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Bradley J. Till, Troy Zerr, Luca Comai, Steven Henikoff
This chapter provides a brief overview of TILLING (Targeting Induced Local Lesion in Genomes; a novel, reverse genetics approach that combines the advantages of point mutations provided by chemical mutagenesis with the advantages of PCR-based mutational screening) and Eco-TILLING [a method that …
Afrique du Sud, us (code pays fourni par la source)
Troy Zerr, Gregory M. Cooper, Evan E. Eichler, Deborah A. Nickerson
SUMMARY: Copy number variants (CNVs) contribute substantially to human genomic diversity, and development of accurate and efficient methods for CNV genotyping is a central problem in exploring human genotype-phenotype associations. SCIMMkit provides a robust, integrated implementation of three previously validated algorithms [SCIMM …
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Heather C Mefford, Gregory M. Cooper, Troy Zerr, Joshua D. Smith et autres
Copy-number variants (CNVs) are substantial contributors to human disease. A central challenge in CNV-disease association studies is to characterize the pathogenicity of rare and possibly incompletely penetrant events, which requires the accurate detection of rare CNVs in large numbers of individuals. Cost …
us (code pays fourni par la source)
Gregory M. Cooper, Troy Zerr, Jeffrey M. Kidd, Evan E. Eichler et autres
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Jeffrey M. Kidd, Gregory M. Cooper, William F. Donahue, Hillary S. Hayden et autres
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Bradley J. Till, Troy Zerr, Luca Comai, Steven Henikoff
us (code pays fourni par la source)
Some popular methods for polymorphism and mutation discovery involve ascertainment of novel bands by the examination of electrophoretic gel images. Although existing strategies for mapping bands work well for specific applications, such as DNA sequencing, these strategies are not well suited for …
Afrique du Sud, us (code pays fourni par la source)
Jeffrey M. Kidd, Gregory M. Cooper, William F. Donahue, Hillary S. Hayden et autres
Abstract Genetic variation among individual humans occurs on many different scales, ranging from gross alterations in the human karyotype to single nucleotide changes. Here we explore variation on an intermediate scale—particularly insertions, deletions and inversions affecting from a few thousand to a …
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