LibreOffice 歷史版本列表 Page3

更新時間：2023-06-10
更新細節：

What's new in this version:

Fixed:
- Bug file is deleted immediately on startup if settings dir (or parent) is a symlink
- Linux: could not launch external tools
- Syntax colors, Comment (dark theme) make a little bit more lighter

更新時間：2023-06-10
更新細節：

What's new in this version:

Features include:
- Tabbed Interface
- Easy and flexible file and folder management
- Choose any folder on your files system as a project
- View subfolders and files list directly within SnapGene via new navigation panel
- Quickly browse all SnapGene supported file types, including DNA, RNA, protein, alignments, chromatograms and gels
- Perform standard file operations directly within SnapGene
- Context-based quick links for easy access to common tools
- -Search for files within the selected project folder based on file or sequence characteristics
- Visualize Primer Annotations in the Add / Edit primer and selected cloning dialogs
- Preview detected features when creating a new sequence
- Get Started pane with easy access to learning resources + recent projects or files
- Directly input selected files into alignments, assembly cloning methods and gel simulations based on the sequence selection in the folder panel.
- Import multi-sequence files to a folder
- Restructures primer dialogs to make it easier to insert into the primer sequence
- Offer the option to insert a non-degenerate recognition sequence into a primer sequence in the primer dialogs.
- Improved binding site information shown in the primer dialogs
- Search for sequences in Dotmatics Bioregister directly from within SnapGene based on the sequence name, Bioregister ID, or using a similar sequence (BLAST search) Import and search Dotmatics Bioregister directly within SnapGene
- Added support for changing methylation when simulating agarose gels
- Improved first launch experience
- Added ladders from Nippon Genetics
- Modern look and feel

Additional changes and fixes:
- New option to apply primers to all agarose gel lanes
- Added ability to extend the selection from a selected feature to an arbitrary position and vice versa
- New option to automatically add upstream bases when inserting 5’ restriction sites into primers
- Added support for undo and redo in the Add / Edit Primer dialog
- Primer annotations created when insertions added automatically during cloning simulations
- Added support for duplicating and editing imported codon usage tables
- Added command line preview in RNA secondary structure settings
- Adjusted the equation used when simulating agarose gels to provide more accurate results
- Added warning for Collections top folder if it has a contents that will not be visible via SnapGene’s Collections UI
- Added setting to hide legacy Collections functionality by default
- Replaced Launch dialog with the ‘Get Started’ space
- Improved look and feel of Windows installer on high resolution displays
- Fixed issues with adjusting the endpoints of multi-segment features
- Fixed an issue that could prevent adjusting the position of point features
- Fixed an issue with garbled text and displaying the dates primers were added in Primers view
- Cmd+W no longer closes the "Save Unsaved Changes?" dialog
- Improved the FASTA importer to reject files that include numerical characters on non-comment lines
- Fixed various issues that prevented opening some Geneious files
- Added support for editing imported genetic codes and duplicating genetic codes
- Fixed a bug where changing the reading frames shown in sequence view or sorting enzymes in Enzymes view had no effect on Windows or Linux.
- Added TaKaRa DL500 ladder
- Added a missing band to the Azura PureView 100 bp DNA Ladder

Known Limitations:
- The file search UI and capabilities are still under development. Updates may change how this works and expand on available search terms, etc. We’d love to hear any feedback or requests you have.
- If a Collection folder is chosen as the project, note that:
- Subfolders and files will be displayed as they are on the file system, which is quite different to how they are displayed within a Collection
- Files added within the Project UI may be rearranged into the appropriate DNA, RNA, Protein or Misc files folder if the Collection is opened later, or some files may not be displayed within the Collection UI.
- -Dropbox online-only files on MacOS cannot be opened in SnapGene. These files will show in the folder panel, but you will need to download or sync a local copy via your file system before opening them in SnapGene.

更新時間：2023-06-10
更新細節：

What's new in this version:

Features include:
- Tabbed Interface
- Easy and flexible file and folder management
- Choose any folder on your files system as a project
- View subfolders and files list directly within SnapGene via new navigation panel
- Quickly browse all SnapGene supported file types, including DNA, RNA, protein, alignments, chromatograms and gels
- Perform standard file operations directly within SnapGene
- Context-based quick links for easy access to common tools
- -Search for files within the selected project folder based on file or sequence characteristics
- Visualize Primer Annotations in the Add / Edit primer and selected cloning dialogs
- Preview detected features when creating a new sequence
- Get Started pane with easy access to learning resources + recent projects or files
- Directly input selected files into alignments, assembly cloning methods and gel simulations based on the sequence selection in the folder panel.
- Import multi-sequence files to a folder
- Restructures primer dialogs to make it easier to insert into the primer sequence
- Offer the option to insert a non-degenerate recognition sequence into a primer sequence in the primer dialogs.
- Improved binding site information shown in the primer dialogs
- Search for sequences in Dotmatics Bioregister directly from within SnapGene based on the sequence name, Bioregister ID, or using a similar sequence (BLAST search) Import and search Dotmatics Bioregister directly within SnapGene
- Added support for changing methylation when simulating agarose gels
- Improved first launch experience
- Added ladders from Nippon Genetics
- Modern look and feel

Additional changes and fixes:
- New option to apply primers to all agarose gel lanes
- Added ability to extend the selection from a selected feature to an arbitrary position and vice versa
- New option to automatically add upstream bases when inserting 5’ restriction sites into primers
- Added support for undo and redo in the Add / Edit Primer dialog
- Primer annotations created when insertions added automatically during cloning simulations
- Added support for duplicating and editing imported codon usage tables
- Added command line preview in RNA secondary structure settings
- Adjusted the equation used when simulating agarose gels to provide more accurate results
- Added warning for Collections top folder if it has a contents that will not be visible via SnapGene’s Collections UI
- Added setting to hide legacy Collections functionality by default
- Replaced Launch dialog with the ‘Get Started’ space
- Improved look and feel of Windows installer on high resolution displays
- Fixed issues with adjusting the endpoints of multi-segment features
- Fixed an issue that could prevent adjusting the position of point features
- Fixed an issue with garbled text and displaying the dates primers were added in Primers view
- Cmd+W no longer closes the "Save Unsaved Changes?" dialog
- Improved the FASTA importer to reject files that include numerical characters on non-comment lines
- Fixed various issues that prevented opening some Geneious files
- Added support for editing imported genetic codes and duplicating genetic codes
- Fixed a bug where changing the reading frames shown in sequence view or sorting enzymes in Enzymes view had no effect on Windows or Linux.
- Added TaKaRa DL500 ladder
- Added a missing band to the Azura PureView 100 bp DNA Ladder

Known Limitations:
- The file search UI and capabilities are still under development. Updates may change how this works and expand on available search terms, etc. We’d love to hear any feedback or requests you have.
- If a Collection folder is chosen as the project, note that:
- Subfolders and files will be displayed as they are on the file system, which is quite different to how they are displayed within a Collection
- Files added within the Project UI may be rearranged into the appropriate DNA, RNA, Protein or Misc files folder if the Collection is opened later, or some files may not be displayed within the Collection UI.
- -Dropbox online-only files on MacOS cannot be opened in SnapGene. These files will show in the folder panel, but you will need to download or sync a local copy via your file system before opening them in SnapGene.

更新時間：2023-05-06
更新細節：

更新時間：2023-05-04
更新細節：

更新時間：2023-04-13
更新細節：

What's new in this version:

Fixed:
- Changes view: synchronized scrolling did not work when searching
- fixed tiny memory leak

Other Noteworthy Changes:
- Compare, Conflict Solver, Find dialog: use text selection if not multiline
- Preferences, Built-in Text Editors: use same control as in File Compare for preview
- Syntax coloring: added TOML

更新時間：2023-04-13
更新細節：

What's new in this version:

Fixed:
- Fixed scrolling in the text representation of History view using a mouse wheel or trackpad
- Ensure dragging DNA, RNA, and protein files into Collections are never placed in the Miscellaneous Items section and ensure they can be opened.
- Fixed issues where detecting common features sometimes failed to identify matches that are not identical at the ends even though the overall match fidelity is above the specified threshold.
- Fixed an issue that sometimes prevented computing the RNA structure when using a non US locale.
- Improved colors of C and G peaks when viewing sequence traces in dark mode
- Fixed an issue that prevented opening FASTQ files on Windows and Linux
- Fixed an issue where moving sequences aligned to a reference up / down could result in them jumping two steps at a time.
- Fixed issues with zooming an RNA secondary structure when using a non-US locale
- Improved display of secondary structure statistics when using a non-US locale
- Improved stability when pasting sequences into the New File dialog
- Updated Windows installer for high resolution displays
- Fixed an issue that prevented opening some EMBL sequences
- Fixed a crash when switching from "Run PCR" to "Use Directory" in the Golden Gate Cloning dialog
- Fixed an issue that could prevent reading in all primers created with upcoming versions of SnapGene

更新時間：2023-04-13
更新細節：

What's new in this version:

Fixed:
- Fixed scrolling in the text representation of History view using a mouse wheel or trackpad
- Ensure dragging DNA, RNA, and protein files into Collections are never placed in the Miscellaneous Items section and ensure they can be opened.
- Fixed issues where detecting common features sometimes failed to identify matches that are not identical at the ends even though the overall match fidelity is above the specified threshold.
- Fixed an issue that sometimes prevented computing the RNA structure when using a non US locale.
- Improved colors of C and G peaks when viewing sequence traces in dark mode
- Fixed an issue that prevented opening FASTQ files on Windows and Linux
- Fixed an issue where moving sequences aligned to a reference up / down could result in them jumping two steps at a time.
- Fixed issues with zooming an RNA secondary structure when using a non-US locale
- Improved display of secondary structure statistics when using a non-US locale
- Improved stability when pasting sequences into the New File dialog
- Updated Windows installer for high resolution displays
- Fixed an issue that prevented opening some EMBL sequences
- Fixed a crash when switching from "Run PCR" to "Use Directory" in the Golden Gate Cloning dialog
- Fixed an issue that could prevent reading in all primers created with upcoming versions of SnapGene

更新時間：2023-03-30
更新細節：

更新時間：2023-03-23
更新細節：

What's new in this version:

New features:
ATEM 4 M/E Constellation HD:
- Includes UVC support for the ATEM 4 M/E Constellation HD
- Corrects headphone output channel swap
- Fixes missing tally for inputs 9 - 4
- General performance and stability updates