Evidence map›Paper›PMID 41882789›Full record

ArticleBMC research notes2026

Whole-genome sequence of a female Loa loa adult worm from Cameroon.

Jeanne A Rajaonarivelo, Cédric Mariac, Philippe Cubry, François Sabot, Sébastien D S Pion

Abstract read
In one paragraph

Article in BMC research notes, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Jeanne A RajaonariveloTransVIHMI, University of Montpellier, INSERM, IRD, Montpellier, France. jeannearline.rajaonarivelo@ird.fr.
Cédric MariacDIADE, Univ Montpellier, CIRAD, IRD, Montpellier, France.
Philippe CubryDIADE, Univ Montpellier, CIRAD, IRD, Montpellier, France.
François SabotDIADE, Univ Montpellier, CIRAD, IRD, Montpellier, France. francois.sabot@ird.fr.
Sébastien D S PionTransVIHMI, University of Montpellier, INSERM, IRD, Montpellier, France.

Funding

Agence Nationale de la Recherche ANR-21-CE17-0008-01
6 · The paper itself

Abstract

objectiveAlthough loiasis affects more than 20 million people and that its associated clinical complications can cause multiple organ failures, this disease remains understudied. Consequently, the elimination of loiasis is not on the agenda of public health services. Defining an effective strategy to tackle this disease is challenging and requires a better understanding of the parasite's biology, including its genetic aspects. Loa loa adult worms provide large amounts of biological tissues for genetic sequencing, but are very difficult to collect. Therefore, limited genomic data are available for this parasite. This study aimed to produce a more complete genome assembly of L. loa worm, which can be used for future research on genetic diversity, population dynamics and immunological processes. DATA DESCRIPTION: A 91.2 Mb genome assembly (150 contigs, N50 = 1.14 Mb, GC content = 30.67%) was generated from a single adult female L. loa worm, sequenced on a PromethION flow cell to a read depth of 147×. Alignment of this assembly with the available Loa reference genome displayed 96.08% identity. BUSCO analysis showed a 98.0% completeness of universally conserved nematode genes. The whole-genome assembly reported in this study were deposited in NCBI under the accession number JBSOQI010000000.

Indexed as

Genome, HelminthLoaWhole Genome SequencingAnimalsCameroonFemaleLoiasisFilarial nematode parasiteLoa loaOxford Nanopore TechnologiesWhole-genome sequencing

Identifiers

PMID41882789
PMCPMC13137628

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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.