Evidence map›Paper›PMID 41993358›Full record

ArticlebioRxiv : the preprint server for biology2026

General, orders-of-magnitude faster whole-genome analysis with genotype representation graphs.

Drew DeHaas, Chris Adonizio, Ziqing Pan, Xinzhu Wei

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

4 authors.

Drew DeHaasDepartment of Computational Biology, Cornell University, Ithaca, NY.
Chris AdonizioDepartment of Computational Biology, Cornell University, Ithaca, NY.
Ziqing PanDepartment of Computational Biology, Cornell University, Ithaca, NY.
Xinzhu WeiDepartment of Computational Biology, Cornell University, Ithaca, NY.

Funding

Dissecting the genetics and evolution of complex traits using whole-genome genealogiesR35GM150579 · NIGMS · CORNELL UNIVERSITY · PI Xinzhu Wei · 2023 to 2026
$1.5M
NIGMS NIH HHS R35 GM150579
6 · The paper itself

Abstract

Whole-genome sequencing (WGS) of biobank-scale cohorts have generated datasets that traditional tabular genotype formats cannot efficiently store or analyze. Genotype Representation Graphs (GRGs) offer a compelling alternative: a biologically-motivated, hierarchical, graph-based representation that compactly and losslessly encodes the genotypes, and that supports computation directly on the graph rather than on a materialized genotype matrix. Here we introduce two advances that together make GRG a practical foundation for biobank-scale population and statistical genetics. First, we present GRG v2, a substantially improved format and construction algorithm that reduces construction time by 10-20×, halves the disk and RAM footprint of the resulting files, and improves load time by more than 20×. Applied to the recently phased UK Biobank WGS dataset (490,541 individuals, 706,556,181 variants), GRG v2 produces files 25 times smaller than

Identifiers

PMID41993358
PMCPMC13081925

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.