Evidence map›Paper›PMID 38895364›Full record

ArticlebioRxiv : the preprint server for biology2024

Comparing statistical learning methods for complex trait prediction from gene expression.

Noah Klimkowski Arango, Fabio Morgante

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. 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

2 authors.

Noah Klimkowski ArangoCenter for Human Genetics, Clemson University, Greenwood, SC, USA.
Fabio MorganteCenter for Human Genetics, Clemson University, Greenwood, SC, USA.ORCID 0000-0003-3285-1988

Funding

Understanding and using gene-by-context interactions in human complex trait geneticsR35GM146868 · NIGMS · CLEMSON UNIVERSITY · PI Fabio Morgante · 2022 to 2026
$1.9M
NIGMS NIH HHS R35 GM146868
6 · The paper itself

Abstract

Accurate prediction of complex traits is an important task in quantitative genetics that has become increasingly relevant for personalized medicine. Genotypes have traditionally been used for trait prediction using a variety of methods such as mixed models, Bayesian methods, penalized regressions, dimension reductions, and machine learning methods. Recent studies have shown that gene expression levels can produce higher prediction accuracy than genotypes. However, only a few prediction methods were used in these studies. Thus, a comprehensive assessment of methods is needed to fully evaluate the potential of gene expression as a predictor of complex trait phenotypes. Here, we used data from the

Identifiers

PMID38895364
PMCPMC11185554

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.