MultiQC is a reporting tool that aggregates results from multiple bioinformatics analyses and samples into a single report. It scans directories for recognised log files, extracts their statistics and presents the results using interactive plots.
This is free and open source software.
Key Features
- Combines results from many bioinformatics tools and samples.
- Automatically scans directories for recognised log files.
- Generates a single HTML report with interactive plots.
- Summarises multiple stages of an analysis within one report.
- Supports a large collection of bioinformatics tools.
- Accepts appropriately formatted results from custom scripts.
- Exports underlying data in tab-delimited, YAML or JSON format.
- Offers extensive report customisation through YAML configuration.
- Supports custom modules, plugins and report templates.
- Available through PyPI, Bioconda, containers and Galaxy wrappers.
Website: github.com/MultiQC/MultiQC
Support:
Developer: Phil Ewels
License: GNU General Public License v3.0
MultiQC is written in JavaScript and Python. Learn JavaScript with our recommended free books and free tutorials. Learn Python with our recommended free books and free tutorials.
Related Software
| Bioinformatics Tools | |
|---|---|
| Bioconductor | Analysis and comprehension of high-throughput genomic data |
| Biopython | Tools for biological computation written in Python |
| UGENE | Set of integrated bioinformatics software |
| BioPerl | Perl tools for computational molecular biology |
| GROMACS | Versatile package to perform molecular dynamics |
| IGV | High-performance visualization genome browser tool |
| GATK | Genomic analysis toolkit focused on variant discovery |
| BioJava | Provides Java tools for processing biological data |
| InterMine | Integrate biological data sources |
| bedtools | Powerful toolset for genome arithmetic |
| EMBOSS | The European Molecular Biology Open Software Suite |
| BLAST | Algorithm for comparing primary biological sequence information |
| Galaxy | Web-based platform for data-intensive computational research |
| minimap2 | Versatile sequence alignment program |
| Scanpy | Scalable analysis of single-cell gene expression data |
| Jalview | Multiple sequence alignment editing, visualisation and analysis |
| SeqKit | Fast toolkit for manipulating FASTA and FASTQ sequence files |
| samtools | Manipulate next-generation sequencing data |
| MultiQC | Aggregates results from multiple bioinformatics analyses |
| BCFtools | Variant calling and manipulating files in the Variant Call Format |
| Foldseek | Fast searching and comparison of large protein structure datasets |
| FastQC | Quality control tool for high throughput sequence data |
| SPAdes | Versatile toolkit for assembling and analysing sequencing data |
| GenomeTools | Collection of bioinformatics tools |
| AliView | Alignment viewer and editor |
| mothur | Analyze microbial communities |
| Bandage | Visualising de novo assembly graphs |
| cramino | BAM/CRAM quality evaluation |
| abPOA | Adaptive banded Partial Order Alignment |
Read our verdict in the software roundup.
Explore our carefully curated directory of recommended free and open source software, covering every major software category.The directory forms part of our extensive collection of articles for Linux enthusiasts. It includes hundreds of detailed reviews, together with free and open source alternatives to proprietary software from companies such as Google, Microsoft, Apple, Adobe, IBM, Cisco, Oracle, and Autodesk. LinuxLinks also covers interesting projects worth exploring, Linux-compatible hardware, free programming books and tutorials, and much more. Know a useful free and open source Linux application that we haven’t covered? Tell us about it using our submission form. |


Please read our Comment Policy before commenting.