SnapGene Viewer 5.2.0 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
Romain Petges 免費軟體 評價 60 分 檔案下載
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 5.2.0

snapgene_viewer_5.2.0_win.exe

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

免費軟體

Romain Petges

http://www.petges.lu/home/

2020-10-14

What's new in this version:

New Functionality:
- Enabled visualization of GC content as a color plot in Map view or base colors in Sequence view
- Added support for finding similar DNA sequences with mismatches or indels compared to the search query
- Added support for simulating the migration of supercoiled DNA molecules in agarose gels using TBE, TAE or SB buffer
- Added support for single-stranded DNA (ssDNA) sequences
- Enabled import of Sequencher project files (*.spf)
- Enabled "Undo" for edits in large sequences
- Added DNA ladders from DyneBio
- Added supercoiled MW markers from ELPIS BIOTECH and New England Biolabs
- Added BsmBI-v2 to the list of enzymes available from New England BioLabs
- Added fields for username and email address in the license registration dialog

Enhancements:
- Optimized storage of history for the following operations: Change Methylation, Change Transformation Strain, Set Origin, Flip, Insert/Delete/Replace, Linearize, Circularize
- Updated the supported protein feature types by adding new types (NonStdRes, Protein, Precursor, SecStr, Het, CDS, gene, misc_feature, unsure, variation), promoting Region subtypes to types, and adding new Site and Bond subtypes
- Added a note in Features view to indicate the presence of internal stop codons in a translated feature
- Enhanced the Preferences tools to allow more flexible default options for displaying ORFs
- Enabled carrying over feature qualifiers when creating a protein sequence using "Make Protein" or "Reverse Translate"
- Added the option to merge segments when using "Make Protein" on a multi-segment DNA feature
- Added a "Hide noncutters" check box in the Choose Enzymes dialog
- Enabled importing features from any supported file type when using "Import Features from a SnapGene File"
- Enabled more flexible batch conversion of chromatogram traces to other formats
- Improved search performance for large DNA sequences
- Configured the minimap to show both scrolled areas when two copies of Sequence view are visible
- Updated the format of the Preferences dialog, and added an "Agarose Gels" tab
- Added the option to designate a new collection as the Main Collection
- Enabled saving imported online sequences directly to a collection
- Added shortcuts in a collection Overview for navigating to the DNA Files, Protein Files, or Miscellaneous Files sections
- Enabled symbols to be entered in search queries when searching SnapGene Online Sequences
- Increased the size of the length indicator in the map label at the "Small" font size
- Consolidated all Fisher MW Markers for agarose gels in the Fisher Scientific set
- Configured the Nonredundant Commercial enzyme set to include similar enzymes that differ by methylation sensitivity
- Configured SnapGene to show the Launch dialog on macOS when the SnapGene icon in the Dock is clicked, if no SnapGene windows are open
- Changed the icon for enabling interrupted circle format for a linear DNA sequence in Map view
- Configured the "Export Map" and "Export History" options to be always enabled
- Improved the wording of various menu options and dialogs to provide greater clarity and consistency
- Added a message informing the user that files can be dragged into the list when using Align Multiple Sequences

Fixed:
- Fixed an issue that prevented cloning dialogs from allowing the use of hidden enzymes
- Corrected an issue in "Protein Search" whereby terminal stop codons were not included in the search query
- Ensured that edits in an alignment window do not cause inappropriate scrolling
- Corrected an issue that could prevent alignment of a high-quality sequence trace
- Ensured that the "Find" control in the Enzymes view chooser always shows a message to indicate if the enzyme is not in the chosen set
- Corrected an issue in which U's in overhangs resulting from linearizing were not preserved
- Configured "Select All" in the trace viewer context menu to actually select all
- Ensured that History view reflects changes after editing DNA ends
- Ensured that case changes in the "Find" entry field are preserved when the search is executed
- Ensured that imported RNA alignments are converted to DNA rather than protein alignments
- Corrected the license inactivity countdown to displays seconds rather than milliseconds
- Ensured that the "Accession Number:" label remains next to its entry field in the collection Search dialog
- Ensured that a "Sequence Name" search in the Protein Files area of a collection also searches the map labels and aliases
- Corrected an issue that resulted in alignment and collection windows not showing unsaved changes in the title bar on Windows and Linux
- Ensured more consistent sorting of enzymes in the Choose Enzymes dialog
- Streamlined the substitution matrix options presented when computing pairwise alignments
- Ensured that open alignments can be used as profiles when computing new alignments
- Corrected an issue that could result in the "Kind" column disappearing when viewing a collection
- Ensured that crisp screenshots are shown when detecting updates
- Improved import of the full publication date from PubMed
- Made various stability fixes

Attribute Changer 相關參考資料

Download SnapGene 5.2.0 - Softpedia
Download SnapGene - Plan and simulate DNA manipulations, visualize ORFs and ... in Map view, and bases can be colored by GC or AT in Sequence view. https://www.softpedia.com
SnapGene Viewer - 下載
SnapGene Viewer, 免費下載. SnapGene ... SnapGene Viewer 是在由GSL Biotech LLC開發類別Miscellaneous Shareware 軟體。 ... 2020/10/08, Calibre 5.2.0 ... https://snapgene-viewer.update
SnapGene Viewer | Free software for plasmid mapping, primer ...
SnapGene Viewer is revolutionary software that allows molecular biologists to create, browse, and share richly annotated DNA sequence files up to 1 Gbp in ... https://www.snapgene.com
SnapGene | Software for everyday molecular biology
SnapGene Viewer · SnapGene is so easy to use that my lab adopted it instantly. · SnapGene is AMAZING. · SnapGene is awesome. · SnapGene is a most excellent ... https://www.snapgene.com