Evidence map›Paper›PMID 40593801›Full record

ArticleScientific data2025

De novo transcriptome assembly of Acartia tonsa adults using Nanopore long-read sequencing.

Florencia Mohamed, Marco Picone, Greta Battaggia, Ilenia Urso, Elisa Camatti, Alessandro Vezzi, Gabriele Sales

Abstract readDataset
In one paragraph

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

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0citing papers in PubMed
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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

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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

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5 · Who and what money

Authors and funding

7 authors.

Florencia MohamedDepartment of Biology, University of Padua, Padua, Italy.
Marco PiconeDepartment of Environmental Sciences, Ca' Foscari University of Venice, Venice, Italy.
Greta BattaggiaDepartment of Biology, University of Padua, Padua, Italy.
Ilenia UrsoDepartment of Biology, University of Padua, Padua, Italy.
Elisa CamattiInstitute of Marine Science, National Research Council (CNR ISMAR), Venice, Italy.
Alessandro VezziDepartment of Biology, University of Padua, Padua, Italy. alessandro.vezzi@unipd.it.ORCID 0000-0002-8629-6644
Gabriele SalesDepartment of Biology, University of Padua, Padua, Italy. gabriele.sales@unipd.it.ORCID 0000-0003-2078-5661

Funding

Università degli Studi di Padova (University of Padova) SALE_VIRD21_01
6 · The paper itself

Abstract

Acartia tonsa is a calanoid copepod with a cosmopolitan distribution. Its ecological relevance makes it a useful bioindicator organism for assessing the toxicity of various compounds. However, transcriptomic assemblies of A. tonsa using long-read technologies have not yet been described. The use of long-read sequencing technologies in transcriptomics allows the study of alternative splicing, structural variations and alternative polyadenylation sites. In this study, we present a de novo transcriptome of A. tonsa adult copepods exposed to different neonicotinoids obtained from Nanopore sequences. This transcriptome (261,560 total transcripts, with 31,291 representative sequences) exhibits 88.3% completeness and an N50 of 2,580 bases, showing better results than previous assemblies of the same organism. We also performed a full annotation by sequence homology (NR database), domain identification (InterProScan) and functional classification (Gene Ontology); 54.3% of representative transcripts were annotated in at least one database. Our transcriptome represents a solid baseline for further transcriptomic studies on A. tonsa and, specifically, its response to currently used pesticides.

Indexed as

CopepodaTranscriptomeAnimalsMolecular Sequence AnnotationNanopore SequencingNeonicotinoidsNeonicotinoids

Identifiers

PMID40593801
PMCPMC12219298

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