Evidence map›Paper›PMID 23979584›Full record

ArticleGenetics2013

Quantifying population genetic differentiation from next-generation sequencing data.

Matteo Fumagalli, Filipe G Vieira, Thorfinn Sand Korneliussen, Tyler Linderoth, Emilia Huerta-Sánchez, Anders Albrechtsen, Rasmus Nielsen

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Genetics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 99 papers.

0numbers the graph read from it
0cells of the map it votes in
99citing papers in PubMed
11.4field-weighted citation impact, top 1% 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

99 citing papers in PubMed, 220 citations in OpenAlex.

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  17. Horticulture research · 2024
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39 more citing papers are in PubMed but not listed here.

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 at 2 institutions in 2 countries.

Matteo FumagalliDepartment of Integrative Biology, University of California, Berkeley, California 94720.
Filipe G Vieira
Thorfinn Sand Korneliussen
Tyler Linderoth
Emilia Huerta-Sánchez
Anders Albrechtsen
Rasmus Nielsen
University of California, Berkeley · USUniversity of Copenhagen · DK

Funding

GENOMICST32HG000047 · NHGRI · UNIVERSITY OF CALIFORNIA BERKELEY · PI RASMUS NIELSEN, Daniel Soleyman Rokhsar · 2000 to 2026
$13.5M
Population Genetic Inferences From Dense Genotype DataR01HG003229 · NHGRI · CORNELL UNIVERSITY ITHACA · PI BUSTAMANTE, CARLOS DANIEL, CLARK, ANDREW G · 2004 to 2013
$4.8M
NHGRI NIH HHS 3R01HG03229-07NHGRI NIH HHS 3R01HG03229-08S2NHGRI NIH HHS R01 HG003229NHGRI NIH HHS T32 HG000047NHGRI NIH HHS T32HG000047-13
6 · The paper itself

Abstract

Over the past few years, new high-throughput DNA sequencing technologies have dramatically increased speed and reduced sequencing costs. However, the use of these sequencing technologies is often challenged by errors and biases associated with the bioinformatical methods used for analyzing the data. In particular, the use of naïve methods to identify polymorphic sites and infer genotypes can inflate downstream analyses. Recently, explicit modeling of genotype probability distributions has been proposed as a method for taking genotype call uncertainty into account. Based on this idea, we propose a novel method for quantifying population genetic differentiation from next-generation sequencing data. In addition, we present a strategy for investigating population structure via principal components analysis. Through extensive simulations, we compare the new method herein proposed to approaches based on genotype calling and demonstrate a marked improvement in estimation accuracy for a wide range of conditions. We apply the method to a large-scale genomic data set of domesticated and wild silkworms sequenced at low coverage. We find that we can infer the fine-scale genetic structure of the sampled individuals, suggesting that employing this new method is useful for investigating the genetic relationships of populations sampled at low coverage.

Indexed as

AnimalsBombyxComputational BiologyComputer SimulationData Interpretation, StatisticalGenetic DriftGenetics, PopulationGenetic VariationGenotypeHigh-Throughput Nucleotide SequencingLikelihood FunctionsModels, GeneticMutationPrincipal Component AnalysisSelection, GeneticFSTnext-generation sequencingprincipal components analysis

Identifiers

PMID23979584
PMCPMC3813878
OpenAlexW2112902627

What OpenQuestion holds

Textmetadata
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.