Titlebook: Cardiovascular Disease, Volume 1; Genetics Qing K. Wang Book 2007 Humana Press 2007 Chromosom.bioinformatics.cardiovascular.gene therapy.ge

遺留之物

Linkage Analysis for Complex Diseases Using Variance Component Analysis,actors, or the joint analysis of multiple phenotypes in the analysis. In this chapter, we present as an introduction the statistical background of variance component analysis as implemented in the genetic analysis package SOLAR.

morale

Genome Resources and Comparative Analysis Tools for Cardiovascular Research,ingle-nucleotide polymorphisms and comparative genomics within and between species. This chapter illustrates the major genome resources, associated bioinformatics tools, and their potential application in cardiovascular research.

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有偏見

Genome-Wide Association Study to Identify Single-Nucleotide Polymorphisms Conferring Risk of Myocar have identified functional SNPs within the lymphotoxin-α gene located on chromosome 6p21 conferred susceptibility to MI. This chapter describes a detailed protocol for performing a genome-wide association study as used in our MI study.

initiate

Highbrow

Spin States and Spin Polarizationbnormal human chromosomes involved in a chromosomal disorder can be successfully isolated and cloned. These hybrid cells serve as an excellent tool with which to define the exact chromosomal breakpoints involved in a cytogenetic abnormality and to identify genes at the breakpoints.

佛刊

concise

Nutrient

Accolade

Construction of Somatic Cell Hybrid Lines,bnormal human chromosomes involved in a chromosomal disorder can be successfully isolated and cloned. These hybrid cells serve as an excellent tool with which to define the exact chromosomal breakpoints involved in a cytogenetic abnormality and to identify genes at the breakpoints.