Charles 歷史版本列表 Page4

更新時間：2020-08-09
更新細節：

更新時間：2020-08-06
更新細節：

What's new in this version:

- Fixed a crash on Windows 7 that started happening in version 1.8.9.2
- Fixed a problem where the screen saver would stop working on the RDP client PC after an RDP session
- Added Uninstall button on the Settings tab
- Miscellaneous internal stability improvements

更新時間：2020-07-24
更新細節：

更新時間：2020-07-21
更新細節：

What's new in this version:

New Functionality:
- Added a "Copy Rich Text" command for selections in alignments, to provide the option of copying either simple sequences or sequences with metadata

Enhancements:
- Added Invitrogen's "pScreen-iT LacZ-Dest" to the list of Gateway® Destination vectors
- Modified the statistics in pairwise alignments to show two digits after the decimal point instead of one
- Added time estimates to various progress dialogs
- Improved the order of "Copy" actions in the Edit menu
- Made various textual, alignment, and spacing improvements
- Enabled export of a map or history while viewing any tab

Fixes:
- Ensured reliable import of primers copied to the clipboard using Microsoft Office
- Added support for dragging and dropping FASTA archives into the Assemble Contigs dialog
- Preserved zoom and split view display options when switching between files in a collection
- Enhanced the Gene Construction Kit importer to capture the full set of notes in the "General Info" section
- Improved stability when computing and viewing multiple sequence alignments
- Corrected an issue that could cause features to be erroneously detected around the numerical origin of a linear sequence
- Ensured that proper file extensions were included when batch converting files from one format to another
- Ensured correct setting of the default button in the Find controls when pressing and releasing Shift in a sequence trace window
- Corrected a regression with the navigation buttons when viewing an alignment to a reference sequence
- Addressed issues with the purple bar and the Tm column when importing primers from another file
- Corrected the displayed molecular weight when adding a translated feature to the common features database
- Removed the colors button in cloning dialogs, and streamlined the side toolbar in the Edit DNA Ends, Browse Common Features, and Mutageneis dialogs
- Improved the display of long sequence names within circular maps
- Corrected a regression by removing cut locations for ancestral restriction sites in History view
- Removed the inappropriate "Preserve feature annotations" control from the New File dialog, and the inappropriate "Detect common features" control when inserting or replacing bases in a sequence trace window
- Improved stability when assembling contigs using FASTQ data
- Disabled the Show/Hide All Enzymes commands when viewing protein files
- Corrected an issue in which the endpoints of a selection were not updated in the selection bar after renumbering the origin of a linear sequence
- Fixed an issue that prevented immediately using SnapGene without restarting after activating a Flexera-based shared license
- Corrected an issue with computing % GC when partially degenerate residues (B, D, H, and V) were present
- Ensured that only the zoomed region is shown for the root map in History view
- Addressed an issue in which the Save As dialog would vanish immediately when attempting to choose a different name instead of saving over an existing file
- Ensured that enzyme set menus are refreshed after using Manage Enzyme Sets
- Ensured that the desired endpoint modifications are correctly applied when designing a synthetic construct
- Improved the registration of file associations on macOS

更新時間：2020-07-21
更新細節：

What's new in this version:

New Functionality:
- Added a "Copy Rich Text" command for selections in alignments, to provide the option of copying either simple sequences or sequences with metadata

Enhancements:
- Added Invitrogen's "pScreen-iT LacZ-Dest" to the list of Gateway® Destination vectors
- Modified the statistics in pairwise alignments to show two digits after the decimal point instead of one
- Added time estimates to various progress dialogs
- Improved the order of "Copy" actions in the Edit menu
- Made various textual, alignment, and spacing improvements
- Enabled export of a map or history while viewing any tab

Fixes:
- Ensured reliable import of primers copied to the clipboard using Microsoft Office
- Added support for dragging and dropping FASTA archives into the Assemble Contigs dialog
- Preserved zoom and split view display options when switching between files in a collection
- Enhanced the Gene Construction Kit importer to capture the full set of notes in the "General Info" section
- Improved stability when computing and viewing multiple sequence alignments
- Corrected an issue that could cause features to be erroneously detected around the numerical origin of a linear sequence
- Ensured that proper file extensions were included when batch converting files from one format to another
- Ensured correct setting of the default button in the Find controls when pressing and releasing Shift in a sequence trace window
- Corrected a regression with the navigation buttons when viewing an alignment to a reference sequence
- Addressed issues with the purple bar and the Tm column when importing primers from another file
- Corrected the displayed molecular weight when adding a translated feature to the common features database
- Removed the colors button in cloning dialogs, and streamlined the side toolbar in the Edit DNA Ends, Browse Common Features, and Mutageneis dialogs
- Improved the display of long sequence names within circular maps
- Corrected a regression by removing cut locations for ancestral restriction sites in History view
- Removed the inappropriate "Preserve feature annotations" control from the New File dialog, and the inappropriate "Detect common features" control when inserting or replacing bases in a sequence trace window
- Improved stability when assembling contigs using FASTQ data
- Disabled the Show/Hide All Enzymes commands when viewing protein files
- Corrected an issue in which the endpoints of a selection were not updated in the selection bar after renumbering the origin of a linear sequence
- Fixed an issue that prevented immediately using SnapGene without restarting after activating a Flexera-based shared license
- Corrected an issue with computing % GC when partially degenerate residues (B, D, H, and V) were present
- Ensured that only the zoomed region is shown for the root map in History view
- Addressed an issue in which the Save As dialog would vanish immediately when attempting to choose a different name instead of saving over an existing file
- Ensured that enzyme set menus are refreshed after using Manage Enzyme Sets
- Ensured that the desired endpoint modifications are correctly applied when designing a synthetic construct
- Improved the registration of file associations on macOS

更新時間：2020-06-20
更新細節：

更新時間：2020-06-20
更新細節：

更新時間：2020-06-18
更新細節：

What's new in this version:

- This version includes multiple fixes and improvements

更新時間：2020-06-18
更新細節：

What's new in this version:

New Functionality:
- Added support for importing protein features from the GFF3 format
- Enabled features to be preserved when a replacement leaves the sequence length unchanged

Enhancements:
- Enabled the import of custom user fields from Vector NTI databases
- Increased the 3' match length limit to 25 bases when importing primers from a list
- Enabled capture of the history of a protein translated from DNA when importing from Vector NTI Advance
- Enhanced primer tooltips to include % GC for the annealed region
- Improved copy and paste of sequence alignments into text editors and other programs
- Increased the size of the DOI field when editing references
- Made various color, layout, and textual enhancements

Fixes:
- Mandated use of the proper default font size when creating new files, importing from online, and opening non-native files
- Corrected an issue that prevented importing primers into multiple files in a collection
- Corrected a regression with displaying translations and the "Original Sequence" when no sequences are aligned to the reference DNA sequence
- Enabled changing methylation for placeholder files
- Fixed various issues when working with placeholder files
- Implemented automatic correction of invalid alignments to a reference sequence computed with prior versions
- Fixed an issue that prevented manually specifying the zoomed range
- Corrected the "+" symbol in plasmid names when importing from "SnapGene Online Sequences"
- Ensured correct updating of the zoomed range when navigating to matches with the Find tool
- Addressed an issue with specifying the position of protein interchain bond locations
- Removed the "Codons" cascading menu when interacting with protein sequences
- Corrected an issue that prevented importing multi-sequence GenBank and GenPept files into a collection
- Ensured that translation numbering is maintained when using Make Protein from multiple selected translated features
- Ensured that the match threshold controls are listed only once when importing features from a SnapGene file
- Corrected an issue that could cause file names to be clipped in source menus
- Fixed an issue that caused files to be marked as modified after hovering over hyperlinks in the Description Panel
- Ensured that stop codons present in protein query strings are included in the search results
- Improved the import of multi-part qualifiers from Geneious
- Fixed an issue with undo of sequence color changes that are limited to a single strand
- Corrected the "Copy" shortcut when viewing a protein sequence or multi-protein alignment
- Ensured more robust behavior when adding primers to DNA sequences
- Turned on the display of truncated primer description data when full descriptions are toggled off in Primers view
- Corrected an issue in which simplified primer binding sites were not shown after modifying hybridization parameters
- Ensured that sufficient space is always allocated above displays of complex primer binding sites in Sequence view
- Turned on display of the parental enzyme set when viewing Nicking Endonucleases in Sequence and Map views
- Improved reliability when importing from Addgene
- Improved the import of Addgene sequences that contain slashes in their names
- Ensured that side toolbar buttons in dialogs are not hidden
- Corrected a regression in which two copies of common features such as EGFP were sometimes annotated when detecting common features
- Removed "Match Threshold" controls from the "Add to Common Features" dialog

更新時間：2020-05-23
更新細節：