What's New in MacVector?
Learn about changes in MacVector since the previous release.
Support
Learn more about this help and where to get additional help if needed.
MacVector Overview
Introduction to MacVector
Bringing Sequences into MacVector
How to bring your sequences into MacVector.
Using MacVector
Basic principles of MacVector.
Analyzing sequences
Restriction enzyme, alignments, primer design and subsequence searches.
Searching Databases
Accessing online databases, BLAST searches and local sequence searches.
Sequence Assembly
Contig Assembly, align cDNAs against genomic sequences and find SNPs.
How do I check the orientation of a ligated fragment.
How do I subclone digested fragments into a vector
How do I design Gibson Assembly/LIC strategies.
How do I determine RE sites for cloning.
How do I show/hide the RE Picker tool?
How do I import Genbank data from a web browser
How to do an online keyword search for sequences.
How do I bring sequences into MacVector.
How do I optimize codon usage.
How do I generate a transcript.
How do I translate a sequence.
How do I automatically annotate blank sequences or change the style of a sequence map.
How do I display missing features, predicted ORFs and restriction sites on my sequence.
How do I annotate a gene feature to my sequence.
How do I change the default appearance of features.
How do I import Features from a Genome Browser.
How do I determine RE sites for cloning.
How do I add a primer to the Primer Database
How do I design primers with tails and mismatches.
How do I design a pair of primers to amplify a gene?
How do I design a primer to match an existing primer
How do I make a permanent note of where my primer binds on a sequence
How do I test a pair of primers?
How do I quickly align sequencing reads against a reference sequence.
How Do I Map NGS data against a reference genome
How do I create a de novo assembly using Velvet
How do I create a de novo assembly using SPAdes
How do I assemble PacBio and NanoPore reads using Flye
How Do I start an Assembly Project
How do I finish a genome assembly
How do I extract specific reads from a FASTQ dataset.
How do I do compare read coverage of different reference assemblies?
How do I automatically sort a sequencing dataset into subprojects
How Do I identify important differences between two genomes
How Do I visually align a pair of sequences.