Literature DB >> 22130889

ChIP-Seq data analysis: identification of protein-DNA binding sites with SISSRs peak-finder.

Leelavati Narlikar1, Raja Jothi.   

Abstract

Protein-DNA interactions play key roles in determining gene-expression programs during cellular development and differentiation. Chromatin immunoprecipitation (ChIP) is the most widely used assay for probing such interactions. With recent advances in sequencing technology, ChIP-Seq, an approach that combines ChIP and next-generation parallel sequencing is fast becoming the method of choice for mapping protein-DNA interactions on a genome-wide scale. Here, we briefly review the ChIP-Seq approach for mapping protein-DNA interactions and describe the use of the SISSRs peak-finder, a software tool for precise identification of protein-DNA binding sites from sequencing data generated using ChIP-Seq.

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Year:  2012        PMID: 22130889      PMCID: PMC4783134          DOI: 10.1007/978-1-61779-400-1_20

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  25 in total

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6.  AIControl: replacing matched control experiments with machine learning improves ChIP-seq peak identification.

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10.  RORγ directly regulates the circadian expression of clock genes and downstream targets in vivo.

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