Literature DB >> 15108269

Approaches for analyzing human mutations and nucleotide sequence variation: a report from the Seventh International Mutation Detection meeting, 2003.

Ann-Christine Syvänen1, Graham R Taylor.   

Abstract

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. This meeting report summarizes the presentations and cites related articles from the special issue of Human Mutation (Volume 23#5, May 2004; available online at www.wiley.com/humanmutation). Copyright 2004 Wiley-Liss, Inc.

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Year:  2004        PMID: 15108269     DOI: 10.1002/humu.20031

Source DB:  PubMed          Journal:  Hum Mutat        ISSN: 1059-7794            Impact factor:   4.878


  1 in total

1.  2. Post-Natal Molecular Diagnosis of Inherited Diseases.

Authors:  Maurizio Ferrari; Laura Cremonesi; Stefania Stenirri
Journal:  EJIFCC       Date:  2008-04-03
  1 in total

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