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Translational utility is the ability of certain biomedical imaging features to capture useful subject-level characteristics in clinical settings, yielding sensible descriptions and/or predictions for individualized treatment trajectory. An important step in achieving translational utility is to demonstrate the association between imaging features and individual characteristics, such as sex, age, and other relevant assessments, on a large out-of-sample unaffected population (no diagnosed illnesses). This initial step then provides a strong normative basis for comparison with patient populations in clinical settings. Detailed information. Website.

 

 

The aim is to provide a formal framework for evaluating the current state of the art, gather researchers in the field and provide high quality data with protocols for validating endoscopic vision algorithms.

The aim of this challenge is to learn effective machine learning models that can estimate a set of clinical significant LV indices (regional wall thicknesses, cavity dimensions, area of cavity and myocardium, cardiac phase) directly from MR images. No intermediate segmentation is required in the whole procedure.

This challenge aims at creating an open and fair competition for various research groups to test and validate their methods, particularly for the multi-sequence ventricle and myocardium segmentation.

Skin cancer is the most common cancer globally, with melanoma being the most deadly form. Dermoscopy is a skin imaging modality that has demonstrated improvement for diagnosis of skin cancer compared to unaided visual inspection. However, clinicians should receive adequate training for those improvements to be realized.

BraTS has always been focusing on the evaluation of state-of-the-art methods for the segmentation of brain tumors in multimodal magnetic resonance imaging (MRI) scans. BraTS 2019 utilizes multi-institutional pre-operative MRI scans and focuses on the segmentation of intrinsically heterogeneous (in appearance, shape, and histology) brain tumors, namely gliomas.

The goal of the challenge is to evaluate new and existing algorithms for automated detection of liver cancer in whole-slide images (WSIs). There are two tasks and therefore two leaderboards for evaluating the performance of the algorithms. Participants can choose to join both or either tasks according to their interests.

CHAOS has two separate but related aims:

  1. Segmentation of liver from computed tomography (CT) data sets, which are acquired at portal phase after contrast agent injection for pre-evaluation of living donated liver transplantation donors (15 training + 15 test sets).
  2. Segmentation of four abdominal organs (i.e. liver, spleen, right and left kidneys) from magnetic resonance imaging (MRI) data sets acquired with two different sequences (T1-DUAL and T2-SPIR) (15 training + 15 test sets).

Digital pathology has been gradually introduced in clinical practice. Although the digital pathology scanner could give very high resolution whole-slide images (WSI) (up to 160nm per pixel), the manual analysis of WSI is still a time-consuming task for the pathologists. Automatic analysis algorithms offer a way to reduce the burden for pathologists. Our proposed challenge will focus on automatic detection and classification of lung cancer using Whole-slide Histopathology. This subject is highly clinical relevant because lung cancer is the top cause of cancer-related death in the world.

In digital pathology, it is often useful to align spatially close but differently stained tissue sections in order to obtain the combined information. The images are large, in general, their appearance and their local structure are different, and they are related through a nonlinear transformation. The proposed challenge focuses on comparing the accuracy and approximative speed of automatic non-linear registration methods for this task. Registration accuracy will be evaluated using manually annotated landmarks.

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