Titlebook: Chromatin Immunoprecipitation Assays; Methods and Protocol Philippe Collas Book 2009 Humana Press 2009 ChIP.DNA.DNA microarray.Genome-wide

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書目名稱Chromatin Immunoprecipitation Assays影響因子(影響力)




書目名稱Chromatin Immunoprecipitation Assays影響因子(影響力)學(xué)科排名




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書目名稱Chromatin Immunoprecipitation Assays網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Chromatin Immunoprecipitation Assays被引頻次




書目名稱Chromatin Immunoprecipitation Assays被引頻次學(xué)科排名




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書目名稱Chromatin Immunoprecipitation Assays年度引用學(xué)科排名




書目名稱Chromatin Immunoprecipitation Assays讀者反饋




書目名稱Chromatin Immunoprecipitation Assays讀者反饋學(xué)科排名

flimsy

Désordres sévères de l’avant-piedlysis of ChIP-chip data very challenging. In this chapter, we review some of the issues involved in the analysis of ChIP-chip data and present a few statistical methods that can be used to overcome these issues and improve the detection of DNA–protein binding sites.

fiscal

aplomb

Chivalrous

Chen Peng,Chuanliang Cheng,Ling Wangecipitation of histone proteins or transcription factors under cross-linking conditions. We describe here a rapid micro (μ)ChIP assay suited for multiple parallel ChIPs from a single chromatin batch from 1,000 cells. The assay is also applicable to a single immunoprecipitation from 100 cells.

儀式

Désordres sévères de l’avant-pieder, such expression is no longer endogenous. To surmount this problem, we have successfully developed a facile method to knock in a 3xFlag epitope into the endogenous gene loci of transcription factors. The knock-in approach provides a general solution for the study of proteins for which antibodies are substandard or not available.

儀式

Quelques pathologies du 5e rayonation of human myoblasts into myotubes. The findings have been validated by the observation of a significant correlation between the detected histone modifications and the expression of the nearby genes, as measured by DNA expression microarrays. This chapter focuses on the computational analysis of the data.

多骨

palliate

Diskectomy

Epitope Tagging of Endogenous Proteins for Genome-Wide Chromatin Immunoprecipitation Analysis,er, such expression is no longer endogenous. To surmount this problem, we have successfully developed a facile method to knock in a 3xFlag epitope into the endogenous gene loci of transcription factors. The knock-in approach provides a general solution for the study of proteins for which antibodies are substandard or not available.