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Although macOS 11 Big Sur has been released, the following problems have been reported regarding our products when the version is upgraded to the OS.
1. The dongle does not work properly. The Corresponding Dongle Driver has not released from the maker yet.
The workaround is either of the following.
In Frame Lane, if you select a region where the stop codon does not appear and register that region as a new feature by right-clicking the mouse, that region will be complemented in the Description Window even though it is in Forward Strand.However, it occurs in the case of new registration from the 3rd frame of Forward Strand. Registration from the 1st and 2nd frames works normally.
Uncheck Complement in the Description Window and register.
Bug fix Version IMC Ver.7.46 has been released (2020/12/09).
Extract the GBFF file consisting of many single GanBank format files into a tree-like directory according to the Taxonomy description of each GenBank file and place it in IMC so that it can be handled easily.
The sequence data of GenBank and RefSeq are compiled into a large compressed file at each release time.
Each entry consists of a header file (*. Gbff) and an array part (* fna). In order to make a single GenBank file, it is necessary to combine these two kinds of files.
GenBank File Expander decompresses these files of GenBank and RefSeq, synthesizes them, and unfolds them as a phylogenetic tree-like directory in an arbitrary place.
If you specify this expanded directory as IMC's root directory, it can be displayed and loaded in IMC's directory tree.
Click "Tools -> Multiple GenBank File Expander" from the menu.
To rebuild the designed gene cluster, fragment the cluster optimally.
After each fragment is chemically synthesized, each fragment is reconstituted by OGAB method to prepare a long chain DNA cluster.
This function is implemented in the following edition.
IMCDS
Extract the core genome from a pan genome.
Load one genome into the current main feature map.
Load multiple genomes to compare to the current reference feature map.
Detects one base mutation between closely related genomes and generates a list of all mutations. In addition, from the list you can display the variation of the reference feature map and the base position of the corresponding main feature map.
Load the base stock genome into the current main feature map.
Load multiple closely related genomes to compare with the current reference feature map.