Evidence map›Paper›PMID 38011285›Full record

ArticlePLoS genetics2023

Transfer learning with false negative control improves polygenic risk prediction.

Xinge Jessie Jeng, Yifei Hu, Vaishnavi Venkat, Tzu-Pin Lu, Jung-Ying Tzeng

Abstract read
In one paragraph

Article in PLoS genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
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  4. Review
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

5 authors.

Xinge Jessie JengDepartment of Statistics, North Carolina State University, Raleigh, North Carolina, United States of America.
Yifei HuDepartment of Statistics, North Carolina State University, Raleigh, North Carolina, United States of America.
Vaishnavi VenkatBioinformatics Research Center, North Carolina State University, Raleigh, North Carolina, United States of America.ORCID 0009-0004-8206-9403
Tzu-Pin LuInstitute of Health Data Analytics and Statistics, National Taiwan University, Taipei, Taiwan.
Jung-Ying TzengDepartment of Statistics, North Carolina State University, Raleigh, North Carolina, United States of America.ORCID 0000-0002-5505-1775

Funding

THE NIA GENETICS OF ALZHEIMER'S DISEASE DATA STORAGE SITEU24AG041689 · NIA · UNIVERSITY OF PENNSYLVANIA · PI LI-SAN WANG · 2012 to 2026
$42.3M
Copy Number Variation Identification and Association Study on Alzheimer's Disease Whole Genome Sequencing DataRF1AG074328 · NIA · UNIVERSITY OF PENNSYLVANIA · PI LEE, WAN-PING, TZENG, JUNG-YING · 2021 to 2021
$2.3M
NIA NIH HHS RF1 AG074328NIA NIH HHS U24 AG041689
6 · The paper itself

Abstract

Polygenic risk score (PRS) is a quantity that aggregates the effects of variants across the genome and estimates an individual's genetic predisposition for a given trait. PRS analysis typically contains two input data sets: base data for effect size estimation and target data for individual-level prediction. Given the availability of large-scale base data, it becomes more common that the ancestral background of base and target data do not perfectly match. In this paper, we treat the GWAS summary information obtained in the base data as knowledge learned from a pre-trained model, and adopt a transfer learning framework to effectively leverage the knowledge learned from the base data that may or may not have similar ancestral background as the target samples to build prediction models for target individuals. Our proposed transfer learning framework consists of two main steps: (1) conducting false negative control (FNC) marginal screening to extract useful knowledge from the base data; and (2) performing joint model training to integrate the knowledge extracted from base data with the target training data for accurate trans-data prediction. This new approach can significantly enhance the computational and statistical efficiency of joint-model training, alleviate over-fitting, and facilitate more accurate trans-data prediction when heterogeneity level between target and base data sets is small or high.

Indexed as

Genome-Wide Association StudyPolymorphism, Single NucleotideGenetic Predisposition to DiseaseHumansMachine LearningMultifactorial InheritancePhenotypeRisk Factors

Identifiers

PMID38011285
PMCPMC10723713

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.