Literature DB >> 22686305

Integrative analyses for omics data: a Bayesian mixture model to assess the concordance of ChIP-chip and ChIP-seq measurements.

Martin Schäfer1, Otgonzul Lkhagvasuren, Hans-Ulrich Klein, Christian Elling, Torsten Wüstefeld, Carsten Müller-Tidow, Lars Zender, Steffen Koschmieder, Martin Dugas, Katja Ickstadt.   

Abstract

The analysis of different variations in genomics, transcriptomics, epigenomics, and proteomics has increased considerably in recent years. This is especially due to the success of microarray and, more recently, sequencing technology. Apart from understanding mechanisms of disease pathogenesis on a molecular basis, for example in cancer research, the challenge of analyzing such different data types in an integrated way has become increasingly important also for the validation of new sequencing technologies with maximum resolution. For this purpose, a methodological framework for their comparison with microarray techniques in the context of smallest sample sizes, which result from the high costs of experiments, is proposed in this contribution. Based on an adaptation of the externally centered correlation coefficient ( Schäfer et al. 2009 ), it is demonstrated how a Bayesian mixture model can be applied to compare and classify measurements of histone acetylation that stem from chromatin immunoprecipitation combined with either microarray (ChIP-chip) or sequencing techniques (ChIP-seq) for the identification of DNA fragments. Here, the murine hematopoietic cell line 32D, which was transduced with the oncogene BCR-ABL, the hallmark of chronic myeloid leukemia, was characterized. Cells were compared to mock-transduced cells as control. Activation or inhibition of other genes by histone modifications induced by the oncogene is considered critical in such a context for the understanding of the disease.

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Year:  2012        PMID: 22686305     DOI: 10.1080/15287394.2012.674914

Source DB:  PubMed          Journal:  J Toxicol Environ Health A        ISSN: 0098-4108


  6 in total

1.  Bayesian integrative analysis of epigenomic and transcriptomic data identifies Alzheimer's disease candidate genes and networks.

Authors:  Hans-Ulrich Klein; Martin Schäfer; David A Bennett; Holger Schwender; Philip L De Jager
Journal:  PLoS Comput Biol       Date:  2020-04-07       Impact factor: 4.475

Review 2.  Techniques and Approaches to Genetic Analyses in Nephrological Disorders.

Authors:  Laurel K Willig
Journal:  J Pediatr Genet       Date:  2015-08-13

3.  A decision theory paradigm for evaluating identifier mapping and filtering methods using data integration.

Authors:  Roger S Day; Kevin K McDade
Journal:  BMC Bioinformatics       Date:  2013-07-15       Impact factor: 3.169

4.  Functional genetics-directed identification of novel pharmacological inhibitors of FAS- and TNF-dependent apoptosis that protect mice from acute liver failure.

Authors:  A P Komarov; E A Komarova; K Green; L R Novototskaya; P S Baker; A Eroshkin; A L Osterman; A A Chenchick; C Frangou; A V Gudkov
Journal:  Cell Death Dis       Date:  2016-03-17       Impact factor: 8.469

5.  Differential roles of STAT1 and STAT2 in the sensitivity of JAK2V617F- vs. BCR-ABL-positive cells to interferon alpha.

Authors:  Claudia Schubert; Manuel Allhoff; Stefan Tillmann; Tiago Maié; Ivan G Costa; Daniel B Lipka; Mirle Schemionek; Kristina Feldberg; Julian Baumeister; Tim H Brümmendorf; Nicolas Chatain; Steffen Koschmieder
Journal:  J Hematol Oncol       Date:  2019-04-02       Impact factor: 17.388

6.  StereoGene: rapid estimation of genome-wide correlation of continuous or interval feature data.

Authors:  Elena D Stavrovskaya; Tejasvi Niranjan; Elana J Fertig; Sarah J Wheelan; Alexander V Favorov; Andrey A Mironov
Journal:  Bioinformatics       Date:  2017-10-15       Impact factor: 6.937

  6 in total

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