CITE-seq (cellular indexing of transcriptomes and epitopes) is an RNA sequencing-based method that simultaneously quantifies cell surface protein and transcriptomic data within a single cell readout. The ability to study cells concurrently offers unprecedented insights into new cell types, disease states or other conditions.
While CITE-seq solves the problem of detecting a limited number of proteins while using single-cell sequencing in an unbiased way, one of its limitations is the high levels of background noise that can hinder analysis.
To rectify this problem, researchers from Boston University Chobanian & Avedisian School of Medicine and College of Arts & Sciences have developed a novel tool which can identify and remove unwanted background noise that comes from various sources.
“We created DecontPro, a statistical model that decontaminates two sources of contamination that were observed empirically in CITE-seq data,” explains corresponding author Joshua Campbell, PhD, associate professor of medicine at the School. “It can be used as an important quality assessment tool that will aid in the downstream analysis and help researchers to better understand the molecular cause of disease,” he said.

The researchers examined several publicly available datasets that profiled different types of tissue with CITE-seq and found a novel type of artifact, which they called a “spongelet.” The spongelets contributed a large amount of background noise in several datasets. The researchers found that DecontPro can estimate and remove different sources of background noise, including contamination from spongelets, from ambient material that may be present in the cell suspension, or from non-specific binding of antibodies.
Masanao Yajima, PhD, professor of the practice in the department of mathematics and statistics states, “DecontPro is a Bayesian hierarchical model. We carefully constructed it so that it can tease apart the signals from noise in single-cell datasets without being overly aggressive.”
Source – Boston University School of Medicine
Availability – DecontPro is freely available as an R package on GitHub: https://github.com/campbio/decontX.
Yin Y, Yajima M, Campbell JD. (2023) Characterization and decontamination of background noise in droplet-based single-cell protein expression data with DecontPro. Nucleic Acids Res [Epub ahead of print]. [article]
CITE-seq (cellular indexing of transcriptomes and epitopes) is an RNA sequencing-based method that simultaneously quantifies cell surface protein and transcriptomic data within a single cell readout. The ability to study cells concurrently offers unprecedented insights into new cell types, disease states or other conditions.
While CITE-seq solves the problem of detecting a limited number of proteins while using single-cell sequencing in an unbiased way, one of its limitations is the high levels of background noise that can hinder analysis.
To rectify this problem, researchers from Boston University Chobanian & Avedisian School of Medicine and College of Arts & Sciences have developed a novel tool which can identify and remove unwanted background noise that comes from various sources.
The researchers examined several publicly available datasets that profiled different types of tissue with CITE-seq and found a novel type of artifact, which they called a “spongelet.” The spongelets contributed a large amount of background noise in several datasets. The researchers found that DecontPro can estimate and remove different sources of background noise, including contamination from spongelets, from ambient material that may be present in the cell suspension, or from non-specific binding of antibodies.
Source – Boston University School of Medicine
Availability – DecontPro is freely available as an R package on GitHub: https://github.com/campbio/decontX.
Yin Y, Yajima M, Campbell JD. (2023) Characterization and decontamination of background noise in droplet-based single-cell protein expression data with DecontPro. Nucleic Acids Res [Epub ahead of print]. [article]
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CITE-seq (cellular indexing of transcriptomes and epitopes) is an RNA sequencing-based method that simultaneously quantifies cell surface protein and transcriptomic data within a single cell readout. The ability to study cells concurrently offers unprecedented insights into new cell types, disease states or other conditions.
While CITE-seq solves the problem of detecting a limited number of proteins while using single-cell sequencing in an unbiased way, one of its limitations is the high levels of background noise that can hinder analysis.
To rectify this problem, researchers from Boston University Chobanian & Avedisian School of Medicine and College of Arts & Sciences have developed a novel tool which can identify and remove unwanted background noise that comes from various sources.
The researchers examined several publicly available datasets that profiled different types of tissue with CITE-seq and found a novel type of artifact, which they called a “spongelet.” The spongelets contributed a large amount of background noise in several datasets. The researchers found that DecontPro can estimate and remove different sources of background noise, including contamination from spongelets, from ambient material that may be present in the cell suspension, or from non-specific binding of antibodies.
Source – Boston University School of Medicine
Availability – DecontPro is freely available as an R package on GitHub: https://github.com/campbio/decontX.
Yin Y, Yajima M, Campbell JD. (2023) Characterization and decontamination of background noise in droplet-based single-cell protein expression data with DecontPro. Nucleic Acids Res [Epub ahead of print]. [article]
Related Posts
Benchmarking RNA sequencing for more accurate alternative splicing analysis
RNA Sequencing identifies new tick-borne virus that causes flu-like illness
Small RNA sequencing reveals regulatory roles for sdRNAs in acute myeloid leukemia
POND-seq enables non-destructive RNA sequencing in living cells
Worm’s radical transformation shows metamorphosis can change the functions of cells
New method allows scientists to follow gene activity over time in the same cells
Single-cell and single-embryo RNA sequencing
RNA sequencing reveals functional chimeric mRNAs in mammalian immunity
Deep learning improves microRNA target prediction from sequence
Atlas of the brain’s striatum could guide researchers to new drug treatments
scLS – a computationally efficient differentially expressed gene detection algorithm
Spatial mapping of RNA turnover kinetics in the mouse brain
Immune cells offer insights on billion-dollar virus
SPIDER improves spatial transcriptomics data using single-cell RNA sequencing
Ultrafast and reference-free sequence discovery in single-cell data
ARCADIA combines RNA sequencing and spatial proteomics to reveal how tissue location shapes cell behavior
An end-to-end computational framework for “Record-seq” transcriptional recording data
A functionally integrated cross-tissue alternative splicing program during short-term calorie restriction
ExoShorkie – predicting RNA-seq coverage of exogenous genomes in yeast by transfer learning
Dietary oxidized plant sterol shifts macrophage state to fuel aortic inflammation
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