Evidence map›Paper›PMID 38559266›Full record

ArticlebioRxiv : the preprint server for biology2024

Genotype prediction of 336,463 samples from public expression data.

Afrooz Razi, Christopher C Lo, Siruo Wang, Jeffrey T Leek, Kasper D Hansen

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. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

5 authors.

Afrooz RaziDepartment of Genetic Medicine, Johns Hopkins University School of Medicine.ORCID 0000-0003-4556-9383
Christopher C LoDepartment of Biostatistics, Johns Hopkins Bloomberg School of Public Health.
Siruo WangDepartment of Biostatistics, Johns Hopkins Bloomberg School of Public Health.
Jeffrey T LeekBiostatistics Program, Division of Public Health Sciences, Fred Hutchinson Cancer Center.ORCID 0000-0002-2873-2671
Kasper D HansenDepartment of Genetic Medicine, Johns Hopkins University School of Medicine.ORCID 0000-0003-0086-0687

Funding

Implementing the Genomic Data Science Analysis, Visualization, and Informatics Lab-space (AnVIL)U24HG010263 · NHGRI · JOHNS HOPKINS UNIVERSITY · PI Enis Afgan, VINCENT JAMES CAREY · 2018 to 2026
$23.8M
Predoctoral Training Program in Human GeneticsT32GM148383 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI Kimberly F Doheny, ANDREW S MCCALLION · 2023 to 2026
$2.4M
Analysis of genomics datasets at a massive scaleR01GM121459 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI HANSEN, KASPER DANIEL · 2017 to 2021
$2.3M
Data analysis tools for leveraging massive public data to improve hypothesis-driven researchR35GM144128 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI Jeffrey T. Leek · 2022 to 2026
$2.2M
Data Science Tools to Increase Insight in Genomics DataR35GM149323 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI Kasper Daniel Hansen · 2023 to 2026
$1.8M
NHGRI NIH HHS U24 HG010263NIGMS NIH HHS R01 GM121459NIGMS NIH HHS R35 GM144128NIGMS NIH HHS R35 GM149323NIGMS NIH HHS T32 GM148383
6 · The paper itself

Abstract

Tens of thousands of RNA-sequencing experiments comprising hundreds of thousands of individual samples have now been performed. These data represent a broad range of experimental conditions, sequencing technologies, and hypotheses under study. The Recount project has aggregated and uniformly processed hundreds of thousands of publicly available RNA-seq samples. Most of these samples only include RNA expression measurements; genotype data for these same samples would enable a wide range of analyses including variant prioritization, eQTL analysis, and studies of allele specific expression. Here, we developed a statistical model based on the existing reference and alternative read counts from the RNA-seq experiments available through Recount3 to predict genotypes at autosomal biallelic loci in coding regions. We demonstrate the accuracy of our model using large-scale studies that measured both gene expression and genotype genome-wide. We show that our predictive model is highly accurate with 99.5% overall accuracy, 99.6% major allele accuracy, and 90.4% minor allele accuracy. Our model is robust to tissue and study effects, provided the coverage is high enough. We applied this model to genotype all the samples in Recount 3 and provide the largest ready-to-use expression repository containing genotype information. We illustrate that the predicted genotype from RNA-seq data is sufficient to unravel the underlying population structure of samples in Recount3 using Principal Component Analysis.

Identifiers

PMID38559266
PMCPMC10979922

What Socratic holds

Textmetadata
LicenceCC BY-ND
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 Socratic graph.