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High-resolution SNP mapping by denaturing HPLC.

Nairz, K; Stocker, H; Schindelholz, B; Hafen, E (2002). High-resolution SNP mapping by denaturing HPLC. Proceedings of the National Academy of Sciences of the United States of America (PNAS), 99(16):10575-10580.

Abstract

With the availability of complete genome sequences, new rapid and reliable strategies for positional cloning become possible. Single-nucleotide polymorphisms (SNPs) permit the mapping of mutations at a resolution not amenable to classical genetics. Here we describe a SNP mapping procedure that relies on resolving polymorphisms by denaturing HPLC without the necessity of determining the nature of the SNPs. With the example of mapping mutations to the Drosophila nicastrin locus, we discuss the benefits of this method, evaluate the frequency of closely linked and potentially misleading second site mutations, and demonstrate the use of denaturing high-performance liquid chromatography to identify mutations in the candidate genes and to fine-map chromosomal breakpoints. Furthermore, we show that recombination events are not uniformly dispersed over the investigated region but rather occur at hot spots.

Additional indexing

Item Type:Journal Article, refereed
Communities & Collections:07 Faculty of Science > Institute of Zoology (former)
Dewey Decimal Classification:570 Life sciences; biology
590 Animals (Zoology)
Scopus Subject Areas:Health Sciences > Multidisciplinary
Language:English
Date:6 August 2002
Deposited On:11 Feb 2008 12:16
Last Modified:01 Nov 2024 02:35
Publisher:National Academy of Sciences
ISSN:0027-8424
OA Status:Hybrid
Free access at:PubMed ID. An embargo period may apply.
Publisher DOI:https://doi.org/10.1073/pnas.162136299
PubMed ID:12149455

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