a simple optimization can improve the performance of single feature polymorphism detection by affymetrix expression arrays一个简单的优化可以提高单一功能多态性检测的性能通过affymetrix表达式数组.pdfVIP
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a simple optimization can improve the performance of single feature polymorphism detection by affymetrix expression arrays一个简单的优化可以提高单一功能多态性检测的性能通过affymetrix表达式数组
Horiuchi et al. BMC Genomics 2010, 11:315
/1471-2164/11/315
RESEARCH ARTICLE Open Access
A simple optimization can improve the
performance of single feature polymorphism
detection by Affymetrix expression arrays
1,3 1,3* 2,3 1 2,4
Youko Horiuchi , Yoshiaki Harushima , Hironori Fujisawa , Takako Mochizuki , Masanori Kawakita ,
Takayuki Sakaguchi2,3,5, Nori Kurata1,3
Abstract
Background: High-density oligonucleotide arrays are effective tools for genotyping numerous loci simultaneously.
In small genome species (genome size: ~300 Mb), whole-genome DNA hybridization to expression arrays has
been used for various applications. In large genome species, transcript hybridization to expression arrays has been
used for genotyping. Although rice is a fully sequenced model plant of medium genome size (~400 Mb), there are
a few examples of the use of rice oligonucleotide array as a genotyping tool.
Results: We compared the single feature polymorphism (SFP) detection performance of whole-genome and
transcript hybridizations using the Affymetrix GeneChip® Rice Genome Array, using the rice cultivars with full
genome sequence, japonica cultivar Nipponbare and indica cultivar 93-11. Both genomes were surveyed for all
probe target sequences. Only completely matched 25-mer single copy probes of the Nipponbare genome were
extracted, and SFPs between them and 93-11 sequences were predicted. We investigated optimum conditions for
SFP detection in both whole genome and transcript hybridization using differences between perfect match and
mismatch probe intensities of non-polymorphic targets, assuming that these differences are representative of those
between mismatch and perfect targets. Several stat
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