixed "There is already a track on this sequence with name..." error message when running various operations such as cloning and SAM import · Fixed out of memory error when viewing some sequences · Fixed a bug where the Csv importer wasn't importing Date fields correctly. · Fixed an error that would occur when searching a server database using a number field · Fixed an issue with Sassafras licenses not working |
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... suite for manipulating, finding, sharing, and exploring biological data such as DNA sequences or proteins, phylogenies, 3D ... design with degeneracy support * Keep a primer database and search for primers which match new sequences. ...
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