SnapGene 5.2.4 軟體資訊介紹&下載

Attribute Changer,軟體教學,軟體下載,電腦問題,電腦教學
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

Attribute Changer Screenshot 1
Attribute Changer Screenshot 2
Attribute Changer Screenshot 3

SnapGene 5.2.4


Windows XP / Vista / Windows 7 / Windows 8 / Windows 10


Romain Petges


What's new in this version:

New Functionality:
- Added DNA ladders from GeneBio Systems

- Improved application stability when dragging out selections
- Corrected a regression to ensure detection of restriction sites whose recognition sequences span the numerical origin
- Populate the "Description" fields when pasting GenBank content into the New File dialogs
- Improved the detection of sequence type when importing DNASTAR SeqBuilder files
- Corrected a regression to restore transfer of primers when pasting a copied DNA sequence
- Fixed an issue that could result in editing-induced disappearance of a sequence aligned to a reference DNA sequence
- Enabled simulation of Gateway BP and LR recombination around the numerical origin
- Improved application stability when searching for enzymes, features, and primers
- Corrected a misleading message that was shown when a problem occurred during program activation
- Ensured that the enzyme set indicator does not occlude content after scrolling to the bottom of Sequence view
- Streamlined the side toolbar in the Insert Codons, Choose Alternative Codons, Browse Common Features and Insert Feature dialogs
- Restored highlighting of the called base under the mouse when viewing sequence traces
- Improved application stability when using the "Find similar DNA sequences" command
- Improved performance when showing the Add Primer dialog and other dialogs that provide controls for choosing files
- Ensured highlighting of the inserted region for Gateway BP cloning in the Insert tab, and of the ancestral insert in History view for the resulting product file
- Restored import of ssRNA sequences as double-stranded rather than single-stranded DNA
- Prevented repetitive alignment to a reference sequence when making simple edits such as insertions, deletions, and same-size replacements
- Ensured that the Next button is the default control after searching a sequence trace
- Ensured correct scrolling of Sequence, Features, and Primers views in response to a change in the selection, but only when appropriate
- Improved application stability when quitting
- Improved application stability when hovering over aligned sequences
- Improved application stability when mousing over features
- Improved application tability when searching a collection for a named feature
- Improved application stability when importing primers
- Improved reliability when importing from NCBI

Attribute Changer 相關參考資料