Welcome to a revolution in Geneious!

With Geneious, you can:

Generate vector
Import and align DNA and RNA sequences
Generate protein sequence alignments
Generate, edit, and align protein topology models
Generate, edit, and align protein structure diagrams
Streamline traditional gene editing
Convert, edit, and inspect multiple sequence alignments
Query sequence databases from within Geneious

Enhance your knowledge of Geneious:

Enhanced help document
New Tips & Tricks with Geneious videos
Interactive help cards inside the editor window

Why choose Geneious over other gene editing programs?

With Geneious, you control the entire editing experience.
You always work directly inside the program, and your custom changes are never lost.
Convert and inspect your sequence alignments with a detailed editor view.
The integrated sequence comparison feature will save you time and simplify your research.
Seamlessly convert and edit DNA and RNA sequences with support for all types of nucleic acid reference and sequence datasets.
Create, edit, and compare protein topology diagrams.
Edit and interact with protein structure diagrams.
View and edit multiple alignments in three dimensions.
See how your changes look in context to the sequence, the alignment, and the structure diagram.
Use the advanced merging features to quickly produce a more in-depth sequence.

Geneious Cloud-Based
Online Help for Geneious

Access help for the latest version of Geneious from the cloud

Geneious Cloud-Based
Online Help for Geneious allows you to get help as you need it, whenever you need it.

Never lose your changes.

Any custom changes you make in Geneious are saved in the cloud.

Never lose your changes.

Data is always safe.

As soon as you have saved a file to the cloud, it is instantly available to you from any of your devices.

Data is always safe.

Data is always safe.

We promise:

We value your privacy.

Data is always safe.

Data is always safe.

We promise:

We value your privacy.

Never lose your changes.

Data is always safe.

Data is always safe.

We promise:

We value your privacy.

We value your privacy.

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Bioinformatics is the new phylum of biology, and much like other pursuits, there are countless resources online to help you carry out your bioinformatics research, and one of them is BioTools. The bioinformatics program enables you to research the basis of life, formulate hypotheses, and discover the latest discoveries.
The program’s core functions include organizing and managing different sequences (including those extracted from the DNA and RNA databases, as well as in-house data), detecting and recognizing similarities, determining and managing nucleotide variations, examining conformational abnormalities, and ultimately, evaluating the success rate of sequencing technologies.
With BioTools, you can perform molecular analyses, identify multiple sequence alignments, identify short sequences, extract peptides, process base differences, and create nucleic acid alignments.
BioTools also facilitates protein bioinformatics analyses by providing you with a space for sequencing your own protein data. Moreover, it also allows you to compare protein sequences, discover short sequences, predict proteins, examine protein-protein interactions, and analyze the primary sequences. You can also view sequences and construct protein-DNA superimposed structures using this program’s integrated molecular viewer, as well as identify protein isoforms.
In short, BioTools enables you to find the answers you are seeking quickly and efficiently, and it’s available in the form of free or trialware versions.

Since there’s a growing number of strains of the virus circulating around the globe, the growing need for accurate diagnostic tools is bigger than ever. All this means that the testing methods have to keep improving so that we can have a reasonably sure grip on what kind of epidemic we are dealing with. In the past, diagnostic kits relied on visual tests, namely the identification of forms of visible infection, such as the formation of plaques, or the formation of cell bodies. But those were soon unable to deliver on their promise because they lacked the accuracy required to provide the necessary information.
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CLC Sequence Viewer is an all-in-one bioinformatics application created by the company MAJIQ. Among its primary features, the application helps you handle multiple sequence alignments, detect conserved regions in homologous sequences, display multiple sequence alignments, and perform genetic translations. In addition, it helps you do many of the things needed to complete popular bioinformatics analyses, as well as record meta data.
To be more specific, the software supports the following: RNA multiple alignments, DNA multiple alignments, protein multiple alignments, and protein sequence alignments; reverse complement sequences; consensus sequences; genetic translations; alignment window options; left-align, right-align, and center-align; and the molecular weight, the number of amino acids, isoelectric point, and the codon.
It is especially designed to make bioinformatics analyses go smoothly by providing an intuitive user interface based on which you can easily explore the various options and complete all the tasks demanded.
The CLC Sequence Viewer setup package installs a user manual that explains all the features of the program in plain and simple language.
CLC Sequence Viewer Requirements:
It is neither difficult to start using CLC Sequence Viewer, as it provides a set of instructions for using it in the user manual, nor is it difficult to use on Windows XP/7/8, as the software works on both of them.
CLC Sequence Viewer User Interface:
In terms of the user interface, CLC Sequence Viewer provides a number of tabs, the first of which is called navigation. Right below the navigation area, it sports a toolbox, which provides access to a number of useful tools. The middle panel serves as the view, while the side panel is where you can make adjustments to the tabs in the view.

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CLC Sequence Viewer is a user-friendly DNA analysis software. It is a GUI software for visualization and analysis of nucleic acid sequences. With CLC Sequence Viewer, you can:
• View nucleotide sequences.
• View nucleotide alignments.
• Use multiple sequence alignment.
• Annotate sequences.
• Calculate DNA/RNA secondary structure.
• Create DNA/RNA sequence alignments for sequence similarity searches (BLAST).
• Calculate molecular weight, composition, and iso electric point.
CLC Sequence Viewer is the first available GUI version of CLC Sequence Viewer from CLC Bio.. It is written in C++ and delivered as both 32-bit and 64-bit version. It was developed by CLC Bio. CLC Sequence Viewer can be used on Windows operating systems. It is available for purchase on CodePlex.
CLC Sequence Viewer supports the following file formats:
• BAM
• CAB
• DNA (dna/rdna/rdna_part)
• FASTA
• GFF
• GenBank
• IDNA
• Index
• IDP
• InterPro
• LASTA
• MAF
• Mate
• PDB
• SAM
• WIG
• WIG.gz
• ZIP
Program Features:
• Import and export sequences in the following formats:
> FASTA
> FASTQ
> GFF
> FASTGFF
> FASTQ.gz
> FASTA.gz
> FASTQ.gz.gz
> GenBank
> GenBank.txt
> GFF.gz
> FASTGFF.gz
> FASTA.xml
> GenBank.xml
> GenBank.xslt
> GenBank.xml.gz
> WIG.sam
> WIG.inf
> GenBank.tsv
> GenBank.xml.gz.tsv
> GFF.sam
> GFF.inf
> GFF.xml
> GFF.xml.gz
> GFF.xml.gz.tsv
> GFF.txt
> GenBank.tsv.gz
> GenBank.txt.gz
• RNA/RDNA
• IDNA/RIDNA
• PARS
• BLASTN/WU-BLASTN
• Predict
•

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