Evidence map›Paper›PMID 31565556›Full record

ArticlePeerJ2019

Genome skimming is a low-cost and robust strategy to assemble complete mitochondrial genomes from ethanol preserved specimens in biodiversity studies.

Bruna Trevisan, Daniel M C Alcantara, Denis Jacob Machado, Fernando P L Marques, Daniel J G Lahr

Open access · goldAbstract read
In one paragraph

Article in PeerJ, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
3.0field-weighted citation impact, top 8% of its field
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

33 citing papers in PubMed, 88 citations in OpenAlex.

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  13. Cryptic diversity patterns of subterranean estuaries.Proceedings. Biological sciences · 2024
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  15. Article
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  18. The complete mitochondrial genome ofMitochondrial DNA. Part B, Resources · 2023
    Article
  19. The complete mitochondrial genome ofMitochondrial DNA. Part B, Resources · 2023
    Article
  20. The complete mitochondrial genome ofMitochondrial DNA. Part B, Resources · 2023
    Article
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 at 2 institutions in 2 countries.

Bruna Trevisan *Department of Zoology, Institute of Biosciences, University of São Paulo, São Paulo, São Paulo, Brazil.
Daniel M C Alcantara *Department of Zoology, Institute of Biosciences, University of São Paulo, São Paulo, São Paulo, Brazil.
Denis Jacob MachadoDepartment of Zoology, Institute of Biosciences, University of São Paulo, São Paulo, São Paulo, Brazil.
Fernando P L MarquesDepartment of Zoology, Institute of Biosciences, University of São Paulo, São Paulo, São Paulo, Brazil.
Daniel J G LahrDepartment of Zoology, Institute of Biosciences, University of São Paulo, São Paulo, São Paulo, Brazil.
Universidade de São Paulo · BRUniversity of North Carolina at Charlotte · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Global loss of biodiversity is an ongoing process that concerns both local and global authorities. Studies of biodiversity mainly involve traditional methods using morphological characters and molecular protocols. However, conventional methods are a time consuming and resource demanding task. The development of high-throughput sequencing (HTS) techniques has reshaped the way we explore biodiversity and opened a path to new questions and novel empirical approaches. With the emergence of HTS, sequencing the complete mitochondrial genome became more accessible, and the number of genome sequences published has increased exponentially during the last decades. Despite the current state of knowledge about the potential of mitogenomics in phylogenetics, this is still a relatively under-explored area for a multitude of taxonomic groups, especially for those without commercial relevance, non-models organisms and with preserved DNA. Here we take the first step to assemble and annotate the genomes from HTS data using a new protocol of genome skimming which will offer an opportunity to extend the field of mitogenomics to under-studied organisms. We extracted genomic DNA from specimens preserved in ethanol. We used Nextera XT DNA to prepare indexed paired-end libraries since it is a powerful tool for working with diverse samples, requiring a low amount of input DNA. We sequenced the samples in two different Illumina platform (MiSeq or NextSeq 550). We trimmed raw reads, filtered and had their quality tested accordingly. We performed the assembly using a baiting and iterative mapping strategy, and the annotated the putative mitochondrion through a semi-automatic procedure. We applied the contiguity index to access the completeness of each new mitogenome. Our results reveal the efficiency of the proposed method to recover the whole mitogenomes of preserved DNA from non-model organisms even if there are gene rearrangement in the specimens. Our findings suggest the potential of combining the adequate platform and library to the genome skimming as an innovative approach, which opens a new range of possibilities of its use to obtain molecular data from organisms with different levels of preservation.

Indexed as

Automated annotationAutomated assemblyCestodaDipteraHigh-coverage genomeMitochondrial genomePoorly preserved samples

Identifiers

PMID31565556
PMCPMC6746217
OpenAlexW2972874364

What OpenQuestion 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 OpenQuestion graph.