Experimental and Bioinformatic Approaches to Studying DNA Methylation in Cancer
被引:8
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作者:
Merkel, Angelika
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Josep Carreras Leukemia Res Inst IJC, Bioinformat Unit, Barcelona 08916, SpainJosep Carreras Leukemia Res Inst IJC, Bioinformat Unit, Barcelona 08916, Spain
Merkel, Angelika
[1
]
Esteller, Manel
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机构:
Josep Carreras Leukemia Res Inst IJC, Canc Epigenet Grp, Barcelona 08916, Spain
Ctr Invest Biomed Red Canc CIBERONC, Madrid 28029, Spain
Inst Catalana Recerca Avancats ICREA, Barcelona 08010, Spain
Univ Catalonia, Sch Med & Hlth Sci, Dept Physiol Sci, Barcelona 08017, SpainJosep Carreras Leukemia Res Inst IJC, Bioinformat Unit, Barcelona 08916, Spain
Esteller, Manel
[2
,3
,4
,5
]
机构:
[1] Josep Carreras Leukemia Res Inst IJC, Bioinformat Unit, Barcelona 08916, Spain
[2] Josep Carreras Leukemia Res Inst IJC, Canc Epigenet Grp, Barcelona 08916, Spain
[3] Ctr Invest Biomed Red Canc CIBERONC, Madrid 28029, Spain
[4] Inst Catalana Recerca Avancats ICREA, Barcelona 08010, Spain
[5] Univ Catalonia, Sch Med & Hlth Sci, Dept Physiol Sci, Barcelona 08017, Spain
Simple Summary Aberrations of normal DNA methylation patterns are observed in many cancers and are associated with chromatin alterations, changes in gene expression and genomic instability, making the study of DNA methylation paramount to our understanding of cancer biology and evolution and the development of biomarkers. Here, we present an overview of genome-wide approaches for the analysis of DNA methylation with relevance to cancer research and clinics. DNA methylation is an essential epigenetic mark. Alterations of normal DNA methylation are a defining feature of cancer. Here, we review experimental and bioinformatic approaches to showcase the breadth and depth of information that this epigenetic mark provides for cancer research. First, we describe classical approaches for interrogating bulk DNA from cell populations as well as more recently developed approaches for single cells and multi-Omics. Second, we focus on the computational analysis from primary data processing to the identification of unique methylation signatures. Additionally, we discuss challenges such as sparse data and cellular heterogeneity.
机构:
Technion, Fac Comp Sci, Haifa, IsraelTechnion, Fac Comp Sci, Haifa, Israel
Lagziel, Shoval
Lee, Won Dong
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机构:
Technion, Fac Biol, Haifa, IsraelTechnion, Fac Comp Sci, Haifa, Israel
Lee, Won Dong
Shlomi, Tomer
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机构:
Technion, Fac Comp Sci, Haifa, Israel
Technion, Fac Biol, Haifa, Israel
Technion, Lokey Ctr Life Sci & Engn, Haifa, IsraelTechnion, Fac Comp Sci, Haifa, Israel
机构:
Taibah Univ, Coll Appl Med Sci, Dept Med Lab Technol, Al Medinah Al Monawara, Saudi ArabiaIslamia Coll Peshawar, Dept Chem, Peshawar, Kpk, Pakistan