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dc.creatorOmar Salem Nasser, Baans
dc.date2018
dc.date.accessioned2022-12-07T00:59:29Z
dc.date.available2022-12-07T00:59:29Z
dc.identifier.urihttp://dspace.unimap.edu.my:80/xmlui/handle/123456789/77417
dc.descriptionMaster of Science in Electronic Engineeringen_US
dc.description.abstractMicroarray has several thousands of spots that represent various parts of human genes on a slide. Each of the spot consists of two samples (normal as a reference and cancer as a target). The samples are labeled into green (reference) and red (target) dyes. If the spot is indicating green dye, it shows a high expression of the normal sample whereas red dye shows a high expression of the target spotted on that gene. In order to indicate the percentage of red and green intensity for every spot, microarray undergoes image processing where there are huge amount of data that increase the probability of error and consume much time. Applying the image processing clears unwanted residues on the microarray image and solves the spot finding problem with high accuracy and short time consumption. The image processing involves gridding, segmentation, intensity extraction and normalization. Gridding addresses the spots on the microarray image. Then segmentation can perform separation between the foreground and background pixels. Thirdly, the averages of the foreground and background intensity for each spot are computed. Fourthly, unwanted balance of the colors is balanced to cut back the noises. The aim of this work is to improve the intensity extraction and normalization step for DNA microarray image processing algorithm using MATLAB. Three methods for allocating and calculating the background intensity values were discussed and compared. These methods were GenePix, ScanAlyze, and QuantArry. Besides that, five alternatives for intensity extraction were applied to a microarray slide image in order to find the most accurate intensity value for each spot in the two-color microarray. These alternatives were Standard, Kooperberg, Edward, Morph and No-background. Based on the results, Edward method shows the most accurate results to extract foreground and background intensity and to calculate the ultimate intensity for each spot by 39.7 dB in term of PSNR. An improved method was proposed for intensity extraction by increasing background locations, where this method showed very accurate results by 41.36 dB in term of PSNR and 2.2 in term of RMSE. Besides that, using the proposed method the MAE is around 9 while it is very high for the other intensity extraction existing algorithms. On the other hand, five normalization algorithms, Global, Lowess, Housekeeping, Quantile, and Print-tip, have been tested and compared to find the most suitable approach for normalization process. Print Tip normalization was chosen for normalization because of its high accuracy which was around 32.89 dB in term of PSNR and its final MA graph shape was well normalized. In relation to this matter, a proposed method for normalization was applied. It increases the accuracy by 33.15 dB in term of PSNR, 32.63 in term of MSE and the occurrence of errors become very small by around 12 in term of MAE. Finally, algorithm profiling has been done, it proved that the proposed algorithm consumes less time than the Bemis project by around 347.7 milliseconds.en_US
dc.language.isoenen_US
dc.publisherUniversiti Malaysia Perlis (UniMAP)en_US
dc.rightsUniversiti Malaysia Perlis (UniMAP)en_US
dc.subjectDNA microarraysen_US
dc.subjectImage processingen_US
dc.subjectImage processing -- Digital techniquesen_US
dc.titleIntensity extraction and normalization algorithm development for DNA microarray image processingen_US
dc.typeThesisen_US
dc.contributor.advisorAsral, Bahari Jambek, Assoc. Prof. Dr.
dc.publisher.departmentSchool of Microelectronic Engineeringen_US


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