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Approaches for analyzing human mutations and nucleotide sequence variation: a report from the Seventh International Mutation Detection meeting, 2003
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Medical Sciences, Molecular Medicine.
2004 (English)In: Human Mutation, ISSN 1059-7794, E-ISSN 1098-1004, Vol. 23, no 5, 401-405 p.Article in journal (Other academic) Published
Abstract [en]

The Seventh International Symposium on Mutations in the Human Genome, Mutation Detection 2003, was held during 2–6 July 2003 in Palm Cove near Cairns, Australia. The meeting was organized under the auspices of the Human Genome Organisation (HUGO) as a satellite meeting of the International World Congress of Genetics, held in Melbourne the following week. Meeting participants reported on advances in mutation detection technologies, including advances in high-throughput detection systems for SNP genotyping applicable to the international haplotype mapping project (HapMap); and bioinformatics tools, including databases for handling and processing growing amounts of genome variation data.

Place, publisher, year, edition, pages
2004. Vol. 23, no 5, 401-405 p.
Keyword [en]
Base Sequence, DNA Mutational Analysis/*methods/trends, DNA Probes, Databases; Nucleic Acid, Genotype, Haplotypes, Humans, Microfluidics/instrumentation, Nucleotides/genetics, Oligonucleotide Array Sequence Analysis/methods, Polymerase Chain Reaction, Polymorphism; Single Nucleotide, Variation (Genetics)
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Medical and Health Sciences
Identifiers
URN: urn:nbn:se:uu:diva-76893DOI: 10.1002/humu.20031PubMedID: 15108269OAI: oai:DiVA.org:uu-76893DiVA: diva2:104805
Available from: 2006-03-09 Created: 2006-03-09 Last updated: 2017-12-14Bibliographically approved

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Syvänen, Ann-Christine

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