Polymorphism, human genome sequence

The International SNP Map Working Group 2001. A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms. Nature 2001 409 928-933. 

Sachidanandam, R., et al., "A Map of Human Genome Sequence Variation Containing 1. Million Single Nucleotide Polymorphisms," Nature, 409, 928-933 (2001). 

Potentially polymorphic novel VNTRs can be identified direcdy from genomic sequence using tools such as Tandem repeat finder (TRF) or Tandyman [17] (http //www.stdgen.lanl.gov/tandyman/docs/index.html). A complete analysis of microsatellites in the human genome sequence using both TRF and Tandyman has been presented in the UCSC human genome browser in the simple repeats and microsatellites tracks [7]. 

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