DesktopOK (64-bit)

最新版本 SnapGene 5.2.3

SnapGene 5.2.3

SnapGene 5.2.3
DesktopOK 64 位是一個小而有效的解決方案,用戶必須經常更改屏幕分辨率。對於經常需要在筆記本電腦(例如筆記本電腦或平板電腦)上使用投影儀的 Windows 用戶來說也是很好的選擇。

更改屏幕分辨率後,您可以在 Windows 桌面上找到一個圖標混亂,就好像一枚炸彈擊中了它。圖標位置將會移動,Windows 將不能正確恢復桌面圖標的位置。 DesktopOK 64 位的也有其他有用的功能,你可以找到這一點,在主菜單中,Tools.

DesktopOK 特點:
保存每個屏幕分辨率您喜歡的圖標的位置。輕鬆最小化屏幕上的所有窗口在 Windows 啟動時啟動。每個用戶可以有自己的安排。便攜式 Windows 應用程序自動保存桌面圖標佈局更改語言最大化 Windows 桌面圖標的數量更改 Windows 桌面圖標大小最小化為托盤區域以便於訪問。多種語言自動隱藏和顯示桌面圖標

ScreenShot

軟體資訊
檔案版本 SnapGene 5.2.3

檔案名稱 snapgene_5.2.3_win.exe
檔案大小
系統 Windows XP 64 / Vista 64 / Windows 7 64 / Windows 8 64 / Windows 10 64
軟體類型 免費軟體
作者 Nenad Hrg
官網 http://www.softwareok.com/?seite=Freeware/DesktopOK
更新日期 2020-11-24
更新日誌

What's new in this version:

- Corrected a regression to enable the "Copy" command when a portion of an aligned sequence is selected
- Corrected an issue that could prevent protein search results from being shown
- Improved the size and placement of the License Agreement and Align Multiple Sequences windows
- Ensured proper opening of GenBank files that omit the molecule type in the LOCUS line
- Fixed an issue that could prevent using a attR Gateway site that lacks an optional leading nucleic acid
- Fixed an issue with using Gateway fragments whose junctions lie at or very near the numerical origin
- Ensured that files and collections located on network drives are included in the Open Recent File and Open Collection menus
- Fixed various glitches with displaying codon and ORF selections in Sequence view
- Improved the appearance of tabs on macOS 11 Big Sur
- Corrected a regression to ensure auto-scrolling in Sequence view for selections made using the minimap or another view
- Corrected a regression to ensure display of restriction sites in sequences aligned to a reference DNA sequence
- Fixed an issue that resulted in ORFs sometimes not being shown
- Ensured that "Find" matches remain highlighted after switching away from and then back to Sequence view or Map view
- Ensured that "Find" matches are shown after restoring the "Find similar DNA sequences" controls
- Ensured that palindromic "Find" matches are highlighted in both strands
- Ensured proper display of "Find similar DNA sequences" matches that wrap around the numerical origin
- Improved the behavior of the search box in the Choose Enzymes window when searching for a noncutter while the "Hide noncutters" checkbox is checked
- Fixed an issue with detecting Gateway sites that have been customized by the user
- Fixed an issue with annotating Gateway sites that lie near the numerical origin after performing BP or LR cloning
- Ensured reliable import of features from SwissProt files
- Ensured reliable opening of SwissProt files that contain limited header information
- Corrected a regression to force use of the correct font in the New DNA File and New Protein File dialogs
- Ensured accurate display of multiple sequence alignment file names in the Window menu on Linux
- Improved reliability when installing software updates on macOS Big Sur

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Changes in version 5.2.3 (Nov 23, 2020). Fixes. Corrected a regression to enable the "Copy" command when a portion of an aligned sequence is selected.

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SnapGene offers the fastest and easiest way to plan, visualize, and document DNA cloning and PCR. You can easily annotate features and design primers.

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