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DNA microarray and array data analysis Some of the slides are adapted from the lecture notes of Dr. Patrick Leahy of the Gene Expression Array Core Facility at CWRU What is DNA Microarray DNA microarray is a new technology to measure the level of the mRNA gene products of a living cell. A microarray chip is a rectangular chip on which is imposed a grid of DNA spots. These spots form a two dimensional array. Each spot in the array contains millions of copies of some DNA strand, bonded to the chip. Chips are made tiny so that a small amount of RNA is needed from experimental cells. DNA Microarray Many applications in both basic and clinical research determining the role a gene plays in a pathway, disease, diagnostics and pharmacology, … There are three main platforms for performing microarray analyses. cDNA arrays (generic, multiple manufacturers) Oligonucleotide arrays (genechips) (Affymetrix) cDNA membranes (radioactive detection) cDNA Microarray Spot cloned cDNAs onto a glass/nylon microscope slide usually PCR amplified segments of plasmids Complementary hybridization -- CTAGCAGG actual gene -- GATCGTCC cDNA (Reverse transcriptase) -- CUAGCAGG mRNA Label 2 mRNA samples with 2 different colors of fluorescent dye -- control vs. experimental Mix two labeled mRNAs and hybridize to the chip Make two scans - one for each color Combine the images to calculate ratios of amounts of each mRNA that bind to each spot Spotted Microarray Process CTRL TEST cDNA Array Experiment Movie http://www.bio.davidson.edu/courses/genomic s/chip/chip.html “Long Oligos” Like cDNAs, but instead of using a cloned gene, design a 40-70 base probe to represent each gene Relies on genome sequence database and bioinformatics Reduces cross hybridization Cheaper and possibly more sensitive than Affy. system Affymetrix Uses 25 base oligos synthesized in place on a chip (20 pairs of oligos for each gene) cRNA labeled and scanned in a single “color” one sample per chip Can have as many as 47,000 probes on a chip (HG-U133 Plus 2.0 Array) Arrays get smaller every year (more genes) Chips are expensive (about $400/chip) Proprietary system: “black box” software, can only use their chips Affymetrix Genome Arrays ® Affymetrix GeneChip Probe Array ® Affymetrix GeneChip Probe Arrays Hybridized Probe Cell GeneChip Probe Array Single stranded, fluorescently labeled cRNA target * * * * * * Oligonucleotide probe 24~50µm 1.28cm Each probe cell or feature contains millions of copies of a specific oligonucleotide probe BGT108_DukeUniv Image of Hybridized Probe Array Affymetrix GeneChip Probe: 25 bases long single stranded DNA oligos Probe Cell: Single square-shaped feature on an array containing one type of probe. Contains millions of probe molecules Probe Pair: Probe Set Perfect Match/Mismatch Array Design 5’ Twenty oligo probes are selected from the last 600 bases from the 3’ end of the gene 3’ For each probe selected, a partner containing a central mutation is also made Perfect Match 25 mer DNA oligo Mismatch Probe Set Perfect Match Mismatch 24m For each gene a total of 20 probe pairs are arrayed on the chip PM MM Probe Pair 24m Probe Cell Probe Sub-types on chips Known genes Specific transcripts Exemplars Consensus Housekeeping genes Expressed sequence tags (ESTs) Spiked control transcripts cRNA preparation Total RNA (5-8 g) AAAAAAAAA cDNA Strand 1 synthesis SS II reverse transcriptase AAAAAAAAA TTTTTTTTTNNNNNNNNN T7RNA pol. promoter E. coli DNA pol. I cDNA Strand 2 synthesis AAAAAAAAANNNNN TTTTTTTTTNNNNNNNNN T7RNA pol. promoter ……….. ……….. ……….. …… ……….. UUUUUUUUUU UUUUUUUUUU UUUUUUUUUU UUUUUUUUUU UUUUUUUUUU IVT cRNA synthesis amplifies and labels transcripts with Biotin T7 RNA pol. Fragmented cRNA cRNA is now ready for hybridization to test chip AAAAAAAAAAAAAAN NNNNNNNNNNNNN TNNNNNNNN T T TT TTTTTTT T cRNA labeled targets B B B B B B B B Post hybridiz -ation washes B B B B B cRNA labeled targetsB Specific Binding B NonSpecific Binding B B B B B B FL B B B S B B B B B BS B B B cDNA probes FL B S FL B B FL BS BS FL FL BS FL B S FL BS FL B S Streptavidin Microarray experiment Biotin-Labeled cRNA transcript Cells AAAA Poly (A)+ RNA IVT cDNA B B B B (B-UTP) Fragment (heat, Mg2+) B Hybridize Scan Wash Stain (1-18 hours) B B B Biotin-Labeled cRNA fragments .dat file Probe set The chip image data file (or “.dat” file) is the first part of data acquisition and appears on the computer screen upon completion of the laser scan. Here, we zoom in to see an individual probe set that has been highlighted The first image is “sample1.dat.” note the pixel to pixel variation within a probe cell A “*.cel.” file is automatically generated when the “*.dat” image first appears on the screen. Note that this derivative file has homogenous signal intensity within its probe cells .cel file Affymetrix Algorithms All MMs < PMs, No adjustment necessary Few MMs > PMs, change MMs based on weighted mean of other MMs Most MMs > PMs, change MMs to be slightly lesss than PM 1. Signal 1.1 Adjusting MMs to purge negative values Signal Calculation. Affymetrix Algorithms PM 1000 MM 900 PM-MM 100 5000 2000 430 230 Calculate the signal 765 25 355 331 98 40 3005 1200 413 20333 203 6197 Having adjusted the MM values, we 3000now200 740 the24 1805 210 14136 calculate signal58 Unweighted mean = 2063 The unweighted mean is vulnerable to outlier data. In order to protect against this, we dampen the effect of outliers by using the Tukey bi-weight mean. PM-MM values that are a number of standard deviations away from the mean are given low weights in accordance with the graph shown here. Individual PM-MM data are multiplied by the weight factor before calculation of the mean. The weighted mean is then called the “signal.” The PM values. The MM values. The PM-MM values are calculated. Weight factor 1 1 2 3 4 5 6 Standard deviations Using Tukey’s biweight mean = 1780 Signal (expression level) = 1780 590 230 360 .xls file ALL_vs_AML_train_set_38_sorted.res ALL_vs_AML_train_set_38_sorted.cls 38 2 1 00000000000000000000000000011111111111 27 11