Evidence map›Paper›PMID 39528918›Full record

ArticleBMC genomics2024

Comparative transcriptomic analyses of thymocytes using 10x Genomics and Parse scRNA-seq technologies.

Igor Filippov, Chinna Susan Philip, Leif Schauser, Pärt Peterson

Abstract readComparative Study
In one paragraph

Article in BMC genomics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
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  3. Review
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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

4 authors.

Igor Filippov *Molecular Pathology Research Group, Institute of Biomedicine and Translational Medicine, University of Tartu, Tartu, Estonia. ihor.filippov@ut.ee.
Chinna Susan Philip *Molecular Pathology Research Group, Institute of Biomedicine and Translational Medicine, University of Tartu, Tartu, Estonia. chinna.susan.philip@ut.ee.
Leif SchauserQIAGEN Aarhus A/S, Aarhus, Denmark.
Pärt PetersonMolecular Pathology Research Group, Institute of Biomedicine and Translational Medicine, University of Tartu, Tartu, Estonia.

Funding

Eesti Teadusagentuur PRG2011Horizon 2020 Framework Programme 955321
6 · The paper itself

Abstract

backgroundSingle-cell RNA sequencing experiments commonly use 10x Genomics (10x) kits due to their high-throughput capacity and standardized protocols. Recently, Parse Biosciences (Parse) introduced an alternative technology that uses multiple in-situ barcoding rounds within standard 96-well plates. Parse enables the analysis of more cells from multiple samples in a single run without the need for additional reagents or specialized microfluidics equipment. To evaluate the performance of both platforms, we conducted a benchmark study using biological and technical replicates of mouse thymus as a complex immune tissue.

resultsWe found that Parse detected nearly twice the number of genes compared to 10x, with each platform detecting a distinct set of genes. The comparison of multiplexed samples generated from 10x and Parse techniques showed 10x data to have lower technical variability and more precise annotation of biological states in the thymus compared to Parse.

conclusionOur results provide a comprehensive comparison of the suitability of both single-cell platforms for immunological studies.

Indexed as

Gene Expression ProfilingGenomicsSingle-Cell AnalysisThymocytesAnimalsMiceRNA-SeqSequence Analysis, RNASingle-Cell Gene Expression AnalysisTranscriptome10xParsescRNA-seqThymusTranscriptomics

Identifiers

PMID39528918
PMCPMC11552371

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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.