SnapGene Viewer 5.1.4 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 Viewer 5.1.4


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


Romain Petges


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

- 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

- 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

Attribute Changer 相關參考資料