ArticleNature genetics2007
What is the human variome project?
Article in Nature genetics, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.
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
12 citing papers in PubMed.
- Living systematic reviews: an emerging opportunity to narrow the evidence-practice gap.PLoS medicine · 2014Article
- Interpreting cancer genomes using systematic host network perturbations by tumour virus proteins.Nature · 2012Article
- Towards an Ecology of Collective Innovation: Human Variome Project (HVP), Rare Disease Consortium for Autosomal Loci (RaDiCAL) and Data-Enabled Life Sciences Alliance (DELSA).Current pharmacogenomics and personalized medicine · 2011Article
- Mutation (variation) databases and registries: a rationale for coordination of efforts.Nature reviews. Genetics · 2011Article
- The value of data.Nature genetics · 2011Article
- Crowdsourcing human mutations.Nature genetics · 2011Article
- Collection of variation causing disease--the Human Variome Project.Human genomics · 2009Article
- Human Splicing Finder: an online bioinformatics tool to predict splicing signals.Nucleic acids research · 2009Article
- System-wide molecular evidence for phenotypic buffering in Arabidopsis.Nature genetics · 2009Article
- VariVis: a visualisation toolkit for variation databases.BMC bioinformatics · 2008Article
- Recommendations for locus-specific databases and their curation.Human mutation · 2008Article
- Structures for clinical follow-up: newborn screening.Journal of inherited metabolic disease · 2007Article
Corrections and comments
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Authors and funding
0 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
PubMed holds no abstract for this paper.
Indexed as
Identifiers
17392793What 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.