Titlebook: Single Nucleotide Polymorphisms; Methods and Protocol Pui-Yan Kwok Book 20031st edition Springer Science+Business Media New York 2003

radionuclides

书目名称Single Nucleotide Polymorphisms影响因子(影响力)




书目名称Single Nucleotide Polymorphisms影响因子(影响力)学科排名




书目名称Single Nucleotide Polymorphisms网络公开度




书目名称Single Nucleotide Polymorphisms网络公开度学科排名




书目名称Single Nucleotide Polymorphisms被引频次




书目名称Single Nucleotide Polymorphisms被引频次学科排名




书目名称Single Nucleotide Polymorphisms年度引用




书目名称Single Nucleotide Polymorphisms年度引用学科排名




书目名称Single Nucleotide Polymorphisms读者反馈




书目名称Single Nucleotide Polymorphisms读者反馈学科排名

异常

Book 20031st editionlity to disease and have clearly become the focus of the next phase of the human genome project. In Single Nucleotide Polymorphisms: Methods and Protocols, Pui-Yan Kwok, MD, PhD, has assembled a collection of robust techniques for the difficult process of SNP discovery and genotyping. These cutting-

ADORE

SNP Detection and Allele Frequency Determination by SSCP,essary to sequence the STSs in individuals with different genotypes. However, once an SNP sequence is correlated with the corresponding fragment mobility in an SSCP analysis, sequencing may not be necessary for genotyping, because SSCP electrophoresis is highly reproducible (.,.).

Camouflage

SNP Discovery by Direct DNA Sequencing,cupy the same site. The uneven peak pattern makes it difficult sometimes to discern these composite peaks because one of the two polymorphic bases may be disproportionately smaller than the other base and the base-calling algorithm of the automatic DNA sequencer misses the correct call (.–.).

Inelasticity

外向者

SNPs: ,, With recent technologies for DNA sequencing and the detection of single-base differences, we are approaching the time when all differences in DNA sequence among individuals can be found. The next challenge is to relate these genetic differences to phenotypes such as disease risk and response to therapies.

易改变

commensurate

Homogeneous Allele-Specific PCR in SNP Genotyping,NP) genotyping assay presented here combines AS PCR amplification with kinetic, realtime monitoring (.–.). It is robust, rapid, inexpensive, and allows accurate measurement of allele frequencies in pools of DNA, facilitating large-scale gene mapping.

的’

Oligonucleotide Ligation Assay,scribe two protocols for solid-phase detection of reaction products in the oligonucleotide ligation assay (OLA), although there are several other detection schemes in use. However, the general considerations of ligase-based sequence distinction are the same, and they will be described in some detail.

或者发神韵

Denaturing High-Performance Liquid Chromatography,e range of 48-67°C; they are retained less on the chromatographic separation matrix, allowing the separation of homo- and heteroduplex species by ion-pair reversed-phase HPLC (IP-RP-HPLC) (.). Characteristic peak patterns both for homozygous and heterozygous samples are obtained.