Evidence map›Paper›PMID 38915693›Full record

ArticlebioRxiv : the preprint server for biology2025

Analysis-ready VCF at Biobank scale using Zarr.

Eric Czech, Timothy R Millar, Will Tyler, Tom White, Benjamin Elsworth, Jérémy Guez, Jonny Hancox, Ben Jeffery, Konrad J Karczewski, Alistair Miles and 6 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. 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

16 authors.

Eric CzechOpen Athena AI Foundation, Lincoln, New Zealand.ORCID 0000-0002-4254-4255
Timothy R MillarThe New Zealand Institute for Plant & Food Research Ltd, Lincoln, New Zealand.ORCID 0000-0002-5142-8811
Will TylerIndependent researcher, Manchester, UK.
Tom WhiteTom White Consulting Ltd., Manchester, UK.
Benjamin ElsworthOur Future Health, Manchester, UK.ORCID 0000-0001-7328-4233
Jérémy GuezProgram in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, Massachusetts 02142, USA.ORCID 0009-0007-6406-5187
Jonny HancoxNVIDIA Ltd, Reading, UK.ORCID 0009-0003-5799-5299
Ben JefferyBig Data Institute, Li Ka Shing Centre for Health Information and Discovery, University of Oxford, UK.ORCID 0000-0002-1982-6801
Konrad J KarczewskiProgram in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, Massachusetts 02142, USA.ORCID 0000-0003-2878-4671
Alistair MilesWellcome Sanger Institute, National Bioinformatics Infrastructure Sweden, Science for Life Laboratory, Uppsala University, Uppsala, Sweden.ORCID 0000-0001-9018-4680
Sam TallmanGenomics England, National Bioinformatics Infrastructure Sweden, Science for Life Laboratory, Uppsala University, Uppsala, Sweden.ORCID 0000-0001-7183-6276
Per UnnebergDepartment of Cell and Molecular Biology, National Bioinformatics Infrastructure Sweden, Science for Life Laboratory, Uppsala University, Uppsala, Sweden.ORCID 0000-0001-5735-3315
Rafal WojdylaOpen Athena AI Foundation, Lincoln, New Zealand.ORCID 0009-0005-0735-7090
Shadi ZabadSchool of Computer Science, McGill University, Montreal, QC, Canada.ORCID 0000-0002-8003-9284
Jeff HammerbacherOpen Athena AI Foundation, Lincoln, New Zealand.ORCID 0000-0001-6596-8563
Jerome KelleherBig Data Institute, Li Ka Shing Centre for Health Information and Discovery, University of Oxford, UK.ORCID 0000-0002-7894-5253

Funding

Scaling up computational genomics with tree sequencesR01HG012473 · NHGRI · UNIVERSITY OF OREGON · PI PETER Lochhead RALPH · 2023 to 2026
$2.3M
Scaling up computational genomics with tree sequencesR56HG011395 · NHGRI · UNIVERSITY OF OREGON · PI RALPH, PETER LOCHHEAD · 2021 to 2021
$557k
Gates Foundation INV-001927NHGRI NIH HHS R01 HG012473NHGRI NIH HHS R56 HG011395Wellcome Trust
6 · The paper itself

Abstract

Background: Variant Call Format (VCF) is the standard file format for interchanging genetic variation data and associated quality control metrics. The usual row-wise encoding of the VCF data model (either as text or packed binary) emphasises efficient retrieval of all data for a given variant, but accessing data on a field or sample basis is inefficient. Biobank scale datasets currently available consist of hundreds of thousands of whole genomes and hundreds of terabytes of compressed VCF. Row-wise data storage is fundamentally unsuitable and a more scalable approach is needed. Results: Zarr is a format for storing multi-dimensional data that is widely used across the sciences, and is ideally suited to massively parallel processing. We present the VCF Zarr specification, an encoding of the VCF data model using Zarr, along with fundamental software infrastructure for efficient and reliable conversion at scale. We show how this format is far more efficient than standard VCF based approaches, and competitive with specialised methods for storing genotype data in terms of compression ratios and single-threaded calculation performance. We present case studies on subsets of three large human datasets (Genomics England: Conclusions: Large row-encoded VCF files are a major bottleneck for current research, and storing and processing these files incurs a substantial cost. The VCF Zarr specification, building on widely-used, open-source technologies has the potential to greatly reduce these costs, and may enable a diverse ecosystem of next-generation tools for analysing genetic variation data directly from cloud-based object stores, while maintaining compatibility with existing file-oriented workflows.

Indexed as

Analysis ready dataVariant Call FormatZarr

Identifiers

PMID38915693
PMCPMC11195102

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.