Evidence map›Paper›PMID 37066144›Full record

ArticlebioRxiv : the preprint server for biology2023

Tree-based QTL mapping with expected local genetic relatedness matrices.

Vivian Link, Joshua G Schraiber, Caoqi Fan, Bryan Dinh, Nicholas Mancuso, Charleston W K Chiang, Michael D Edge

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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0citing 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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Vivian LinkDepartment of Quantitative and Computational Biology, University of Southern California.
Joshua G SchraiberDepartment of Quantitative and Computational Biology, University of Southern California.
Caoqi FanDepartment of Quantitative and Computational Biology, University of Southern California.
Bryan DinhDepartment of Quantitative and Computational Biology, University of Southern California.
Nicholas MancusoDepartment of Quantitative and Computational Biology, University of Southern California.
Charleston W K ChiangDepartment of Quantitative and Computational Biology, University of Southern California.
Michael D EdgeDepartment of Quantitative and Computational Biology, University of Southern California.

Funding

Leveraging the Evolutionary History to Improve Identification of Trait-Associated Alleles and Risk Stratification Models in Native HawaiiansR01HG011646 · NHGRI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Charleston Chiang · 2022 to 2026
$4.0M
Characterizing the evolutionary architecture of complex disease within and across diverse populationsR01HG012133 · NHGRI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI MANCUSO, NICHOLAS · 2021 to 2025
$3.6M
Traits on trees: Population genomics for understanding complex phenotypesR35GM137758 · NIGMS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Michael Donald Edge · 2020 to 2026
$2.5M
An evolutionary framework to elucidate and interpret the genetic architecture of complex traits in diverse populations - diversity supplementR35GM142783 · NIGMS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI CHIANG, CHARLESTON · 2021 to 2025
$2.2M
Genomic resources and references for genetic investigation of an understudied populationF31HG012159 · NHGRI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI DINH, BRYAN LY · 2021 to 2024
$143k
NHGRI NIH HHS F31 HG012159NHGRI NIH HHS R01 HG011646NHGRI NIH HHS R01 HG012133NIGMS NIH HHS R35 GM137758NIGMS NIH HHS R35 GM142783
6 · The paper itself

Abstract

Understanding the genetic basis of complex phenotypes is a central pursuit of genetics. Genome-wide Association Studies (GWAS) are a powerful way to find genetic loci associated with phenotypes. GWAS are widely and successfully used, but they face challenges related to the fact that variants are tested for association with a phenotype independently, whereas in reality variants at different sites are correlated because of their shared evolutionary history. One way to model this shared history is through the ancestral recombination graph (ARG), which encodes a series of local coalescent trees. Recent computational and methodological breakthroughs have made it feasible to estimate approximate ARGs from large-scale samples. Here, we explore the potential of an ARG-based approach to quantitative-trait locus (QTL) mapping, echoing existing variance-components approaches. We propose a framework that relies on the conditional expectation of a local genetic relatedness matrix given the ARG (local eGRM). Simulations show that our method is especially beneficial for finding QTLs in the presence of allelic heterogeneity. By framing QTL mapping in terms of the estimated ARG, we can also facilitate the detection of QTLs in understudied populations. We use local eGRM to identify a large-effect BMI locus, the

Identifiers

PMID37066144
PMCPMC10104234

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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.