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== Affymetrix Microarray Data == * CEL files: contain processed intensity values, higher intensity (transcript abundance) more active genes |
1. Affymetrix Microarray Data * CEL files: contain intensity values, higher intensity (transcript abundance) more active genes |
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== Microarray Experimental Designs == | 2. Microarray Experimental Designs |
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* Pooling (biological averaging), blocking | * Pooling (biological averaging), blocking, randomized |
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== Data Exploration == | 3. Data Exploration |
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4. Data Preprocessing * Approaches: background correction, normalization, PM correction, and summarization * Background correction methods: * rma: robust multiarray average method (Irizarry et al. 2003) * mas: Affymetrix Microarray Suite background correction method (2002) * GCRMA: modified RMA to estimate nonspecific binding (Wu et al. 2004) * Normalization methods: * quantile, contrast and loess: discussed and compared by Bolstad et al. (2003) * constant (scaling): taken by Affymetrix, usually done after summarization * invariantset: used in the dChip software (Li and Wong 2001) * qspline: normalized by fitting splines to the quantiles (Workman et al. 2002). * PM correction methods: * mas: an ideal mismatch subtracted from PM (Affymetrix 2002) * pmonly: no adjustment to the PM values. * subtractmm: subtract MM from PM (Affymetrix MAS 4.0 1999) * Summarization methods: * avgdiff: the average (Affymetrix MAS 4.0 1999) * mas: Tukey biweight on log2(PM-CM) (Affymetrix MAS 5.0 2002) * liwong: model-based expression index (MBEI) (Li and Wong 2001), fitting the following multi-chip model to each probeset: * y_ij = theta_i * phi_j + epsilon_ij, where y_ij = PM_ij - MM_ij * y_ij = mu_i + theta_i * phi_j + epsilon_ij, where y_ij = PM_ij * medianpolish: used in the RMA expression summary (Irizarry et al. 2003). A multichip linear model is fit to data from each probeset * y_ij = alpha_i + beta_j + epsilon_ij, where y_ij are the background-adjusted, normalized, and log-transformed PM intensities * playerout: Lazaridis et al. (2002) * Popular methods || Popular methods || Background correction || Normalization || PM correction || Summarization || || RMA || rma || quantile || pmonly || medianpolish (log2 scale)|| || MAS5 || mas || constant || mas || mas (log2 scale)|| || MBEI || PM only || invariantset || pmonly or subtractmm || liwong || |
Summary of Affymetrix Microarray Data Analysis
1. Affymetrix Microarray Data
- CEL files: contain intensity values, higher intensity (transcript abundance) more active genes
- CDF (chip description file) files: specify the probe and probe set to which each cell belongs
- Terms:
- Probe: oligonucleotides of 25 base (pair) length used to probe RNA targets (25 base sequence)
- Probe pair: a unit composed of a perfect match (PM) and its mismatch (MM)
- Probe pair set: PMs and MMs related to a common affyID (a group of probe pairs corresponds to a particular gene or a fraction of a gene. Some genes are represented by more than one probe set.)
- affyID: an identification for a probe set (which can be a gene or a fraction of a gene) represented on the array
2. Microarray Experimental Designs
- Biological and technical replicates
- Pooling (biological averaging), blocking, randomized
- Sample size determination
3. Data Exploration
- MA plots
- M values are log fold changes, M=log2(T/C)=log2(T)-log2(C)
- A values are average log intensities between two arrays, A=(log2(T)+log2(C))/2
- Images, residual images
- Histograms, boxplots
- RNA degradation plots
4. Data Preprocessing
- Approaches: background correction, normalization, PM correction, and summarization
- Background correction methods:
- rma: robust multiarray average method (Irizarry et al. 2003)
- mas: Affymetrix Microarray Suite background correction method (2002)
- GCRMA: modified RMA to estimate nonspecific binding (Wu et al. 2004)
- Normalization methods:
- quantile, contrast and loess: discussed and compared by Bolstad et al. (2003)
- constant (scaling): taken by Affymetrix, usually done after summarization
- invariantset: used in the dChip software (Li and Wong 2001)
- qspline: normalized by fitting splines to the quantiles (Workman et al. 2002).
- PM correction methods:
- mas: an ideal mismatch subtracted from PM (Affymetrix 2002)
- pmonly: no adjustment to the PM values.
- subtractmm: subtract MM from PM (Affymetrix MAS 4.0 1999)
- Summarization methods:
- avgdiff: the average (Affymetrix MAS 4.0 1999)
- mas: Tukey biweight on log2(PM-CM) (Affymetrix MAS 5.0 2002)
- liwong: model-based expression index (MBEI) (Li and Wong 2001), fitting the following multi-chip model to each probeset:
- y_ij = theta_i * phi_j + epsilon_ij, where y_ij = PM_ij - MM_ij
- y_ij = mu_i + theta_i * phi_j + epsilon_ij, where y_ij = PM_ij
- medianpolish: used in the RMA expression summary (Irizarry et al. 2003). A multichip linear model is fit to data from each probeset
- y_ij = alpha_i + beta_j + epsilon_ij, where y_ij are the background-adjusted, normalized, and log-transformed PM intensities
- playerout: Lazaridis et al. (2002)
- Background correction methods:
- Popular methods
Popular methods
Background correction
Normalization
PM correction
Summarization
RMA
rma
quantile
pmonly
medianpolish (log2 scale)
MAS5
mas
constant
mas
mas (log2 scale)
MBEI
PM only
invariantset
pmonly or subtractmm
liwong