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Publication : Use of denaturing HPLC to map human and murine genes and to validate single-nucleotide polymorphisms.

First Author  Schriml LM Year  2000
Journal  Biotechniques Volume  28
Issue  4 Pages  740-5
PubMed ID  10769753 Mgi Jnum  J:62634
Mgi Id  MGI:1859354 Doi  10.2144/00284rr03
Citation  Schriml LM, et al. (2000) Use of denaturing HPLC to map human and murine genes and to validate single-nucleotide polymorphisms. Biotechniques 28(4):740-5
abstractText  Linkage mapping has been extensively applied in the murine and human genomes. It remains a powerful approach to mapping genes and identifying genetic variants. As genome efforts identify large numbers of single-nucleotide polymorphisms, it will be critical to validate these polymorphisms and confirm their gene assignment and chromosomal location. The presence of pseudogenes can confuse such efforts. We have used denaturing HPLC to identify polymorphisms in human genes and to genotype individuals in selected CEPH pedigrees. The same approach has been applied to the mapping of murine genes in interspecies backcross animals. This strategy is rapid, accurate and superior in several respects to other technologies.
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