ArticleMemorias do Instituto Oswaldo Cruz2026
Comprehensive identification and co-expression analysis of long non-coding RNAs across eight timepoints of Schistosoma mansoni life cycle
Article in Memorias do Instituto Oswaldo Cruz, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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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.
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Who cites it
1 citing paper in PubMed.
- Long Non-Coding RNAs Identified as Hub Genes by Weighted Gene Co-Expression Network Analysis inInternational journal of molecular sciences · 2026Article
Corrections and comments
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Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundLong non-coding RNAs (lncRNAs) are important regulatory molecules that can be considered potential biomarkers for schistosomiasis. However, the identification and characterisation of these molecules in such complex organism as Schistosoma mansoni, remains very challenging.
objectivesThis study aimed to identify novel lncRNAs in S. mansoni using RNA-seq libraries representative of six developmental stages (eggs, miracidia, sporocysts, cercariae, schistosomula, and juveniles).
methodsA pipeline for lncRNAs identification was defined and applied to 41 RNA-seq libraries of eggs, miracidia, 1-day, 5-days, 32-days sporocysts, cercariae, schistosomula, and juveniles of S. mansoni. Novel identified lncRNAs and annotated mRNAs were submitted to a weighted co-expression network analysis (WGCNA) to establish lncRNA-mRNAs correlation.
findingsWe identified 1,082 novel lncRNAs, mostly presenting stage-specific expression. Co-expression analysis demonstrate that MSTRG.5305.1 can potentially target MEGs and tetraspanin, essential for juvenile worm survival, making it a promising candidate for further functional studies. MAIN
conclusionsThese findings expand the current catalog of S. mansoni lncRNAs and provide new insights into their potential roles in parasite development and host adaptation. Further functional validation could reveal new molecular targets for schistosomiasis control.
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