#SERIAL CLONER FEATURE IMPORT GENBANK HOW TO#
#SERIAL CLONER FEATURE IMPORT GENBANK PDF#
#SERIAL CLONER FEATURE IMPORT GENBANK SERIAL#

Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.) Filing date Publication date Family has litigation Priority to US201261652086P priority Critical Priority to US201261716256P priority Priority to US201361757640P priority Priority to US201361765576P priority Priority to US13/842,859 priority patent/US10266850B2/en Application filed by Universitaet Wien, University of California filed Critical Universitaet Wien Assigned to UNIVERSITY OF VIENNA reassignment UNIVERSITY OF VIENNA ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Original Assignee Universitaet Wien University of California Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.) DOUDNA Martin Jinek Emmanuelle Charpentier Krzysztof Chylinski James Harrison Doudna Cate Wendell Lim Lei Qi Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.) Granted Application number US13/842,859 Other versions US10266850B2

#SERIAL CLONER FEATURE IMPORT GENBANK PDF#

Google Patents Methods and compositions for rna-directed target dna modification and for rna-directed modulation of transcriptionĭownload PDF Info Publication number US20140068797A1 US20140068797A1 US13/842,859 US201313842859A US2014068797A1 US 20140068797 A1 US20140068797 A1 US 20140068797A1 US 201313842859 A US201313842859 A US 201313842859A US 2014068797 A1 US2014068797 A1 US 2014068797A1 Authority US United States Prior art keywords dna activity cell site targeting rna Prior art date Legal status (The legal status is an assumption and is not a legal conclusion. Google Patents US20140068797A1 - Methods and compositions for rna-directed target dna modification and for rna-directed modulation of transcription

Getting Started with MacVector: An overview of primer design workflows in MacVector.US20140068797A1 - Methods and compositions for rna-directed target dna modification and for rna-directed modulation of transcription.

Melissa Caimano on HOW DO I video guides to common molecular biology workflows.

admin on HOW DO I video guides to common molecular biology workflows.

mariam abdelmalak on Major release details – Summary.

Brian on Designing primers and documenting In-Fusion Cloning with MacVector.

Chris on Designing primers and documenting In-Fusion Cloning with MacVector.

Simulating DNA electrophoresis in agarose gels using MacVector’s Agarose Gel tool.

#SERIAL CLONER FEATURE IMPORT GENBANK HOW TO#

MacVectorTip: How to copy a specific short amino acid translation of a sequence.MacVectorTip: Trimming trace files by quality.MacVectorTip: Identifying, Selecting and Assembling NGS reads with a variant genotype.

#SERIAL CLONER FEATURE IMPORT GENBANK SERIAL#

MacVector will directly import many file formats such as common sequence formats such as Genbank, FASTA, FASTQ plus from software packages such as Sequencher Projects and Serial Cloner, For example you may prefer features to be displayed on just those two levels instead of being distributed over the multiple levels as per the default settings. However, MacVector’s graphics are highly customizable and you can adjust the graphical settings to display the plasmid exactly as you want. This sequence was opened using the MacVector defaults. It’s been opened directly in MacVector by double clicking the file. Here’s a plasmid sequence downloaded from the Addgene website in Snapgene format. However, Snapgene will always place features on the same two levels and so features sometimes overlap. For example MacVector has multiple levels (up to six) outside and inside a plasmid and will always try to place features so that no feature overlaps another. However, there are some aspects to the display that are not the same between the two applications. The colors of features will be the same as the original. When you import a Snapgene file the appearance will be very similar.

This is very useful when downloading plasmid sequences from the wonderful Addgene plasmid repository. You just need to use FILE | OPEN or double click the file. MacVector will directly import SnapGene DNA files.

Serial cloner feature import genbank