Evidence map›Paper›PMID 35084033›Full record

ArticleGigaScience2022

Comparative analysis of common alignment tools for single-cell RNA sequencing.

Ralf Schulze Brüning, Lukas Tombor, Marcel H Schulz, Stefanie Dimmeler, David John

Open access · goldAbstract read
In one paragraph

Article in GigaScience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.7field-weighted citation impact, top 9% of its field
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

22 citing papers in PubMed, 37 citations in OpenAlex.

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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

5 authors at 2 institutions in 2 countries.

Ralf Schulze BrüningInstitute of Cardiovascular Regeneration, Theodor-Stern-Kai 7, 60590 Frankfurt, Germany.
Lukas TomborInstitute of Cardiovascular Regeneration, Theodor-Stern-Kai 7, 60590 Frankfurt, Germany.ORCID 0000-0002-5867-576X
Marcel H SchulzInstitute of Cardiovascular Regeneration, Theodor-Stern-Kai 7, 60590 Frankfurt, Germany.ORCID 0000-0002-1252-3656
Stefanie DimmelerInstitute of Cardiovascular Regeneration, Theodor-Stern-Kai 7, 60590 Frankfurt, Germany.ORCID 0000-0002-1045-2436
David JohnInstitute of Cardiovascular Regeneration, Theodor-Stern-Kai 7, 60590 Frankfurt, Germany.ORCID 0000-0003-3217-5449
German Centre for Cardiovascular Research · DERegenerative Medicine Institute · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWith the rise of single-cell RNA sequencing new bioinformatic tools have been developed to handle specific demands, such as quantifying unique molecular identifiers and correcting cell barcodes. Here, we benchmarked several datasets with the most common alignment tools for single-cell RNA sequencing data. We evaluated differences in the whitelisting, gene quantification, overall performance, and potential variations in clustering or detection of differentially expressed genes. We compared the tools Cell Ranger version 6, STARsolo, Kallisto, Alevin, and Alevin-fry on 3 published datasets for human and mouse, sequenced with different versions of the 10X sequencing protocol.

resultsStriking differences were observed in the overall runtime of the mappers. Besides that, Kallisto and Alevin showed variances in the number of valid cells and detected genes per cell. Kallisto reported the highest number of cells; however, we observed an overrepresentation of cells with low gene content and unknown cell type. Conversely, Alevin rarely reported such low-content cells. Further variations were detected in the set of expressed genes. While STARsolo, Cell Ranger 6, Alevin-fry, and Alevin produced similar gene sets, Kallisto detected additional genes from the Vmn and Olfr gene family, which are likely mapping artefacts. We also observed differences in the mitochondrial content of the resulting cells when comparing a prefiltered annotation set to the full annotation set that includes pseudogenes and other biotypes.

conclusionOverall, this study provides a detailed comparison of common single-cell RNA sequencing mappers and shows their specific properties on 10X Genomics data.

Indexed as

Computational BiologyGenomicsAnimalsCluster AnalysisMiceRNASequence Analysis, RNASingle-Cell AnalysisSoftwareRNAalignersbenchmarkingmappersmapping-algorithmssingle-cell RNA sequencingtranscriptomics

Identifiers

PMID35084033
PMCPMC8848315
OpenAlexW4225680935

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.