A SNP Resource for Human Chromosome 22: Extracting Dense Clusters of SNPs From the Genomic Sequence

The recent publication of the complete sequence of human chromosome 22 provides a platform from which to investigate genomic sequence variation. We report the identification and characterization of 12,267 potential variants (SNPs and other small insertions/deletions) of human chromosome 22, discover...

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Detalhes bibliográficos
Main Authors: Dawson, Elisabeth, Chen, Yuan, Hunt, Sarah, Smink, Luc J., Hunt, Adrienne, Rice, Kate, Livingston, Simon, Bumpstead, Suzannah, Bruskiewich, Richard, Sham, Pak, Ganske, Rocky, Adams, Mark, Kawasaki, Kazuhiko, Shimizu, Nobuyoshi, Minoshima, Shinsei, Roe, Bruce, Bentley, David, Dunham, Ian
Formato: Artigo
Idioma:Inglês
Publicado em: Cold Spring Harbor Laboratory Press 2001
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC311026/
https://ncbi.nlm.nih.gov/pubmed/11156626
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