ArticleMethods in molecular biology (Clifton, N.J.)2010
Nonparametric methods for molecular biology.
Article in Methods in molecular biology (Clifton, N.J.), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.
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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.
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Who cites it
9 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Meta-analysis derived atopic dermatitis (MADAD) transcriptome defines a robust AD signature highlighting the involvement of atherosclerosis and lipid metabolism pathways.BMC medical genomics · 2015Pooled it
- TIGA: target illumination GWAS analytics.Bioinformatics (Oxford, England) · 2021Article
- CrAssphage as a Novel Tool to Detect Human Fecal Contamination on Environmental Surfaces and Hands.Emerging infectious diseases · 2020Article
- Allelic Variation in a Single Genomic Region Alters the Microbiome of the Snail Biomphalaria glabrata.The Journal of heredity · 2018Article
- Complex polymorphisms in endocytosis genes suggest alpha-cyclodextrin as a treatment for breast cancer.PloS one · 2018Article
- Conditional long-term survival following minimally invasive robotic mitral valve repair: a health services perspective.Annals of cardiothoracic surgery · 2015Article
- Whole blood gene expression profiles to assess pathogenesis and disease severity in infants with respiratory syncytial virus infection.PLoS medicine · 2013Article
- From single-SNP to wide-locus: genome-wide association studies identifying functionally related genes and intragenic regions in small sample studies.Pharmacogenomics · 2013Article
- The evolutionary rate of antibacterial drug targets.BMC bioinformatics · 2013Article
Corrections and comments
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Authors and funding
2 authors.
Funding
Abstract
In 2003, the completion of the Human Genome Project (1) together with advances in computational resources (2) were expected to launch an era where the genetic and genomic contributions to many common diseases would be found. In the years following, however, researchers became increasingly frustrated as most reported 'findings' could not be replicated in independent studies (3). To improve the signal/noise ratio, it was suggested to increase the number of cases to be included to tens of thousands (4), a requirement that would dramatically restrict the scope of personalized medicine. Similarly, there was little success in elucidating the gene-gene interactions involved in complex diseases or even in developing criteria for assessing their phenotypes. As a partial solution to these enigmata, we here introduce a class of statistical methods as the 'missing link' between advances in genetics and informatics. As a first step, we provide a unifying view of a plethora of nonparametric tests developed mainly in the 1940s, all of which can be expressed as u-statistics. Then, we will extend this approach to reflect categorical and ordinal relationships between variables, resulting in a flexible and powerful approach to deal with the impact of (1) multiallelic genetic loci, (2) poly-locus genetic regions, and (3) oligo-genetic and oligo-genomic collaborative interactions on complex phenotypes.
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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.