Brave Browser (64-bit)

最新版本 SnapGene Viewer 6.0.0

SnapGene Viewer 6.0.0

SnapGene Viewer 6.0.0
新的勇敢的瀏覽器 64 位自動阻止廣告和跟踪器,使其比目前的瀏覽器更快,更安全。除了真實的內容,一切頁面的加載速度都是驚人的。最多 60%的網頁加載時間是由每次在您最喜歡的新聞網站上打開頁面時加載到各個位置的基礎廣告技術引起的。其中 20%的時間花在加載試圖了解更多關於你的東西上。下載勇敢的瀏覽器 64 位脫機安裝程序安裝程序!

Brave 底層是一個基於 Chromium 的網絡瀏覽器,這意味著它的性能和網絡兼容性是非常相似的基於 Chromium 的其他瀏覽器.

Brave 瀏覽器功能:

Browse 更快 61225896Brave 塊跟踪和侵入性的廣告,可以放慢你在網絡上.

瀏覽更安全
Brave 64 位讓你和你的信息更安全,有效地屏蔽你從第三方跟踪和 malletin.

Browse Better
With 勇敢,你可以選擇是否看到廣告,尊重您的隱私或支付網站直接。無論哪種方式,您都可以在幫助資助內容創作者方面感覺良好.

阻止有害的廣告
在城裡有一個新的廣告遊戲。這就是所謂的“惡意廣告”。最新的展示廣告技術可以在您不知情的情況下在您的筆記本電腦上安裝惡意程但不能與勇敢的看著你的後背.

Brave 將網站重定向到 HTTPS
“我們已經將 HTTPS Everywhere 集成到每個勇敢的瀏覽器中,以確保您始終將您的位移到最安全的管道。下載勇敢的瀏覽器 64 位離線安裝程序安裝程序!

阻止塊跟踪像素和跟踪 Cookie
您是否曾經有過這樣的感覺,即當您看到某個廣告前幾天購買了某個東西時,有人在註視著您?當您在網上購物並瀏覽您最喜愛的網站時,我們確保您沒有被追踪.

也可用:下載 Brave Browser for Mac

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軟體資訊
檔案版本 SnapGene Viewer 6.0.0

檔案名稱 snapgene_viewer_6.0.0_win.exe
檔案大小
系統 Windows 7 64 / Windows 8 64 / Windows 10 64
軟體類型 開源軟體
作者 Brave Software Inc.
官網 https://www.brave.com
更新日期 2021-11-30
更新日誌

What's new in this version:

New Functionality:
- Added a tool for adding enzymes sites to a coding sequence by silent mutation
- Added a tool for removing an enzyme site from a coding sequence by silent mutation
- Added support for custom features types not included in the standard set of GenBank feature types
- Enabled changing the default color of standard Genbank feature types
- Added support for saving and loading Agarose gel simulations as .gel files
- Added support for features within pairwise alignments
- Enabled adding, editing and deleting features in alignments
- Added a features table when viewing pairwise and multiple sequence alignments
- Enabled searching an alignment to find features
- Enhanced Gibson, InFusion and NEBuilder HiFi Assembly simulation tools to allow the vector to be flipped
- Enhanced cloning simulation tools to support adding, removing and re-ordering sequences
- Included controls to filter the set of chosen enzymes based on the number of times and relative location an enzyme cleaves with respect to its recognition sequence
- Enabled setting a default Codon Usage Table
- Added tool for converting ng/uL to nM in the DNA Calculations dialog
- Added base counts to the DNA Calculations dialog

Enhancements:
- Enhanced the 'Blocks of 3' Sequence view format to enable aligning nucleotide triplets with the reading frame
- Support for optionally displaying sequence names alongside the sequences when printing pairwise and multiple sequence alignments
- Switched from "?" to "X/Xaa" in translations to represent ambiguous amino acids
- Added Tm for the selected region in ssDNA sequences
- Added a locking mechanism which sets files as read only to other instances of SnapGene when being edited. Note that the locking mechanism is not available on large files, and has short delay, so is not effective when files are opened simultaneously
- Convert Psi to U when importing or creating a new RNA sequence
- Added support for including binding site locations when exporting primer data
- Added Gateway Cloning destination vectors pEXP3-DEST and pEXP4-DEST, and updated cross-references in descriptions for pEXP-DEST Vectors
- Features and custom numbering are now retained when copying and pasting into the New Protein File dialog, or inserting or replacing residues in a protein sequence
- Added support for pasting copied complementary primer pairs to configure an Agarose Gel lane
- Improved explanation for how to change sequence methylation when an enzyme is blocked during Restriction Cloning
- Added support for adjusting the resolution (ppi) and creating a transparent image when exporting maps from the command line interface
- Included various textual enhancements

Fixed:
- Included Nicking enzymes in the 6+ Cutters enzyme set
- Remove secondary recognition sequence for TaqII as this does not result in cleavage
- Restore last shown enzyme variant when returning to a previously viewed enzyme in the Restriction Enzymes window.
- Reduced file size and sped up loading files by omitting features in History view for large ancestral sequences
- Added support for the following non-standard qualifiers for all translatable feature types: calculated_mol_wt, codon, codon_start, exception, protein_id, transl_except, transl_table, translation
- Non-standard qualifiers are now retained when importing and exporting (previously they were converted to /note)
- Added support for /transl_table and /codon_start qualifiers with CDS features in protein sequences
- Fixed an occasional issue on macOS where an empty SnapGene window appears which cannot be closed except by restarting SnapGene
- Disabled subsidiary check boxes when appropriate in Preferences
- Corrected mouse-over effects for Site features with multiple segments
- Fixed an issue that prevented setting a protein point feature type to misc_feature, unsure, or variation.
- Automatically change feature color when changing the type when adding a point feature if the color has not been manually adjusted.
- Fixed an issue where U's were not converted to T's if either end of a linear DNA sequence is modified to be covalently closed.
- Fixed an issue where unsaved files added to the align sequence tools were listed using the wrong name
- Fixed an issue that sometimes prevented run-on translations from being shown in alignments
- Ensured it is always possible to scroll to the last base in DNA files
- Removed inappropriate methylation message which was shown when opening the features tab for some protein files
- Corrected an issue that prevented pliancy from being shown when using the "Choose Alternative Codons" tool
- Corrected various display issues when switching a lane in an agarose gel simulation to using a MW marker
- Fixed an issue that prevented point features from being added to protein sequences
- Require a product name to be specified when using the Mutagenesis tool
- Ensured bases are always visible when history colors are shown
- Always show shared codons in adjacent translated features within Sequence view
- Fixed Align to Reference DNA sequence so that undoing sequences edits no longer hides the aligned sequences
- Reliably display ORF's that wrap around the numerical origin in circular sequences
- Fixed an issue that prevented some keyboard shortcuts from working while the launch dialog was visible on Linux
- Correctly show the Description Panel by default when this preference is toggled on
- Ensured the navigation buttons in the Choose Alternative Codons tool are properly enabled
- Corrected an issue with searching for features in protein sequences when Region features are not shown
- Fixed an issue where qualifier selections in Features view were lost when switching tabs
- Fixed an issue where using undo while viewing an alignment to a reference sequence resulted in expanded aligned sequences being collapsed.
- Fixed issues with Make Protein and Copy Translation with two abutting in-frame translated Features for which a codon spans the feature boundaries
- Fixed lagging selection of checkboxes on windows when importing primers
- Enabled jumping to next/previous regions across the origin using "Next/Previous Aligned Region" buttons
- Clarified dialogs to indicate Java 8 is supported for Vector NTI Express database import
- Fixed the default folder in Preferences > Files for opening being ignored by Open Files
- Corrected an issue that resulted in primer names not being included in default document name when creating a new file from a primer pair selection
- Fixed an issue that prevented using the NEBuilder tool with primers that are separated by less than 50 bp
- Corrected an issue with refreshing the list of sequences after clearing the search control when using the Import SnapGene Online Sequences tool
- Fixed an issue that prevented using preexisting non-overlapping PCR primers for the vector when using the NEBuilder tool
- Corrected an issue that prevented dragging and dropping files onto Agarose Gel windows
- Corrected an issue that prevented shown chosen enzymes when switching between documents in a collection
- Removed unnecessary horizontal lines that remained after removing references in the Edit References window
- Improved default size of the Edit References window
- Corrected an issue with displaying the selection length for selections with sticky overhangs
- Improved stability when making selections in sequences aligned to a reference
- Removed ambiguous codons when using the Insert Codon and Choose Alternative Codons tools
- Improved stability when using Opt-click to close all files
- Improved overall stability and corrected various memory leaks
- Restore selected history operation and display of history colors after undoing hiding an operation.
- Corrected an issue where an erroneous message was shown indicating a purchase was required before installing an available software update.
- Improved the name and icon shown for alignment documents in Window menus
- Fixed an issue that prevented correctly displaying where sequences align to a reference sequence in Map view.
- (Reported by Lauri Lintott)
- Improved the appearance of simulated agarose gels on screen and when exporting to a file
- Improved stability when saving multiple files in a collection
- Improved the appearance of site features in linear maps when printing and copying to the clipboard.
- Ignore collection index conflict flies created by OneDrive.
- (Reported by Andras Solt)
- Fixed an issue that prevented using selected primers to pre-populate controls in PCR-driven cloning dialogs.
- Fixed position where the add/edit/duplicate protein feature dialogs appear
- Improved stability when clicking on Save to Main Collection without a file selected
- Correctly display the sequence name above enzyme sets that are associated with a single sequence in the side toolbar menu
- Stability fixes when using splice to remove intros and new file from selection
- Fixed wrong shortcut showing on Windows in search type combo box for search bar (Meta→Alt)

SnapGene Viewer 6.0.0 相關參考資料
Adjust the Configuration - User Guides

2020年2月11日 — How can SnapGene be configured to adjust or disable some functionality? 1. Windows or Linux. Open the SnapGene settings file in a text editor.

https://help.snapgene.com

Command Line: Installation and Activation - User Guides

2021年8月30日 — Learn how to use the command line to install and manage SnapGene licenses. ... View License Information (Windows).

https://help.snapgene.com

Download SnapGene Viewer 6.0.0 - Softpedia

Download SnapGene Viewer - A user-friendly software solution that can come in handy for previewing your created DNA maps and analyzing enzymes or other ...

https://www.softpedia.com

Installation - User Guides

User GuidesSnapGene User GuideInstallation ... Line: Installation and Activation · Manage A SnapGene Subscription or Permanent License ... View all chapters ...

https://help.snapgene.com

Search for an Exact DNA Sequence - User Guides

2020年9月1日 — SnapGene will find matches to either GGTCTACTTC or GGTCTGCTTC. ... In Map view, a matching DNA sequence will be highlighted in blue.

https://help.snapgene.com

SnapGene User Guide

Change View Options for DNA Sequences · Display a Circular Plasmid as a Linear (Horizontal) Map · Show or Hide DNA Feature Labels · Show Restriction Site or ...

https://help.snapgene.com

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 lets you see your data for free with the same rich visualization, annotation, and sharing capabilities as the fully enabled SnapGene ...

https://www.snapgene.com

View an AB1 or SCF Trace File - User Guides

2021年9月14日 — Learn how to view a sequence trace/chromatogram file in SnapGene.

https://help.snapgene.com