Evidence map›Paper›PMID 38045347›Full record

ArticlebioRxiv : the preprint server for biology2023

Inferring a directed acyclic graph of phenotypes from GWAS summary statistics.

Rachel Zilinskas, Chunlin Li, Xiaotong Shen, Wei Pan, Tianzhong Yang

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
0cells of the map it votes in
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

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

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

5 authors.

Rachel ZilinskasStatistics and Data Corporation, Tempe, Arizona 85288, U.S.A.
Chunlin LiDepartment of Statistics, Iowa State University, Ames, Iowa 50011, U.S.A.ORCID 0000-0003-2989-8785
Xiaotong ShenSchool of Statistics, University of Minnesota, Minneapolis, Minnesota 55455, U.S.A.ORCID 0000-0003-1300-1451
Wei PanDivision of Biostatistics and Health Data Science, University of Minnesota, Minneapolis, Minnesota 55455, U.S.A.ORCID 0000-0002-1159-0582
Tianzhong YangDivision of Biostatistics and Health Data Science, University of Minnesota, Minneapolis, Minnesota 55455, U.S.A.ORCID 0000-0002-0162-7740

Funding

Causal and integrative deep learning for Alzheimer's disease geneticsU01AG073079 · NIA · UNIVERSITY OF MINNESOTA · PI PAN, WEI · 2021 to 2025
$3.5M
Deep Learning with Neuroimaging Genetic Data for Alzheimer's DiseaseR01AG069895 · NIA · UNIVERSITY OF MINNESOTA · PI PAN, WEI, SHEN, XIAOTONG TOM · 2020 to 2024
$3.4M
Association analysis of rare variants with sequencing dataR01HL116720 · NHLBI · UNIVERSITY OF MINNESOTA · PI PAN, WEI, WEI, PENG · 2013 to 2020
$3.3M
Discovering causal genes, brain regions and other risk factors for Alzheimer's DiseaseR01AG065636 · NIA · UNIVERSITY OF MINNESOTA · PI PAN, WEI · 2020 to 2024
$3.1M
Integrating Alzheimer's disease GWAS with proteomic and metabolomic QTL dataRF1AG067924 · NIA · UNIVERSITY OF MINNESOTA · PI PAN, WEI · 2020 to 2020
$1.9M
Estimation and Inference of Gene Regulatory NetworksR01GM126002 · NIGMS · UNIVERSITY OF MINNESOTA · PI PAN, WEI, SHEN, XIAOTONG TOM · 2017 to 2020
$1.4M
NHLBI NIH HHS R01 HL116720NIA NIH HHS R01 AG065636NIA NIH HHS R01 AG069895NIA NIH HHS RF1 AG067924NIA NIH HHS U01 AG073079NIGMS NIH HHS R01 GM126002
6 · The paper itself

Abstract

Estimating phenotype networks is a growing field in computational biology. It deepens the understanding of disease etiology and is useful in many applications. In this study, we present a method that constructs a phenotype network by assuming a Gaussian linear structure model embedding a directed acyclic graph (DAG). We utilize genetic variants as instrumental variables and show how our method only requires access to summary statistics from a genome-wide association study (GWAS) and a reference panel of genotype data. Besides estimation, a distinct feature of the method is its summary statistics-based likelihood ratio test on directed edges. We applied our method to estimate a causal network of 29 cardiovascular-related proteins and linked the estimated network to Alzheimer's disease (AD). A simulation study was conducted to demonstrate the effectiveness of this method. An R package sumdag implementing the proposed method, all relevant code, and a Shiny application are available at https://github.com/chunlinli/sumdag.

Indexed as

Alzheimer’s disease (AD)directed acyclic graph (DAG)genome-wide association study (GWAS)likelihood ratio testproteomics

Identifiers

PMID38045347
PMCPMC10690198

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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.