In clinical cardiology, both anatomy and physiology are needed to diagnose cardiac pathologies. CT imaging and computer simulations provide valuable and complementary data for this purpose. However, it remains challenging to gain useful information from the large amount of high-dimensional diverse data. The current tools are not adequately integrated to visualize anatomic and physiologic data from a complete yet focused perspective. We introduce a new computer-aided diagnosis framework, which allows for comprehensive modeling and visualization of cardiac anatomy and physiology from CT imaging data and computer simulations, with a primary focus on ischemic heart disease. The following visual information is presented: (1) Anatomy from CT imaging: geometric modeling and visualization of cardiac anatomy, including four heart chambers, left and right ventricular outflow tracts, and coronary arteries; (2) Function from CT imaging: motion modeling, strain calculation, and visualization of four heart chambers; (3) Physiology from CT imaging: quantification and visualization of myocardial perfusion and contextual integration with coronary artery anatomy; (4) Physiology from computer simulation: computation and visualization of hemodynamics (e.g., coronary blood velocity, pressure, shear stress, and fluid forces on the vessel wall). Substantially, feedback from cardiologists have confirmed the practical utility of integrating these features for the purpose of computer-aided diagnosis of ischemic heart disease.

Image-based, high throughput genome-wide RNA interference (RNAi) experiments are increasingly carried out to facilitate the understanding of gene functions in intricate biological processes. Robust automated segmentation of the large volumes of output images generated from image-based screening is much needed for data analyses. In this paper, we propose a new automated segmentation technique to fill the void. The technique consists of two steps: nuclei and cytoplasm segmentation. In the former step, nuclei are extracted, labeled and used as starting points for the latter. A new force obtained from rough segmentation is introduced into the classical level set curve evolution to improve the performance for odd shapes, such as spiky or ruffly cells. A scheme of preventing curves from crossing is proposed to treat the difficulty of segmenting touching cells. We apply it to three types of drosophila cells in RNAi fluorescence images. In all cases, greater than 92% accuracy is obtained.