Evidence map›Paper›PMID 31424552›Full record

ArticleMolecular biology and evolution2019

Contemporary Demographic Reconstruction Methods Are Robust to Genome Assembly Quality: A Case Study in Tasmanian Devils.

Austin H Patton, Mark J Margres, Amanda R Stahlke, Sarah Hendricks, Kevin Lewallen, Rodrigo K Hamede, Manuel Ruiz-Aravena, Oliver Ryder, Hamish I McCallum, Menna E Jones and 2 more

Abstract readEvaluation Study
In one paragraph

Article in Molecular biology and evolution, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing 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

55 citing papers in PubMed.

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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

12 authors.

Austin H PattonSchool of Biological Sciences, Washington State University, Pullman, WA.
Mark J MargresSchool of Biological Sciences, Washington State University, Pullman, WA.
Amanda R StahlkeInstitute for Bioinformatics and Evolutionary Studies, University of Idaho, Moscow, ID.
Sarah HendricksInstitute for Bioinformatics and Evolutionary Studies, University of Idaho, Moscow, ID.
Kevin LewallenInstitute for Bioinformatics and Evolutionary Studies, University of Idaho, Moscow, ID.
Rodrigo K HamedeSchool of Natural Sciences, University of Tasmania, Hobart, Australia.
Manuel Ruiz-AravenaSchool of the Environment, Griffith University, Nathan, Australia.
Oliver RyderInstitute for Conservation Research, San Diego, CA.
Hamish I McCallumSchool of the Environment, Griffith University, Nathan, Australia.
Menna E JonesSchool of Natural Sciences, University of Tasmania, Hobart, Australia.
Paul A HohenloheInstitute for Bioinformatics and Evolutionary Studies, University of Idaho, Moscow, ID.
Andrew StorferSchool of Biological Sciences, Washington State University, Pullman, WA.

Funding

Genomics Resources Core (GRC)P30GM103324 · NIGMS · UNIVERSITY OF IDAHO · PI FORNEY, LARRY J · 2013 to 2017
$5.0M
Evolution of cancer transmissionR01GM126563 · NIGMS · WASHINGTON STATE UNIVERSITY · PI STORFER, ANDREW T · 2017 to 2020
$2.3M
NIGMS NIH HHS P30 GM103324NIGMS NIH HHS R01 GM126563
6 · The paper itself

Abstract

Reconstructing species' demographic histories is a central focus of molecular ecology and evolution. Recently, an expanding suite of methods leveraging either the sequentially Markovian coalescent (SMC) or the site-frequency spectrum has been developed to reconstruct population size histories from genomic sequence data. However, few studies have investigated the robustness of these methods to genome assemblies of varying quality. In this study, we first present an improved genome assembly for the Tasmanian devil using the Chicago library method. Compared with the original reference genome, our new assembly reduces the number of scaffolds (from 35,975 to 10,010) and increases the scaffold N90 (from 0.101 to 2.164 Mb). Second, we assess the performance of four contemporary genomic methods for inferring population size history (PSMC, MSMC, SMC++, Stairway Plot), using the two devil genome assemblies as well as simulated, artificially fragmented genomes that approximate the hypothesized demographic history of Tasmanian devils. We demonstrate that each method is robust to assembly quality, producing similar estimates of Ne when simulated genomes were fragmented into up to 5,000 scaffolds. Overall, methods reliant on the SMC are most reliable between ∼300 generations before present (gbp) and 100 kgbp, whereas methods exclusively reliant on the site-frequency spectrum are most reliable between the present and 30 gbp. Our results suggest that when used in concert, genomic methods for reconstructing species' effective population size histories 1) can be applied to nonmodel organisms without highly contiguous reference genomes, and 2) are capable of detecting independently documented effects of historical geological events.

Indexed as

GenomeAnimalsDemographyFemaleGenomicsMarsupialiademographic historySFSsimulationSMCTasmanian devilwhole-genome assembly

Identifiers

PMID31424552
PMCPMC6878949

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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.