cqn
The "cqn" software tool addresses a critical challenge in molecular biology: the unwanted variability in gene expression data derived from genome-wide assays, including microarrays and RNA sequencing (RNA-seq) technologies. Despite initial excitement over RNA-seq's potential for reduced variability compared to microarrays, cqn highlights that RNA-seq data exhibit sample-specific variability, notably influenced by guanine-cytosine (GC) content. This variability, if not corrected, can lead to false positives in downstream analyses, undermining the reliability of the data.
Topic
RNA-seq
Detail
Operation: Standardisation and normalisation;RNA-Seq analysis
Software interface: Command-line user interface,Library
Language: R
License: Artistic License 2.0
Cost: Free
Version name: 1.48.0
Credit: The National Institutes of Health, National Science Foundation.
Input: -
Output: -
Contact: Kasper Daniel Hansen kasperdanielhansen@gmail.com
Collection: -
Maturity: Stable
Publications
- Removing technical variability in RNA-seq data using conditional quantile normalization.
- Hansen KD, et al. Removing technical variability in RNA-seq data using conditional quantile normalization. Removing technical variability in RNA-seq data using conditional quantile normalization. 2012; 13:204-16. doi: 10.1093/biostatistics/kxr054
- https://doi.org/10.1093/biostatistics/kxr054
- PMID: 22285995
- PMC: PMC3297825
Download and documentation
Source: https://bioconductor.org/packages/release/bioc/src/contrib/cqn_1.48.0.tar.gz
Documentation: https://bioconductor.org/packages/release/bioc/manuals/cqn/man/cqn.pdf
Home page: http://bioconductor.org/packages/release/bioc/html/cqn.html
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