SnapGene Viewer 5.1.4 軟體資訊介紹&下載

Canvas X,軟體教學,軟體下載,電腦問題,電腦教學
Canvas X 是一個繪圖,成像和發布計算機軟件從 ACD 系統的 Windows PC!作為尋求溝通的工程師,小型企業主和技術圖形專業人員的最佳資源,Canvas X 2017 提供了一個多元化,功效驅動的設計環境。這個可靠的軟件支持 64 位操作系統,並能夠處理超過 100 萬個對象的文檔。迎合廣泛的專業人士— 從圖形設計師到地震學家— Canvas X 2017 對性能進行了微調,並以閃電般的速度通過項目進行分解.

以優化的啟動,加載和保存速度,Canvas X 2017 具有豐富的用戶體驗,為長期用戶的可訪問性和舒適性而精心打造。憑藉其獨特的一體化設計環境,Canvas X 2017 使得圖形元素和高端效果更加直接的結合在一起,得益於各種效率驅動的增強功能。輕鬆訪問常用功能,實現更流暢的工作流程,輕鬆計算,動態編輯等等。為了取得成就,方便和總體易用性而開發,Canvas X 2017 提出了許多 UI 改進,以允許流體對象編輯。



只需右鍵單擊並從上下文菜單中選擇一個選項即可添加和刪除 SpriteEffects。


Rely 在 Canvas X 為桌面立即計算對象的尺寸,甚至無需定義開始和結束點。為了清晰和美觀,移動或刪除測量值.

Shrewd Shuffling

享受動態更新對其對象所做更改的影子的輕鬆感。自定義對象的顯示效果,以何種角度,多麼模糊,以及使用什麼顏色。Windows PC 的跨平台靈活性
Canvas X 允許您跨操作系統工作,支持為 Mac 文件導入 Canvas Draw。

Into Your Own Hands
Canvas X 2017 現在支持觸摸屏選擇,繪畫,繪畫等功能,所以即使在旅途中也可以創建。另外,雙指放大和平移!

敏捷和 Able
在記錄時間結束!更快,更強大,Canvas X 2017 擁有優化的啟動,保存和加載文件的速度.

注意:30 天試用版.

Canvas X Screenshot 1
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SnapGene Viewer 5.1.4


33.48 MB

Windows 7 / Windows 7 64 / Windows 8 / Windows 8 64 / Windows 10 / Windows 10 64


ACD Systems Inc


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

Canvas X 相關參考資料