Evidence map›Paper›PMID 39038848›Full record

ArticleGenome research2024

Scalable summary-statistics-based heritability estimation method with individual genotype level accuracy.

Moonseong Jeong, Ali Pazokitoroudi, Zhengtong Liu, Sriram Sankararaman

Abstract read
In one paragraph

Article in Genome research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Unravelling the genetic architecture of cerebral small vessel disease in the context of stroke.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2026
    Review
  2. Article
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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.

Moonseong JeongDepartment of Computer Science, University of California, Los Angeles, Los Angeles, California 90095, USA; bronsonj@cs.ucla.edu sriram@cs.ucla.edu.ORCID 0009-0009-3836-2676
Ali PazokitoroudiDepartment of Computer Science, University of California, Los Angeles, Los Angeles, California 90095, USA.ORCID 0000-0002-2839-2291
Zhengtong LiuDepartment of Computer Science, University of California, Los Angeles, Los Angeles, California 90095, USA.ORCID 0009-0008-2467-9376
Sriram SankararamanDepartment of Computer Science, University of California, Los Angeles, Los Angeles, California 90095, USA; bronsonj@cs.ucla.edu sriram@cs.ucla.edu.ORCID 0000-0003-1586-9641

Funding

Methods for Genome-wide Association Studies in Admixed PopulationsR01HG006399 · NHGRI · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI PRICE, ALKES L · 2011 to 2024
$6.3M
Statistical Models for Dissecting Human Population Admixture and its Role in Evolution and DiseaseR35GM125055 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SANKARARAMAN, SRIRAM · 2017 to 2021
$1.6M
Expressive and scalable statistical models for genomic and biomedical dataR35GM153406 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Sriram Sankararaman · 2024 to 2026
$1.0M
NHGRI NIH HHS R01 HG006399NIGMS NIH HHS R35 GM125055NIGMS NIH HHS R35 GM153406
6 · The paper itself

Abstract

SNP heritability, the proportion of phenotypic variation explained by genotyped SNPs, is an important parameter in understanding the genetic architecture underlying various diseases and traits. Methods that aim to estimate SNP heritability from individual genotype and phenotype data are limited by their ability to scale to Biobank-scale data sets and by the restrictions in access to individual-level data. These limitations have motivated the development of methods that only require summary statistics. Although the availability of publicly accessible summary statistics makes them widely applicable, these methods lack the accuracy of methods that utilize individual genotypes. Here we present a SUMmary-statistics-based Randomized Haseman-Elston regression (SUM-RHE), a method that can estimate the SNP heritability of complex phenotypes with accuracies comparable to approaches that require individual genotypes, while exclusively relying on summary statistics. SUM-RHE employs Genome-Wide Association Study (GWAS) summary statistics and statistics obtained on a reference population, which can be efficiently estimated and readily shared for public use. Our results demonstrate that SUM-RHE obtains estimates of SNP heritability that are substantially more accurate compared with other summary statistic methods and on par with methods that rely on individual-level data.

Indexed as

Genome-Wide Association StudyGenotypePolymorphism, Single NucleotideHumansModels, GeneticPhenotypeQuantitative Trait, Heritable

Identifiers

PMID39038848
PMCPMC11529871

What OpenQuestion holds

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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.