Qualimap 2: advanced multi-sample quality control for high-throughput sequencing data
Open accessAbstract
Motivation: Detection of random errors and systematic biases is a crucial step of a robust pipeline for processing high-throughput sequencing (HTS) data. Bioinformatics software tools capable of performing this task are available, either for general analysis of HTS data or targeted to a specific sequencing technology. However, most of the existing QC instruments only allow processing of one sample at a time. Results: Qualimap 2 represents a next step in the QC analysis of HTS data. Along with comprehensive single-sample analysis of alignment data, it includes new modes that allow simultaneous processing and comparison of multiple samples. As with the first version, the new features are available via both graphical and command line interface. Additionally, it includes a large number of improvements proposed by the user community. Availability and implementation: The implementation of the software along with documentation is freely available at http://www.qualimap.org. Contact: meyer@mpiib-berlin.mpg.de Supplementary information: Supplementary data are available at Bioinformatics online.
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Alignment quality was verified using QualiMap v2.2.1.
“Alignment quality was verified using QualiMap v2.2.155.”
From Integrative genomic analyses identify candidate causal genes for calcific aortic valve stenosis involving tissue-specific regulation (2024) · cites this paper as [55]
Alignment quality was evaluated using Qualimap.
“Alignment quality was evaluated using qualimap (v2.3) [76].”
From Mechanical stiffness orchestrates distinct regulation of <scp>MRTFs</scp> and <scp>YAP</scp> / <scp>TAZ</scp> transcriptional cofactors in hepatocytes (2026) · cites this paper as [76]
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Research works printed but not linked: 11
- Adams D. (2012) BLUEPRINT to decode the epigenetic signature written in blood. Nat. Biotechnol. 30, 224– 226. 22398613
- Anders S. (2013) Count-based differential expression analysis of RNA sequencing data using R and Bioconductor. Nat. Protoc. 8, 1765– 1786. 23975260
- DeLuca D.S. (2012) RNA-SeQC: RNA-seq metrics for quality control and process optimization. Bioinformatics, 28, 1530– 1532. 22539670 PMC3356847
- García-Alcalde F. (2012) Qualimap: evaluating next-generation sequencing alignment data. Bioinformatics, 28, 2678– 2679. 22914218
- Koeppel M. (2015) Helicobacter pylori infection causes characteristic DNA damage patterns in human cells. Cell Rep., 11, 1703– 1713. 26074077
- Patel R.K. Mukesh J. (2012) NGS QC toolkit: a toolkit for quality control of next generation sequencing data. PLoS One, 7, e30619. 22312429 PMC3270013
- Ramirez-Gonzalez R.H. (2013) StatsDB: platform-agnostic storage and understanding of next generation sequencing run metrics. F1000Res. 2, 248. 24627795 PMC3938176
- Rosenbloom K.R. (2013) ENCODE data in the UCSC Genome Browser: year 5 update. Nucleic Acids Res., 41, D56– D63. 23193274 PMC3531152
- Ross M.G. (2013) Characterizing and measuring bias in sequence data. Genome Biol., 14, R51. 23718773 PMC4053816
- Sims D. (2014) Sequencing depth and coverage: key considerations in genomic analyses. Nat. Rev. Genet., 15, 121– 132. 24434847
- Wang L. (2012) RSeQC: quality control of RNA-seq experiments. Bioinformatics, 28, 2184– 2185. 22743226
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Torres‐Ortiz, B. S., Pérez‐Calixto, D., Carretero‐Ortega, J., Guzman‐López, A. G., Pinto‐Dueñas, D. C., Hernández‐Juárez, M., Jiménez‐Escobar, A., Rodríguez‐Hernández, A., Díaz‐Bello, B., Serna‐Márquez, N., et al. (2026) · The FEBS Journal · doi:10.1111/febs.70570
- Authors
- Okonechnikov, K., Conesa, A., & García-Alcalde, F.
- Affiliations
- Max Planck Institute for Infection Biology (DE)
- University of Florida (US)
- Corresponding author
- García-Alcalde, Fernando
- Venue
- Bioinformatics
- Publisher
- Oxford University Press (OUP)
- Published
- 2015-10-01
- Volume
- 32
- Issue
- 2
- Pages
- 292-294
- ISSN
- 1367-4803 (ISSN-L)
- 1367-4811
- PMC
- PMC4708105
- OpenAlex
- W2111281047
- Cited by
- 2,145
- References
- 0
- Citations by year
- 2026: 271 · 2025: 295 · 2024: 352 · 2023: 274 · 2022: 267 · 2021: 228 · 2020: 175 · 2019: 114 · 2018: 92 · 2017: 56 · 2016: 20 · 2015: 1
- FWCI
- 24.47
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Locations
- Bioinformatics (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- MPG.PuRe (Max Planck Society) (submittedVersion, cc-by)
- HighWire Press Open Archive (submittedVersion)
- Funders
- European Commission (217768)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Single-cell and spatial transcriptomics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gene expression and cancer classification
- Keywords
- high-throughput sequencing data, quality control, multi-sample analysis, random error, systematic bias, bioinformatics software
- MeSH terms
- Algorithms, Humans, Quality Control, Software, Sequence Alignment, Sequence Analysis, DNA, Genomics, High-Throughput Nucleotide Sequencing
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