ArticleNucleic acids research2026
Genome Variation Map: a platform for the analysis and integration of genomic variation.
Article in Nucleic acids research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
- YanHuang Paternal Genomic Resource Suggests A Weakly-differentiated Multi-source Admixture in the Formation of Han Founding Ancestral Lineages.Genomics, proteomics & bioinformatics · 2025Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
11 authors.
Funding
Abstract
The Genome Variation Map (GVM; https://ngdc.cncb.ac.cn/gvm) serves as a public repository for genetic variation data. This version represents a major upgrade to GVM, integrating rigorously curated high-quality DNA resequencing data from a wide range of species and delivering significant enhancements over previous releases. Specifically, the current release encompasses ~2.14 billion standardized variants across 73 species and archives 898 genetic variation projects originating from 79 species, contributed by 180 organizations globally. Furthermore, GVM innovatively incorporates a public variant aggregation pipeline that consolidates in-house curated datasets, user-submitted data, and records from the European Variation Archive to generate comprehensive reference variant sets for each organism. A new module has also been introduced to provide deleterious variant annotations and population genetic selection signals based on population genetic analyses. Additionally, newly implemented online tools support population-specific haplotype analysis and cross-mapping between genome assemblies, serving as integral features of GVM. Collectively, this resource remains essential for archiving and utilizing genomic variation data and for catalyzing advancements in evolutionary biology, disease etiology research, and agricultural genomics.
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Identifiers
What OpenQuestion holds
Registered trials
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.