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Published byToby Carter Modified over 9 years ago
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ChIP-chip Data
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DNA-binding proteins Constitutive proteins (mostly histones) –Organize DNA –Regulate access to DNA –Have many modifications Acetylation, methylation, … Sporadic proteins (Transcription Factors) –Mediate docking of transcription apparatus –Modify histones –Methylate DNA
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Histones Histones are an ancient family of proteins which serve as the scaffold for DNA Four types of histones assemble in pairs to form a nucleosome DNA is wrapped twice around each nucleosome
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Histones and Modifications DNA contacts histones on their tails Histone tails can be modified Histones can stay loose or assemble tightly – this compacts the DNA
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Transcription Factors General – help to set up transcription of many genes Specific – draw in general factors or RNA Pol II to specific genes TATA Binding Protein
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DNA Methylation Adding a Methyl to Cytosine Cytosine methylation is passed on to daughter cells
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Chromatin Immuno-precipitation
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Tiling Array One probe every n base pairs over some length of chromosome –Interrupted by repeat regions Promoter array: each (known) promoter tiled An Affymetrix tiling design
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What the data look like histone acetylation on 15 samples over one promoter (raw)
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Multiple Promoters
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Normalized by Medians
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Methods and Issues Normalization –Different enrichment ratios –Different probe thermodynamics –Dye and probe bias Estimation –Categorical or continuous? –Individual values are noisy: For TF binding: where is the peak?
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Normalization Basic idea: compensate technical variables Technique differences should affect different probes differently Try to estimate what part of signal can be attributed to technical factors Easiest variable to access: sequence
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MAT One color Affy array –Needs separate array for comparison Normalizes probe thermodynamics & enrichment ratio Estimation by (robust) moving average
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Normalized Data – Rare Event
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Normalized Data – Common Event
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Estimation Try to build an intelligent moving average Not all neighbors will be similar Typical TF binds to 8bp –Pol II may spread wider Typical fragment is 100-200 bp Cannot resolve < 200 bp Pol II binding on a 100 bp grid
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TileMap Ignores normalization ‘Shrinkage’ estimator of variance –Improves individual scores Smooths noise by moving average
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