Evidence map›Paper›PMID 37369060›Full record

ArticleHuman molecular genetics2023

Integrating GWAS summary statistics, individual-level genotypic and omic data to enhance the performance for large-scale trait imputation.

Jingchen Ren, Zhaotong Lin, Wei Pan

Abstract read
In one paragraph

Article in Human molecular genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

3 authors.

Jingchen RenSchool of Statistics, University of Minnesota, Minneapolis, MN 55455, USA.
Zhaotong LinDivision of Biostatistics, School of Public Health, University of Minnesota, Minneapolis, MN 55455, USA.ORCID 0000-0001-8723-4392
Wei PanDivision of Biostatistics, School of Public Health, University of Minnesota, Minneapolis, MN 55455, USA.ORCID 0000-0002-1159-0582

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 AG067924NIGMS NIH HHS R01 GM126002NIH HHS U01 AG073079
6 · The paper itself

Abstract

Recently, a non-parametric method has been proposed to impute the genetic component of a trait for a large set of genotyped individuals based on a separate genome-wide association study (GWAS) summary dataset of the same trait (from the same population). The imputed trait may contain linear, non-linear and epistatic effects of genetic variants, thus can be used for downstream linear or non-linear association analyses and machine learning tasks. Here, we propose an extension of the method to impute both genetic and environmental components of a trait using both single nucleotide polymorphism (SNP)-trait and omics-trait association summary data. We illustrate an application to a UK Biobank subset of individuals (n ≈ 80K) with both body mass index (BMI) GWAS data and metabolomic data. We divided the whole dataset into two equally sized and non-overlapping training and test datasets; we used the training data to build SNP- and metabolite-BMI association summary data and impute BMI on the test data. We compared the performance of the original and new imputation methods. As by the original method, the imputed BMI values by the new method largely retained SNP-BMI association information; however, the latter retained more information about BMI-environment associations and were more highly correlated with the original observed BMI values.

Indexed as

Genome-Wide Association StudyPolymorphism, Single NucleotideGenotypeHumansPhenotype

Identifiers

PMID37369060
PMCPMC10460491

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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.