ILLUMINA SEQUENCING Whole-Genome Chromatin IP Sequencing (ChIP-Seq) Illumina ChIP-Seq combines chromatin immunoprecipitation (ChIP) with massively parallel DNA sequencing to identify binding sites of DNA-associated proteins. Illumina ChIP-Seq technology precisely and cost-effectively maps global binding sites for a protein of interest
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INTRODUCTION Transcription factors and other chromatin-associated proteins are essential phenotype-influencing mechanisms. Determining how proteins interact with DNA to regulate gene expression is essential for fully understanding many biological processes and disease states. This epigenetic information is complimentary to genotype and expression analysis. Traditional methods have successfully identified transcription factor binding sites and specific DNA-associated protein modifications and their roles in regulating specific genes, but these experiments are limited in scale and resolution. The powerful Illumina Whole-Genome Chromatin IP Sequencing (ChIP-Seq) application allows researchers to easily expand the scale of their studies to identify binding sites across the entire genome simultaneously with high resolution and without constraints. Specific DNA sites in direct physical interaction with transcription factors and other proteins can be isolated by chromatin immunoprecipitation (ChIP). ChIP produces a library of target DNA sites that a given factor was bound to in vivo. The revolutionary Solexa Sequencing technology is an ideal method to identify isolated DNA sites from ChIP. This massively parallel sequence analysis in the context of easy access to whole-genome sequence databases has made analyzing the interaction pattern of any protein with DNA, or the pattern of any epigenetic chromatin modifications, across the entire genome fast and cost-effective. The Illumina Genome Analyzer determines the sequences of ChIP-isolated DNA fragments to identify and quantify the sites bound by a protein of interest. ChIP-Seq technology supports virtually unconstrained selection of any ChIP-able protein and modifications HIGHLIGHTS OF ILLUMINA CHIP-SEQ
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ILLUMINA SEQUENCING Whole-Genome Chromatin IP Sequencing (ChIP-Seq) Illumina ChIP-Seq combines chromatin immunoprecipitation (ChIP) with massively parallel DNA sequencing to identify binding sites of DNA-associated proteins. Illumina ChIP-Seq technology precisely and cost-effectively maps global binding sites for a protein of interest
INTRODUCTION Transcription factors and other chromatin-associated proteins are essential phenotype-influencing mechanisms. Determining how proteins interact with DNA to regulate gene expression is essential for fully understanding many biological processes and disease states. This epigenetic information is complimentary to genotype and expression analysis. Traditional methods have successfully ...
متن کاملComputational analysis of ChIP-seq data.
Chromatin immunoprecipitation followed by massively parallel sequencing (ChIP-seq) is a new technology to map protein-DNA interactions in a genome. The genome-wide transcription factor binding site and chromatin modification data produced by ChIP-seq provide invaluable information for studying gene regulation. This chapter reviews basic characteristics of ChIP-seq data and introduces a computat...
متن کاملGenome-wide identification of in vivo protein–DNA binding sites from ChIP-Seq data
ChIP-Seq, which combines chromatin immunoprecipitation (ChIP) with ultra high-throughput massively parallel sequencing, is increasingly being used for mapping protein-DNA interactions in-vivo on a genome scale. Typically, short sequence reads from ChIP-Seq are mapped to a reference genome for further analysis. Although genomic regions enriched with mapped reads could be inferred as approximate ...
متن کاملDe novo motif identification improves the accuracy of predicting transcription factor binding sites in ChIP-Seq data analysis
Dramatic progress in the development of next-generation sequencing technologies has enabled accurate genome-wide characterization of the binding sites of DNA-associated proteins. This technique, baptized as ChIP-Seq, uses a combination of chromatin immunoprecipitation and massively parallel DNA sequencing. Other published tools that predict binding sites from ChIP-Seq data use only positional i...
متن کاملTELP, a sensitive and versatile library construction method for next-generation sequencing
Next-generation sequencing has been widely used for the genome-wide profiling of histone modifications, transcription factor binding and gene expression through chromatin immunoprecipitated DNA sequencing (ChIP-seq) and cDNA sequencing (RNA-seq). Here, we describe a versatile library construction method that can be applied to both ChIP-seq and RNA-seq on the widely used Illumina platforms. Stan...
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تاریخ انتشار 2007