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The SNPforID browser: an online tool for query and display of frequency data from the SNPforID project

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Abstract

The SNPforID browser is a web-based tool for the query and visualization of the SNP allele frequency data generated by the SNPforID consortium (http://www.snpforid.org/). From this project, validated panels of single nucleotide polymorphisms (SNPs) for a variety of forensic applications have been generated with the browser concentrating on the single-tube identification SNP set comprising 52 markers. A web interface allows the visitor to review the allele frequencies of the studied markers from all the available populations used by SNPforID to validate global SNP variability. The interface has been designed to offer the useful facility of combining populations into appropriate geographic groups for visual comparison of populations individually or amongst user-defined groupings and with equivalent HapMap data.

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References

  1. Altshuler D, Brooks LD, Chakravarti A, Collins FS, Daly MJ, Donnelly P, The International HapMap Consortium (2005) A haplotype map of the human genome. Nature 437:1299–1320

    Article  Google Scholar 

  2. Brandstatter A, Salas A, Niederstatter H, Gassner C, Carracedo A, Parson W (2006) Dissection of mitochondrial superhaplogroup H using coding region SNPs. Electrophoresis 27:2541–2550

    Article  PubMed  Google Scholar 

  3. Brion M, Sanchez JJ, Balogh K et al (2005) Introduction of an single nucleotide polymorphism-based “major Y-chromosome haplogroup typing kit” suitable for predicting the geographical origin of male lineages. Electrophoresis 26:4411–4420

    Article  CAS  PubMed  Google Scholar 

  4. Cann HM, de Toma C, Cazes L et al (2002) A human genome diversity cell line panel. Science 296:261–262

    Article  CAS  PubMed  Google Scholar 

  5. Emerson J (2006) DIY Map: a clickable and zoomable map written in Flash. Available at http://www.backspace.com/mapapp/

  6. Lowe AL, Urquhart A, Foreman LA, Evett IW (2001) Inferring ethnic origin by means of an STR profile. Forensic Sci Int 119:17–22

    Article  CAS  PubMed  Google Scholar 

  7. Parson W, Brandstatter A, Alonso A et al (2004) The EDNAP mitochondrial DNA population database (EMPOP) collaborative exercises: organisation results and perspectives. Forensic Sci Int 139:215–226

    Article  CAS  PubMed  Google Scholar 

  8. Phillips C, Lareu V, Salas A, Carracedo A (2004) Non binary single-nucleotide polymorphism markers. In: Doutremepuich C, Morling N (eds) Progress in forensic genetics, 10. Elsevier, Amsterdam, pp 30–32

    Google Scholar 

  9. Phillips C, Salas A, Sanchez JJ et al (2007) Inferring ancestral origin using a single multiplex assay of ancestry-informative marker SNPs. Forensic Sci Int Genetics 1:233–235

    Google Scholar 

  10. Roewer L, Krawczak M, Willuweit S et al (2001) Online reference database of European Y–chromosomal short tandem repeat (STR) haplotypes. Forensic Sci Int 118:106–113

    Article  CAS  PubMed  Google Scholar 

  11. Rosenberg NA, Pritchard JK, Weber JL, Cann HM, Kidd KK, Zhivotovsky LA, Feldman MW (2002) Genetic structure of human populations. Science 298:2381–2385

    Article  CAS  PubMed  Google Scholar 

  12. Ruitberg CM, Reeder DJ, Butler JM (2001) STRBase: a short tandem repeat DNA database for the human identity testing community. Nucleic Acids Res 29:320–322

    Article  CAS  PubMed  Google Scholar 

  13. Sanchez JJ, Phillips C, Borsting C et al (2006) A multiplex assay with 52 single nucleotide polymorphisms for human identification. Electrophoresis 27:1713–1724

    Article  CAS  PubMed  Google Scholar 

  14. Thorisson GA, Smith AV, Krishnan L, Stein LD (2005) The international HapMap project web site. Genome Res 15:1592–1593

    Article  CAS  PubMed  Google Scholar 

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Acknowledgements

The authors wish to thank Albert Vernon Smith and Lalitha Krishnan of the HapMap Project for their guidance in helping us link the browser to the HapMap SNP dataset, and Antonio Salas for his help with the genotyping quality assessment. We also would like to thank the Centro de Supercomputación de Galicia (CESGA) for their web hosting service and technical support. Funding from Xunta de Galicia: PGIDTIT06PXIB228195PR and Ministerio de Educación y Ciencia: proyecto BIO2006-06178 given to ML partially supported this work.

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Correspondence to Jorge Amigo.

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Accessibility: web access to this tool is granted at http://spsmart.cesga.es/snpforid.php

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Amigo, J., Phillips, C., Lareu, M. et al. The SNPforID browser: an online tool for query and display of frequency data from the SNPforID project. Int J Legal Med 122, 435–440 (2008). https://doi.org/10.1007/s00414-008-0233-7

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  • DOI: https://doi.org/10.1007/s00414-008-0233-7

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