Evidence map›Paper›PMID 40860566›Full record

ArticleISME communications2025

CleanBar: a versatile demultiplexing tool for split-and-pool barcoding in single-cell omics.

Vicente Arnau, Alicia Ortiz-Maiques, Juan Valero-Tebar, Lucas Mora-Quilis, Vaida Kurmauskaite, Lorea Campos Dopazo, Pilar Domingo-Calap, Mária Džunková

Abstract read
In one paragraph

Article in ISME communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Vicente ArnauInstitute for Integrative Systems Biology (I2SysBio), University of Valencia and Spanish National Research Council (CSIC), 46980, Paterna, Valencia, Spain.
Alicia Ortiz-MaiquesInstitute for Integrative Systems Biology (I2SysBio), University of Valencia and Spanish National Research Council (CSIC), 46980, Paterna, Valencia, Spain.
Juan Valero-TebarInstitute for Integrative Systems Biology (I2SysBio), University of Valencia and Spanish National Research Council (CSIC), 46980, Paterna, Valencia, Spain.
Lucas Mora-QuilisInstitute for Integrative Systems Biology (I2SysBio), University of Valencia and Spanish National Research Council (CSIC), 46980, Paterna, Valencia, Spain.
Vaida KurmauskaiteAtrandi Biosciences, Savanorių pr. 178C-101, LT-03154 Vilnius, Lithuania.
Lorea Campos DopazoAtrandi Biosciences, Savanorių pr. 178C-101, LT-03154 Vilnius, Lithuania.
Pilar Domingo-CalapInstitute for Integrative Systems Biology (I2SysBio), University of Valencia and Spanish National Research Council (CSIC), 46980, Paterna, Valencia, Spain.
Mária DžunkováInstitute for Integrative Systems Biology (I2SysBio), University of Valencia and Spanish National Research Council (CSIC), 46980, Paterna, Valencia, Spain.ORCID https://orcid.org/0000-0002-1765-0697

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Split-and-pool barcoding generates thousands of unique barcode strings through sequential ligations in 96-well plates, making single-cell omics more accessible, thus advancing microbial ecology, particularly in studies of bacterial interactions with plasmids and bacteriophages. While the wet-lab aspects of the split-and-pool barcoding are well-documented, no universally applicable bioinformatic tool exists for demultiplexing single cells barcoded with this approach. We present CleanBar (https://github.com/tbcgit/cleanbar), a flexible tool for demultiplexing reads tagged with sequentially ligated barcodes, accommodating variations in barcode positions and linker lengths while preventing misclassification of natural barcode-like sequences and handling diverse ligation errors. It also provides statistics useful for optimizing laboratory procedures. We demonstrate CleanBar's performance with the Atrandi platform for microbial single-cell genomics, coupled with PacBio sequencing, to reach a cell throughput comparable with traditional bulk metagenomics, but overcoming its limitations in studying phage-bacteria interactions. In four

Indexed as

Atrandidemultiplexingmicrobial single-cell genomicsPacBiophage-bacteria interactionssplit-and-pool barcoding

Identifiers

PMID40860566
PMCPMC12376035

What OpenQuestion holds

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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.