ArticleNature2010
Genomics: In search of rare human variants.
Article in Nature, 2010. 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.
- DiNAMO: highly sensitive DNA motif discovery in high-throughput sequencing data.BMC bioinformatics · 2018Article
- Assessing mutant p53 in primary high-grade serous ovarian cancer using immunohistochemistry and massively parallel sequencing.Scientific reports · 2016Article
- Article
- The relevance of HLA sequencing in population genetics studies.Journal of immunology research · 2014Review
- Adjustment of familial relatedness in association test for rare variants.BMC proceedings · 2014Article
- Clinical review: Genome-wide association studies of skeletal phenotypes: what we have learned and where we are headed.The Journal of clinical endocrinology and metabolism · 2012Review
- A novel genome-information content-based statistic for genome-wide association analysis designed for next-generation sequencing data.Journal of computational biology : a journal of computational molecular cell biology · 2012Article
- Manifold learning for human population structure studies.PloS one · 2012Article
- CallSim: Evaluation of Base Calls Using Sequencing Simulation.ISRN bioinformatics · 2012Article
- Methods for adjusting population structure and familial relatedness in association test for collective effect of multiple rare variants on quantitative traits.BMC proceedings · 2011Article
- Identification and correction of systematic error in high-throughput sequence data.BMC bioinformatics · 2011Article
- Rare and common regulatory variation in population-scale sequenced human genomes.PLoS genetics · 2011Article
Corrections and comments
- Comment on
Authors and funding
1 author.
Funding
No grant is acknowledged in the PubMed record.
Abstract
PubMed holds no abstract for this paper.
Indexed as
Identifiers
20981085What 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.