Transcriptomic data of piglet blood compartments with 3′ mRNA sequencing

This article reports transcriptomic dataset generated by rationalized sequencing of the 3' ends of messenger RNAs (3' mRNA-Seq) in porcine samples. Libraries were prepared from whole blood, plasma, serum, and exosome-enriched fractions derived from plasma and serum. This approach was applied to whole blood, with porcine globin blockers being used to minimise the impact of the large quantity of globin transcripts. In addition, serum and plasma-derived RNA were processed without globin depletion, allowing a direct assessment of transcriptome profiles from these biofluids. Although the library preparation protocol employed was not originally designed for plasma or serum samples, we successfully produced libraries from RNA extracted from these different compartments. More unexpectedly, libraries could also be generated from exosome-enriched fractions. While expression profiles from plasma and serum fractions display distinctive characteristics compared to whole blood, a quite high proportion of genes were detected in these extracts. The resulting data provide comprehensive transcriptomic information across multiple sample types, including minimally invasive compartments, and are made available to support further exploration of 3' mRNA-Seq in biomedical and veterinary research.

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Publication Details

Journal
Data in Brief
Published
2026-03-11
DOI
https://doi.org/10.1016/j.dib.2026.112679
Primary Topic
Molecular Biology Techniques and Applications
Type
article
Field-Weighted Citation Impact
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article

Transcriptomic data of piglet blood compartments with 3′ mRNA sequencing

Gaëlle Payros, Yannick Lippi, Laure Gress, Laurence Liaubet Liaubet et al.
Data in Brief
Molecular Biology Techniques and Applications
article

Transcriptomic data of piglet blood compartments with 3′ mRNA sequencing

Gaëlle Payros, Yannick Lippi, Laure Gress, Laurence Liaubet Liaubet, Maëlle Gusmini, Kory Jason
article en

Abstract

This article reports transcriptomic dataset generated by rationalized sequencing of the 3' ends of messenger RNAs (3' mRNA-Seq) in porcine samples. Libraries were prepared from whole blood, plasma, serum, and exosome-enriched fractions derived from plasma and serum. This approach was applied to whole blood, with porcine globin blockers being used to minimise the impact of the large quantity of globin transcripts. In addition, serum and plasma-derived RNA were processed without globin depletion, allowing a direct assessment of transcriptome profiles from these biofluids. Although the library preparation protocol employed was not originally designed for plasma or serum samples, we successfully produced libraries from RNA extracted from these different compartments. More unexpectedly, libraries could also be generated from exosome-enriched fractions. While expression profiles from plasma and serum fractions display distinctive characteristics compared to whole blood, a quite high proportion of genes were detected in these extracts. The resulting data provide comprehensive transcriptomic information across multiple sample types, including minimally invasive compartments, and are made available to support further exploration of 3' mRNA-Seq in biomedical and veterinary research.

Data in BriefVol. 66
École Nationale Vétérinaire de Toulouse (FR), Université Fédérale de Toulouse Midi-Pyrénées (FR), Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement (FR), Toxicologie Alimentaire (FR), Génétique Physiologie et Systèmes d'Elevage (FR)
Openalex Percentile: Top 25%
Molecular Biology Techniques and Applications
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