Evidence map›Paper›PMID 41993395›Full record

ArticlebioRxiv : the preprint server for biology2026

African Pan Genome Contigs Expose Biologically Relevant Sequence Still Hidden from Human Reference Frameworks.

Rachel Martini, Abdulfatai Tijjani, Kyriaki Founta, Daniel Cha, Alexandria Awai, Sebastian Maurice, Jason A White, Christopher E Mason, Isidro Cortes-Ciriano, Nicolas Robine and 3 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 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

13 authors.

Rachel MartiniInstitute of Translational Genomic Medicine, Morehouse School of Medicine, Atlanta, GA.ORCID 0000-0002-8921-0041
Abdulfatai TijjaniNorthwell, New Hyde Park, NY.ORCID 0000-0002-0793-9059
Kyriaki FountaNorthwell, New Hyde Park, NY.ORCID 0009-0007-5389-7615
Daniel ChaCarnegie Mellon University, Pittsburgh, PA.
Alexandria AwaiInstitute of Translational Genomic Medicine, Morehouse School of Medicine, Atlanta, GA.
Sebastian MauriceCity College of New York, New York, NY.
Jason A WhiteInstitute of Translational Genomic Medicine, Morehouse School of Medicine, Atlanta, GA.ORCID 0000-0002-2725-5009
Christopher E MasonWeill Cornell Medicine, New York, NY.ORCID 0000-0002-1850-1642
Isidro Cortes-CirianoEuropean Molecular Biology Laboratory, European Bioinformatics Institute, Hinxton, Cambridge CB10 1SD, UK.ORCID 0000-0002-2036-494X
Nicolas RobineNew York Genome Center, New York, NY.ORCID 0000-0001-5698-8183
Onyinye BalogunWeill Cornell Medicine, New York, NY.
Nyasha ChambweNorthwell, New Hyde Park, NY.ORCID 0000-0002-2812-0122
Melissa B DavisInstitute of Translational Genomic Medicine, Morehouse School of Medicine, Atlanta, GA.ORCID 0000-0002-6124-6923

Funding

Project 4 Green-DavisP01CA272295 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI Christopher Edward Mason · 2024 to 2026
$9.3M
Workforce Development CoreU54HG013595 · NHGRI · MOREHOUSE SCHOOL OF MEDICINE · PI Robert Meller · 2024 to 2026
$6.4M
BAF complex deregulation in lymphomaR01CA266279 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Michael Richard Green, Christopher Edward Mason · 2022 to 2026
$3.4M
The DARC side of Breast Cancer Disparities - African Ancestry and Cancer- Related Immune ResponseR01CA259396 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI DAVIS, MELISSA B, YATES, CLAYTON · 2021 to 2025
$2.4M
CANCER GRAND CHALLENGES 2024 SOCIETAL, ANCESTRY, MOLECULAR AND BIOLOGICAL ANALYSES OF INEQUALITIES (SAMBAI) Morehouse School of MedicineOT2CA297574 · NCI · MOREHOUSE SCHOOL OF MEDICINE · PI DAVIS, MELISSA B · 2024 to 2024
$614k
Graphical Processing Units and a Large-Memory Compute Node for Applications in Genomics, Neuroscience, and Structural BiologyS10OD028632 · OD · COLD SPRING HARBOR LABORATORY · PI SIEPEL, ADAM CHARLES · 2020 to 2020
$437k
NCI NIH HHS OT2 CA297574NCI NIH HHS P01 CA272295NCI NIH HHS R01 CA259396NCI NIH HHS R01 CA266279NHGRI NIH HHS U54 HG013595NIH HHS S10 OD028632
6 · The paper itself

Abstract

Human reference genomes underpin biomedical discovery but remain incomplete and biased toward European populations, constraining interpretation of genetic variation in underrepresented populations. Here we characterize African Pan Genome (APG) contigs totaling 296.5 Mb to define the sequence and functional landscape of genomic regions absent from current references. Most contigs align to the telomere-to-telomere (T2T-CHM13) genome and across 47 haplotype-resolved Human Pangenome Reference Consortium (HPRC) assemblies, with T2T-CHM13 placements enriched in centromeric and satellite repeats and overlapping 373 genes, including disease-associated loci. Mapping across HPRC assemblies revealed ancestry-associated contig enrichment, particularly in African genomes. Notably, 742 contigs remained unmapped under both stringent and relaxed criteria. These sequences are largely nonrepetitive and exhibit strong functional potential, including predicted protein-coding genes, CpG islands and transcriptional activity. Together, these results demonstrate that functionally relevant, ancestry-enriched genomic sequences remain absent from current references, with important implications for disease variant interpretation and precision medicine.

Indexed as

African Pan-genomeancestry-associated genomic variationcentromeric and satellite repeatsnovel transcriptsreference bias

Identifiers

PMID41993395
PMCPMC13082152

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.