Microarray II
What is a microarray
Microarray Experiment RT-PCR LASER DNA “Chip” High glucose Low glucose
Raw data – images Red (Cy5) dot – overexpressed or up-regulated Green (Cy3) dot – underexpressed or down- regulated Yellow dot –equally expressed Intensity - “absolute” level cDNA plotted microarray
Levels of analysis Level 1: Which genes are induced / repressed? Gives a good understanding of the biology Methods: Factor-2 rule, t-test. Level 2: Which genes are co-regulated? Inference of function. -Clustering algorithms. Level 3: Which genes regulate others? Reconstruction of networks. - Transcriptions factor binding sites.
Level 1 2-fold rule: Is a gene 2-fold up (or down) regulated? Students t-test: Is the regulation significantly different from background variation? (Needs repeated measurements)
T-test X ~ N( ), Cannot reject H 0 Reject H 0 The p-value is the probability of drawing the wrong conclusion by rejecting a null hypothesis
Multiple testing In a microarray experiment, we perform 1 test / gene Prob (correct) = 1 - c Prob (globally correct) = (1 – c n Prob (wrong somewhere) = 1 - (1 – c n e = 1 - (1 – c n For small e : c e n Bonferroni correction
Multiple Experiments: Time course (Chu et al) Explore changes in gene expression during a biological process. Extract mRNA at time points 0, 0.5, 2, 5, 7, 9, and 11 hours and wish to compare expression profiles across time points. Compensate for array variability by using the 0 time point as common reference (green channel).
Experiment: time course Time 0 Genes Sample annotations Gene annotations Intensity (Red) Intensity (Green)
Experiment: time course Time 0.5 Genes Intensity (Red) Intensity (Green) Time 0
Experiment: time course Genes Time (hours)
Gene expression database Genes Gene expression levels Samples Sample annotations Gene annotations Gene expression matrix
Gene expression database Samples Genes Gene expression matrix Timeseries, Conditions A, B, … Mutants in genes a, b … Etc.
Data normalization expression of gen x in experiment i expression of gen x in reference Logarithm of ratio - treats induction and repression of identical magnitude as numerical equal but with opposite sign. red/green - ratio of expression – 2 - 2x overexpressed – x underexpressed log 2 ( red/green ) - “log ratio” – 1 2x overexpressed – -1 2x underexpressed
Analysis of multiple experiments Expression of gene x in m experiments can be represented by an expression vector with m elements Z-transformation: If X ~ N( ),
Clustering Hierachical clustering: - Transforms n (genes) * m (experiments) matrix into a diagonal n * n similarity (or distance) matrix Similarity (or distance) measures: Euclidic distance Pearsons correlation coefficent Eisen et al PNAS 95:
Most Common Minkowski Metrics
An Example 4 3 x y
Similarity Measures: Correlation Coefficient
Time Gene A Gene B Gene A Time Gene B Expression Level Time Gene A Gene B
Clustering of Genes and Conditions Unsupervised: –Hierarchical clustering –K-means clustering –Self Organizing Maps (SOMs)
Clustering Hierachical clustering: - Transforms n (genes) * m (experiments) matrix into a diagonal n * n similarity (or distance) matrix Similarity (or distance) measures: Euclidic distance Pearsons correlation coefficent Eisen et al PNAS 95:
Distance Measures: Minkowski Metric r r m i ii m m yxyxd yyyy xxxx myx ||),( )( )( by defined is metric Minkowski The :features have both and objects two Suppose
Most Common Minkowski Metrics ||max),( ||),( 1 ||),( ii m i m i ii m i ii yxyxd r yxyxd r yxyxd r )distance sup"(" 3, distance) (Manhattan 2, ) distance (Euclidean 1,
An Example 4 3 x y
Similarity Measures: Correlation Coefficient. and :averages )()( ))(( ),( m i i m m i i m m i m i ii m i ii yyxx yyxx yyxx yxs
Similarity Measures: Correlation Coefficient Time Gene A Gene B Gene A Time Gene B Expression Level Time Gene A Gene B
Distance-based Clustering Assign a distance measure between data Find a partition such that: –Distance between objects within partition (i.e. same cluster) is minimized –Distance between objects from different clusters is maximized Issues: –Requires defining a distance (similarity) measure in situation where it is unclear how to assign it –What relative weighting to give to one attribute vs another? –Number of possible partition is super-exponential
Clustering of Genes and Conditions Unsupervised: –Hierarchical clustering –K-means clustering –Self Organizing Maps (SOMs)
Ordered dendrograms Hierachical clustering: Hypothesis: guilt-by-association Common regulation -> common function Eisen98
Hierarchical Clustering Techniques At the beginning, each object (gene) is a cluster. In each of the subsequent steps, two closest clusters will merge into one cluster until there is only one cluster left.
Hierarchical Clustering Given a set of n items to be clustered, and an n*n distance (or similarity) matrix, the basic process hierarchical clustering is this: 1.Start by assigning each item to its own cluster, so that if you have n items, you now have n clusters, each containing just one item. Let the distances (similarities) between the clusters equal the distances (similarities) between the items they contain. 2.Find the closest (most similar) pair of clusters and merge them into a single cluster, so that now you have one less cluster. 3.Compute distances (similarities) between the new cluster and each of the old clusters. 4.Repeat steps 2 and 3 until all items are clustered into a single cluster of size N.
Merge two clusters by: Single-Link Method / Nearest Neighbor (NN): minimum of pairwise dissimilarities Complete-Link / Furthest Neighbor (FN): maximum of pairwise dissimilarities Unweighted Pair Group Method with Arithmetic Mean (UPGMA): average of pairwise dissimilarities
Single-Link Method Diagonal n*n distance Matrix Euclidean Distance b a cd (1) cd a,b (2) a,b,c d (3) a,b,c,d
Complete-Link Method b a Distance Matrix Euclidean Distance (1) (2) (3) a,b ccd d c,d a,b,c,d
Compare Dendrograms Single-LinkComplete-Link
Serum stimulation of human fibroblasts (24h) Cholesterol biosynthesis Celle cyclus I-E response Signalling/ Angiogenesis Wound healning
Partitioning k-means clustering Self organizing maps (SOMs)
k-means clustering Tavazoie et al Nature Genet. 22:
k-Means Clustering Algorithm 1) Select an initial partition of k clusters 2) Assign each object to the cluster with the closest centre 3) Compute the new centres of the clusters 4) Repeat step 2 and 3 until no object changes cluster
1. centroide
2. centroide 3. centroide 4. centroide 5. centroide 6. centroide k = 6
1. centroide 2. centroide 3. centroide 5. centroide 6. centroide k = 6
1. centroide 2. centroide 3. centroide 4. centroide 5. centroide 6. centroide k = 6
Self organizing maps Tamayo et al PNAS 96:
1. centroide2. centroide3. centroide 4. centroide 5. centroide6. centroide k = (2,3) = 6
k = 6
Cluster Co-regulation (DeRisi et al, 1997)
Cluster of co-expressed genes, pattern discovery in regulatory regions 600 basepairs Expression profiles Upstream regions Retrieve Pattern over-represented in cluster
Some Discovered Patterns Pattern Probability ClusterNo.Total ACGCG 6.41E ACGCGT 5.23E CCTCGACTAA 5.43E GACGCG 7.89E TTTCGAAACTTACAAAAAT 2.08E TTCTTGTCAAAAAGC 2.08E ACATACTATTGTTAAT 3.81E GATGAGATG 5.60E TGTTTATATTGATGGA 1.90E GATGGATTTCTTGTCAAAA 5.04E TATAAATAGAGC 1.51E GATTTCTTGTCAAA 3.40E GATGGATTTCTTG 3.40E GGTGGCAA 4.18E TTCTTGTCAAAAAGCA 5.10E Vilo et al. 2001
Results Over 6000 “interesting” patterns Many from homologous upstreams - removed –Leaves 1500 patterns These patterns clustered into 62 groups –Found alignments, consensus, and profiles Of 62 clusters - 48 had patterns matching SCPD (experimentally mapped) binding site database
The " GGTGGCAA " Cluster
Clustering and promoter elements Harmer et al Science 290:
Two sided Clustering
-Deletion mutations Vector Chromosomes Homologous recombination
Transcriptional profiling of mutants -Mutants Genes
Microarray and cancer Alizadeh et al Nature 403:
Diffuse large B-cell lymphoma
Human tumor patient and normal cells; various conditions Cluster genes across tumors Classify tumors according to genes
Regulatory pathways: KEGG
Regulatory pathway reconstruction Ideker et al Science 2001
Perturbations Selected genes are deleted. RNA is extracted from -strains and from WT under +/- Galactose conditions Repeated measurements enable estimation of statistical significance Compare data – model –Design new experiments Clustering : Self Organizing Maps Protein – mRNA correlations Network correlations –Protein-DNA (Promoter analysis) –Protein-Protein
Correlation mRNA – protein levels Mass-spectrometry
ICAT reagent Isotope coded affinity tags
ICAT procedure
Mapping of gene expression changes onto interaction network Yellow: Protein-DNA Blue: Protein-protein
Hierarchical clustering of -perturbations
Conclusion Significance Database (matrix), data normalization Distances HCL, SOM, k-means Two-sided clustering Promoter elements Metabolic / regulatory pathways Deletion mutants ICAT technology; MS/MS