Plex Media Server

最新版本 SnapGene Viewer 5.3.0

SnapGene Viewer 5.3.0

SnapGene Viewer 5.3.0
Plex Media Server 連接您所有的本地和在線媒體 Plex 客戶端。集中的圖書館管理,在線內容的流式傳輸和轉碼功能的結合提供了靈活性和易用性。 Plex Media Server 在 Mac,PC 或兼容的 NAS 設備上運行,並向您的所有 Plex 客戶端(包括啟用 Plex 的移動設備和智能電視)提供媒體服務。

Plex Media Server 功能:

讓您的媒體更加美麗
Plex 為您提供了一個簡單的界面, :您的電影和電視收藏,音樂庫以及所有照片和家庭視頻。 Plex 通過添加說明,劇情總結,海報和專輯封面來豐富媒體庫。在家中或任何移動設備上的每台電視機上享受您的媒體。

Plex 跟踪您的媒體
最近添加的內容顯示在前面和中心,因此您可以立即看到什麼是新的。 Plex 也知道你正在觀看哪些電影和節目,所以你可以輕鬆地拿起你離開的地方或播放下一集.

在大多數設備上可用
在你的 Windows,Mac 或 Linux 計算機上運行 Plex Media Server 並流到你的 iOS,Android,Windows 電話 8 或 Windows 8.1 設備。你家有多台電視機?沒問題,Plex 也適用於 Chromecast,Amazon Fire TV,Roku,Google TV,Xbox,PlayStation®,VIZIO 以及許多新型智能電視。 Plex 甚至可以在大多數網絡連接的存儲設備上使用.

播放列表,用於無盡的娛樂
創建自己的自定義音樂或視頻播放列表,以適應任何場合,包括基於流派,收藏等的智能播放列表。您甚至可以導入現有的 iTunes 播放列表,智能播放列表,評分,曲目計數和其他詳細信息!播放列表可在 iOS 和 Web 應用程序中使用,但 Plex 團隊將努力將其帶入所有平台.

您的大屏幕最好的朋友
Plex 將您從單屏查看中解放出來。借助 Plex Companion,您可以將精彩內容從手機投射到電視上。當你上床睡覺的時候,請繼續在平板電腦上看電影。當電話鈴響時,暫停一個插曲,跳過你聽過太多次的曲目或者只是了解更多關於你正在用世界上最好的遙控器觀看的東西.

與朋友和家人分享你的媒體
輕鬆地在朋友之間分享媒體,所以你們都可以一起發現和享受更多的內容。通過分享您的度假照片和家庭視頻,與遙遠的家庭成員交換珍貴的回憶。現在,你也可以看到你的朋友是從你的收藏中流出的,因為每個人都有自己的觀點進入你的圖書館。

訪問你最喜歡的在線內容
Plex 頻道提供訪問眾多的在線內容來源,如 TED 講座,Vimeo,修訂 3,等等。無論您的興趣是什麼,您都可以找到很棒的東西來觀看或推薦給您的朋友,所有這一切都在 Plex 華麗的界面中呈現出來.

世界級的 DLNA 支持內置於
Plex 讓您的媒體在成千上萬的 DLNA 認證設備像 PS3,Xbox 360 和 WDTV Live 設備,而無需安裝專用應用程序。利用最複雜 DLNA 服務器的強大功能,輕鬆將任何格式的流式傳輸到您的設備,開箱即用.

立即保存,稍後觀看
輕鬆保存您喜愛的網站的在線視頻,稍後即使在大屏幕上觀看。或通過向朋友推薦視頻來分享體驗.

注意:Plex Pass 需要使用同步功能,將用戶添加到您的家中,查看預告片和其他附加內容,從移動設備上傳內容,使用 Gracenote Music Magic.

ScreenShot

軟體資訊
檔案版本 SnapGene Viewer 5.3.0

檔案名稱 snapgene_viewer_5.3.0_win.exe
檔案大小
系統 Windows 7 / Windows 8 / Windows 10
軟體類型 免費軟體
作者 Plex, Inc
官網 https://plex.tv/downloads
更新日期 2021-05-14
更新日誌

What's new in this version:

New Functionality:
- Added support for viewing features in multiple sequence alignments
- Enhanced History view with a Text format tab, and with an option to show the entire history
- Added support for RNA sequences as .rna files
- Enabled viewing files of all types simultaneously in a Collection using a new "All Files" area
- Enabled gaps to be displayed every 10th base for protein sequences, and every 10th or 3rd base for nucleotide sequences
- Added support for filling in DNA ends of annealed oligos to create a double-stranded DNA sequence
- Added support for annotating primers that anneal at the 5’ end but not the 3’ end
- Enabled viewing and printing chromatogram files in a wrapped multi-line format
- Improved the conversion of .geneious nucleotide and protein sequences and alignments
- Added DNA Ladders from Ecogen, TIANGEN, and Vazyme

Enhancements:
- Extended the range for the minimum required 3' match for primers from 25 to 35 bases
- Enabled export of alignments to rich text format .rtf files
- Enhanced the visualization of mutagenesis simulations and mutagenic primers
- Enhanced the response to mousing over a primer so that the binding site is now highlighted in gray
- Added support for /protein_id qualifiers for mat_peptide features
- Enabled printing to PDF on macOS when no printers are installed
- Added an indicator in the selection bar to show "DNA" or "RNA" as the sequence type
- Enhanced enzyme, feature, and primer label layout in Map view for linear sequences
- Added clickable "contact support" links to messages that pop up in various places
- Made terminator features directional in the common features database
- Added the keyboard shortcuts Cmd+1 / Cmd+2 / Cmd+3 for switching between tabs in chromatogram windows
- Enhanced cursor placement, highlighting, and trace data tooltips when the mouse cursor is between bases
- Changed the "Replace" button label in Collections to "Bulk Edit" for improved clarity and accuracy
- Improved primer binding sites to avoid bulges if a 5' N tail is present in the primer sequence
- Updated the MAFFT aligner to version 7.471
- Updated the Parasail aligner to version 2.4.2
- Added a shortcut (Shift + Spacebar) for scrolling one page up in multiple sequence alignments
- Streamlined toolbar on macOS

Fixed:
- Rationalized the View menu to show options relevant to the file type
- Removed the "Browse..." menu action that had no effect in the "Import Primers from a SnapGene File" dialog
- Adjusted the tooltips for buttons in the "Find" bar to make them more consistent with other tooltips
- Changed the heading in the Collection search dialog for Protein Files to say "Names" rather than "Names & Numbers"
- Ensured that only a single /mod_base qualifier is allowed for modified_base features
- Added a ruler for protein sequences when viewing in compact format
- Fixed a bug with selection of the last item in Features, Primers, and Enzymes views
- Implemented immediate update of the version listed on the account administrator page after SnapGene is updated
- Corrected a regression in which sequence selection was lost after clicking in the Description Panel
- Corrected a regression with enzyme site selection in Lines mode of Enzymes view
- Ensured consistent display of the selection when switching to Sequence view
- Fixed an issue in which spaces were not shown after commas on macOS Big Sur
- Fixed a non-functional "Choose Enzymes..." command in the "Choose enzyme set" dropdown menu
- Corrected a regression that caused overtyping of characters in the primer name fields of the Simulate Agarose Gel dialog
- Ensured correct refreshing of primer binding sites when changing hybridization parameters
- Prevented truncation of 3' overhangs that extend beyond the end of a circular sequence
- Prevented input of an invalid location in the Go To dialog for sequences aligned to a reference DNA sequence
- Fixed some tabs that displayed as white text on a white background on macOS Big Sur
- Ensured that features are not lost from inserts in cloning operations when windows are opened or closed
- Corrected the color of the gray bar below the list box in the Collection interface
- Prevented "< Please choose >" from being propagated from the Anneal Oligos dialog to the oligo names in the resulting history
- Ensured that in the Anneal Oligos dialog, a double-click on a compatible enzyme is needed to transfer focus to the Restriction Enzymes dialog
- Configured the pull-down menus in the Anneal Oligos dialog to refresh when documents are opened or closed
- Ensured that the specified font size is used when printing the Description Panel
- Fixed an issue with the folder location used when exporting standard common features
- Improved scrolling performance in Enzymes view
- Fixed the default file name chosen when exporting a single file from a Collection
- Improved the reliability of displaying the warning in the Print dialog on Windows about printing to PDF
- Ensured that tabbed window controls on macOS are reliably shown
- Improved the background color display in Map view
- Fixed issue in which keywords could be used as the construct name for some GenBank/GenPept files
- Improved the opening of SeqBuilder files
- Addressed issues with importing references from another file
- Improved the quality when exporting maps at high resolutions
- Updated Map, Sequence, and other views when protein sequences are zoomed
- Implemented hiding of zoom controls in a collection when switching from a long sequence that supports zooming to a shorter one that does not
- Prevented unnecessary display of a message about unsupported qualifiers during NCBI import when the content includes nonstandard qualifiers (e.g., /UniProtKB_evidence) that are deliberately converted to /note qualifiers
- Corrected an issue in which some line breaks in /note qualifiers were not preserved when opening GenBank or GenPept files
- Addressed a potential stability issue when viewing protein files
- Fixed copying of maps and histories on macOS, and improved the quality when pasting such content into applications such as Microsoft Word or PowerPoint on macOS
- Improved the message shown when attempting to use a sequence over 1 Mbp to compute a pairwise alignment
- Ensured correct identification of macOS Big Sur when sending anonymous user statistics
- Ensured correct display of a trace file icon in the Windows menu
- Fixed various issues with specifying and displaying the /collection_date qualifier
- Addressed an issue that could result in sequence characters moving slightly after periods of no mouse activity on Windows and Linux
- Simplified the choice of a destination folder during import into a collection by making the "Add" button the default
- Improved the display of feature names on Windows during pliancy and selection
- Fixed the Redo shortcut on Linux
- Improved margins and alignment in various windows and dialogs
- Improved the default placement of a window created via File → Open when no document was previously open
- Improved stability while viewing collections
- Avoided duplication of DNA documents in the Window menu after converting to single- or double-stranded format
- Corrected the shortcut for Overlap Extension PCR of two fragments
- Ensured that if the side toolbar button is used to show alignments and there are no currently aligned sequences, the software asks which files to import to align to the reference sequence
- Corrected an issue in which unmodified alignment documents sometimes indicated unsaved changes
- Corrected issues with dragging collection files onto other applications
- Fixed a crash when saving an alignment to a collection
- Disabled "Actions → Convert to Single-Stranded..." when viewing alignments
- Corrected an issue that prevented conversion of a feature translation to upper- or lowercase if the last selected codon was located at the end of the sequence
- Fixed a bug in which an open document might not be listed in the Window menu or in the lists of open documents in cloning dialogs, while the launch dialog would remain visible
- Fixed an issue that could result in two copies of the application running on macOS
- Ensured correct rendering of multi-region Site features that span multiple rows in Sequence view
- Addressed a stability issue when exporting and opening the alignment consensus
- Removed the dead "Browse..." action in the source menu when importing features from BED, GFF3, or GTF files
- Ensured that "Primers → Sort Primer List..." executes the desired sort
- Updated outdated web links to online resources
- Ensured correct residue numbering for Smith-Waterman (local) pairwise alignments

SnapGene Viewer 5.3.0 相關參考資料
Download SnapGene 5.3.0 - Softpedia

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Release Notes - SnapGene

Release Notes &middot; View Features in Multiple Sequence Alignments &middot; View and Export History in Text Format &middot; RNA Sequence Files &middot; New &#39;All Files&#39; Area in Collections.

https://www.snapgene.com

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SnapGene Viewer 5.3.0 Free Download 2021 Latest - BytesIn

SnapGene Viewer is an excellent tool for viewing DNA maps with ease. It works very well in conjunction with Snapgene, a software that lets you create and...

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SnapGene Viewer is revolutionary software that allows molecular biologists to create, browse, and share richly annotated DNA sequence files up to 1 Gbp in&nbsp;...

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