High-throughput, parallel gene expression analysis by means of microarray technology has become a widely used technique in recent years. There are currently two main dye-labelling strategies for microarray studies based on custom-spotted cDNA or oligonucleotides arrays: (I) Dye-labelling of a single target sample with a particular dye, followed by subsequent hybridisation to a single microarray slide, (II) Dye-labelling of two different target samples with two different dyes, followed by subsequent co-hybridisation to a single microarray slide. The two dyes most frequently used for either method are Cy3 and Cy5. We propose and evaluate a novel experiment set-up utilising three differently labelled targets co-hybridised to one microarray slide. In addition to Cy3 and Cy5, this incorporates Alexa 594 as a third dye-label. We evaluate this approach in line with current data processing and analysis techniques for microarrays, and run separate analyses on Alexa 594 used in single-target, dual-target and the intended triple-target experiment set-ups (a total of 18 microarray slides). We follow this by pointing out practical applications and suitable analysis methods, and conclude that triple-target microarray experiments can add value to microarray research by reducing material costs for arrays and related processes, and by increasing the number of options for pragmatic experiment design.
The addition of Alexa 594 as a dye-label for an additional – third – target sample works within the framework of more commonplace Cy5/Cy3 labelled target sample combinations. Standard normalisation methods are still applicable, and the resulting data can be expected to allow identification of expression differences in a biological experiment, given sufficient levels of biological replication (as is necessary for most microarray experiments).
The use of three dye-labelled target samples can be a valuable addition to the standard repertoire of microarray experiment designs. The method enables direct comparison between two experimental populations as well as measuring these two populations in relation to a third reference sample, allowing comparisons within the slide and across slides. These benefits are only offset by the added level of consideration required in the experimental design and data processing of a triple-target study design. Common methods for data processing and analysis are still applicable, but there is scope for the development of custom models for triple-target data. In summary, we do not consider the triple-target approach to be a new standard, but a valuable addition to the existing microarray study toolkit.
Microarray technology is a high-throughput and parallel platform that enables research on whole genomes, thereby helping to increase our understanding of the regulation of biological systems. All variations of this technique involve the deposition of a large number of probe sequences (e.g. oligonucleotides, cDNA) – representing a whole genome or subsets thereof – in a regular grid-like array on a physical substrate, usually a glass slide for custom spotted arrays. Microarray studies are costly in terms of equipment, consumables and time, therefore careful design and replication are particularly important if the resulting experiment is to be maximally informative. As opposed to high-density arrays like Affymetrix (probes produced in-situ in a process resembling lithography), standard experiments using spotted arrays on glass slides usually involve the co-hybridisation of two differently labelled targets to one slide. This is normally referred to as dual-target or dual-dye arrays. In such a cDNA microarray dual-target experiment, it is usually the fluorescent dyes Cy5 and Cy3 that are used in tandem. One of the dyes is used to label an experimental target sample, the other to label a reference or control sample. After measuring the fluorescence of each dye-label channel separately, the scan images are processed and this results in a numerical value of abundance (often termed expression) of this gene in the experimental sample and the reference sample. The relative abundance of each gene is usually presented as the log-ratio of these two values, and used as the measure of gene expression for an array. There are practical issues concerning this experimental approach, in that constraints on the number of arrays processed and/or the amount of RNA available can have a detrimental effect on the experimental design .
We have introduced a third dye-label (Alexa 594) in an attempt to improve on such practical limitations without sacrificing data quality. This novel experimental strategy was specifically developed to investigate, using cDNA microarrays, the changes in gene expression patterns during the normal development of spermatogenesis in wild type mouse, and in parallel, in a known fertility mutant (Dazl-null mouse) . We envisage this approach to be useful in similar complex multi-factorial experiments, e.g., time-series data with comparisons between different genotypes, or cancer studies where comparisons are required both in a single patient (e.g. before and after therapy) and across a population of patients. In each case, the benefit lies in producing more than one on-chip measurement of relative expression. For example, using a common reference sample in combination with a test sample of type A and type B on one array allows a direct comparison of the relative gene expression levels in both test samples, without having to compare relative expression values from two or more dual-target arrays containing only a reference and one of the test samples. With a suitable laboratory protocol, and including the necessary levels of replication, this considerably reduces the number of arrays required for a microarray study without having to reduce the complexity of the biology under study.
There have been previous publications [3, 4] investigating the use of three dye-labels per microarray, but it must be stressed here that the third dye was used to label the probes rather than a third target sample. This is a different objective to the one described here, and, due to the manipulation of the actual array platform, has larger requirements in terms of repeat array hybridisations. To avoid confusion between these different concepts and aims, we refer to the approach described in this paper as "triple-target" rather than "triple-dye".
In this paper, we report on the methodology and evaluation of using three dye-labelled target samples per array, specifically Cy3, Cy5 and Alexa 594.
Results and Discussion
In order to assess both the use of Alexa 594 in combination with the other two dyes and the use of Alexa 594 by itself or in combination with only one of the other dyes, three separate analyses were performed. The first is based on the analysis of arrays which have been co-hybridised with three differently labelled target samples, with n = 5 arrays. The second analysis is based on arrays which have been co-hybridised with only two of the available three dye-labels, with n = 2 arrays for each of the three possible dye-label combinations. The third analysis involves arrays that have been hybridised with only one dye-labelled target sample, with n = 3 arrays for Alexa594, n = 2 arrays for Cy5 and n = 2 arrays for Cy3. The only difference imposed on these three analyses was the use of a different print-run of slides for the single-target analysis. There was one consistent pool of target sample material for all hybridisations and labellings. QuantArray software was used to convert the images to numerical data, and all interpretation of data is done on these numerical data. The parameter values for the QuantArray algorithm were chosen based on manufacturer recommendations and kept consistent for all arrays and dye-label samples. Any choice of algorithm and parameter values results in some level of observed discrepancy between image and numerical presentation of the image (e.g. background estimates). Where such differences are apparent, they have been pointed out in the evaluation.
Triple-target self hybridisations
For dual-target experiments, any setup involving one sample dye-labelled with both dyes and hybridised to one array is referred to as self-to-self hybridisation, and in building on this terminology the experimental setup for this evaluation experiment will be referred to as triple-self hybridisations. The theoretical outcome of any self-to-self experiment is clear: absolute expression values for genes should be identical across array dye-label channels. Similarly, relative expression value for every gene should be 1 (or 0 on a log scale), independent of the dye-label combination in question. Evaluation of the validity of adding a third dye-labelled sample therefore consists of testing to which degree this theoretical outcome is true, and if it is different to outcomes from standard dual-target arrays. In practice, the ideal theoretical outcome is normally not achieved in experimental data, due to factors like differences in RNA extraction, dye-label incorporation, hybridisation quality, slide quality and scanning parameters etc., all of which increase variance in the data . To minimise dye-label incorporation differences, aminoallyl labelling has been used, which results in higher labelling efficiency and improved incorporation of the different dyes compared to the direct labelling method [6–8]. Normalisation algorithms have been devised to further limit the effect of such sources of variation, and as a result, any self-to-self hybridisation should then approximate the ideal outcome. In the following section this statement is evaluated.
A first investigation of the expression values obtained from the three individual samples on an array (Fig. 1, Table 1) shows that, across all probes on an array, Cy3 and Alexa594 share similar average expression and spread of values before applying any normalisation methods. Cy5 labelled samples appear to have a greater spread of data values, with differences apparent in the lower signal intensities. This may be caused by dye-label incorporation differences, which are known to occur in most common Cy5/Cy3 dual-target experiments. These differences are not evident for Cy3/Alexa594 combinations here. Before normalisation, log-ratios for pair-wise sample comparisons on the arrays are therefore showing slightly greater variance for those combinations that involve Cy5 (Fig. 2a), in addition to global differences that systematically move the ratios away from zero 0. Subsequent location and scale normalisation reduces these systematic differences and results in very comparable data distributions, all gene probes on an array contained in the Inter-Quartile-Range having log-ratios within the interval [+0.25; -0.25] (Fig. 2b).
The sample-to-sample differences for all three samples on an array were also assessed by visualising their standard deviation in relation to the average level of expression, both calculated across all gene-probes in a dye-label channel (Fig. 3). Due to the limitation of only having three dye-label observations per gene per array, the calculation of the relative standard deviation is not a statistically relevant procedure, and influenced by outlier values. Here it only serves as a global quality indicator. Nonetheless, this exercise clearly emphasises that most variance in the expression levels of a gene on an array is occurring at lower levels of expression. The majority of medium and high expressed genes have a relative standard deviation <0.05 even before applying normalisation methods.
A common visualisation method for dual-target arrays is the MA plot (in a similar version often referred to as R-I plot), which combines information about the log-ratio of a gene probe with its expression level, and this is also used as the basis for a LoWeSS normalisation. A standard dual-target array will obviously have only one such plot, whereas a triple-target array increases the number of possible sample-combinations on the array to 3. In a real biological experiment, the interest may be focused on only two of these, but for the purpose of this evaluation we examine all possible relationships (Fig. 4). All five arrays show reproducible patterns of dependence or non-dependence of the log-ratio on the log-intensity. The dye-incorporation differences discussed above are clearly visible for the standard Cy5/Cy3 combination as well as for the Cy5/Alexa594 combination. The relationship between Cy3 and Alexa594 is equally reproducible, but, in contrast to the other two pairings, there is no evidence of pronounced differences between the two labels at low expression levels. After removing systematic linear and non-linear differences between any two dye-labelled samples, the resulting log-ratios for all dye-label combinations are centred around 0 (Fig. 5). Since the LoWeSS normalisation needs to apply a greater change to log-ratios involving Cy5, at least at lower levels of signal intensity, it could be surmised that the corrected log-ratios from the Cy3/Alexa combination will be associated with less introduced bias.
Dual-target self hybridisations
Whereas triple-target self hybridisations are ideal for testing the validity of adding a third dye-labelled sample on an array, to further evaluate Alexa 594, we performed dual-target self hybridisations. Such an experiment allows a) to examine the effect of the new dye-label Alexa594 without the presence of a third dye-labelled sample (which may have unknown effects), and b) to examine a standard dual-target experiment in the same system as is used for the triple-target hybridisations. The third scan for each array was still performed although no material had been hybridised for this dye. In theory, this blank channel should produce no signal values, and deviations from this show potential "signal bleed" from one dye-label (or rather, the laser frequency it is scanned at) to another. Limitations of target sample material and printed arrays did not allow for the inclusion of more than two arrays per dual-target combination, which limits the statistical interpretability of these results. However, for the purposes of this study, they serve as supporting evidence and should identify gross problems with the inclusions of a third dye.
All arrays confirm the results obtained from analysis I: Cy5 is associated with more gene probes values in the low expression range (Fig. 6). The dependence of log-ratio on log-intensity of a gene probe is also consistent with the triple-target arrays, in that the use of Cy5 with either of the other two dyes leads to non-linear effects (Fig. 7). A positive aspect of Cy5 are the very small signal values close to zero when it is the blank channel, which cannot be said for Alexa594 and Cy3, both of which result in low level signal values even if no sample has been hybridised to the array with the corresponding dye-label. This is probably an indication of the relative closeness of the dye-labels in the light frequency spectrum, leading for example to fluorescence of the Cy3 channel when the array is subjected with the laser frequency corresponding to Alexa594. However, the level of signal obtained from these blank channels is small in proportion to the hybridised channels, with linear slopes between 0.02 and 0.03 and intercept signal values between 52 and 115. Given the assumption that this effect is also present in the triple-target hybridisation, it does not present itself as a large or non-systematic problem. It does not cause signal interpretation problems that are greater than those created by using two dyes with a non-linear relationship (i.e. Cy5 vs. Cy3) at comparable low levels of expression.
The hybridisation of only one dye-labelled sample to an array allows a closer investigation of signal "bleeding" from one dye-labelled sample to another, as described above. For this analysis, spike controls were included for all three dye-labels to allow calibration between channels, and their relation to the other gene probes on the array is shown in figure 8. Visual inspection of the images obtained from this experiment revealed that there is some visible signal bleeding between Alexa594 and Cy3, as well as between Alexa594 and Cy5. However, the results of this visual inspection differ from the numerical analysis, where Cy5 also has a similar level of bleed into the other channels (see below). This is most likely due to the image conversion algorithm interpreting pixels and features differently from the human eye. Although the number of replicates is not sufficient to draw statistical conclusions, the results are supporting those of the dual-target hybridisations. If Alexa594 is the hybridised sample, there is little to no signal present if scanning the blank Cy5 channel, whereas the scan for the blank Cy3 channel is resulting in consistent, but low levels of signal values (Fig. 9). The same is true where Cy3 is the hybridised sample: the blank Cy5 channel exhibits little to no signal, Alexa594 results in a low level of signal values. However, the current standard situation of dual-target hybridisations involving the combination of Cy5 and Cy3 appears to be subject to the same problem, as indicated by the single-target hybridisation with Cy5. The scans for the two blank channels Alexa594 and Cy3 have a low level of signal of the same relative proportion as the blank channels in the other single-target and dual-target hybridisations. This would seem to show that it is not just the relative closeness of Cy3 and Alexa594 in the light emission spectrum which results in signal bleeding to the other channel. The blank Cy5 channel in a Cy3-labelled single-target hybridisation remains unaffected by signal bleeding, whereas in the reverse situation the blank Cy3 channels is affected and shows some signal. In all of the above cases of signal bleed into other channels, this occurs at the intensity level around the detection threshold.
Evaluation of combined self hybridisation results
In order to provide quantitative indicators in addition to the graphical evaluation, tables 2 and 3 present comparative estimates of centrality and spread for log-ratios obtained from triple-self and self-to-self arrays after normalisation. There is good agreement in those estimates between the triple-self and self-self arrays for each of the three combinations of dye-label log-ratios. The theoretical centre of the log-ratio distributions is 0, and this value is approximately met by the majority of gene probes on the array, with only small differences between the different dye-label combinations. The combination of Cy5/Cy3 is marginally worse in its approximation of the theoretical ideal, and this is likely to be the result of the LoWeSS normalisation having to make greater adjustments to low expressed genes.
In light of the triple-, dual- and single-target hybridisation experiments carried out, it is clear that the addition of Alexa 594 does not introduce negative effects that are not already present or smaller than in the commonly used combination of Cy5 and Cy3. The triple-self hybridisations have shown that, for low levels of signal, there is less inherent difference between Cy3 and Alexa 594 than there is between Cy5 and Cy3. The problem of differential dye-label incorporation in traditional dual-target Cy5/Cy3 hybridisations seems largely due to Cy5, at least where low-level signal values are concerned. Co-hybridisation of Cy3/Alexa594 does not present this problem and in theory does not require a non-linear approach to normalisation (although there is no harm in using it). A non-linear normalisation like LoWeSS will make more of a numerical adjustment at this level of expression for the Cy5/Cy3 combination. However, following a successful normalisation, all three dye-label combinations have comparable log-ratio data, with only minor differences between them (tables 2 and 3). In cases where low levels of signal are relevant to the question under study, these different levels of noise/error in the low expression regions must be accounted for in the usual way by biological replication of the experiment.
With the dual- and single-target hybridisations, we investigated the issue of inherent signal bleeding between channels. The outcome of these has shown that in any hybridisations with Cy3 or Alexa 594, Cy5 will not suffer from this problem. On the other hand, both Cy3 and Alexa 594 will present this problem in any hybridisation involving Cy5. Although to our knowledge this has not been investigated before, it may therefore be present in most 'standard' experiments with Cy5/Cy3 dual-target hybridisations. Our data do not show that this is either a serious or a non-systematic problem. It usually occurs below or at the safe detection level of an array (as identified by negative control probes, data not shown), and contributes only a small amount of signal to one channel which is corrected together with other systematic dye-label and hybridisation differences during the normalisation procedure.
Experimental design issues
The ability to directly compare two target samples to a third condition (be it treatment or reference) on one array is of potentially great use for experiments that include multiple factors. However, such an approach also requires good planning of logistics and analysis. It is important to consider which dye is used to label a particular biological target, the logistics of using dye-labelling kits, and the allocation of dye-labelled samples to particular arrays [9, 10]. Simple reference designs can be extended to include a third-dye label in a straightforward manner. However, loop-designs will require a larger extent of planning to identify all necessary target sample combinations, with an inherent property of being inflexible in terms of adding more conditions/arrays or removing individual arrays due to hybridisation failure.
Dye-swap arrays also require consideration, since it is possible to only perform a dye-swap on two of the samples, or on all three. For our study of mouse spermatogenesis , Cy3 and Cy5 dye-swaps were only performed on the target samples of interest (wild type and Dazl-null mouse, from different developmental time-points), while the reference sample was always labelled with Alexa 594. This partial swap design was chosen to reduce the number of slides, cutting costs and time. To increase the reliability of the data, an extra level of replication was added by repeating this process with a second independent pool of mice. Although it could be argued that residual colour bias is introduced because the reference sample was not dye-swapped, in our experimental design this was not critical. The main focus of the experiment is on the relative changes in sample expression across the six developmental time-points and not in comparison to the reference.
Data processing and analysis issues
With respect to data normalisation and analysis, current software packages or analysis modules are geared towards the analysis of single- or dual-dye experiments, providing little facility to deal effectively with three samples per array. Although either working around these problems or customising analyses could be time-consuming, in the practical application of the triple-target method we found that data processing works well if the triple-target results are split into two files; file one contains the signal and background measurements of the wild type and the reference sample, and file two contains the signal and background measurements of the Dazl knock-out and the same reference sample.
For the purposes of this paper, we have used existing methods for normalisation and visualisation. If triple-target approaches are to be used on a regular basis, there is scope for developing statistical models that include all three dye-labels rather than multiple pair-wise combinations. This also applies to visualisation techniques. Naturally, assumptions applying to dual-hybridisation experiments still apply to our approach. The majority of genes in all samples need to be biologically unaffected by an experimental condition in order to allow global normalisation methods to be applied. Where this assumption is not met, control probes on the array are a necessity.
In summary, there has been no evidence that the inclusion of Alexa594 as a third dye-label causes additional noise or unexpected results in the data. We used a theoretically well-controlled system of replicated triple-self hybridisations to evaluate any effect this addition may have on the expression of gene probes on an array. In conjunction with Cy5 and Cy3, this dye has shown similar levels of inherent quality of labelling and subsequent data acquisition. Standard normalisation methods work as well as they do for single- or dual-dye experiments, and the resulting data can be expected to allow identification of expression differences in a biological experiment, given sufficient levels of biological replication (as is necessary for most microarray experiments). We consider this novel triple-target hybridisation strategy to be useful for the analysis of complex multifactorial experiments. As such, it provides an additional option to the current choice of array experimental designs. On a solely technical basis there is little reason not to include a third dye-label (although we have to limit this conclusion to Alexa594) for two-factorial experiments, the only prerequisite being a working laboratory protocol for using three dyes and good planning of logistics. Triple-target hybridisations can be performed within the same technological framework as current conventional approaches and, since they perform more than one absolute or relative gene expression assay per array, constitute a possible solution to practical constraints of finance, logistics or availability of biological sample material in the design of an experiment.
The use of triple-target microarray experiments is a valid addition to the experiment design toolbox. Although the method adds complexity to the experiment planning stage and the later data handling, this is offset by the benefits for studies where there are multiple experimental factors to consider, for example a combined time-series and treatment study. We limit this conclusion to the dye-labels and combination of biological system (adult mouse testes) and platform (custom spotted mouse array) used for this proof of concept, although in theory the same approach is usable in other experiments. We have developed in-house standards for the specifics of using three dye-labels for microarrays, but this may have to be adapted by other researchers working on different systems. Given further and more widespread use of the triple-target approach, it may prove a valuable tool that can be standardised for multiple biological systems and dye-labels.
An in-house created, subtracted and normalised adult mouse testis cDNA library consisting of 5,225 clones with an average insert size of 500 base pairs, plus 118 negative control (buffer spots) and 32 positive control spots, was deposited in duplicate (resulting in 10,750 individual features) onto glass slides. All were produced to the same standards and coated with poly-L-lysine according to a protocol available online at http://cmgm.stanford.edu/pbrown/protocols/1_slides.html. A detailed description of the probe cDNA library generation and characterisation, along with the microarray construction, is provided elsewhere . In total, 18 arrays were used in this study. These are comprised of 5 arrays (a sixth one failed to hybridise) for triple-self hybridisations, 6 arrays for dual-self hybridisations and 7 arrays for single-target hybridisations. Target samples for all hybridisations were drawn from one pool of adult mouse testes RNA.
Tissue collection, labelling and hybridisation
Male C57BL/6 mice were housed under standard conditions and fed ad libitum. Testes were removed, immediately frozen in liquid nitrogen and stored at -70°C until used for RNA extraction. Total RNA was isolated from individual adult mouse whole testes using Tri Reagent (Sigma, St. Louis, MO, USA), according to the manufacturer's instructions. RNA quality was confirmed by spectrophotometry, using an Ultrospec 3000 pro UV spectrophotometer (Amersham Biosciences, Freiburg, Germany) and denaturing gel electrophoresis. Array hybridisations were performed using Alexa Fluor 594 carboxylic acid succinimidyl ester (Molecular Probes, Leiden, the Netherlands), and the Cy3- and Cy5-Monofunctional Reactive dyes (Amersham Pharmacia Biotech, Buckinghamshire, UK). The three dyes were selected for their separate spectral spacing to avoid cross-talk problems during image acquisition (Cy3 excitation 543 nm, emission 570 nm; Cy5 excitation 633 nm, emission 670 nm; Alexa 594 excitation 594 nm, emission 614 nm) and were captured by separate lasers using a ScanArray 4000 confocal laser scanner (Packard BioScience). 15 μg of mRNA were aminoallyl labelled and resuspended in 27% deionised Formamide; 2.7 x SSC; 0.68%SDS, containing 8 μg of poly dA(40–60) (Amersham Pharmacia Biotech, Buckinghamshire, UK), 10 μg of yeast t-RNA (Sigma, Saint Louis, Missouri, USA) and 4 μg of Cot-1 mouse DNA (Invitrogen, Carlsbad, CA, USA). Hybridisation was carried out at 50°C for ~16 h in a humid CMT-Hybridisation chamber (Corning, Acton, MA, USA). Slides were washed for 15 min at 55°C with 2x SSC, 0.2% SDS, followed by 10 min at room temperature with 2x SSC and 10 min at room temperature with 0.2x SSC.
Image files on all arrays were collected with a ScanArray 4000 scanner (Packard BioScience, Billerica, MA, USA). Multiple scans constituting a series of parameter settings were performed for each array and dye-label channel in order to allow for subsequent selection of the dataset best representing the array (i.e. a large dynamic range of data values without saturation of relevant spots).
QuantArray microarray analysis software (version 3.0; Packard Bioscience) was used for quantification of scan images. Existing in-house standards and long-term experience with this software enabled us to obtain a good numerical representation of the image data. Parameter values were kept constant for all arrays, and only manual fine tuning for grid alignment added. Specifically, the chosen quantitation method was "Fixed Circle", since in our experience, the "Adaptive" method performs less well for the spot morphology on this array type. Background under this method was estimated using the 5th to 55th percentile pixel intensities, signal was estimated using the 45th to 95th percentile; in both cases output quantification was "Mean Intensity". No further filters or corrections were applied within QuantArray. This generates a numerical dataset containing intensity values Ii and background values Bi for each gene per array and channel. Data transformation, LoWeSS normalisation, MAD (Median Absolute Deviation) scaling, visualisation and computation of CVs, log-ratios and other statistics following on from here were performed using custom R http://www.r-project.org scripts.
The numerical raw data obtained were evaluated for background noise effects by means of 'signal maps' based on QuantArray signal and background values displayed by location on the array (data not shown). No background spatial effects were evident after application of the chosen QuantArray image processing algorithm. As a consequence, no additional data manipulation in form of a signal intensity correction was carried out.
Any values Ii < 1 or Ii < Bi (see image conversion) were removed from the dataset in order to facilitate analysis for the triple-self hybridisations. Note that for experiments on real biological systems it is recommended to follow more specific filtering procedures which determine suitable detection-thresholds or spot quality scores [12, 13].
Microarray data are subject to data variation from other sources than the biological difference of interest between test samples. Hybridisation conditions, dye-label properties, RNA extraction process etc. are such sources of variation, and normalisation of data adjusts for these and is a required step. For this validation experiment, current methods for location and scale normalisations of log-ratio values were used [14–16]. Location normalisation methods like LoWeSS are used to (non-linearly) normalise log ratios within an array, additional methods for normalisation of scale are used to compare log-ratios across multiple arrays.
Log-ratio location normalisation
Aij and Bij denote the j th spot value on the i th array for two dye-label channels. The LoWeSS function estimating the dependence of log-ratio y on log-intensity x for a given array is denoted by y(ij) .
yij = log2 (Aij / Bij)
xij = log2 (Aij * Bij)
NLRij = yij - y(xi)
For the triple-target self-hybridisation arrays this method was used for three dye-label combinations per array: Cy5/Cy3, C5/Alexa594 and Cy3/Alexa594.
Log-ratio scale normalisation
Median Average Deviation (MAD)
NLRij denotes the already location normalised log-ratios for the j th spot on the i th array. SLRij denotes the scale normalised log-ratios.
MADi = medianj (| NLRij - medianj (NLRij) |)
Three separate analyses were performed, one for the triple-target self-hybridisations, one for the dual-target self-hybridisations and one for single-target hybridisations. They were performed on dye-label channels, i.e. data for each differently labelled sample on an array, and on ratio data, i.e. the relative values between two such dye-label channels. Analyses were carried out on log2-transformed intensities and ratios. In addition to graphical output for evaluation of data distributions and global effects of variation, pooled and by-gene medians and median average distances (MAD) were computed for all log-ratios of interest across the replicate arrays, i.e. Cy5 vs. Alexa594, Cy3 vs. Alexa594 and Cy5 vs. Cy3.
A complete MIAME-compliant catalogue of this data, including a complete listing of annotated gene content and clone sequences for this microarray, together with all raw and normalized expression measurement files, will be made available at the MRC Human Genetics Unit web site http://www.hgu.mrc.ac.uk/Research/Cooke/germline.html. Experimental data will also be made available on the EBI ArrayExpress database http://www.ebi.ac.uk/arrayexpress.
Yang YH, Speed T: Design issues for cDNA microarray experiments. Nat Rev Genet. 2002, 3: 579-588.
Maratou K, Forster T, Costa Y, Taggart M, Speed R, Ireland J, Teague P, Roy D, Cooke HJ: Expression profiling of the developing testis in wild type and Dazl knockout mice. Mol Reprod Dev. 2004, 67: 26-54. 10.1002/mrd.20010.
Hessner MJ, Wang X, Khan S, Meyer L, Schlicht M, Tackes J, Datta MW, Jacob HJ, Ghosh S: Use of a three-color cDNA microarray platform to measure and control support-bound probe for improved data quality and reproducibility. Nucleic Acids Res. 2003, 31: e60-10.1093/nar/gng059.
Hessner MJ, Wang X, Hulse K, Meyer L, Wu Y, Nye S, Guo SW, Ghosh S: Three color cDNA microarrays: quantitative assessment through the use of fluorescein-labeled probes. Nucleic Acids Res. 2003, 31: e14-10.1093/nar/gng014.
Richter A, Schwager C, Hentze S, Ansorge W, Hentze MW, Muckenthaler M: Comparison of fluorescent tag DNA labeling methods used for expression analysis by DNA microarrays. Biotechniques. 2002, 33: 620-630.
Wang X, Hessner MJ, Wu Y, Pati N, Ghosh S: Quantitative quality control in microarray experiments and the application in data filtering, normalization and false positive rate prediction. Bioinformatics. 2003, 19: 1341-1347. 10.1093/bioinformatics/btg154.
Yang IV, Chen E, Hassemann JP, Liang W, Frank BC, Wang S, Sharov V, Saeed AI, White J, Li J, Lee NH, Yeatman TJ, Quackenbush J: Within the fold: assessing differential expression measures and reproducibility in microarray assays. Genome Biol. 2002, 3: 0062.1-0062.12.
We thank Mary Taggart and Robert M. Speed who assisted us in sample collection. We are grateful to Klemens Vierlinger, Elisabet Gudmundsdottir and Alan Ross of the Scottish Centre for Genomic Technology and Informatics for their help on printing the microarrays. This research was funded by the UK Medical Research Council.
Authors and Affiliations
Scottish Centre for Genomic Technology and Informatics, University of Edinburgh, The Chancellor's Building, College of Medicine, 49 Little France Crescent, Edinburgh, EH16 4SB, UK
Thorsten Forster & Douglas Roy
MRC Human Genetics Unit, The Department of Chromosome Biology, Western General Hospital, Crewe Road, Edinburgh, EH4 2XU, UK
TF performed data analysis and drafted the manuscript. YC carried out most of the laboratory work required for producing arrays and target samples. DR and HC provided the technology platform (array production and laboratory procedures) and advice relating to it, KM conceived of and planned the experiment implemented in the biological paper, produced the extensive clone library used for the arrays, performed all hybridisations and arrays scans and drafted parts of this manuscript.
Additional File 1: Tab-delimited ASCII data file. Column 1 refers to the sequential spot number in the original Quantarray output file. Columns 2–5 determine the spot position on the array by meta-row, meta-column, row and column. Column 6 is the name of the gene probe (this is a text field and needs to be specified as such when importing into other software). Columns 7–8 indicate the precise center of the spot on the array. All subsequent columns contain the raw data, s20 etc is the number of the slide, followed by the dye used for this column. In the manuscript, these have been numbered sequentially. An additional 'BG' indicates background measurements. Columns are arranged by slides, i.e. all three dye-label channels and corresponding background measurements are in adjacent columns. (TXT 5 MB)