ArticleBMC bioinformatics2008
Snagger: a user-friendly program for incorporating additional information for tagSNP selection.
Article in BMC bioinformatics, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.
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Who cites it
34 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Fine-mapping of prostate cancer susceptibility loci in a large meta-analysis identifies candidate causal variants.Nature communications · 2018Pooled it
- Germline genetic variants in ABCB1, ABCC1 and ALDH1A1, and risk of hematological and gastrointestinal toxicities in a SWOG Phase III trial S0221 for breast cancer.The pharmacogenomics journal · 2014Trial
- Nicotinic acetylcholine receptor beta2 subunit gene implicated in a systems-based candidate gene study of smoking cessation.Human molecular genetics · 2008Trial
- Growth factor genes and change in mammographic density after stopping combined hormone therapy in the California Teachers Study.BMC cancer · 2018Article
- Evaluating the association of single-nucleotide polymorphisms with tenofovir exposure in a diverse prospective cohort of women living with HIV.The pharmacogenomics journal · 2018Article
- A population-based case-control study of genetic variation in cytokine genes associated with risk of cervical and vulvar cancers.Gynecologic oncology · 2015Article
- Hormone metabolism pathway genes and mammographic density change after quitting estrogen and progestin combined hormone therapy in the California Teachers Study.Breast cancer research : BCR · 2014Article
- Risk of squamous cell skin cancer after organ transplant associated with antibodies to cutaneous papillomaviruses, polyomaviruses, and TMC6/8 (EVER1/2) variants.Cancer medicine · 2014Article
- Comprehensive analyses of DNA repair pathways, smoking and bladder cancer risk in Los Angeles and Shanghai.International journal of cancer · 2014Article
- Genetic variation in the TLR and NF-κB pathways and cervical and vulvar cancer risk: a population-based case-control study.International journal of cancer · 2014Article
- Epigenetic genes and emotional reactivity to daily life events: a multi-step gene-environment interaction study.PloS one · 2014Article
- Nucleotide variation in IL-10 and IL-12 and their receptors and cervical and vulvar cancer risk: a hybrid case-parent triad and case-control study.International journal of cancer · 2013Article
- Five linkage regions each harbor multiple type 2 diabetes genes in the African American subset of the GENNID Study.Journal of human genetics · 2013Article
- Genetic variation in TLR or NFkappaB pathways and the risk of breast cancer: a case-control study.BMC cancer · 2013Article
- Genetic variation in transforming growth factor beta 1 and mammographic density in Singapore Chinese women.Cancer research · 2013Article
- Variation in inflammatory cytokine/growth-factor genes and mammographic density in premenopausal women aged 50-55.PloS one · 2013Article
- Genetic variations in SMAD7 are associated with colorectal cancer risk in the colon cancer family registry.PloS one · 2013Article
- Association of ANXA11 genetic variation with sarcoidosis in African Americans and European Americans.Genes and immunity · 2013Article
- Common sequence variants in chemokine-related genes and risk of breast cancer in post-menopausal women.International journal of molecular epidemiology and genetics · 2013Article
- Gender-stratified gene and gene-treatment interactions in smoking cessation.The pharmacogenomics journal · 2012Article
Corrections and comments
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Authors and funding
5 authors.
Funding
Abstract
backgroundThere has been considerable effort focused on developing efficient programs for tagging single-nucleotide polymorphisms (SNPs). Many of these programs do not account for potential reduced genomic coverage resulting from genotyping failures nor do they preferentially select SNPs based on functionality, which may be more likely to be biologically important.
resultsWe have developed a user-friendly and efficient software program, Snagger, as an extension to the existing open-source software, Haploview, which uses pairwise r2 linkage disequilibrium between single nucleotide polymorphisms (SNPs) to select tagSNPs. Snagger distinguishes itself from existing SNP selection algorithms, including Tagger, by providing user options that allow for: (1) prioritization of tagSNPs based on certain characteristics, including platform-specific design scores, functionality (i.e., coding status), and chromosomal position, (2) efficient selection of SNPs across multiple populations, (3) selection of tagSNPs outside defined genomic regions to improve coverage and genotyping success, and (4) picking of surrogate tagSNPs that serve as backups for tagSNPs whose failure would result in a significant loss of data. Using HapMap genotype data from ten ENCODE regions and design scores for the Illumina platform, we show similar coverage and design score distribution and fewer total tagSNPs selected by Snagger compared to the web server Tagger.
conclusionSnagger improves upon current available tagSNP software packages by providing a means for researchers to select tagSNPs that reliably capture genetic variation across multiple populations while accounting for significant genotyping failure risk and prioritizing on SNP-specific characteristics.
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