Medical image computing

Last updated

Medical image computing (MIC) is an interdisciplinary field at the intersection of computer science, information engineering, electrical engineering, physics, mathematics and medicine. This field develops computational and mathematical methods for solving problems pertaining to medical images and their use for biomedical research and clinical care.

Contents

The main goal of MIC is to extract clinically relevant information or knowledge from medical images. While closely related to the field of medical imaging, MIC focuses on the computational analysis of the images, not their acquisition. The methods can be grouped into several broad categories: image segmentation, image registration, image-based physiological modeling, and others. [1]

Data forms

Medical image computing typically operates on uniformly sampled data with regular x-y-z spatial spacing (images in 2D and volumes in 3D, generically referred to as images). At each sample point, data is commonly represented in integral form such as signed and unsigned short (16-bit), although forms from unsigned char (8-bit) to 32-bit float are not uncommon. The particular meaning of the data at the sample point depends on modality: for example a CT acquisition collects radiodensity values, while an MRI acquisition may collect T1 or T2-weighted images. Longitudinal, time-varying acquisitions may or may not acquire images with regular time steps. Fan-like images due to modalities such as curved-array ultrasound are also common and require different representational and algorithmic techniques to process. Other data forms include sheared images due to gantry tilt during acquisition; and unstructured meshes, such as hexahedral and tetrahedral forms, which are used in advanced biomechanical analysis (e.g., tissue deformation, vascular transport, bone implants).

Segmentation

A T1 weighted MR image of the brain of a patient with a meningioma after injection of an MRI contrast agent (top left), and the same image with the result of an interactive segmentation overlaid in green (3D model of the segmentation on the top right, axial and coronal views at the bottom). MeningiomaMRISegmentation.png
A T1 weighted MR image of the brain of a patient with a meningioma after injection of an MRI contrast agent (top left), and the same image with the result of an interactive segmentation overlaid in green (3D model of the segmentation on the top right, axial and coronal views at the bottom).

Segmentation is the process of partitioning an image into different meaningful segments. In medical imaging, these segments often correspond to different tissue classes, organs, pathologies, or other biologically relevant structures. [2] Medical image segmentation is made difficult by low contrast, noise, and other imaging ambiguities. Although there are many computer vision techniques for image segmentation, some have been adapted specifically for medical image computing. Below is a sampling of techniques within this field; the implementation relies on the expertise that clinicians can provide.

However, there are some other classification of image segmentation methods which are similar to above categories. Moreover, we can classify another group as "Hybrid" which is based on combination of methods. [20]

Registration

CT image (left), PET image (center) and overlay of both (right) after correct registration. CT-PET.jpg
CT image (left), PET image (center) and overlay of both (right) after correct registration.

Image registration is a process that searches for the correct alignment of images. [21] [22] [23] [24] In the simplest case, two images are aligned. Typically, one image is treated as the target image and the other is treated as a source image; the source image is transformed to match the target image. The optimization procedure updates the transformation of the source image based on a similarity value that evaluates the current quality of the alignment. This iterative procedure is repeated until a (local) optimum is found. An example is the registration of CT and PET images to combine structural and metabolic information (see figure).

Image registration is used in a variety of medical applications:

There are several important considerations when performing image registration:

Visualization

Volume rendering (left), axial cross-section (right top), and sagittal cross-section (right bottom) of a CT image of a subject with multiple nodular lesions (white line) in the lung. Visualization of Medical Imaging.png
Volume rendering (left), axial cross-section (right top), and sagittal cross-section (right bottom) of a CT image of a subject with multiple nodular lesions (white line) in the lung.

Visualization plays several key roles in Medical Image Computing. Methods from scientific visualization are used to understand and communicate about medical images, which are inherently spatial-temporal. Data visualization and data analysis are used on unstructured data forms, for example when evaluating statistical measures derived during algorithmic processing. Direct interaction with data, a key feature of the visualization process, is used to perform visual queries about data, annotate images, guide segmentation and registration processes, and control the visual representation of data (by controlling lighting rendering properties and viewing parameters). Visualization is used both for initial exploration and for conveying intermediate and final results of analyses.

The figure "Visualization of Medical Imaging" illustrates several types of visualization: 1. the display of cross-sections as gray scale images; 2. reformatted views of gray scale images (the sagittal view in this example has a different orientation than the original direction of the image acquisition; and 3. A 3D volume rendering of the same data. The nodular lesion is clearly visible in the different presentations and has been annotated with a white line.

Atlases

Medical images can vary significantly across individuals due to people having organs of different shapes and sizes. Therefore, representing medical images to account for this variability is crucial. A popular approach to represent medical images is through the use of one or more atlases. Here, an atlas refers to a specific model for a population of images with parameters that are learned from a training dataset. [33] [34]

The simplest example of an atlas is a mean intensity image, commonly referred to as a template. However, an atlas can also include richer information, such as local image statistics and the probability that a particular spatial location has a certain label. New medical images, which are not used during training, can be mapped to an atlas, which has been tailored to the specific application, such as segmentation and group analysis. Mapping an image to an atlas usually involves registering the image and the atlas. This deformation can be used to address variability in medical images.

Single template

The simplest approach is to model medical images as deformed versions of a single template image. For example, anatomical MRI brain scans are often mapped to the MNI template [35] as to represent all the brain scans in common coordinates. The main drawback of a single-template approach is that if there are significant differences between the template and a given test image, then there may not be a good way to map one onto the other. For example, an anatomical MRI brain scan of a patient with severe brain abnormalities (i.e., a tumor or surgical procedure), may not easily map to the MNI template.

Multiple templates

Rather than relying on a single template, multiple templates can be used. The idea is to represent an image as a deformed version of one of the templates. For example, there could be one template for a healthy population and one template for a diseased population. However, in many applications, it is not clear how many templates are needed. A simple albeit computationally expensive way to deal with this is to have every image in a training dataset be a template image and thus every new image encountered is compared against every image in the training dataset. A more recent approach automatically finds the number of templates needed. [36]

Statistical analysis

Statistical methods combine the medical imaging field with modern Computer Vision, Machine Learning and Pattern Recognition. Over the last decade, several large datasets have been made publicly available (see for example ADNI, 1000 functional Connectomes Project), in part due to collaboration between various institutes and research centers. This increase in data size calls for new algorithms that can mine and detect subtle changes in the images to address clinical questions. Such clinical questions are very diverse and include group analysis, imaging biomarkers, disease phenotyping and longitudinal studies.

Group analysis

In the Group Analysis, the objective is to detect and quantize abnormalities induced by a disease by comparing the images of two or more cohorts. Usually one of these cohorts consist of normal (control) subjects, and the other one consists of abnormal patients. Variation caused by the disease can manifest itself as abnormal deformation of anatomy (see Voxel-based morphometry). For example, shrinkage of sub-cortical tissues such as the Hippocampus in brain may be linked to Alzheimer's disease. Additionally, changes in biochemical (functional) activity can be observed using imaging modalities such as Positron Emission Tomography.

The comparison between groups is usually conducted on the voxel level. Hence, the most popular pre-processing pipeline, particularly in neuroimaging, transforms all of the images in a dataset to a common coordinate frame via (Medical Image Registration) in order to maintain correspondence between voxels. Given this voxel-wise correspondence, the most common Frequentist method is to extract a statistic for each voxel (for example, the mean voxel intensity for each group) and perform statistical hypothesis testing to evaluate whether a null hypothesis is or is not supported. The null hypothesis typically assumes that the two cohorts are drawn from the same distribution, and hence, should have the same statistical properties (for example, the mean values of two groups are equal for a particular voxel). Since medical images contain large numbers of voxels, the issue of multiple comparison needs to be addressed,. [37] [38] There are also Bayesian approaches to tackle group analysis problem. [39]

Classification

Although group analysis can quantify the general effects of a pathology on an anatomy and function, it does not provide subject level measures, and hence cannot be used as biomarkers for diagnosis (see Imaging Biomarkers). Clinicians, on the other hand, are often interested in early diagnosis of the pathology (i.e. classification, [40] [41] ) and in learning the progression of a disease (i.e. regression [42] ). From methodological point of view, current techniques varies from applying standard machine learning algorithms to medical imaging datasets (e.g. Support Vector Machine [43] ), to developing new approaches adapted for the needs of the field. [44] The main difficulties are as follows:

Clustering

Image-based pattern classification methods typically assume that the neurological effects of a disease are distinct and well defined. This may not always be the case. For a number of medical conditions, the patient populations are highly heterogeneous, and further categorization into sub-conditions has not been established. Additionally, some diseases (e.g., autism spectrum disorder (ASD), schizophrenia, mild cognitive impairment (MCI)) can be characterized by a continuous or nearly-continuous spectra from mild cognitive impairment to very pronounced pathological changes. To facilitate image-based analysis of heterogeneous disorders, methodological alternatives to pattern classification have been developed. These techniques borrow ideas from high-dimensional clustering [49] and high-dimensional pattern-regression to cluster a given population into homogeneous sub-populations. The goal is to provide a better quantitative understanding of the disease within each sub-population.

Shape analysis

Shape Analysis is the field of Medical Image Computing that studies geometrical properties of structures obtained from different imaging modalities. Shape analysis recently become of increasing interest to the medical community due to its potential to precisely locate morphological changes between different populations of structures, i.e. healthy vs pathological, female vs male, young vs elderly. Shape Analysis includes two main steps: shape correspondence and statistical analysis.

Longitudinal studies

In longitudinal studies the same person is imaged repeatedly. This information can be incorporated both into the image analysis, as well as into the statistical modeling.

Image-based physiological modelling

Traditionally, medical image computing has seen to address the quantification and fusion of structural or functional information available at the point and time of image acquisition. In this regard, it can be seen as quantitative sensing of the underlying anatomical, physical or physiological processes. However, over the last few years, there has been a growing interest in the predictive assessment of disease or therapy course. Image-based modelling, be it of biomechanical or physiological nature, can therefore extend the possibilities of image computing from a descriptive to a predictive angle.

According to the STEP research roadmap, [50] [51] the Virtual Physiological Human (VPH) is a methodological and technological framework that, once established, will enable the investigation of the human body as a single complex system. Underlying the VPH concept, the International Union for Physiological Sciences (IUPS) has been sponsoring the IUPS Physiome Project for more than a decade,. [52] [53] This is a worldwide public domain effort to provide a computational framework for understanding human physiology. It aims at developing integrative models at all levels of biological organization, from genes to the whole organisms via gene regulatory networks, protein pathways, integrative cell functions, and tissue and whole organ structure/function relations. Such an approach aims at transforming current practice in medicine and underpins a new era of computational medicine. [54]

In this context, medical imaging and image computing play an increasingly important role as they provide systems and methods to image, quantify and fuse both structural and functional information about the human being in vivo. These two broad research areas include the transformation of generic computational models to represent specific subjects, thus paving the way for personalized computational models. [55] Individualization of generic computational models through imaging can be realized in three complementary directions:

In addition, imaging also plays a pivotal role in the evaluation and validation of such models both in humans and in animal models, and in the translation of models to the clinical setting with both diagnostic and therapeutic applications. In this specific context, molecular, biological, and pre-clinical imaging render additional data and understanding of basic structure and function in molecules, cells, tissues and animal models that may be transferred to human physiology where appropriate.

The applications of image-based VPH/Physiome models in basic and clinical domains are vast. Broadly speaking, they promise to become new virtual imaging techniques. Effectively more, often non-observable, parameters will be imaged in silico based on the integration of observable but sometimes sparse and inconsistent multimodal images and physiological measurements. Computational models will serve to engender interpretation of the measurements in a way compliant with the underlying biophysical, biochemical or biological laws of the physiological or pathophysiological processes under investigation. Ultimately, such investigative tools and systems will help our understanding of disease processes, the natural history of disease evolution, and the influence on the course of a disease of pharmacological and/or interventional therapeutic procedures.

Cross-fertilization between imaging and modelling goes beyond interpretation of measurements in a way consistent with physiology. Image-based patient-specific modelling, combined with models of medical devices and pharmacological therapies, opens the way to predictive imaging whereby one will be able to understand, plan and optimize such interventions in silico.

Mathematical methods in medical imaging

A number of sophisticated mathematical methods have entered medical imaging, and have already been implemented in various software packages. These include approaches based on partial differential equations (PDEs) and curvature driven flows for enhancement, segmentation, and registration. Since they employ PDEs, the methods are amenable to parallelization and implementation on GPGPUs. A number of these techniques have been inspired from ideas in optimal control. Accordingly, very recently ideas from control have recently made their way into interactive methods, especially segmentation. Moreover, because of noise and the need for statistical estimation techniques for more dynamically changing imagery, the Kalman filter [56] and particle filter have come into use. A survey of these methods with an extensive list of references may be found in. [57]

Modality specific computing

Some imaging modalities provide very specialized information. The resulting images cannot be treated as regular scalar images and give rise to new sub-areas of Medical Image Computing. Examples include diffusion MRI, functional MRI and others.

Diffusion MRI

A mid-axial slice of the ICBM diffusion tensor image template. Each voxel's value is a tensor represented here by an ellipsoid. Color denotes principal orientation: red = left-right, blue=inferior-superior, green = posterior-anterior DiffusionMRI glyphs.png
A mid-axial slice of the ICBM diffusion tensor image template. Each voxel's value is a tensor represented here by an ellipsoid. Color denotes principal orientation: red = left-right, blue=inferior-superior, green = posterior-anterior

Diffusion MRI is a structural magnetic resonance imaging modality that allows measurement of the diffusion process of molecules. Diffusion is measured by applying a gradient pulse to a magnetic field along a particular direction. In a typical acquisition, a set of uniformly distributed gradient directions is used to create a set of diffusion weighted volumes. In addition, an unweighted volume is acquired under the same magnetic field without application of a gradient pulse. As each acquisition is associated with multiple volumes, diffusion MRI has created a variety of unique challenges in medical image computing.

In medicine, there are two major computational goals in diffusion MRI:

The diffusion tensor, [58] a 3 × 3 symmetric positive-definite matrix, offers a straightforward solution to both of these goals. It is proportional to the covariance matrix of a Normally distributed local diffusion profile and, thus, the dominant eigenvector of this matrix is the principal direction of local diffusion. Due to the simplicity of this model, a maximum likelihood estimate of the diffusion tensor can be found by simply solving a system of linear equations at each location independently. However, as the volume is assumed to contain contiguous tissue fibers, it may be preferable to estimate the volume of diffusion tensors in its entirety by imposing regularity conditions on the underlying field of tensors. [59] Scalar values can be extracted from the diffusion tensor, such as the fractional anisotropy, mean, axial and radial diffusivities, which indirectly measure tissue properties such as the dysmyelination of axonal fibers [60] or the presence of edema. [61] Standard scalar image computing methods, such as registration and segmentation, can be applied directly to volumes of such scalar values. However, to fully exploit the information in the diffusion tensor, these methods have been adapted to account for tensor valued volumes when performing registration [62] [63] and segmentation. [64] [65]

Given the principal direction of diffusion at each location in the volume, it is possible to estimate the global pathways of diffusion through a process known as tractography. [66] However, due to the relatively low resolution of diffusion MRI, many of these pathways may cross, kiss or fan at a single location. In this situation, the single principal direction of the diffusion tensor is not an appropriate model for the local diffusion distribution. The most common solution to this problem is to estimate multiple directions of local diffusion using more complex models. These include mixtures of diffusion tensors, [67] Q-ball imaging, [68] diffusion spectrum imaging [69] and fiber orientation distribution functions, [70] [71] which typically require HARDI acquisition with a large number of gradient directions. As with the diffusion tensor, volumes valued with these complex models require special treatment when applying image computing methods, such as registration [72] [73] [74] and segmentation. [75]

Functional MRI

Functional magnetic resonance imaging (fMRI) is a medical imaging modality that indirectly measures neural activity by observing the local hemodynamics, or blood oxygen level dependent signal (BOLD). fMRI data offers a range of insights, and can be roughly divided into two categories:

There is a rich set of methodology used to analyze functional neuroimaging data, and there is often no consensus regarding the best method. Instead, researchers approach each problem independently and select a suitable model/algorithm. In this context there is a relatively active exchange among neuroscience, computational biology, statistics, and machine learning communities. Prominent approaches include

When working with large cohorts of subjects, the normalization (registration) of individual subjects into a common reference frame is crucial. A body of work and tools exist to perform normalization based on anatomy (FSL, FreeSurfer, SPM). Alignment taking spatial variability across subjects into account is a more recent line of work. Examples are the alignment of the cortex based on fMRI signal correlation, [84] the alignment based on the global functional connectivity structure both in task-, or resting state data, [85] and the alignment based on stimulus specific activation profiles of individual voxels. [86]

Software

Software for medical image computing is a complex combination of systems providing IO, visualization and interaction, user interface, data management and computation. Typically system architectures are layered to serve algorithm developers, application developers, and users. The bottom layers are often libraries and/or toolkits which provide base computational capabilities; while the top layers are specialized applications which address specific medical problems, diseases, or body systems.

Additional notes

Medical Image Computing is also related to the field of Computer Vision. An international society, The MICCAI Society represents the field and organizes an annual conference and associated workshops. Proceedings for this conference are published by Springer in the Lecture Notes in Computer Science series. [87] In 2000, N. Ayache and J. Duncan reviewed the state of the field. [88]

See also

Related Research Articles

<span class="mw-page-title-main">Image registration</span> Mapping of data into a single system

Image registration is the process of transforming different sets of data into one coordinate system. Data may be multiple photographs, data from different sensors, times, depths, or viewpoints. It is used in computer vision, medical imaging, military automatic target recognition, and compiling and analyzing images and data from satellites. Registration is necessary in order to be able to compare or integrate the data obtained from these different measurements.

Functional integration is the study of how brain regions work together to process information and effect responses. Though functional integration frequently relies on anatomic knowledge of the connections between brain areas, the emphasis is on how large clusters of neurons – numbering in the thousands or millions – fire together under various stimuli. The large datasets required for such a whole-scale picture of brain function have motivated the development of several novel and general methods for the statistical analysis of interdependence, such as dynamic causal modelling and statistical linear parametric mapping. These datasets are typically gathered in human subjects by non-invasive methods such as EEG/MEG, fMRI, or PET. The results can be of clinical value by helping to identify the regions responsible for psychiatric disorders, as well as to assess how different activities or lifestyles affect the functioning of the brain.

<span class="mw-page-title-main">Neuroimaging</span> Set of techniques to measure and visualize aspects of the nervous system

Neuroimaging is the use of quantitative (computational) techniques to study the structure and function of the central nervous system, developed as an objective way of scientifically studying the healthy human brain in a non-invasive manner. Increasingly it is also being used for quantitative research studies of brain disease and psychiatric illness. Neuroimaging is highly multidisciplinary involving neuroscience, computer science, psychology and statistics, and is not a medical specialty. Neuroimaging is sometimes confused with neuroradiology.

In neuroimaging, spatial normalization is an image processing step, more specifically an image registration method. Human brains differ in size and shape, and one goal of spatial normalization is to deform human brain scans so one location in one subject's brain scan corresponds to the same location in another subject's brain scan.

<span class="mw-page-title-main">FreeSurfer</span> Brain imaging software package

FreeSurfer is brain imaging software originally developed by Bruce Fischl, Anders Dale, Martin Sereno, and Doug Greve. Development and maintenance of FreeSurfer is now the primary responsibility of the Laboratory for Computational Neuroimaging at the Athinoula A. Martinos Center for Biomedical Imaging. FreeSurfer contains a set of programs with a common focus of analyzing magnetic resonance imaging (MRI) scans of brain tissue. It is an important tool in functional brain mapping and contains tools to conduct both volume based and surface based analysis. FreeSurfer includes tools for the reconstruction of topologically correct and geometrically accurate models of both the gray/white and pial surfaces, for measuring cortical thickness, surface area and folding, and for computing inter-subject registration based on the pattern of cortical folds.

<span class="mw-page-title-main">Voxel-based morphometry</span> Computational neuroanatomy method

Voxel-based morphometry is a computational approach to neuroanatomy that measures differences in local concentrations of brain tissue, through a voxel-wise comparison of multiple brain images. In traditional morphometry, volume of the whole brain or its subparts is measured by drawing regions of interest (ROIs) on images from brain scanning and calculating the volume enclosed. However, this is time consuming and can only provide measures of rather large areas. Smaller differences in volume may be overlooked. The value of VBM is that it allows for comprehensive measurement of differences, not just in specific structures, but throughout the entire brain. VBM registers every brain to a template, which gets rid of most of the large differences in brain anatomy among people. Then the brain images are smoothed so that each voxel represents the average of itself and its neighbors. Finally, the image volume is compared across brains at every voxel.

<span class="mw-page-title-main">Computer-aided diagnosis</span> Type of diagnosis assisted by computers

Computer-aided detection (CADe), also called computer-aided diagnosis (CADx), are systems that assist doctors in the interpretation of medical images. Imaging techniques in X-ray, MRI, endoscopy, and ultrasound diagnostics yield a great deal of information that the radiologist or other medical professional has to analyze and evaluate comprehensively in a short time. CAD systems process digital images or videos for typical appearances and to highlight conspicuous sections, such as possible diseases, in order to offer input to support a decision taken by the professional.

<span class="mw-page-title-main">ITK-SNAP</span> Medical imaging software

ITK-SNAP is an interactive software application that allows users to navigate three-dimensional medical images, manually delineate anatomical regions of interest, and perform automatic image segmentation. The software was designed with the audience of clinical and basic science researchers in mind, and emphasis has been placed on having a user-friendly interface and maintaining a limited feature set to prevent feature creep. ITK-SNAP is most frequently used to work with magnetic resonance imaging (MRI), cone-beam computed tomography (CBCT) and computed tomography (CT) data sets.

<span class="mw-page-title-main">3D Slicer</span> Image analysis and scientific visualization software

3D Slicer (Slicer) is a free and open source software package for image analysis and scientific visualization. Slicer is used in a variety of medical applications, including autism, multiple sclerosis, systemic lupus erythematosus, prostate cancer, lung cancer, breast cancer, schizophrenia, orthopedic biomechanics, COPD, cardiovascular disease and neurosurgery.

Brain morphometry is a subfield of both morphometry and the brain sciences, concerned with the measurement of brain structures and changes thereof during development, aging, learning, disease and evolution. Since autopsy-like dissection is generally impossible on living brains, brain morphometry starts with noninvasive neuroimaging data, typically obtained from magnetic resonance imaging (MRI). These data are born digital, which allows researchers to analyze the brain images further by using advanced mathematical and statistical methods such as shape quantification or multivariate analysis. This allows researchers to quantify anatomical features of the brain in terms of shape, mass, volume, and to derive more specific information, such as the encephalization quotient, grey matter density and white matter connectivity, gyrification, cortical thickness, or the amount of cerebrospinal fluid. These variables can then be mapped within the brain volume or on the brain surface, providing a convenient way to assess their pattern and extent over time, across individuals or even between different biological species. The field is rapidly evolving along with neuroimaging techniques—which deliver the underlying data—but also develops in part independently from them, as part of the emerging field of neuroinformatics, which is concerned with developing and adapting algorithms to analyze those data.

Anders Martin Dale is a prominent neuroscientist and professor of radiology, neurosciences, psychiatry, and cognitive science at the University of California, San Diego (UCSD), and is one of the world's leading developers of sophisticated computational neuroimaging techniques. He is the founding Director of the Center for Multimodal Imaging Genetics (CMIG) at UCSD.

<span class="mw-page-title-main">Amira (software)</span> Software platform for 3D and 4D data visualization

Amira is a software platform for visualization, processing, and analysis of 3D and 4D data. It is being actively developed by Thermo Fisher Scientific in collaboration with the Zuse Institute Berlin (ZIB), and commercially distributed by Thermo Fisher Scientific — together with its sister software Avizo.

<span class="mw-page-title-main">CONN (functional connectivity toolbox)</span>

CONN is a Matlab-based cross-platform imaging software for the computation, display, and analysis of functional connectivity in fMRI in the resting state and during task.

Statistical shape analysis and statistical shape theory in computational anatomy (CA) is performed relative to templates, therefore it is a local theory of statistics on shape. Template estimation in computational anatomy from populations of observations is a fundamental operation ubiquitous to the discipline. Several methods for template estimation based on Bayesian probability and statistics in the random orbit model of CA have emerged for submanifolds and dense image volumes.

Large deformation diffeomorphic metric mapping (LDDMM) is a specific suite of algorithms used for diffeomorphic mapping and manipulating dense imagery based on diffeomorphic metric mapping within the academic discipline of computational anatomy, to be distinguished from its precursor based on diffeomorphic mapping. The distinction between the two is that diffeomorphic metric maps satisfy the property that the length associated to their flow away from the identity induces a metric on the group of diffeomorphisms, which in turn induces a metric on the orbit of shapes and forms within the field of Computational Anatomy. The study of shapes and forms with the metric of diffeomorphic metric mapping is called diffeomorphometry.

<span class="mw-page-title-main">Ron Kikinis</span> American physician and scientist (born 1956)

Ron Kikinis is an American physician and scientist best known for his research in the fields of imaging informatics, image guided surgery, and medical image computing. He is a professor of radiology at Harvard Medical School. Kikinis is the founding director of the Surgical Planning Laboratory in the Department of Radiology at Brigham and Women's Hospital, in Boston, Massachusetts. He is the vice-chair for Biomedical Informatics Research in the Department of Radiology.

U-Net is a convolutional neural network that was developed for image segmentation. The network is based on a fully convolutional neural network whose architecture was modified and extended to work with fewer training images and to yield more precise segmentation. Segmentation of a 512 × 512 image takes less than a second on a modern (2015) GPU using the U-Net architecture.

Arterial spin labeling (ASL), also known as arterial spin tagging, is a magnetic resonance imaging technique used to quantify cerebral blood perfusion by labelling blood water as it flows throughout the brain. ASL specifically refers to magnetic labeling of arterial blood below or in the imaging slab, without the need of gadolinium contrast. A number of ASL schemes are possible, the simplest being flow alternating inversion recovery (FAIR) which requires two acquisitions of identical parameters with the exception of the out-of-slice saturation; the difference in the two images is theoretically only from inflowing spins, and may be considered a 'perfusion map'. The ASL technique was developed by John S. Leigh Jr, John A. Detre, Donald S. Williams, and Alan P. Koretsky in 1992.

Elastix is an image registration toolbox built upon the Insight Segmentation and Registration Toolkit (ITK). It is entirely open-source and provides a wide range of algorithms employed in image registration problems. Its components are designed to be modular to ease a fast and reliable creation of various registration pipelines tailored for case-specific applications. It was first developed by Stefan Klein and Marius Staring under the supervision of Josien P.W. Pluim at Image Sciences Institute (ISI). Its first version was command-line based, allowing the final user to employ scripts to automatically process big data-sets and deploy multiple registration pipelines with few lines of code. Nowadays, to further widen its audience, a version called SimpleElastix is also available, developed by Kasper Marstal, which allows the integration of elastix with high level languages, such as Python, Java, and R.

References

  1. Perera Molligoda Arachchige, Arosh S.; Svet, Afanasy (2021-09-10). "Integrating artificial intelligence into radiology practice: undergraduate students' perspective". European Journal of Nuclear Medicine and Molecular Imaging. 48 (13): 4133–4135. doi:10.1007/s00259-021-05558-y. ISSN   1619-7089. PMID   34505175. S2CID   237459138.
  2. Forghani, M.; Forouzanfar, M.; Teshnehlab, M. (2010). "Parameter optimization of improved fuzzy c-means clustering algorithm for brain MR image segmentation". Engineering Applications of Artificial Intelligence. 23 (2): 160–168. doi:10.1016/j.engappai.2009.10.002.
  3. J Gee; M Reivich; R Bajcsy (1993). "Elastically Deforming a Three-Dimensional Atlas to Match Anatomical Brain Images". Journal of Computer Assisted Tomography. 17 (1): 225–236. doi:10.1097/00004728-199303000-00011. PMID   8454749. S2CID   25781937.
  4. MR Sabuncu; BT Yeo; K Van Leemput; B Fischl; P Golland (June 2010). "A Generative Model for Image Segmentation Based on Label Fusion". IEEE Transactions on Medical Imaging. 29 (10): 1714–1729. doi:10.1109/TMI.2010.2050897. PMC   3268159 . PMID   20562040.
  5. Cootes TF, Taylor CJ, Cooper DH, Graham J (1995). "Active shape models-their training and application". Computer Vision and Image Understanding. 61 (1): 38–59. doi:10.1006/cviu.1995.1004. S2CID   15242659.
  6. Cootes, T.F.; Edwards, G.J.; Taylor, C.J. (2001). "Active appearance models". IEEE Transactions on Pattern Analysis and Machine Intelligence. 23 (6): 681–685. CiteSeerX   10.1.1.128.4967 . doi:10.1109/34.927467.
  7. G. Zheng; S. Li; G. Szekely (2017). Statistical Shape and Deformation Analysis. Academic Press. ISBN   9780128104941.
  8. R. Goldenberg, R. Kimmel, E. Rivlin, and M. Rudzsky (2001). "Fast geodesic active contours" (PDF). IEEE Transactions on Image Processing. 10 (10): 1467–1475. Bibcode:2001ITIP...10.1467G. CiteSeerX   10.1.1.35.1977 . doi:10.1109/83.951533. PMID   18255491.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  9. Karasev, P.; Kolesov I.; Chudy, K.; Vela, P.; Tannenbaum, A. (2011). "Interactive MRI segmentation with controlled active vision". IEEE Conference on Decision and Control and European Control Conference. pp. 2293–2298. doi:10.1109/CDC.2011.6161453. ISBN   978-1-61284-801-3. PMC   3935399 . PMID   24584213.
  10. K. Mikula, N. Peyriéras, M. Remešíková, A.Sarti: 3D embryogenesis image segmentation by the generalized subjective surface method using the finite volume technique. Proceedings of FVCA5 – 5th International Symposium on Finite Volumes for Complex Applications, Hermes Publ., Paris 2008.
  11. A. Sarti, G. Citti: Subjective surfaces and Riemannian mean curvature flow graphs. Acta Math. Univ. Comenian. (N.S.) 70 (2000), 85–103.
  12. A. Sarti, R. Malladi, J.A. Sethian: Subjective Surfaces: A Method for Completing Missing Boundaries. Proc. Natl. Acad. Sci. mi 12, No. 97 (2000), 6258–6263.
  13. A. Sarti, R. Malladi, J.A. Sethian: Subjective Surfaces: A Geometric Model for Boundary Completion, International Journal of Computer Vision, mi 46, No. 3 (2002), 201–221.
  14. Badrinarayanan, Vijay; Kendall, Alex; Cipolla, Roberto (2015-11-02). "SegNet: A Deep Convolutional Encoder-Decoder Architecture for Image Segmentation". arXiv: 1511.00561 [cs.CV].
  15. Ronneberger, Olaf; Fischer, Philipp; Brox, Thomas (2015-05-18). "U-Net: Convolutional Networks for Biomedical Image Segmentation". arXiv: 1505.04597 [cs.CV].
  16. He, Kaiming; Zhang, Xiangyu; Ren, Shaoqing; Sun, Jian (June 2016). "Deep Residual Learning for Image Recognition". 2016 IEEE Conference on Computer Vision and Pattern Recognition (CVPR). Las Vegas, NV, USA: IEEE. pp. 770–778. doi:10.1109/CVPR.2016.90. ISBN   978-1-4673-8851-1. S2CID   206594692.
  17. Ahmad, Ibtihaj; Xia, Yong; Cui, Hengfei; Islam, Zain Ul (2023-05-01). "AATSN: Anatomy Aware Tumor Segmentation Network for PET-CT volumes and images using a lightweight fusion-attention mechanism". Computers in Biology and Medicine. 157: 106748. doi:10.1016/j.compbiomed.2023.106748. ISSN   0010-4825. PMID   36958235. S2CID   257489603.
  18. Vaswani, Ashish; Shazeer, Noam; Parmar, Niki; Uszkoreit, Jakob; Jones, Llion; Gomez, Aidan N.; Kaiser, Lukasz; Polosukhin, Illia (2017-06-12). "Attention Is All You Need". arXiv: 1706.03762 [cs.CL].
  19. Sorin, Vera; Barash, Yiftach; Konen, Eli; Klang, Eyal (August 2020). "Creating Artificial Images for Radiology Applications Using Generative Adversarial Networks (GANs) – A Systematic Review". Academic Radiology. 27 (8): 1175–1185. doi:10.1016/j.acra.2019.12.024. ISSN   1076-6332. PMID   32035758. S2CID   211072078.
  20. Ehsani Rad, Abdolvahab; Mohd Rahim Mohd Shafry; Rehman Amjad; Altameem Ayman; Saba Tanzila (May 2013). "Evaluation of Current Dental Radiographs Segmentation Approaches in Computer-aided Applications". IETE Technical Review. 30 (3): 210. doi: 10.4103/0256-4602.113498 (inactive 1 November 2024). S2CID   62571134.{{cite journal}}: CS1 maint: DOI inactive as of November 2024 (link)
  21. Lisa Gottesfeld Brown (1992). "A survey of image registration techniques". ACM Computing Surveys. 24 (4): 325–376. CiteSeerX   10.1.1.35.2732 . doi:10.1145/146370.146374. S2CID   14576088.
  22. J. Maintz; M. Viergever (1998). "A survey of medical image registration". Medical Image Analysis. 2 (1): 1–36. CiteSeerX   10.1.1.46.4959 . doi:10.1016/S1361-8415(01)80026-8. PMID   10638851.
  23. J. Hajnal; D. Hawkes; D. Hill (2001). Medical Image Registration. Baton Rouge, Florida: CRC Press.
  24. Barbara Zitová; Jan Flusser (2003). "Image registration methods: a survey". Image Vision Comput. 21 (11): 977–1000. doi:10.1016/S0262-8856(03)00137-9. hdl:10338.dmlcz/141595.
  25. J. P. W. Pluim; J. B. A. Maintz; M. A. Viergever (2003). "Mutual information based registration of medical images: A survey". IEEE Trans. Med. Imaging. 22 (8): 986–1004. CiteSeerX   10.1.1.197.6513 . doi:10.1109/TMI.2003.815867. PMID   12906253. S2CID   2605077.
  26. Grenander, Ulf; Miller, Michael I. (1998). "Computational anatomy: an emerging discipline". Q. Appl. Math. LVI (4): 617–694. doi: 10.1090/qam/1668732 .
  27. P. A. Viola (1995). Alignment by Maximization of Mutual Information (Thesis). Massachusetts Institute of Technology.
  28. C. Wachinger; T. Klein; N. Navab (2011). "Locally adaptive Nakagami-based ultrasound similarity measures". Ultrasonics. 52 (4): 547–554. doi:10.1016/j.ultras.2011.11.009. PMID   22197152.
  29. C. Wachinger; N. Navab (2012). "Entropy and Laplacian images: structural representations for multi-modal registration". Medical Image Analysis. 16 (1): 1–17. doi:10.1016/j.media.2011.03.001. PMID   21632274.
  30. Hill, Derek LG; Hawkes, David J (1994-04-01). "Medical image registration using knowledge of adjacency of anatomical structures". Image and Vision Computing. 12 (3): 173–178. CiteSeerX   10.1.1.421.5162 . doi:10.1016/0262-8856(94)90069-8. ISSN   0262-8856.
  31. Toth, Daniel; Panayiotou, Maria; Brost, Alexander; Behar, Jonathan M.; Rinaldi, Christopher A.; Rhode, Kawal S.; Mountney, Peter (2016-10-17). "Registration with Adjacent Anatomical Structures for Cardiac Resynchronization Therapy Guidance". Statistical Atlases and Computational Models of the Heart. Imaging and Modelling Challenges (Submitted manuscript). Lecture Notes in Computer Science. Vol. 10124. pp. 127–134. doi:10.1007/978-3-319-52718-5_14. ISBN   9783319527178. S2CID   1698371.
  32. Pielawski, N., Wetzer, E., Ofverstedt, J., Lu, J., Wählby, C., Lindblad, J., & Sladoje, N. (2020). CoMIR: Contrastive Multimodal Image Representation for Registration. In Advances in Neural Information Processing Systems (pp. 18433–18444). Curran Associates, Inc.
  33. M. De Craene; A. B. d Aische; B. Macq; S. K. Warfield (2004). "Multi-subject Registration for Unbiased Statistical Atlas Construction" (PDF). Medical Image Computing and Computer-Assisted Intervention – MICCAI 2004. Lecture Notes in Computer Science. Vol. 3216. pp. 655–662. doi: 10.1007/978-3-540-30135-6_80 . ISBN   978-3-540-22976-6.
  34. C. J. Twining; T. Cootes; S. Marsland; V. Petrovic; R. Schestowitz; C. Taylor (2005). "A Unified Information-Theoretic Approach to Groupwise Non-rigid Registration and Model Building". Information Processing in Medical Imaging. Lecture Notes in Computer Science. Vol. 19. pp. 1–14. doi:10.1007/11505730_1. ISBN   978-3-540-26545-0. PMID   17354680.
  35. "The MNI brain and the Talairach atlas".
  36. M. Sabuncu; S. K. Balci; M. E. Shenton; P. Golland (2009). "Image-driven Population Analysis through Mixture Modeling". IEEE Transactions on Medical Imaging. 28 (9): 1473–1487. CiteSeerX   10.1.1.158.3690 . doi:10.1109/TMI.2009.2017942. PMC   2832589 . PMID   19336293.
  37. J. Ashburner; K.J. Friston (2000). "Voxel-Based Morphometry – The Methods". NeuroImage. 11 (6): 805–821. CiteSeerX   10.1.1.114.9512 . doi:10.1006/nimg.2000.0582. PMID   10860804. S2CID   16777465.
  38. C. Davatzikos (2004). "Why voxel-based morphometric analysis should be used with great caution when characterizing group differences". NeuroImage. 23 (1): 17–20. doi:10.1016/j.neuroimage.2004.05.010. PMID   15325347. S2CID   7452089.
  39. K.J. Friston; W.D. Penny; C. Phillips; S.J. Kiebel; G. Hinton; J. Ashburner (2002). "Classical and Bayesian Inference in Neuroimaging: Theory". NeuroImage. 16 (2): 465–483. CiteSeerX   10.1.1.128.8333 . doi:10.1006/nimg.2002.1090. PMID   12030832. S2CID   14911371.
  40. Yong Fan; Nematollah Batmanghelich; Chris M. Clark; Christos Davatzikos (2008). "Spatial patterns of brain atrophy in MCI patients, identified via high-dimensional pattern classification, predict subsequent cognitive decline". NeuroImage. 39 (4): 1731–1743. doi:10.1016/j.neuroimage.2007.10.031. PMC   2861339 . PMID   18053747.
  41. Rémi Cuingnet; Emilie Gerardin; Jérôme Tessieras; Guillaume Auzias; Stéphane Lehéricy; Marie-Odile Habert; Marie Chupin; Habib Benali; Olivier Colliot (2011). "The Alzheimer's Disease Neuroimaging Initiative, Automatic classification of patients with Alzheimer's disease from structural MRI: A comparison of ten methods using the ADNI database" (PDF). NeuroImage. 56 (2): 766–781. doi:10.1016/j.neuroimage.2010.06.013. PMID   20542124. S2CID   628131.
  42. Y. Wang; Y. Fan; P. Bhatt P; C. Davatzikos (2010). "High-dimensional pattern regression using machine learning: from medical images to continuous clinical variables". NeuroImage. 50 (4): 1519–35. doi:10.1016/j.neuroimage.2009.12.092. PMC   2839056 . PMID   20056158.
  43. Benoît Magnin; Lilia Mesrob; Serge Kinkingnéhun; Mélanie Pélégrini-Issac; Olivier Colliot; Marie Sarazin; Bruno Dubois; Stéphane Lehéricy; Habib Benali (2009). "Support vector machine-based classification of Alzheimer's disease from whole-brain anatomical MRI". Neuroradiology. 51 (2): 73–83. doi:10.1007/s00234-008-0463-x. PMID   18846369. S2CID   285128.
  44. 1 2 N.K. Batmanghelich; B. Taskar; C. Davatzikos (2012). "Generative-discriminative basis learning for medical imaging". IEEE Trans Med Imaging. 31 (1): 51–69. doi:10.1109/TMI.2011.2162961. PMC   3402718 . PMID   21791408.
  45. 1 2 Glenn Fung; Jonathan Stoeckel (2007). "SVM feature selection for classification of SPECT images of Alzheimer's disease using spatial information". Knowledge and Information Systems. 11 (2): 243–258. CiteSeerX   10.1.1.62.6245 . doi:10.1007/s10115-006-0043-5. S2CID   9901011.
  46. 1 2 R. Chaves; J. Ramírez; J.M. Górriz; M. López; D. Salas-Gonzalez; I. Álvarez; F. Segovia (2009). "SVM-based computer-aided diagnosis of the Alzheimer's disease using t-test NMSE feature selection with feature correlation weighting". Neuroscience Letters. 461 (3): 293–297. doi:10.1016/j.neulet.2009.06.052. PMID   19549559. S2CID   9981775.
  47. 1 2 Yanxi Liu; Leonid Teverovskiy; Owen Carmichael; Ron Kikinis; Martha Shenton; Cameron S. Carter; V. Andrew Stenger; Simon Davis; Howard Aizenstein; James T. Becker (2004). "Discriminative MR Image Feature Analysis for Automatic Schizophrenia and Alzheimer's Disease Classification" (PDF). Medical Image Computing and Computer-Assisted Intervention – MICCAI 2004. Lecture Notes in Computer Science. Vol. 3216. pp. 393–401. doi: 10.1007/978-3-540-30135-6_48 . ISBN   978-3-540-22976-6.{{cite book}}: |journal= ignored (help)
  48. Savio A.; Graña M. (2013). "Deformation based feature selection for Computer Aided Diagnosis of Alzheimer's Disease". Expert Systems with Applications. 40 (5): 1619–1628. doi:10.1016/j.eswa.2012.09.009. ISSN   0957-4174.
  49. R. Filipovych; S. M. Resnick; C. Davatzikos (2011). "Semi-supervised cluster analysis of imaging data". NeuroImage. 54 (3): 2185–2197. doi:10.1016/j.neuroimage.2010.09.074. PMC   3008313 . PMID   20933091.
  50. STEP research roadmap Archived 2008-08-28 at the Wayback Machine . europhysiome.org
  51. J. W. Fenner; B. Brook; G. Clapworthy; P. V. Coveney; V. Feipel; H. Gregersen; D. R. Hose; P. Kohl; P. Lawford; K. M. McCormack; D. Pinney; S. R. Thomas; S. Van Sint Jan; S. Waters; M. Viceconti (2008). "The EuroPhysiome, STEP and a roadmap for the virtual physiological human" (PDF). Philosophical Transactions of the Royal Society A. 366 (1878): 2979–2999. Bibcode:2008RSPTA.366.2979F. doi:10.1098/rsta.2008.0089. PMID   18559316. S2CID   1211981.
  52. J. B. Bassingthwaighte (2000). "Strategies for the Physiome Project". Annals of Biomedical Engineering. 28 (8): 1043–1058. doi:10.1114/1.1313771. PMC   3425440 . PMID   11144666.
  53. P. J. Hunter; T. K. Borg (2003). "Integration from proteins to organs: The Physiome Project". Nat. Rev. Mol. Cell Biol. 4 (3): 237–243. doi:10.1038/nrm1054. PMID   12612642. S2CID   25185270.
  54. R. L.Winslow; N. Trayanova; D. Geman; M. I. Miller (2012). "Computational medicine: Translating models to clinical care". Sci. Transl. Med. 4 (158): 158rv11. doi:10.1126/scitranslmed.3003528. PMC   3618897 . PMID   23115356.
  55. N. Ayache, J.-P. Boissel, S. Brunak, G. Clapworthy, G. Lonsdale, J. Fingberg, A. F. Frangi, G.Deco, P. J. Hunter, P.Nielsen, M.Halstead, D. R. Hose, I. Magnin, F. Martin-Sanchez, P. Sloot, J. Kaandorp, A. Hoekstra, S. Van Sint Jan, and M. Viceconti (2005) "Towards virtual physiological human: Multilevel modelling and simulation of the human anatomy and physiology". Directorate General INFSO & Directorate General JRC, White paper
  56. Boulfelfel D.; Rangayyan R.M.; Hahn L.J.; Kloiber R.; Kuduvalli G.R. (1994). "Restoration of single photon emission computed tomography images by the Kalman filter". IEEE Transactions on Medical Imaging. 13 (1): 102–109. doi:10.1109/42.276148. PMID   18218487.
  57. Angenent, S.; Pichon, E.; Tannenbaum, A. (2006). "Mathematical methods in medical image processing". Bulletin of the AMS. 43 (3): 365–396. doi:10.1090/S0273-0979-06-01104-9. PMC   3640423 . PMID   23645963.
  58. P Basser; J Mattiello; D LeBihan (January 1994). "MR diffusion tensor spectroscopy, imaging". Biophysical Journal. 66 (1): 259–267. Bibcode:1994BpJ....66..259B. doi:10.1016/S0006-3495(94)80775-1. PMC   1275686 . PMID   8130344.
  59. P Fillard; X Pennec; V Arsigny; N Ayache (2007). "Clinical DT-MRI estimation, smoothing,, fiber tracking with log-Euclidean metrics". IEEE Transactions on Medical Imaging. 26 (11): 1472–1482. CiteSeerX   10.1.1.218.6380 . doi:10.1109/TMI.2007.899173. PMID   18041263.
  60. S-K Song; S-W Sun; M Ramsbottom; C Cheng; J Russell; A Cross (November 2002). "Dysmyelination Revealed through MRI as Increased Radial (but Unchanged Axial) Diffusion of Water". NeuroImage. 13 (3): 1429–1436. doi:10.1006/nimg.2002.1267. PMID   12414282. S2CID   43229972.
  61. P Barzo; A Marmarou; P Fatouros; K Hayasaki; F Corwin (December 1997). "Contribution of vasogenic and cellular edema to traumatic brain swelling measured by diffusion-weighted imaging". Journal of Neurosurgery. 87 (6): 900–907. doi:10.3171/jns.1997.87.6.0900. PMID   9384402.
  62. D Alexander; C Pierpaoli; P Basser (January 2001). "Spatial transformation of diffusion tensor magnetic resonance images" (PDF). IEEE Transactions on Medical Imaging. 20 (11): 1131–1139. doi:10.1109/42.963816. PMID   11700739. S2CID   6559551.
  63. Y Cao; M Miller; S Mori; R Winslow; L Younes (June 2006). "Diffeomorphic Matching of Diffusion Tensor Images". Proceedings of IEEE Computer Society Conference on Computer Vision, Pattern Recognition (CVPR), Workshop on Mathematical Methods in Biomedical Image Analysis (MMBIA 2006). New York. p. 67. doi:10.1109/CVPRW.2006.65. PMC   2920614 .
  64. Z Wang; B Vemuri (October 2005). "DTI segmentation using an information theoretic tensor dissimilarity measure". IEEE Transactions on Medical Imaging. 24 (10): 1267–1277. CiteSeerX   10.1.1.464.9059 . doi:10.1109/TMI.2005.854516. PMID   16229414. S2CID   32724414.
  65. Melonakos, J.; Pichon, E.; Angenent, S.; Tannenbaum, A. (2008). "Finsler active contours". IEEE Trans. Pattern Anal. Mach. Intell. 30 (3): 412–423. doi:10.1109/TPAMI.2007.70713. PMC   2796633 . PMID   18195436.
  66. S Mori; B Crain; V Chacko; P van Zijl (February 1999). "Three-dimensional tracking of axonal projections in the brain by magnetic resonance imaging". Annals of Neurology. 45 (2): 265–269. doi:10.1002/1531-8249(199902)45:2<265::AID-ANA21>3.0.CO;2-3. PMID   9989633. S2CID   334903.
  67. D Tuch; T Reese; M Wiegell; N Makris; J Belliveau; V Wedeen (October 2002). "High angular resolution diffusion imaging reveals intravoxel white matter fiber heterogeneity". Magnetic Resonance in Medicine. 48 (4): 577–582. doi: 10.1002/mrm.10268 . PMID   12353272.
  68. D Tuch (December 2004). "Q-ball imaging". Magnetic Resonance in Medicine. 52 (6): 1358–1372. doi: 10.1002/mrm.20279 . PMID   15562495.
  69. V Wedeen; P Hagmann; W-Y Tseng; T Reese (December 2005). "Mapping complex tissue architecture with diffusion spectrum magnetic resonance imaging". Magnetic Resonance in Medicine. 54 (6): 1377–1386. doi: 10.1002/mrm.20642 . PMID   16247738.
  70. K Jansons; D Alexander (July 2003). "Persistent angular structure: new insights from diffusion magnetic resonance imaging data". Proceedings of Information Processing in Medical Imaging (IPMI) 2003, LNCS 2732. pp. 672–683. doi:10.1007/978-3-540-45087-0_56.
  71. J-D Tournier; F Calamante; D Gadian; A Connelly (2007). "Direct estimation of the fiber orientation density function from diffusion-weighted MRI data using spherical deconvolution". NeuroImage. 23 (3): 1176–1185. doi:10.1016/j.neuroimage.2004.07.037. PMID   15528117. S2CID   24169627.
  72. X Geng; T Ross; W Zhan; H Gu; Y-P Chao; C-P Lin; G Christensen; N Schuff; Y Yang (July 2009). "Diffusion MRI Registration Using Orientation Distribution Functions". Proceedings of Information Processing in Medical Imaging (IPMI) 2009, LNCS 5636. Vol. 21. pp. 626–637. doi:10.1007/978-3-642-02498-6_52. PMC   3860746 .
  73. P-T Yap; Y Chen; H An; Y Yang; J Gilmore; W Lin; D Shen (2011). "SPHERE: SPherical Harmonic Elastic REgistration of HARDI data". NeuroImage. 55 (2): 545–556. doi:10.1016/j.neuroimage.2010.12.015. PMC   3035740 . PMID   21147231.
  74. P Zhang; M Niethammer; D Shen; P-T Yap (2012). "Large Deformation Diffeomorphic Registration of Diffusion-Weighted Images" (PDF). Proceedings of Medical Image Computing and Computer-Assisted Intervention (MICCAI). doi: 10.1007/978-3-642-33418-4_22 .
  75. M Descoteaux; R Deriche (September 2007). "Segmentation of Q-Ball Images Using Statistical Surface Evolution". Proceedings of Medical Image Computing and Computer-Assisted Intervention (MICCAI) 2007, LNCS 4792. pp. 769–776. doi: 10.1007/978-3-540-75759-7_93 .
  76. 1 2 Friston, K.; Holmes, A.; Worsley, K.; Poline, J.; Frith, C.; Frackowiak, R.; et al. (1995). "Statistical parametric maps in functional imaging: a general linear approach". Hum Brain Mapp. 2 (4): 189–210. doi:10.1002/hbm.460020402. S2CID   9898609.
  77. Buckner, R. L.; Andrews-Hanna, J. R.; Schacter, D. L. (2008). "The brain's default network: anatomy, function, and relevance to disease". Annals of the New York Academy of Sciences. 1124 (1): 1–38. Bibcode:2008NYASA1124....1B. CiteSeerX   10.1.1.689.6903 . doi:10.1196/annals.1440.011. PMID   18400922. S2CID   3167595.
  78. 1 2 Yeo, B. T. T.; Krienen, F. M.; Sepulcre, J.; Sabuncu, M. R.; Lashkari, D.; Hollinshead, M.; Roffman, J. L.; Smoller, J. W.; Zöllei, L.; Polimeni, J. R.; Fischl, B.; Liu, H.; Buckner, R. L. (2011). "The organization of the human cerebral cortex estimated by intrinsic functional connectivity". J Neurophysiol. 106 (3): 1125–65. doi:10.1152/jn.00338.2011. PMC   3174820 . PMID   21653723.
  79. J. V. Haxby; M. I. Gobbini; M. L. Furey; A. Ishai; J. L. Schouten; P. Pietrini (2001). "Distributed and overlapping representations of faces and objects in ventral temporal cortex". Science. 293 (5539): 2425–30. Bibcode:2001Sci...293.2425H. CiteSeerX   10.1.1.381.2660 . doi:10.1126/science.1063736. PMID   11577229. S2CID   6403660.
  80. Langs, G.; Menze, B. H.; Lashkari, D.; Golland, P. (2011). "Detecting stable distributed patterns of brain activation using Gini contrast". NeuroImage. 56 (2): 497–507. doi:10.1016/j.neuroimage.2010.07.074. PMC   3960973 . PMID   20709176.
  81. Varoquaux, G.; Gramfort, A.; Pedregosa, F.; Michel, V.; Thirion, B. (2011). "Multi-subject dictionary learning to segment an atlas of brain spontaneous activity". Inf Process Med Imaging. Vol. 22. pp. 562–73.
  82. van den Heuvel, M. P.; Stam, C. J.; Kahn, R. S.; Hulshoff Pol, H. E. (2009). "Efficiency of functional brain networks and intellectual performance". J Neurosci. 29 (23): 7619–24. doi:10.1523/JNEUROSCI.1443-09.2009. PMC   6665421 . PMID   19515930.
  83. Friston, K. (2003). "Dynamic causal modelling". NeuroImage. 19 (4): 1273–1302. doi:10.1016/S1053-8119(03)00202-7. PMID   12948688. S2CID   2176588.
  84. Sabuncu, M. R.; Singer, B. D.; Conroy, B.; Bryan, R. E.; Ramadge, P. J.; Haxby, J. V. (2010). "Function-based Intersubject Alignment of Human Cortical Anatomy". Cerebral Cortex. 20 (1): 130–140. doi:10.1093/cercor/bhp085. PMC   2792192 . PMID   19420007.
  85. Langs, G.; Lashkari, D.; Sweet, A.; Tie, Y.; Rigolo, L.; Golby, A. J.; Golland, P. (2011). "Learning an atlas of a cognitive process in its functional geometry". Inf Process Med Imaging. Vol. 22. pp. 135–46.
  86. Haxby, J. V.; Guntupalli, J. S.; Connolly, A. C.; Halchenko, Y. O.; Conroy, B. R.; Gobbini, M. I.; Hanke, M.; Ramadge, P. J. (2011). "A common, high-dimensional model of the representational space in human ventral temporal cortex". Neuron. 72 (2): 404–416. doi:10.1016/j.neuron.2011.08.026. PMC   3201764 . PMID   22017997.
  87. Wells, William M; Colchester, Alan; Delp, Scott (1998). Lecture Notes in Computer Science (Submitted manuscript). Vol. 1496. doi:10.1007/BFb0056181. ISBN   978-3-540-65136-9. S2CID   31031333.
  88. JS Duncan; N Ayache (2000). "Medical image analysis: Progress over two decades and the challenges ahead". IEEE Transactions on Pattern Analysis and Machine Intelligence. 22: 85–106. CiteSeerX   10.1.1.410.8744 . doi:10.1109/34.824822.

Journals on medical image computing

In addition the following journals occasionally publish articles describing methods and specific clinical applications of medical image computing or modality specific medical image computing