Attribute Changer

最新版本 SnapGene 5.2.3

SnapGene 5.2.3

SnapGene 5.2.3
Attribute Changer 是一個功能強大的 Windows 資源管理器擴展。無論何時在 Windows 資源管理器中右鍵單擊文件,文件夾甚至驅動器,都可以隨時使用。該工具加載了令人興奮的功能,並幫助您在 Microsoft Windows 中管理您的日常任務。

想讓您的文件只讀,以防止修改或需要強制一個特定的文件的新的備份版本,而無需修改內容。可能性是無止境。 Attribute Changer 可以修改像 ReadOnly,隱藏,存檔,系統,壓縮和索引文件和文件夾的標準屬性。如果您將數據存儲在區分大小寫的文件系統(如基於 Linux 的 NAS 系統)上,文件和文件夾的名稱和擴展名可以輕鬆地從大寫轉換為小寫,反之亦然。

Attribute Changer 可以通過手動輸入日期和時間值來修改照片信息(EXIF),或者您可以選擇與時間戳和文件日期同步信息。更高級的選項,如修改日期和時間戳的詳細部分是可用的,如果需要的話。

文件和文件夾過濾器指示 Attribute Changer 根據多個條件(如屬性,日期,時間,大小和文件或文件夾名稱通配符)排除或包含對象。範圍可以為他們大多數定義。可以將多個條件組合在一起以創建一組要應用於文件和文件夾的條件。

支持 Windows XP,Vista,7,8 和 10 的所有 32 位和 64 位版本。它與許多流行的第三方文件管理器集成在一起。

Attribute Changer 功能:
外殼擴展(在 Windows 資源管理器中右鍵單擊文件和文件夾)管理只讀,隱藏,存檔,系統,壓縮和索引屬性管理創建,修改和訪問日期和時間戳管理照片(EXIF)日期和時間戳將絕對值和偏移值應用於日期和時間應用隨機日期和時間戳同步日期和時間戳更改文件和文件夾名稱及擴展名的大小寫在選擇上應用過濾器以限制處理實時和詳細報告模擬模式 PDF 格式的豐富的本地化用戶指南 Attribute Changer 是免費的,即使是商業用途

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 / Vista / Windows 7 / Windows 8 / Windows 10
軟體類型 免費軟體
作者 Romain Petges
官網 http://www.petges.lu/home/
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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