Evidence map›Paper›PMID 41836511›Full record

ArticleResearch square2026

RNAScope-Ancestry: A Cross-Modality Framework for Inferring Genetic Ancestry from RNA-Seq with Application to MECA.

Rashi Verma, Shivam Sharma, Harriet Na Blankson, Emine Guven, Andrea Pearson, Charles D Searles, Peter Baltrus, Tene T Lewis, Priscilla Pemu, Dean Jones and 4 more

Abstract readPreprint
In one paragraph

Article in Research square, 2026. 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

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

14 authors.

Rashi VermaMorehouse School of Medicine.
Shivam SharmaGeorgia Institute of Technology.
Harriet Na BlanksonMorehouse School of Medicine.
Emine GuvenMorehouse School of Medicine.
Andrea PearsonMorehouse School of Medicine.
Charles D SearlesAtlanta VA Health Care System.
Peter BaltrusMorehouse School of Medicine.
Tene T LewisEmory University School of Medicine.
Priscilla PemuMorehouse School of Medicine.
Dean JonesEmory University School of Medicine.
Arshed Ali QuyyumiEmory University School of Medicine.
Herman TaylorMorehouse School of Medicine.
I King JordanGeorgia Institute of Technology.
Robert MellerMorehouse School of Medicine.

Funding

Yerkes National Primate Research Center Role of type-I IFN in regulating COVID-19 induced inflammation and pathogenesisP51OD011132 · OD · EMORY UNIVERSITY · PI Joon Sup Lee · 2012 to 2026
$167.0M
Workforce Development CoreU54HG013595 · NHGRI · MOREHOUSE SCHOOL OF MEDICINE · PI Robert Meller · 2024 to 2026
$6.4M
Blood transcriptomics as CT adjuvant to exclude hemorrhage in acute strokeR01NS112422 · NINDS · MOREHOUSE SCHOOL OF MEDICINE · PI MELLER, ROBERT · 2020 to 2024
$2.8M
Translating genomic profiling to bedside precision medicineRM1HG012334 · NHGRI · MOREHOUSE SCHOOL OF MEDICINE · PI BALTRUS, PETER T, MELLER, ROBERT · 2022 to 2022
$2.5M
Illumina NovaSeq 6000 High Throughput DNA Sequencer for Emory UniversityS10OD026799 · OD · EMORY UNIVERSITY · PI BOSINGER, STEVEN EDWARD · 2019 to 2019
$985k
NHGRI NIH HHS RM1 HG012334NHGRI NIH HHS U54 HG013595NIH HHS P51 OD011132NIH HHS S10 OD026799NINDS NIH HHS R01 NS112422
6 · The paper itself

Abstract

Genetic ancestry inference traditionally relies on genotyping arrays or whole-genome sequencing. We present RNAScope-Ancestry, a computational pipeline that leverages short-read RNA-seq for dual-purpose ancestry and transcriptomic analysis. Using RNA-seq from 490 MECA participants and 1000 Genomes reference populations, we performed variant calling, quality filtering, principal component analysis and retained 230 high-frequency SNPs for ancestry estimation via Rye algorithm for ancestry inferences. MECA participants aligned with African and admixed populations, predominantly West African. Correlation with gene expression identified the top 50 ancestry-associated transcripts. Validation in 109 longitudinal samples confirmed reproducibility. The pipeline is open-source and generalizable: https://github.com/rob-meller/; https://github.com/Vermarashi/.

Indexed as

Cardiovascular DiseaseEthnicityGenetic AncestryRaceShort-Read RNA-Seq

Identifiers

PMID41836511
PMCPMC12980372

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.