2010
DOI: 10.1016/j.cviu.2009.08.003
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Parasite detection and identification for automated thin blood film malaria diagnosis

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Cited by 176 publications
(111 citation statements)
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References 33 publications
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“…When it comes to pre-processing, illumination correction has been implemented by Diaz et al [31], Tek et al [15]. A Kruskal Wallis H test performed on a randomly selected set of three images revealed that there is significant difference in luminance distribution in the images, χ2(2)=21.706, p=0.000<0.01.…”
Section: Limitationsmentioning
confidence: 99%
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“…When it comes to pre-processing, illumination correction has been implemented by Diaz et al [31], Tek et al [15]. A Kruskal Wallis H test performed on a randomly selected set of three images revealed that there is significant difference in luminance distribution in the images, χ2(2)=21.706, p=0.000<0.01.…”
Section: Limitationsmentioning
confidence: 99%
“…Author Halim et al [43], performed parasite detection using a Variance based approach and separately a Colour Based Co-occurrence Matrix based matching technique. Authors Tek et al [15] used RGB histogram and probability density function to determine parasite region. Toha & Ngah [10], calculated a threshold value to identify parasite region followed by calculating the Euclidean distance to differentiate between each parasite cluster.…”
Section: Literature Reviewmentioning
confidence: 99%
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“…According to the World Health Organization, it causes more than 1 million deaths arising from approximately 300 to 500 million infections every year [6]. It is a serious global health problem and rapid, precise determination of parasitemia is necessary for malaria research and in clinical settings.…”
Section: Literature Reviewmentioning
confidence: 99%
“…Furthermore, manual counting from Giemsa-smears is known to vary depending on the personnel engaged and quality of smears involving a high chance of misinterpreting other microorganisms such as bacteria and fungi as Plasmodium parasites and difficulties associated with identifying different Plasmodium strains [31]. Previously, several laboratories explored image processing based automated cell counting for parasitemia estimation, but most of them suffered from high false positive values [32][33][34], inferior accuracy [35], inability to differentiate parasitic stages [36] primarily rings [37] and the requirement of fluorescent dyes [38,39].…”
Section: Introductionmentioning
confidence: 99%