Evidence map›Paper›PMID 30666785›Full record

ArticleMolecular ecology resources2019

LDJump: Estimating variable recombination rates from population genetic data.

Philipp Hermann, Angelika Heissl, Irene Tiemann-Boege, Andreas Futschik

Open access · hybridAbstract read
In one paragraph

Article in Molecular ecology resources, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.2field-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

13 citing papers in PubMed, 28 citations in OpenAlex.

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  7. Chromosome-Level Haplotype Assembly forFrontiers in genetics · 2022
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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

4 authors at 1 institution in 1 country.

Philipp HermannDepartment of Applied Statistics, Johannes Kepler University Linz, Linz, Austria.ORCID https://orcid.org/0000-0003-4556-6297
Angelika HeisslInstitute of Biophysics, Johannes Kepler University Linz, Linz, Austria.
Irene Tiemann-BoegeInstitute of Biophysics, Johannes Kepler University Linz, Linz, Austria.ORCID https://orcid.org/0000-0002-3621-7020
Andreas FutschikDepartment of Applied Statistics, Johannes Kepler University Linz, Linz, Austria.ORCID https://orcid.org/0000-0002-7980-0304
Johannes Kepler University of Linz · AT

Funding

Austrian Academy of Sciences 24529Austrian Science Fund P27698-B22Austrian Science Fund FWF P 27698
6 · The paper itself

Abstract

As recombination plays an important role in evolution, its estimation and the identification of hotspot positions is of considerable interest. We propose a novel approach for estimating population recombination rates based on genotyping or sequence data that involves a sequential multiscale change point estimator. Our method also permits demography to be taken into account. It uses several summary statistics within a regression model fitted on suitable scenarios. Our proposed method is accurate, computationally fast, and provides a parsimonious solution by ensuring a type I error control against too many changes in the recombination rate. An application to human genome data suggests a good congruence between our estimated and experimentally identified hotspots. Our method is implemented in the R-package LDJump, which is freely available at https://github.com/PhHermann/LDJump.

Indexed as

Recombination, GeneticComputational BiologyGenetics, PopulationGenotyping TechniquesHumansSequence Analysis, DNAbioinformaticschange-point estimationpopulation recombination rateregressionR-package

Identifiers

PMID30666785
PMCPMC6519033
OpenAlexW2951087614

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.