Download OmicsBox 3.4
Download here the latest version of OmicsBox for free (on the right). The download contains an executable installer which will install OmicsBox on your computer. Choose between Windows, Mac or Linux based versions.
Get the Installer from here:
How do I get an activation key?
Just click here and register with your name and email and we will send you your key immediately. Registration takes less than 1 minute.
System Requirements
- We recommend at least 8GB of RAM.
- A stable internet connection is required to use many of the application features.
- OmicsBox is available for macOS (12+) Intel or ARM architectures, Windows (10+) and Linux systems (Ubuntu 18.04+, Debian 8+, RedHat Enterprise Linux 8.9+, CentOS 9+). The Linux systems require the library version GTK 3.22+.
- OmicsBox supports automatic updates (write permissions required).
Please find more details in the User Manual under System Requirements.
Release History and Versions
Metagenomics
- New Taxonomic Classifications via Silva, Greengene and GTDB
Single Cell Transcriptomics
- Improved UMAP Performance for Large Datasets
Long Read Transcriptomics
- New Feature to Combine Transcriptomes with TAMA Merge
- Redesigned PacBio IsoSeq Pipeline
Transcriptomics
- Improved Time Course Data Analysis with Masigpro
- Improved Differential Expression Analysis Gene Filtering
- New Feature: Batch Renaming of Feature IDs for Count Tables and Differential Expression Results
- New Feature: Renaming and Deleting of Samples for Count Tables
Genome Analysis
- New Feature: Genome Assembly Completeness Assessment with Busco
General
- New Info Icon in all tabs to view analysis details
Single Cell Transcriptomics
- New: Cell Type Identification with SingleR
- Update: Interactive Single-Cell Visualization and Annotation Tool
- Update: Seurat v.5 – Update: Improved Trajectory Analysis with Monocle
- New: Autocorrelation Analysis via Monocle3
Long Read Transcriptomics
- New: Isoform Definition and Quantification with IsoQuant
- New: Reference-Free Long-Read Transcriptome with isON pipeline
- Update: FLAIR v.2 including Quantification
- Update: Curation of Long-Read Transcriptomes with SQANTI3 v.5
Transcriptomics
- Update: Busco Database – Update: EdgeR v.4
- Improved Gene-Level Quantification with HTSeq Count (now cloud based)
Genetic Variation
- New: Merge and Extract VCF Files
- New: Population Structure Analysis with ADMIXTURE
- New: Imputation and Phasing with Beagle
- New: Filtering for GBS data via dDocent Pipeline
Genome Analysis
- Update: Evidence-based eukaryotic gene predictions with Augustus
Functional Analysis
- New: Find Pathways via Annotations
General
- Improved Trimmomatic Wizard (now cloud based)
- Improved Application Messages
- OmicsBox now available for macOS ARM architecture
Functional Analysis
- Removed MobiDB-Lite from InterProScan due to the lack of GO information
Genetic Variation
- Fixed Issue when Saving MAGMA Objects
Transcriptomics
- Fixed GTF/GFF Input for STAR
- Fixed Issue for Cell-Barcoded and Full-Length Modality in STARsolo
- Fixed Single-cell Dimensionality Check for Count Matrix Import
- Improved STARsolo Chart for Genes Distributions in Percentages
Metagenomics
- Fixed Pairing Factor Issue of the Differential Taxonomic Abundance Analysis.
General
- More Specific Task Error Messages
- New Bubble Plot for GSEA
- Updated GO-Slim Links
- Fixed GO Annotation Taxa Filtering
- Added Single-Cell Count Matrix Dimension Check for MTX Format
- Improved Single-Cell Quantification Summary Report
- Fixed Bug in the STARsolo Wizard
- Changed maSigPro to apply a Negative Binomial Distribution
- Fixed Numeric x-Axis for maSigPro Expression Profiles
- Updated Pfam2GO Links
- Fixed Variant Annotation for Poliploides
- Improved File-Upload Resilience for CloudFiles
- Minor CloudFiles Improvements
Transcriptomics
- New Single Cell RNA-Seq Quantification Feature with StarSolo
- Improved Single Cell RNA-Seq Clustering with Interactive UMAPs
- Improved Single Cell RNA-Seq Trajectory Visualizations: Gene Trends and Expression UMAPS
- New Long-Read Aligner: Minimap2
Genetic Variation
- New Functional Analysis of GWAS Results with MAGMA
- New Variant Calling Option for Mixed-ploidy in Freebayes
- New feature to extract variant information from Variant Annotation using Manhattan Plots
General
- Improved Barcode Demultiplexing Supporting Paired-Ends
- Improved Job Progress and Status Messages
- Improved Proxy Configuration and Authentication
Metagenomics
- Custom Kraken DB Option for Taxonomic Classifications
Functional Analysis
- Custom Diamond Blast DB Option
Genetic Variation Module
- Fast Variant Calling with BCFtools and FreeBayes
- Variant Filtering
- Variant Annotation with Variant Effect Predictor (VEP)
- Guided Genome Wide Association Study
Transcriptomics
- Isoform Definition and Correction with Flair
Functional Analysis
- Faster Functional Annotation with Diamond Blast
- KEGG Pathways Analysis for commercial customers
Genome Analysis
- Genome Assembly Comparision and Qualitiy Assessment with QUAST
General Tools
- Barcode Demultiplexing with Cutadapt
General Improvements
- Redesigned Functional Enrichment Analysis Options throughout OmicsBox
- Improved Message Handling for Cloud Jobs
- Option to share Cloud Files
General Tools
- New Tool for the quality control of Long Read DNA-Seq Data
- New Tool for the quality control of RNA-Seq BAM Files
- New option to merge FastA/Q Files
Transcriptomics Module
General Improvements
- Restructuring of Menus and Side Panel Options for improved usability
- Introduction of CloudStorage
- Improved Workflows
Transcriptomics Module
- New Heatmap and PCA 2D/3D Plots
- New Single Cell Clustering Option
- Coding Potential Assesment now part of the Transcriptomics Module
Genome Analysis Module
- MLST feature as part the Genome Analysis Module
- Genome Browser now part of the Genome Analysis Module
Functional Analysis
- Plant Reactome Database for Combined Pathway Analysis
- New Pathway Analysis Charts
- Subcellular Localization Prediction with Psortb
Functional Analysis
Transcriptomics Module
- De-novo Isoform Discovery for PacBio Long Reads (Iso-Seq)
- Updates for Trinity (2.12.0), BUSCO (5.1.2) and STAR (2.7.8a)
Metagenomics Module
- rRNA Removal with SortMeRNA
- Contaminant Removal with Bowtie2
- Kraken and Pfam (v.34.0) Database Updates
Genome Analysis Module
- New DNA-Seq Alignment with Bowtie 2
- Improved Eukaryotic Gene Finding with Augustus
- Updates for ABySS (2.3.0), SPAdes (3.15.2), Flye (2.8.2), Augustus (3.4.0) and RepeatMasker
General Tools and Improvements
- User Authentication with Account Management
- More interactive charts
- New BAM Tool: Convert BAM to FASTA/Q
Metagenomics Module
- Taxonomic Classification: Kraken2 database update and new parameters
- Taxonomic Classification: New option to add, remove and rename samples
- Taxonomic Classification: Improvements to bar chart
Transcriptomics Module
- RNA-Seq de novo Assembly: Trinity update (v2.10.0), improved performance and new parameters
- GSEA for Pairwise DEA: Ranking is now based on p-values instead of the FDR
- RNA-Seq Alignment: STAR update (v.2.7.5a) and new reference fasta file format (.gz)
- RNA-Seq Alignment: New parameter to include Read Group (@RG) header and tags in BAM output
- Create Count Table Transcript-Level: RSEM update (v.1.3.3)
Genome Analysis Module
- DNA-Seq Polishing: Improved performance due to parallelized analysis
- DNA-Seq Alignment: New reference fasta file format (.gz)
- DNA-Seq Alignment: New parameter to include Read Group (@RG) header and tags in BAM output
- DNA-Seq Assembly (Flye): Flye Update (v.2.8) and support of PacBio HiFi data
- MLST: Database update and wizard improvements
Functional Analysis
- BLAST: New feature “Custom DB Cloud Blast” to run blast against own fasta file
General
- Genome Browser: New reference fasta file format (.gz)
- File Manager: Fixed issue with “Merge Objects”
- Make Blast DB Fix: Internal parameter for win64: BLASTDB_LMDB_MAP_SIZE
- Fisher’s Exact Test: Fixed dialog link and GO selection
- Taxonomic Classification: Improve memory management and improved report formatting
- BWA: Improved name for BAM file output
- Genome Browser: Fixed issue with region selection while scrolling
- FASTQ Preprocessing: Fixed workflow permissions
- Differential Abundance Analysis of Functions and Pathways (EggNOG and Pfam)
- Taxonomic Classification with Kraken: Update to v.2
- RNA-Seq Alignment with BWA
- Sequence Clustering with CD-HIT
- Trinity accepts FASTA read files as input
- Completeness Assessment with BUSCO: Update to v.4 and OrthoDB v.10
- Long-Read De-Novo Assembly and Polishing with Flye and Pilon
- DNA-Seq Alignment with BWA
- DNA-Seq De-Novo Assembly SPAdes: Update to v.3.14
- Filter Fasta by Length
- Convert FastQ to Fasta
- Improved Venn Diagram
Metagenomics Module
- New Taxonomic Classification Statistics: Chao1 OTU Diversity, Rarefaction Curves and PCoA Plot
- OTU Differential Abundance Testing with edgeR
Transcriptomics Module
- Completeness Assessment with BUSCO
- Predict Coding Regions with TransDecoder
- Improved RNA-Seq Alignment Input: GFF is automatically converted to GTF
- New RNA-Seq Alignment Options: 2-Pass mode, Export Spliced Junctions, Export Unmapped Reads
- New RNA-Seq De Novo Assembly Option: SuperTranscripts
- Export Normalised Counts of TimeCourse Results
- Export Normalised Counts of Pairwise Differential Expression Without Replicates Results
Genome Analysis Module
- De-Novo Assembly with SPAdes
- Repeat Masking Database Update DFAM v.3
- Repeat Masking Compatibility with RepBase 2017 and 2018
- Improved Wizard for Sample Selection
General Tools
- Barcode Splitter Tool
- New Example Workflows
General
- Minor visual improvements
Transcriptomics Module
- Create Count Table (Gene-level): Memory usage improvements
- Differential Expression Analysis: Heatmap minor improvements
- RNA-Seq Alignment: Fix bug with fastq files
Metagenomics Module
- Taxonomy Classification: Fix report
- GO Graphs: new option to export the visible region
- Generic Export: new options for start/end query and HSP positions in BlastHits
- Table Viewer: fix scroll issue causing hidden bottom rows
- License: fix the restart loop when using limited mode after key expired
- Blast Results: fix tooltip
- Genome Browser: fix a specific region position issue
- CloudBlast: skip sequences longer than 100k symbols
- Create Count Table: fix download BAM files issue when “Generate Alignment Files” is selected
General
- Fix minor issue regarding citations in wizards
Metagenomics Module
- Fix bug in metagenomics workflows causing tasks to fail
Functional Analysis Module
- Make Blast DB: Taxonomy Map file can be plain text
General
- Allow opening OmicsBox in viewer mode when offline
- Fix: Welcome window sometimes not showing content on MacOS
- Fix: Update previously installed Apps on platform update
- Improvement: Check fastq.gz files for corruption
Transcriptomics Module
- RNA-Seq De Novo Assembly: two additional parameters
- RNA-Seq Alignments: fix output BAM files name
- Differential Expression: improve files parser to skip headers
Genome Analysis Module
- Repeat Masking: unknown species are rejected by the validator
Metagenomics Module
- Fixed problem with white spaces in filenames
- Updated Kraken database to 2019.06
- Improves Krona viewer styling
Functional Analysis Module
- InterProScan: remove deprecated ProDom search option
- Rfam: fix ‘end’ column not showing data
General
- Improved citations in wizards and reports
- Example Data Import option
Transcriptomics Module
- RNA-Seq Alignment against reference genome (STAR)
Genome Analysis Module
- DNA-Seq De Novo Assembly (ABySS 2.0)
- Repeat Masking (RepeatMasker)
Metagenomics Module
- Taxonomic Classification (Kraken)
- Metagenomic Assembly (MEGAHIT and meta-SPAdes)
- Metagenomic Gene Prediction (FragGeneScan and Prodigal)
Functional Analysis Module
- New CloudBlast taxonomy filtering
- Improved CloudIPS speed and resource usage
- New EC class (7)
Jan. 2019
- Blast2GO is now OmicsBox
- Search box for menu actions
- New menu structured by modules
- Bug fixes and improvements
- New Module: Metagenomics
OMICSBOX MODULES
OmicsBox is a bioinformatics software solution which allows to get from reads to insights with ease. Use OmicsBox for the NGS data analysis of genomes, transcriptomics and metagenomes.
OmicsBox is structured in Modules. Depending on your needs you can combine different modules required for your data analysis.
- Quality Control And Assessment
- De-Novo Assembly
- Repeat Masking
- Gene Finding
- Coding Potential
- Fast Variant Calling
- Model & Non-Model Variant Annotation
- Variant Filtering
- Guided Genome-Wide Association Studies
- Quality Control
- Quantify Expression
- De-Novo Assembly
- RNA-Seq Alignment
- Differential Expression Analysis
- High-Throughput Blast and InterProScan
- Gene Ontology Mapping
- Blast2GO Annotation
- Enrichment Analysis
- Functional Interpretation
- Quality Control And Assessment
- Taxonomic Classification
- Metagenomic Assembly
- Gene Prediction
- Functional Annotation
OmicsBox Base Platform
Manage Projects and Files, Access to Cloud Computing, Design, Run and Save Workflows, Visualize Data, Genome Browser, Filter and Sort Large Tables, General Bioinformatics Tools, and More.