Evidence map›Paper›PMID 40642868›Full record

ArticleMolecular ecology resources2025

Conserved Sequence Identification Within Large Genomic Datasets Using 'Unikseq2': Application in Environmental DNA Assay Development.

Mark Louie D Lopez, René L Warren, Michael J Allison, Lauren Coombe, Jacob J Imbery, Inanc Birol, Caren C Helbing

Abstract read
In one paragraph

Article in Molecular ecology resources, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Using environmental DNA to identify emerging Pacific salmon habitats and support Indigenous governance.Ecological applications : a publication of the Ecological Society of America · 2026
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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

7 authors.

Mark Louie D LopezDepartment of Biochemistry and Microbiology, University of Victoria, Victoria, British Columbia, Canada.
René L WarrenCanada's Michael Smith Genome Sciences Centre at BC Cancer, Vancouver, British Columbia, Canada.
Michael J AllisonDepartment of Biochemistry and Microbiology, University of Victoria, Victoria, British Columbia, Canada.
Lauren CoombeCanada's Michael Smith Genome Sciences Centre at BC Cancer, Vancouver, British Columbia, Canada.
Jacob J ImberyDepartment of Biochemistry and Microbiology, University of Victoria, Victoria, British Columbia, Canada.
Inanc BirolCanada's Michael Smith Genome Sciences Centre at BC Cancer, Vancouver, British Columbia, Canada.
Caren C HelbingDepartment of Biochemistry and Microbiology, University of Victoria, Victoria, British Columbia, Canada.ORCID https://orcid.org/0000-0002-8861-1070

Funding

Digital Research Alliance of CanadaGenome British ColumbiaGenome CanadaGenome QuebecLiber Ero FoundationNatural Sciences and Engineering Research Council of Canada
6 · The paper itself

Abstract

Identification of conserved genomic sequences and their utilisation as anchor points for clade detection and/or characterisation is a mainstay in ecological studies. For environmental DNA (eDNA) assays, effective processing of large genomic datasets is crucial for reliable species detection in biodiversity monitoring. While considerable focus has been on developing robust species-targeted assays, eDNA assays with broader taxonomic coverage (e.g., detecting any species within a taxonomic group such as fish), can significantly streamline environmental monitoring, especially when detecting individual species' DNA proves challenging. Designing such assays requires identifying conserved regions representing the target taxonomic group, a chiefly manual task that is often labor-intensive and error-prone, particularly when working with large sequence datasets. To address these challenges, we present unikseq2, an enhanced, alignment-free, k-mer-based tool for identifying unique and conserved sequences. It introduces a new functionality to identify sequence conservation among target species, enabling more informed marker selection for applications such as universal primer design. This automates sequence selection in large-scale mitochondrial genome datasets eliminating the need for manual inspection of computationally costly multiple sequence alignments. Herein, we demonstrate unikseq2's capabilities by developing and validating eDNA assays for various taxa, including Osteichthyes (bony fishes), the Salmonidae family (salmon and trout), Myotis bats and Cervus deer. Unikseq2-based eDNA assays allow for accurate detection across multiple taxonomic levels, from genus to class, enhancing the flexibility, scalability and reliability of eDNA tools in environmental monitoring. By leveraging genomic data from public repositories, unikseq2 supports efficient, reproducible assay design, making it an invaluable tool for a wide range of ecological and biodiversity research applications.

Indexed as

Computational BiologyConserved SequenceDNA, EnvironmentalGenomicsAnimalsFishesSequence Analysis, DNADNA, EnvironmentaleDNA assay designqPCR assaysequence conservationuniversal primer development

Identifiers

PMID40642868
PMCPMC12415942

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Registered trials

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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.