TY - JOUR T1 - Quantitative assessment of eye phenotypes for functional genetic studies using <em>Drosophila melanogaster</em> JF - bioRxiv DO - 10.1101/036368 SP - 036368 AU - Janani Iyer AU - Qingyu Wang AU - Thanh Le AU - Lucilla Pizzo AU - Sebastian Grönke AU - Surendra S. Ambegaokar AU - Yuzuru Imai AU - Ashutosh Srivastava AU - Beatriz Llamusí Troisí AU - Graeme Mardon AU - Ruben Artero AU - George R. Jackson AU - Adrian M. Isaacs AU - Linda Partridge AU - Bingwei Lu AU - Justin P. Kumar AU - Santhosh Girirajan Y1 - 2016/01/01 UR - http://biorxiv.org/content/early/2016/01/15/036368.abstract N2 - About two-thirds of the vital genes in the Drosophila genome are involved in eye development, making the fly eye an excellent genetic system to study cellular function and development, neurodevelopment/degeneration, and complex diseases such as cancer and diabetes. We developed a novel computational method, implemented as Flynotyper software (http://flynotyper.sourceforge.net), to quantitatively assess the morphological defects in the Drosophila eye resulting from genetic alterations affecting basic cellular and developmental processes. Flynotyper utilizes a series of image processing operations to automatically detect the fly eye and the individual ommatidium, and calculates a phenotypic score as a measure of the disorderliness of ommatidial arrangement in the fly eye. As a proof of principle, we tested our method by analyzing the defects due to eye-specific knockdown of Drosophila orthologs of 12 neurodevelopmental genes to accurately document differential sensitivities of these genes to dosage alteration. We also evaluated eye images from six independent studies assessing the effect of overexpression of repeats, candidates from peptide library screens, and modifiers of neurotoxicity and developmental processes on eye morphology, and show strong concordance with the original assessment. We further demonstrate the utility of this method by analyzing 16 modifiers of sine oculis obtained from two genome-wide deficiency screens of Drosophila and accurately quantifying the effect of its enhancers and suppressors during eye development. Our method will complement existing assays for eye phenotypes and increase the accuracy of studies that use fly eyes for functional evaluation of genes and genetic interactions. ER -