Evidence map›Paper›PMID 26977894›Full record

ArticlePLoS genetics2016

S/HIC: Robust Identification of Soft and Hard Sweeps Using Machine Learning.

Daniel R Schrider, Andrew D Kern

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 126 papers.

0numbers the graph read from it
0cells of the map it votes in
126citing papers in PubMed
24.0field-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

126 citing papers in PubMed, 219 citations in OpenAlex.

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  9. Omics Technologies in Molecular Biology.International journal of molecular sciences · 2026
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  12. Neural posterior estimation for population genetics.bioRxiv : the preprint server for biology · 2026
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  17. Global impact of micronutrients in modern human evolution.American journal of human genetics · 2025
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  20. Article

66 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

2 authors at 1 institution in 1 country.

Daniel R SchriderDepartment of Genetics, Rutgers University, Piscataway, New Jersey, United States of America.
Andrew D KernDepartment of Genetics, Rutgers University, Piscataway, New Jersey, United States of America.
Rutgers, The State University of New Jersey · US

Funding

The Population Genetics of DivergenceR01GM078204 · NIGMS · TEMPLE UNIV OF THE COMMONWEALTH · PI HEY, EMANUEL · 2007 to 2016
$1.7M
Human-Specific Gain and Loss of FunctionF32GM105231 · NIGMS · RUTGERS, THE STATE UNIV OF N.J. · PI SCHRIDER, DANIEL R · 2013 to 2015
$153k
NIGMS NIH HHS F32 GM105231NIGMS NIH HHS R01 GM078204NIGMS NIH HHS R01GM078204
6 · The paper itself

Abstract

Detecting the targets of adaptive natural selection from whole genome sequencing data is a central problem for population genetics. However, to date most methods have shown sub-optimal performance under realistic demographic scenarios. Moreover, over the past decade there has been a renewed interest in determining the importance of selection from standing variation in adaptation of natural populations, yet very few methods for inferring this model of adaptation at the genome scale have been introduced. Here we introduce a new method, S/HIC, which uses supervised machine learning to precisely infer the location of both hard and soft selective sweeps. We show that S/HIC has unrivaled accuracy for detecting sweeps under demographic histories that are relevant to human populations, and distinguishing sweeps from linked as well as neutrally evolving regions. Moreover, we show that S/HIC is uniquely robust among its competitors to model misspecification. Thus, even if the true demographic model of a population differs catastrophically from that specified by the user, S/HIC still retains impressive discriminatory power. Finally, we apply S/HIC to the case of resequencing data from human chromosome 18 in a European population sample, and demonstrate that we can reliably recover selective sweeps that have been identified earlier using less specific and sensitive methods.

Indexed as

Genetic DriftGenetics, PopulationMachine LearningChromosomes, Human, Pair 18Genome, HumanHaplotypesHumansSelection, Genetic

Identifiers

PMID26977894
PMCPMC4792382
OpenAlexW2950732129

What OpenQuestion holds

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LicenceCC BY
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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.