Evidence map›Paper›PMID 39117628›Full record

ArticleNature communications2024

Lineage-informative microhaplotypes for recurrence classification and spatio-temporal surveillance of Plasmodium vivax malaria parasites.

Sasha V Siegel, Hidayat Trimarsanto, Roberto Amato, Kathryn Murie, Aimee R Taylor, Edwin Sutanto, Mariana Kleinecke, Georgia Whitton, James A Watson, Mallika Imwong and 12 more

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
–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

22 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Article
  4. UnderstandingiScience · 2026
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  7. Temporal trends inmedRxiv : the preprint server for health sciences · 2026
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  8. Adaptive evolution ofbioRxiv : the preprint server for biology · 2025
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  11. Genetic characterization ofLancet regional health. Americas · 2025
    Article
  12. Article
  13. UnderstandingmedRxiv : the preprint server for health sciences · 2025
    Article
  14. Review
  15. Review
  16. Article
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  18. Article
  19. Population genomics ofbioRxiv : the preprint server for biology · 2024
    Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors.

Sasha V SiegelWellcome Sanger Institute, Hinxton, Cambridge, CB10 1SA, UK.ORCID 0000-0002-1458-4348
Hidayat TrimarsantoMenzies School of Health Research and Charles Darwin University, Darwin, Northern Territory, 0811, Australia.ORCID 0000-0003-2436-8283
Roberto AmatoWellcome Sanger Institute, Hinxton, Cambridge, CB10 1SA, UK.ORCID 0000-0001-8633-9221
Kathryn MurieWellcome Sanger Institute, Hinxton, Cambridge, CB10 1SA, UK.
Aimee R TaylorInstitut Pasteur, University de Paris, Infectious Disease Epidemiology and Analytics Unit, Paris, France.
Edwin SutantoExeins Health Initiative, Jakarta Selatan, 12870, Indonesia.ORCID 0000-0002-2997-4648
Mariana KleineckeMenzies School of Health Research and Charles Darwin University, Darwin, Northern Territory, 0811, Australia.ORCID 0000-0003-0159-371X
Georgia WhittonWellcome Sanger Institute, Hinxton, Cambridge, CB10 1SA, UK.
James A WatsonCentre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, OX3 7LJ, UK.ORCID 0000-0001-5524-0325
Mallika ImwongDepartment of Molecular Tropical Medicine and Genetics, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.ORCID 0000-0003-0857-1855
Ashenafi AssefaEthiopian Public Health Institute, Addis Ababa, Ethiopia.ORCID 0000-0001-6093-6685
Awab Ghulam RahimMahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Bangkok, 10400, Thailand.ORCID 0000-0002-7380-1197
Hoang Chau NguyenOxford University Clinical Research Unit, Hospital for Tropical Diseases, 764 Vo Van Kiet, W.1, Dist.5, Ho Chi Minh City, Vietnam.
Tinh Hien TranOxford University Clinical Research Unit, Hospital for Tropical Diseases, 764 Vo Van Kiet, W.1, Dist.5, Ho Chi Minh City, Vietnam.
Justin A GreenFormerly GlaxoSmithKline, Brentford, UK.
Gavin C K W KohDepartment of Infectious Diseases, Northwick Park Hospital, Harrow, UK.ORCID 0000-0002-7336-1566
Nicholas J WhiteCentre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, OX3 7LJ, UK.
Nicholas DayCentre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, OX3 7LJ, UK.
Dominic P KwiatkowskiWellcome Sanger Institute, Hinxton, Cambridge, CB10 1SA, UK.
Julian C RaynerCambridge Institute for Medical Research, University of Cambridge, Hills Road, Cambridge, CB2 0XY, UK.ORCID 0000-0002-9835-1014
Ric N PriceMenzies School of Health Research and Charles Darwin University, Darwin, Northern Territory, 0811, Australia.ORCID 0000-0003-2000-2874
Sarah AuburnMenzies School of Health Research and Charles Darwin University, Darwin, Northern Territory, 0811, Australia. Sarah.Auburn@Menzies.edu.au.ORCID 0000-0002-4638-536X

Funding

Large Scale systematic priorization of Plasmodium vivax blood stage vaccine antigensR01AI137154 · NIAID · UNIVERSITY OF CAMBRIDGE · PI RAYNER, JULIAN CHARLES · 2018 to 2021
$1.4M
Bill and Melinda Gates Foundation (Bill & Melinda Gates Foundation) INV-043618Bill and Melinda Gates Foundation (Bill & Melinda Gates Foundation) OPP1054404Department of Health | National Health and Medical Research Council (NHMRC) APP2001083NIAID NIH HHS R01 AI137154U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01AI137154Wellcome Trust 200909/Z/16/ZWellcome Trust 204911Wellcome Trust 206194Wellcome Trust (Wellcome) 206194/Z17/ZWellcome Trust (Wellcome) ICRG GR071614MA
6 · The paper itself

Abstract

Challenges in classifying recurrent Plasmodium vivax infections constrain surveillance of antimalarial efficacy and transmission. Recurrent infections may arise from activation of dormant liver stages (relapse), blood-stage treatment failure (recrudescence) or reinfection. Molecular inference of familial relatedness (identity-by-descent or IBD) can help resolve the probable origin of recurrences. As whole genome sequencing of P. vivax remains challenging, targeted genotyping methods are needed for scalability. We describe a P. vivax marker discovery framework to identify and select panels of microhaplotypes (multi-allelic markers within small, amplifiable segments of the genome) that can accurately capture IBD. We evaluate panels of 50-250 microhaplotypes discovered in a global set of 615 P. vivax genomes. A candidate global 100-microhaplotype panel exhibits high marker diversity in the Asia-Pacific, Latin America and horn of Africa (median H

Indexed as

Malaria, VivaxPlasmodium vivaxRecurrenceGenome, ProtozoanGenotypeHaplotypesHumansPolymorphism, Single Nucleotide

Identifiers

PMID39117628
PMCPMC11310204

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.