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1
Intro
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High throughput sequencing
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What is ChIP sequencing
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Differential binding
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RNAseq
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How much does normalization matter
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Library size
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Background bins
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Road map
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Capital T truth
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Factoring
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spiking controls
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symmetry
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Asymmetry
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Size Factors
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Relative Log Expression
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Technical Conditions
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Simulations
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False Discovery Rate
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Symmetrical DNA Binding
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Background Bin
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Entire Genome
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Four Images
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Technical Condition
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Trend
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Data
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Principal Components
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Summary
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Controls
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Biological Experiment
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Conclusion
Description:
Save Big on Coursera Plus. 7,000+ courses at $160 off. Limited Time Only! Grab it Explore the intricacies of selecting between-sample ChIP-Seq normalization methods in this 44-minute conference talk by Jo Hardin at the Computational Genomics Summer Institute (CGSI) 2023. Delve into the assumptions underlying various normalization techniques for ChIP-Seq data analysis, drawing parallels with RNA-Seq normalization methods. Examine the importance of normalization in high-throughput sequencing, focusing on differential binding analysis in ChIP-Seq experiments. Learn about library size adjustments, background bin considerations, and the concept of "capital T truth" in data analysis. Explore various normalization approaches, including size factors, relative log expression, and technical condition adjustments. Understand the impact of symmetry and asymmetry in DNA binding on normalization choices. Evaluate normalization methods through simulations and false discovery rate assessments. Gain insights into the use of controls, biological experiments, and principal component analysis in ChIP-Seq data interpretation. Conclude with a comprehensive understanding of how to select appropriate normalization methods based on experimental design and data characteristics. Read more

Selecting Between-sample ChIP-Seq Normalization Methods - Assumptions and Implications

Computational Genomics Summer Institute CGSI
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