Evidence map›Paper›PMID 39948460›Full record

ArticleBMC bioinformatics2025

Using individual barcodes to increase quantification power of massively parallel reporter assays.

Pia Keukeleire, Jonathan D Rosen, Angelina Göbel-Knapp, Kilian Salomon, Max Schubach, Martin Kircher

Abstract read
In one paragraph

Article in BMC bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Massively parallel reporter assays forbioRxiv : the preprint server for biology · 2026
    Article
  4. Article
  5. Promoter mutagenesis and a massively parallel reporter screen of thebioRxiv : the preprint server for biology · 2026
    Article
  6. Article
  7. Article
  8. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Pia KeukeleireInstitute of Human Genetics, University Hospital Schleswig-Holstein, University of Lübeck, Lübeck, Germany.ORCID https://orcid.org/0000-0002-8828-636X
Jonathan D RosenDepartment of Genetics & Department of Biostatistics, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.ORCID https://orcid.org/0000-0001-6396-4219
Angelina Göbel-KnappInstitute of Human Genetics, University Hospital Schleswig-Holstein, University of Lübeck, Lübeck, Germany.
Kilian SalomonExploratory Diagnostic Sciences, Berlin Institute of Health at Charité - Universitätsmedizin Berlin, Berlin, Germany.ORCID https://orcid.org/0009-0009-3182-7987
Max SchubachExploratory Diagnostic Sciences, Berlin Institute of Health at Charité - Universitätsmedizin Berlin, Berlin, Germany.ORCID https://orcid.org/0000-0002-2032-6679
Martin KircherInstitute of Human Genetics, University Hospital Schleswig-Holstein, University of Lübeck, Lübeck, Germany. martin.kircher@uni-luebeck.de.ORCID https://orcid.org/0000-0001-9278-5471

Funding

Systematic in vivo characterization of disease-associated regulatory variantsUM1HG012003 · NHGRI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Michael Isaiah Love, KAREN L. MOHLKE · 2021 to 2026
$9.9M
Massively parallel characterization of variants and elements impacting transcriptional regulation in dynamic cellular systemsUM1HG011966 · NHGRI · UNIVERSITY OF WASHINGTON · PI Nadav Ahituv, Jay Ashok Shendure · 2021 to 2026
$9.7M
Impact of Genomic Variation on Function (IGVF) 1UM1HG011966Impact of Genomic Variation on Function (IGVF) 1UM1HG012003NHGRI NIH HHS UM1 HG011966NHGRI NIH HHS UM1 HG012003
6 · The paper itself

Abstract

backgroundMassively parallel reporter assays (MPRAs) are an experimental technology for measuring the activity of thousands of candidate regulatory sequences or their variants in parallel, where the activity of individual sequences is measured from pools of sequence-tagged reporter genes. Activity is derived from the ratio of transcribed RNA to input DNA counts of associated tag sequences in each reporter construct, so-called barcodes. Recently, tools specifically designed to analyze MPRA data were developed that attempt to model the count data, accounting for its inherent variation. Of these tools, MPRAnalyze and mpralm are most widely used. MPRAnalyze models barcode counts to estimate the transcription rate of each sequence. While it has increased statistical power and robustness against outliers compared to mpralm, it is slow and has a high false discovery rate. Mpralm, a tool built on the R package Limma, estimates log fold-changes between different sequences. As opposed to MPRAnalyze, it is fast and has a low false discovery rate but is susceptible to outliers and has less statistical power.

resultsWe propose BCalm, an MPRA analysis framework aimed at addressing the limitations of the existing tools. BCalm is an adaptation of mpralm, but models individual barcode counts instead of aggregating counts per sequence. Leaving out the aggregation step increases statistical power and improves robustness to outliers, while being fast and precise. We show the improved performance over existing methods on both simulated MPRA data and a lentiviral MPRA library of 166,508 target sequences, including 82,258 allelic variants. Further, BCalm adds functionality beyond the existing mpralm package, such as preparing count input files from MPRAsnakeflow, as well as an option to test for sequences with enhancing or repressing activity. Its built-in plotting functionalities allow for easy interpretation of the results.

conclusionsWith BCalm, we provide a new tool for analyzing MPRA data which is robust and accurate on real MPRA datasets. The package is available at https://github.com/kircherlab/BCalm .

Indexed as

Genes, ReporterHigh-Throughput Nucleotide SequencingSoftwareHumansElement and variant effect quantificationMassively Parallel Reporter Assays (MPRA)R packageStatistical analysis

Identifiers

PMID39948460
PMCPMC11827149

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.