MPSS is a technique for analyzing gene expression that involves sequencing cDNA fragments cloned onto microbeads. It allows for the simultaneous sequencing of over 1 million cDNA clones. MPSS generates 17-base signature sequences that uniquely identify mRNA transcripts. Gene expression levels are quantified by counting the number of signatures for each gene. MPSS provides a more in-depth analysis of gene expression compared to other methods as it can detect genes expressed at very low levels and does not require prior knowledge of gene sequences.
The rapid increase in throughput of next generation sequencing (NGS) platforms is changing the genomics landscape. Typically, adapters containing sample indexes are added during library construction to allow multiple samples to be sequenced in parallel. Some strategies also introduce a unique molecular identifier (UMI) within the adapter to correct for PCR and sequencing errors. When a UMI is added, reads are assigned to each sample based on their associated sample index, and the UMI is used for error correction during data analysis. For simplicity, a single adapter that is suitable for a variety of applications would be ideal.
xGen® Dual Index UMI Adapters take the guesswork out of adapter design and ordering. These adapters, created for Illumina sequencers, are compatible with standard library preparation methods and may be sequenced in different modes depending on your application. In addition to unique, dual indexes, the adapters contain a molecular barcode in an optional read position. We will discuss how unique, dual indexes mitigate sample index hopping for multiplexed sequencing and demonstrate how UMIs reduce false positives to improve detection of low-frequency variants.
This document discusses next generation sequencing technologies. It provides details on several massively parallel sequencing platforms and describes their advantages over traditional Sanger sequencing such as higher throughput, lower costs, and ability to process millions of reads in parallel. It then outlines several applications of next generation sequencing like mutation discovery, transcriptome analysis, metagenomics, epigenetics research and discovery of non-coding RNAs.
This document discusses cancer genomics and tumor sequencing. It explains that tumor genotyping helps clinicians individualize cancer treatments by matching patients to the best treatment based on their tumor's DNA alterations. Next generation sequencing methods have made it possible to sequence entire cancer genomes and identify additional targets for new cancer therapies. Large-scale projects like The Cancer Genome Atlas and the International Cancer Genome Consortium are analyzing hundreds of cancer genomes to better understand the molecular changes driving different cancer types.
This document discusses clinical and consumer applications of microarrays and genotyping technologies. It provides an overview of genotyping and different technologies like PCR microarrays and SNP microarrays. It describes how microarrays are still useful despite the rise of sequencing due to their low cost, high throughput, and ability to test millions of markers. The document outlines several applications of microarrays like direct-to-consumer testing, pharmacogenetics, and clinical sequencing. It also discusses challenges and trends in these areas like global initiatives to increase genomic data sharing.
Advances in next generation sequencing enable the detection of variants at exceptionally low frequencies. The accurate detection of low-frequency variants is challenging due in part to errors that are introduced during sample preparation, target enrichment, and sequencing. After tagging individual DNA library molecules with adapters containing unique molecular identifiers (UMIs), bioinformatic filters can be applied to identify and correct errors introduced during the sequencing workflow. In this presentation, we walk through the analytical workflows developed at IDT for processing data containing UMIs. We highlight methods to extract UMI information, correct errors, and build consensus among multiple observations of an original source molecule.
Biochemical and molecular methods allow identification and analysis of macromolecules like proteins and nucleic acids. These include hybridization, separation techniques like chromatography and electrophoresis, and using restriction enzymes. Hybridization with labeled probes enables detection and visualization of DNA/RNA locations. Polymerase chain reaction (PCR) is used to selectively amplify DNA or cDNA fragments for cloning and analysis. Northern blotting, ribonuclease protection, and reverse transcription PCR (RT-PCR) analyze mRNA expression levels and locations.
Ion Torrent (Proton/PGM) and SOLiD sequencing are two types of next-generation sequencing technologies. Ion Torrent uses semiconductor sequencing to detect hydrogen ions released during DNA synthesis, while SOLiD uses ligation of octamer probes and fluorescent dyes to determine sequences in color space. Both have advantages such as fast run times and high throughput but also limitations including errors in homopolymers for Ion Torrent and issues with palindromic sequences for SOLiD.
MPSS is a technique for analyzing gene expression that involves sequencing cDNA fragments cloned onto microbeads. It allows for the simultaneous sequencing of over 1 million cDNA clones. MPSS generates 17-base signature sequences that uniquely identify mRNA transcripts. Gene expression levels are quantified by counting the number of signatures for each gene. MPSS provides a more in-depth analysis of gene expression compared to other methods as it can detect genes expressed at very low levels and does not require prior knowledge of gene sequences.
The rapid increase in throughput of next generation sequencing (NGS) platforms is changing the genomics landscape. Typically, adapters containing sample indexes are added during library construction to allow multiple samples to be sequenced in parallel. Some strategies also introduce a unique molecular identifier (UMI) within the adapter to correct for PCR and sequencing errors. When a UMI is added, reads are assigned to each sample based on their associated sample index, and the UMI is used for error correction during data analysis. For simplicity, a single adapter that is suitable for a variety of applications would be ideal.
xGen® Dual Index UMI Adapters take the guesswork out of adapter design and ordering. These adapters, created for Illumina sequencers, are compatible with standard library preparation methods and may be sequenced in different modes depending on your application. In addition to unique, dual indexes, the adapters contain a molecular barcode in an optional read position. We will discuss how unique, dual indexes mitigate sample index hopping for multiplexed sequencing and demonstrate how UMIs reduce false positives to improve detection of low-frequency variants.
This document discusses next generation sequencing technologies. It provides details on several massively parallel sequencing platforms and describes their advantages over traditional Sanger sequencing such as higher throughput, lower costs, and ability to process millions of reads in parallel. It then outlines several applications of next generation sequencing like mutation discovery, transcriptome analysis, metagenomics, epigenetics research and discovery of non-coding RNAs.
This document discusses cancer genomics and tumor sequencing. It explains that tumor genotyping helps clinicians individualize cancer treatments by matching patients to the best treatment based on their tumor's DNA alterations. Next generation sequencing methods have made it possible to sequence entire cancer genomes and identify additional targets for new cancer therapies. Large-scale projects like The Cancer Genome Atlas and the International Cancer Genome Consortium are analyzing hundreds of cancer genomes to better understand the molecular changes driving different cancer types.
This document discusses clinical and consumer applications of microarrays and genotyping technologies. It provides an overview of genotyping and different technologies like PCR microarrays and SNP microarrays. It describes how microarrays are still useful despite the rise of sequencing due to their low cost, high throughput, and ability to test millions of markers. The document outlines several applications of microarrays like direct-to-consumer testing, pharmacogenetics, and clinical sequencing. It also discusses challenges and trends in these areas like global initiatives to increase genomic data sharing.
Advances in next generation sequencing enable the detection of variants at exceptionally low frequencies. The accurate detection of low-frequency variants is challenging due in part to errors that are introduced during sample preparation, target enrichment, and sequencing. After tagging individual DNA library molecules with adapters containing unique molecular identifiers (UMIs), bioinformatic filters can be applied to identify and correct errors introduced during the sequencing workflow. In this presentation, we walk through the analytical workflows developed at IDT for processing data containing UMIs. We highlight methods to extract UMI information, correct errors, and build consensus among multiple observations of an original source molecule.
Biochemical and molecular methods allow identification and analysis of macromolecules like proteins and nucleic acids. These include hybridization, separation techniques like chromatography and electrophoresis, and using restriction enzymes. Hybridization with labeled probes enables detection and visualization of DNA/RNA locations. Polymerase chain reaction (PCR) is used to selectively amplify DNA or cDNA fragments for cloning and analysis. Northern blotting, ribonuclease protection, and reverse transcription PCR (RT-PCR) analyze mRNA expression levels and locations.
Ion Torrent (Proton/PGM) and SOLiD sequencing are two types of next-generation sequencing technologies. Ion Torrent uses semiconductor sequencing to detect hydrogen ions released during DNA synthesis, while SOLiD uses ligation of octamer probes and fluorescent dyes to determine sequences in color space. Both have advantages such as fast run times and high throughput but also limitations including errors in homopolymers for Ion Torrent and issues with palindromic sequences for SOLiD.
Slides presented at the Molecular Med Tri-Con 2018 Precision Medicine, "Emerging Role of Radiomics in Precision Medicine" (http://www.triconference.com/Precision-Medicine/)
Abstract
The goal of this talk is to discuss the role of data standards, and specifically the Digital Imaging and Communication in Medicine (DICOM) standard, in supporting radiomics research. From the clinical images, to the storage of image annotations and results of radiomics analysis, standardization can potentially have transformative effect by enabling discovery, reuse and mining of the data, and integration of the radiomics workflows into the healthcare enterprise.
Lessons Learned from the DICOM Standardization Effort Lessons Learned from ...MedicineAndDermatology
DICOM is an international standard for communicating medical imaging information and related data between devices. It has been developed over 18 years through collaboration between industry and clinical experts. Maintaining and evolving standards like DICOM requires significant organizational infrastructure and ongoing effort. Key aspects of the DICOM standard include its use of tagged data elements, object orientation, network services, privacy/security features, and support for structured reporting.
The document describes a deep learning framework for joint segmentation and classification of lung nodules in CT images. It uses a VGG19 network-assisted VGG-SegNet model for segmentation, extracting deep features from VGG19, and combining with handcrafted features for classification. The methodology involves collecting CT images, segmenting nodules using VGG-SegNet, extracting deep and handcrafted features, concatenating the features, and classifying images using various classifiers. Experimental results on LIDC-IDRI and Lung-PET-CT-Dx datasets show the proposed approach achieves 97.83% accuracy using an SVM-RBF classifier.
3D Slicer is an open-source software platform for medical image computing and visualization that allows users to load, segment, register, and analyze medical images from various modalities like MRI, CT, and DICOM. It provides tools for tasks such as interactive image segmentation, registration, visualization of diffusion tensor images and tractography, and integration of functional and anatomical data. Slicer has been used in applications such as surgical planning, virtual endoscopy, and pre-operative mapping of functional areas to avoid during surgery.
Development of Computational Tool for Lung Cancer Prediction Using Data MiningEditor IJCATR
The requirement for computerization of detection of lung cancer disease arises ever since recent-techniques which involve
manual-examination of the blood smear as the first step toward diagnosis. This is quite time-consuming, and their accurateness depends
upon the ability of operator's. So, prevention of lung cancer is very essential. This paper has surveyed various techniques used by previous
authors like ANN (Artificial Neural Network), image processing, LDA (Linear Dependent Analysis), SOM (Self Organizing Map) etc.
Statistical Feature-based Neural Network Approach for the Detection of Lung C...CSCJournals
Lung cancer, if successfully detected at early stages, enables many treatment options, reduced risk of invasive surgery and increased survival rate. This paper presents a novel approach to detect lung cancer from raw chest X-ray images. At the first stage, we use a pipeline of image processing routines to remove noise and segment the lung from other anatomical structures in the chest X-ray and extract regions that exhibit shape characteristics of lung nodules. Subsequently, first and second order statistical texture features are considered as the inputs to train a neural network to verify whether a region extracted in the first stage is a nodule or not . The proposed approach detected nodules in the diseased area of the lung with an accuracy of 96% using the pixel-based technique while the feature-based technique produced an accuracy of 88%.
1- List of modalities and study types
2- CT/US/DX Study Structure
3- DICOM composite instance IOD information module
4- Storage of DICOM image in PACS server
5- Imaging Data
6- Query and Retrieval from PACS
7- Window Width/ Window Center
8- DCM File Sections
The MAGIC-5 lung CAD system uses three parallel approaches - region growing, virtual ants, and voxel-based neural networks - to detect and classify lung nodules in CT scans. It was validated on three databases and performs competitively with state-of-the-art systems. In the ANODE09 international competition, the three MAGIC-5 CADs achieved scores between 0.25-0.29 for detecting pulmonary nodules, outperforming other participating CAD systems. The MAGIC-5 project aims to support medical diagnosis and allow large-scale image analysis through developing models and algorithms for biomedical image analysis.
The swings and roundabouts of a decade of fun and games with Research Objects Carole Goble
Research Objects and their instantiation as RO-Crate: motivation, explanation, examples, history and lessons, and opportunities for scholarly communications, delivered virtually to 17th Italian Research Conference on Digital Libraries
Lung Cancer Detection using transfer learning.pptx.pdfjagan477830
Lung cancer is one of the deadliest cancers worldwide. However, the early detection of lung cancer significantly improves survival rate. Cancerous (malignant) and noncancerous (benign) pulmonary nodules are the small growths of cells inside the lung. Detection of malignant lung nodules at an early stage is necessary for the crucial prognosis.
The classification of different types of tumors is of great importance in cancer diagnosis and its drug discovery. Cancer classification via gene expression data is known to contain the keys for solving the fundamental problems relating to the diagnosis of cancer. The recent advent of DNA microarray technology has made rapid monitoring of thousands of gene expressions possible. With this large quantity of gene expression data, scientists have started to explore the opportunities of classification of cancer using a gene expression dataset. To gain a profound understanding of the classification of cancer, it is necessary to take a closer look at the problem, the proposed solutions, and the related issues altogether. In this research thesis, I present a new way for Leukemia classification using the latest AI technique of Deep learning using Google TensorFlow on gene expression data.
A discriminative-feature-space-for-detecting-and-recognizing-pathologies-of-t...Damian R. Mingle, MBA
Each year it has become more and more difficult for healthcare providers to determine if a patient has a pathology
related to the vertebral column. There is great potential to become more efficient and effective in terms of quality
of care provided to patients through the use of automated systems. However, in many cases automated systems
can allow for misclassification and force providers to have to review more causes than necessary. In this study, we
analyzed methods to increase the True Positives and lower the False Positives while comparing them against stateof-the-art
techniques in the biomedical community. We found that by applying the studied techniques of a data-driven
model, the benefits to healthcare providers are significant and align with the methodologies and techniques utilized
in the current research community.
Computer-aided diagnostic system kinds and pulmonary nodule detection efficacyIJECEIAES
This paper summarizes the literature on computer-aided detection (CAD) systems used to identify and diagnose lung nodules in images obtained with computed tomography (CT) scanners. The importance of developing such systems lies in the fact that the process of manually detecting lung nodules is painstaking and sequential work for radiologists, as it takes a long time. Moreover, the pulmonary nodules have multiple appearances and shapes, and the large number of slices generated by the scanner creates great difficulty in accurately locating the lung nodules. The handcraft nodules detection process can be caused by messing some nodules spicily when these nodules' diameter be less than 10 mm. So, the CAD system is an essential assistant to the radiologist in this case of nodule detection, and it contributed to reducing time consumption in nodules detection; moreover, it applied more accuracy in this field. The objective of this paper is to follow up on current and previous work on lung cancer detection and lung nodule diagnosis. This literature dealt with a group of specialized systems in this field quickly and showed the methods used in them. It dealt with an emphasis on a system based on deep learning involving neural convolution networks.
Fundamentals and Innovations in medical imaging.pptxHemant Rakesh
1. Medical imaging plays a key role in healthcare but errors can be life threatening or fatal, costing billions per year.
2. Artificial intelligence techniques like deep learning can help reduce errors by automating tasks like lesion detection, image segmentation, report generation from medical scans.
3. However, developing accurate AI systems requires large curated datasets which are currently lacking due to privacy and ethical concerns.
Early detection of cancer is the most promising way to enhance a patient's chance for survival. This paper presents a computer-aided classification method using computed tomography (CT) images of the lung based on ensemble of three classifiers including MLP, KNN and SVM. In this study, the entire lung is first segmented from the CT images and specific features like Roundness, Circularity, Compactness, Ellipticity, and Eccentricity are calculated from the segmented images. These morphological features are used for classification process in a way that each classifier makes its own decision. Finally, majority voting method is used to combine decisions of this ensemble system. The performance of this system is evaluated using 60 CT scans collected by Lung Image Database Consortium (LIDC) and the results show good improvement in diagnosing of pulmonary nodules.
Semantic Web Technologies as a Framework for Clinical InformaticsChimezie Ogbuji
1. The document discusses using semantic web technologies like RDF and SPARQL to store and query patient data from electronic health records to enable cohort identification and clinical research.
2. Each patient record is stored as a named graph in an RDF dataset that can then be queried using SPARQL. This allows parallel processing and optimizing queries to search within patient graphs.
3. Challenges include limitations of SPARQL for representing complex queries and a lack of standard medical ontologies, leading the authors to develop their own patient record ontology.
Exploiting Cognitive Computing and Frame Semantic Features for Biomedical Doc...Syed Muhammad Ali Hasnain
The document discusses using cognitive computing and frame semantic features for biomedical document clustering. Specifically:
- It explores using IBM Watson's Alchemy Language API and Framester to extract concepts, keywords, entities and semantic frames from medical reports to represent them as vectors.
- The vectors are used to cluster the reports using hierarchical and k-means clustering with cosine and Euclidean distance metrics.
- Clustering quality is evaluated using the Silhouette coefficient, showing semantic features led to better clusters than TF-IDF alone.
1. The document discusses applying 3D printing to medical imaging by discussing medical image modeling.
2. It covers topics like virtual surgery modeling, 3D printers, image scanners, requirements for 3D printed medical models, and the medical imaging workflow from acquisition to 3D printing and post-processing.
3. Key aspects of medical image-based 3D printing discussed are image segmentation, surface modeling, and an in-house software for virtual simulated surgery.
Making Radiology AI Models more robust: Federated Learning and other Approachesimgcommcall
Daniel Rubin discusses approaches for making AI models more robust by accessing larger amounts of medical image data. Centralized data pooling is challenging due to data sharing barriers. Federated learning, which trains models across sites without sharing patient data, is presented as an alternative. However, federated learning requires common data standards for image annotations. The talk explores existing annotation standards and tools that could enable federated learning to leverage multi-institutional medical image data for developing more generalizable AI models.
This document provides an agenda for the NCI Imaging Informatics Webinar held on July 6, 2020. The agenda included presentations on distributed learning of deep learning in medical imaging, an update on the MedICI website, an update on The Cancer Imaging Archive, and announcements about future community calls, the community call wiki page, and where recordings could be accessed. The next scheduled community calls were listed as August 3, 2020 and September 14, 2020.
More Related Content
Similar to Standardized representation of the LIDC annotations using DICOM
Slides presented at the Molecular Med Tri-Con 2018 Precision Medicine, "Emerging Role of Radiomics in Precision Medicine" (http://www.triconference.com/Precision-Medicine/)
Abstract
The goal of this talk is to discuss the role of data standards, and specifically the Digital Imaging and Communication in Medicine (DICOM) standard, in supporting radiomics research. From the clinical images, to the storage of image annotations and results of radiomics analysis, standardization can potentially have transformative effect by enabling discovery, reuse and mining of the data, and integration of the radiomics workflows into the healthcare enterprise.
Lessons Learned from the DICOM Standardization Effort Lessons Learned from ...MedicineAndDermatology
DICOM is an international standard for communicating medical imaging information and related data between devices. It has been developed over 18 years through collaboration between industry and clinical experts. Maintaining and evolving standards like DICOM requires significant organizational infrastructure and ongoing effort. Key aspects of the DICOM standard include its use of tagged data elements, object orientation, network services, privacy/security features, and support for structured reporting.
The document describes a deep learning framework for joint segmentation and classification of lung nodules in CT images. It uses a VGG19 network-assisted VGG-SegNet model for segmentation, extracting deep features from VGG19, and combining with handcrafted features for classification. The methodology involves collecting CT images, segmenting nodules using VGG-SegNet, extracting deep and handcrafted features, concatenating the features, and classifying images using various classifiers. Experimental results on LIDC-IDRI and Lung-PET-CT-Dx datasets show the proposed approach achieves 97.83% accuracy using an SVM-RBF classifier.
3D Slicer is an open-source software platform for medical image computing and visualization that allows users to load, segment, register, and analyze medical images from various modalities like MRI, CT, and DICOM. It provides tools for tasks such as interactive image segmentation, registration, visualization of diffusion tensor images and tractography, and integration of functional and anatomical data. Slicer has been used in applications such as surgical planning, virtual endoscopy, and pre-operative mapping of functional areas to avoid during surgery.
Development of Computational Tool for Lung Cancer Prediction Using Data MiningEditor IJCATR
The requirement for computerization of detection of lung cancer disease arises ever since recent-techniques which involve
manual-examination of the blood smear as the first step toward diagnosis. This is quite time-consuming, and their accurateness depends
upon the ability of operator's. So, prevention of lung cancer is very essential. This paper has surveyed various techniques used by previous
authors like ANN (Artificial Neural Network), image processing, LDA (Linear Dependent Analysis), SOM (Self Organizing Map) etc.
Statistical Feature-based Neural Network Approach for the Detection of Lung C...CSCJournals
Lung cancer, if successfully detected at early stages, enables many treatment options, reduced risk of invasive surgery and increased survival rate. This paper presents a novel approach to detect lung cancer from raw chest X-ray images. At the first stage, we use a pipeline of image processing routines to remove noise and segment the lung from other anatomical structures in the chest X-ray and extract regions that exhibit shape characteristics of lung nodules. Subsequently, first and second order statistical texture features are considered as the inputs to train a neural network to verify whether a region extracted in the first stage is a nodule or not . The proposed approach detected nodules in the diseased area of the lung with an accuracy of 96% using the pixel-based technique while the feature-based technique produced an accuracy of 88%.
1- List of modalities and study types
2- CT/US/DX Study Structure
3- DICOM composite instance IOD information module
4- Storage of DICOM image in PACS server
5- Imaging Data
6- Query and Retrieval from PACS
7- Window Width/ Window Center
8- DCM File Sections
The MAGIC-5 lung CAD system uses three parallel approaches - region growing, virtual ants, and voxel-based neural networks - to detect and classify lung nodules in CT scans. It was validated on three databases and performs competitively with state-of-the-art systems. In the ANODE09 international competition, the three MAGIC-5 CADs achieved scores between 0.25-0.29 for detecting pulmonary nodules, outperforming other participating CAD systems. The MAGIC-5 project aims to support medical diagnosis and allow large-scale image analysis through developing models and algorithms for biomedical image analysis.
The swings and roundabouts of a decade of fun and games with Research Objects Carole Goble
Research Objects and their instantiation as RO-Crate: motivation, explanation, examples, history and lessons, and opportunities for scholarly communications, delivered virtually to 17th Italian Research Conference on Digital Libraries
Lung Cancer Detection using transfer learning.pptx.pdfjagan477830
Lung cancer is one of the deadliest cancers worldwide. However, the early detection of lung cancer significantly improves survival rate. Cancerous (malignant) and noncancerous (benign) pulmonary nodules are the small growths of cells inside the lung. Detection of malignant lung nodules at an early stage is necessary for the crucial prognosis.
The classification of different types of tumors is of great importance in cancer diagnosis and its drug discovery. Cancer classification via gene expression data is known to contain the keys for solving the fundamental problems relating to the diagnosis of cancer. The recent advent of DNA microarray technology has made rapid monitoring of thousands of gene expressions possible. With this large quantity of gene expression data, scientists have started to explore the opportunities of classification of cancer using a gene expression dataset. To gain a profound understanding of the classification of cancer, it is necessary to take a closer look at the problem, the proposed solutions, and the related issues altogether. In this research thesis, I present a new way for Leukemia classification using the latest AI technique of Deep learning using Google TensorFlow on gene expression data.
A discriminative-feature-space-for-detecting-and-recognizing-pathologies-of-t...Damian R. Mingle, MBA
Each year it has become more and more difficult for healthcare providers to determine if a patient has a pathology
related to the vertebral column. There is great potential to become more efficient and effective in terms of quality
of care provided to patients through the use of automated systems. However, in many cases automated systems
can allow for misclassification and force providers to have to review more causes than necessary. In this study, we
analyzed methods to increase the True Positives and lower the False Positives while comparing them against stateof-the-art
techniques in the biomedical community. We found that by applying the studied techniques of a data-driven
model, the benefits to healthcare providers are significant and align with the methodologies and techniques utilized
in the current research community.
Computer-aided diagnostic system kinds and pulmonary nodule detection efficacyIJECEIAES
This paper summarizes the literature on computer-aided detection (CAD) systems used to identify and diagnose lung nodules in images obtained with computed tomography (CT) scanners. The importance of developing such systems lies in the fact that the process of manually detecting lung nodules is painstaking and sequential work for radiologists, as it takes a long time. Moreover, the pulmonary nodules have multiple appearances and shapes, and the large number of slices generated by the scanner creates great difficulty in accurately locating the lung nodules. The handcraft nodules detection process can be caused by messing some nodules spicily when these nodules' diameter be less than 10 mm. So, the CAD system is an essential assistant to the radiologist in this case of nodule detection, and it contributed to reducing time consumption in nodules detection; moreover, it applied more accuracy in this field. The objective of this paper is to follow up on current and previous work on lung cancer detection and lung nodule diagnosis. This literature dealt with a group of specialized systems in this field quickly and showed the methods used in them. It dealt with an emphasis on a system based on deep learning involving neural convolution networks.
Fundamentals and Innovations in medical imaging.pptxHemant Rakesh
1. Medical imaging plays a key role in healthcare but errors can be life threatening or fatal, costing billions per year.
2. Artificial intelligence techniques like deep learning can help reduce errors by automating tasks like lesion detection, image segmentation, report generation from medical scans.
3. However, developing accurate AI systems requires large curated datasets which are currently lacking due to privacy and ethical concerns.
Early detection of cancer is the most promising way to enhance a patient's chance for survival. This paper presents a computer-aided classification method using computed tomography (CT) images of the lung based on ensemble of three classifiers including MLP, KNN and SVM. In this study, the entire lung is first segmented from the CT images and specific features like Roundness, Circularity, Compactness, Ellipticity, and Eccentricity are calculated from the segmented images. These morphological features are used for classification process in a way that each classifier makes its own decision. Finally, majority voting method is used to combine decisions of this ensemble system. The performance of this system is evaluated using 60 CT scans collected by Lung Image Database Consortium (LIDC) and the results show good improvement in diagnosing of pulmonary nodules.
Semantic Web Technologies as a Framework for Clinical InformaticsChimezie Ogbuji
1. The document discusses using semantic web technologies like RDF and SPARQL to store and query patient data from electronic health records to enable cohort identification and clinical research.
2. Each patient record is stored as a named graph in an RDF dataset that can then be queried using SPARQL. This allows parallel processing and optimizing queries to search within patient graphs.
3. Challenges include limitations of SPARQL for representing complex queries and a lack of standard medical ontologies, leading the authors to develop their own patient record ontology.
Exploiting Cognitive Computing and Frame Semantic Features for Biomedical Doc...Syed Muhammad Ali Hasnain
The document discusses using cognitive computing and frame semantic features for biomedical document clustering. Specifically:
- It explores using IBM Watson's Alchemy Language API and Framester to extract concepts, keywords, entities and semantic frames from medical reports to represent them as vectors.
- The vectors are used to cluster the reports using hierarchical and k-means clustering with cosine and Euclidean distance metrics.
- Clustering quality is evaluated using the Silhouette coefficient, showing semantic features led to better clusters than TF-IDF alone.
1. The document discusses applying 3D printing to medical imaging by discussing medical image modeling.
2. It covers topics like virtual surgery modeling, 3D printers, image scanners, requirements for 3D printed medical models, and the medical imaging workflow from acquisition to 3D printing and post-processing.
3. Key aspects of medical image-based 3D printing discussed are image segmentation, surface modeling, and an in-house software for virtual simulated surgery.
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Making Radiology AI Models more robust: Federated Learning and other Approachesimgcommcall
Daniel Rubin discusses approaches for making AI models more robust by accessing larger amounts of medical image data. Centralized data pooling is challenging due to data sharing barriers. Federated learning, which trains models across sites without sharing patient data, is presented as an alternative. However, federated learning requires common data standards for image annotations. The talk explores existing annotation standards and tools that could enable federated learning to leverage multi-institutional medical image data for developing more generalizable AI models.
This document provides an agenda for the NCI Imaging Informatics Webinar held on July 6, 2020. The agenda included presentations on distributed learning of deep learning in medical imaging, an update on the MedICI website, an update on The Cancer Imaging Archive, and announcements about future community calls, the community call wiki page, and where recordings could be accessed. The next scheduled community calls were listed as August 3, 2020 and September 14, 2020.
The document discusses the American College of Radiology's (ACR) efforts to advance the appropriate use of data science and artificial intelligence in radiology. It provides details on ACR's Data Science Institute (DSI) programs and initiatives to help define, validate, and monitor AI algorithms. These include ACR Define-AI, ACR Assess-AI, and ACR Certify-AI. The DSI aims to establish ACR as a leader in the radiology AI ecosystem and ensure the safe, effective integration of AI into clinical practice and medical education. The rest of the document discusses ACR's AI-LAB program to pilot AI algorithms and collect clinical feedback at partner sites.
The document summarizes the agenda for an NCI Imaging Informatics Webinar on April 6, 2020. The webinar included presentations on PathPresenter, a web-based digital pathology and image viewer, and an update on The Cancer Imaging Archive. It was announced that the webinar recordings and slides would be made available online on the NCI Imaging Community Call Wiki page and SlideShare account. The next webinars were scheduled for May 4 and June 1, 2020.
The Medical Segmentation Decathlon provides a benchmark for evaluating the generalizability of semantic segmentation algorithms across a variety of anatomical structures and imaging modalities. The Decathlon includes 10 segmentation tasks with over 2,600 unique patient datasets. In Phase 1 of the challenge, participants developed algorithms to segment the structures and submitted results for evaluation. The top performing methods for each task are identified based on Dice scores and boundary accuracy metrics. Phase 2 will involve applying the previously developed algorithms to new datasets without modifications, to further evaluate generalizability.
The January 6, 2020 Imaging Community Call featured presentations on the Medical Segmentation Decathlon, Imaging Data Commons updates, NBIA updates, and TCIA updates. Announcements were made about recording the presentations, the community call wiki page with recordings and slides, and the next scheduled community calls in February and March 2020.
NCI Cancer Research Data Commons - Overviewimgcommcall
The NCI Cancer Research Data Commons aims to enable sharing of diverse cancer research data across institutions by providing easy access to data stored in domain-specific repositories through a common authentication and authorization mechanism. It utilizes a framework of reusable components including data nodes, a cancer data aggregator, and cloud resources to integrate genomic, imaging, proteomic, and other data types while controlling access. The goals are to facilitate discovery and analysis tools as well as sustainably sharing data publicly to advance cancer research.
Imaging Data Commons (IDC) - Introduction and intital approachimgcommcall
The document introduces the Imaging Data Commons (IDC) which will connect researchers to cancer image collections, metadata, and tools for searching, viewing, and analyzing imaging data and related data types. The IDC will build on existing technologies and collaborations, with an initial focus on radiology and pathology images stored in DICOM format. It will utilize public cancer image collections from the Cancer Imaging Archive and integrate with other nodes in the Cancer Research Data Commons. The team has experience with open-source imaging tools, cloud infrastructure, and standards development. The initial implementation phases will focus on defining the data model and use cases, evaluating existing tools, and developing a minimal viable product hosted on the Google Cloud platform.
The document outlines the agenda for an Imaging Community Call on July 1, 2019. The agenda included welcome remarks, overviews of the Clinical Proteomic Tumor Analysis Consortium project and how its image, proteomic, and genomic data can be accessed through various data portals. It concluded with announcements about joining a community call group, an imaging community call wiki, and details on the next call in August 2019 focusing on tissue cytometry presentations.
The document discusses the Office of Cancer Clinical Proteomics Research (OCCPR) and its tumor characterization programs, including the Clinical Proteomic Tumor Analysis Consortium (CPTAC). CPTAC applies proteogenomics to characterize tumors and generate public resources of proteomic and genomic data. It builds on data from The Cancer Genome Atlas (TCGA) by characterizing proteins and genes to understand cancer. CPTAC data, along with clinical and genomic data, can be found on the Genomic Data Commons (GDC) portal. The document provides information on accessing, exploring, and analyzing CPTAC and other proteomic data deposited on the GDC.
CPTAC Data Portal and Proteomics Data Commonsimgcommcall
The CPTAC Data Coordinating Center houses proteomic datasets from CPTAC studies in its public data portal and assay portal. It analyzes data through a common pipeline and enables high-speed access. The Proteomic Data Commons is being developed to provide unified access to mass spectrometry data from multiple sources and allow analysis tools to access data in the cloud. It currently hosts data from CPTAC studies and is working to integrate with other cancer research data clouds. The goal is to improve data sharing, reuse and reproducibility across proteomic studies.
The National Cancer Institute’s Clinical Proteomic Tumor Analysis Consortium (CPTAC) is a national effort to accelerate the understanding of the molecular basis of cancer through the application of large-scale proteome and genome analysis, or proteogenomics.
The PRISM semantic integration approach aims to integrate diverse datasets from The Cancer Imaging Archive by representing data using shared ontologies. This removes obstacles to combining data about the same individuals from different sources. The Arkansas Image Enterprise System (ARIES) is an instance of PRISM that integrates imaging, clinical, and cognitive data from three Parkinson's disease cohorts. Semantic representation allows linking image volumes to cognitive assessments across cohorts. Ongoing work expands data integration and develops semantic query tools.
New manual contours for evaluating lung segmentation algorithms, additional MRI sequences for prostate data, and three new pathology datasets were added to TCIA. Diffusion and dynamic contrast MRI were added to the QIN-Prostate-Repeatability collection. 2018 Crowds Cure Cancer data was also released. The CPTAC lung adenocarcinoma proteomics/clinical discovery cohort data is now available. An upcoming Community Call will discuss the CPTAC program and data access policies. Multiple TCIA datasets were used in an AI cancer detection paper covered by major media outlets. A paper also discussed vulnerabilities in radiomic signature development using the NSCLC dataset. The NBIA data portal was updated with species selection and automatic inclusion of annotation files.
The document summarizes the agenda for an Imaging Community Call on June 3, 2019. The agenda included welcome remarks, updates on the PRISM project and TCIA, and announcements. The announcements section provided information on joining the community call mailing list, the Imaging Community Call Wiki page, and the next scheduled call on July 1, 2019.
This document summarizes the new features and improvements in the NBIA 7.0 GA Community Version release, including a new search interface, support for fielded text search, an improved data retriever application, upgrades for better Java support, and testing of load balancing capabilities. It also provides information on how to obtain the community version release and where to find additional documentation and support resources.
The document summarizes the agenda for an Imaging Community Call on May 6, 2019. The agenda included welcome remarks, updates on ITCR, TCIA, CPTAC SIG, and NBIA 7.0GA, and announcements. Under announcements, it invites the community to future calls, topics for discussion, and links to the community call wiki and SlideShare page for presentation materials. The next scheduled calls were for June 3rd with a PRISM update and July 1st.
Beyond the Basics of A/B Tests: Highly Innovative Experimentation Tactics You...Aggregage
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End-to-end pipeline agility - Berlin Buzzwords 2024Lars Albertsson
We describe how we achieve high change agility in data engineering by eliminating the fear of breaking downstream data pipelines through end-to-end pipeline testing, and by using schema metaprogramming to safely eliminate boilerplate involved in changes that affect whole pipelines.
A quick poll on agility in changing pipelines from end to end indicated a huge span in capabilities. For the question "How long time does it take for all downstream pipelines to be adapted to an upstream change," the median response was 6 months, but some respondents could do it in less than a day. When quantitative data engineering differences between the best and worst are measured, the span is often 100x-1000x, sometimes even more.
A long time ago, we suffered at Spotify from fear of changing pipelines due to not knowing what the impact might be downstream. We made plans for a technical solution to test pipelines end-to-end to mitigate that fear, but the effort failed for cultural reasons. We eventually solved this challenge, but in a different context. In this presentation we will describe how we test full pipelines effectively by manipulating workflow orchestration, which enables us to make changes in pipelines without fear of breaking downstream.
Making schema changes that affect many jobs also involves a lot of toil and boilerplate. Using schema-on-read mitigates some of it, but has drawbacks since it makes it more difficult to detect errors early. We will describe how we have rejected this tradeoff by applying schema metaprogramming, eliminating boilerplate but keeping the protection of static typing, thereby further improving agility to quickly modify data pipelines without fear.
Standardized representation of the LIDC annotations using DICOM
1. Andrey Fedorov, Matthew Hancock, David Clunie,
Mathias Brockhausen, Jonathan Bona, Justin Kirby, John Freymann,
Steve Pieper, Hugo Aerts, Ron Kikinis, Fred Prior
7 January 2019 for CBIIT Imaging Community
Contact: andrey.fedorov@gmail.com
Standardized representation of
the LIDC annotations using DICOM
2. Lung Imaging Database Consortium (LIDC)
● NCI-initiated in 2000, 5 institutions selected through
peer-review process
● Goal: develop a public web-accessible resource
containing
○ an image repository of screening and diagnostic thoracic CT
scans
○ associated metadata such as technical scan parameters (e.g., slice
thickness, tube current, and re- construction algorithm and
patient information (e.g., age, gender, and pathologic diagnosis)
○ nodule truth information based on the subjective assessments of
mul- tiple experienced radiologists (e.g., lesion category, nodule
outlines, and subtlety ratings)
○ .
○
Armato et al. Lung Image Database Consortium: Developing a Resource for the Medical Imaging Research Community1. Radiology 232, 739–748 (2004).
Armato et al. The Lung Image Database Consortium (LIDC) and Image Database Resource Initiative (IDRI): a completed reference database of lung nodules on CT scans.
Med. Phys. 38, 915–931 (2011). 2
3. TCIA LIDC-IDRI collection
● One of the largest and most popular annotated collection of TCIA
● Utilized in numerous challenges
● 1000+ citations, used to enable numerous derivative studies
Kalpathy-Cramer, J., Freymann, J. B., Kirby, J. S., Kinahan, P. E. & Prior, F. W. Quantitative Imaging
Network: Data Sharing and Competitive AlgorithmValidation Leveraging The Cancer Imaging Archive.
Transl. Oncol. 7, 147–152 (2014).
3
https://wiki.cancerimagingarchive.net/display/Public/LIDC-IDRI
4. LIDC groups of findings
1. “nodules ≥ 3 mm”: any lesion considered to be a nodule with greatest
in-plane dimension in the range 3–30 mm regardless of presumed
histology;
2. “nodules < 3 mm”: any lesion considered to be a nodule with greatest
in-plane dimension less than 3 mm that is not clearly benign;
3. “non-nodules ≥ 3 mm”: any other pulmonary lesion, such as an apical
scar, with greatest in-plane dimension greater than or equal to 3 mm
that does not possess features consistent with those of a nodule.
Armato et al. The Lung Image Database Consortium (LIDC) and Image Database Resource Initiative (IDRI): a
completed reference database of lung nodules on CT scans. Med. Phys. 38, 915–931 (2011).
4
5. LIDC expert review process
Each of the four radiologists independently reviewed all of the scans in a
“blinded” phase to identify all of the findings from the three groups
above.
For each finding identified by a given radiologist as a “nodule ≥ 3 mm”,
outlines were constructed in each slice where that nodule appear, while
for the other two categories only the approximate center of mass was
annotated.
In the subsequent “unblinded” read phase each radiologist had access to
the categories assigned and annotations for the nodules, and “a
radiologist’s own marks then could be left unchanged, deleted, switched
in terms of lesion category, or additional marks could be added”.
After the unblinded phase each radiologist assessed subjective
characteristics of “nodules < 3 mm”, such as spiculation, subtlety, etc
Armato et al. The Lung Image Database Consortium (LIDC) and Image Database Resource Initiative (IDRI): a
completed reference database of lung nodules on CT scans. Med. Phys. 38, 915–931 (2011).
5
8. Consequences of using project-specific XML representation
● No single conventional tool that can render annotations over the image
● Annotations need to be managed separately from images
○ Accessed as a ZIP file
● Linked to images via DICOM Study/InstanceUID, patient information separate
from the XML
● Conventions about stored content need to be parsed from the accompanying
documentation and annotated XML example
● Conversion of contours into image-space is error-prone
○ inclusion/exclusion contours, inclusion or exclusion of boundary pixels, coordinate space
conventions
● Representation not harmonized with any conventions for any other TCIA
collection
8
10. DICOM - preparing for the unknown, since 1983
● Standard for images and image-related evidence
● “The HOW”: Fixed syntax, encoding, compression …
○ (hierarchical) list of attribute/value pairs
● “The WHAT”: Object definitions
○ Object-specific required and optional attributes
○ Constraints and values sets
○ Common data elements / lexicons / ontologies
● For all object types
○ Dates, patient IDs, study, series - for every object
○ Unique identifiers
● References to related evidence
○ Provenance of data acquisition, analysis
● + networking, web, de-identification …
10
Horii SC. DICOM. In: Kagadis GC, Langer SG, editors.
Informatics in medical imaging. 2011. p. 41–67.
11. pylidc https://pylidc.github.io/
“pylidc is an Object-relational mapping (using SQLAlchemy) for the data provided in the LIDC dataset. This
means that the data can be queried in SQL-like fashion, and that the data are also objects that add additional
functionality via functions that act on instances of data obtained by querying for particular attributes”
● Open source, python
● Easy to install on any platform
● Used by others!
● More than LIDC parser
● Supported
○ Thanks Matt Hancock!
11
Hancock, M. C. & Magnan, J. F. Lung nodule malignancy classification using only radiologist-quantified image features as inputs to statistical learning
algorithms: probing the Lung Image Database Consortium dataset with two statistical learning methods. J Med Imaging (Bellingham) 3, 044504 (2016).
12. dcmqi https://github.com/qiicr/dcmqi
“dcmqi (DICOM for Quantitative Imaging) is a free, open source library that can help
with the conversion between imaging research formats and the standard DICOM
representation for image analysis results”
● DICOM Segmentation object
● DICOM Parametric map object
● DICOM Region-based measurements Structured Report
12
Herz, C., Fillion-Robin, J.-C., Onken, M., Riesmeier, J., Lasso, A., Pinter, C., Fichtinger, G., Pieper, S., Clunie, D., Kikinis, R. & Fedorov, A. dcmqi: An
Open Source Library for Standardized Communication of Quantitative Image Analysis Results Using DICOM. Cancer Res. 77, e87–e90 (2017).
13. LIDC nodule segmentations
● (x,y) coordinates of the contour points for image slices defined by DICOM
SOPInstanceUID
● Contours can be “inclusion” or exclusion
● Contour points are not part of the segmentation!
13
https://github.com/notmatthancock/pylidc/issues/15 https://wiki.cancerimagingarchive.net/display/Public/LIDC-IDRI
14. Image Segmentations - as DICOM
14
Spatial labeling of the voxels of
interest +
● Patient information
● Unique identifiers
● References to the segmented
image
● Ontology-enabled semantics
(SNOMED-CT, RadLex, etc)
● Segmentation algorithm
● Single file, efficient storage,
multiple occupancy voxels
● Presentation color
15. LIDC segmentations: conversion process
● One nodule annotation per DICOM Segmentation object
● Use pylidc to get numpy array for each nodule segmentation
○ Also use pylidc clustering functionality to assign segmentations to individual nodules
● Use ITK-python to reorient the array, add origin/spacing/directions and save
as a 3D volume
● Populate metadata JSON
● Use dcmqi to write DICOM Segmentation object
● Conversion process includes pointer to the source CT series
○ Propagate composite context
○ Establish references to the source series analyzed
15https://itkpythonpackage.readthedocs.io
18. DICOM Structured Reporting (SR)
● Extends the DICOM standard beyond attributes in
"image header”
● Into a “tree” of structured content
● Each tree node (“content item”) is a "name-value"
pair
● Or a “container” (provides an outline of “headings”)
● Name is always coded, value may or may not be
● Generic framework - recursively nested content of
unbounded complexity
● Complexity constrained for specific use cases by
"templates"
18
19. DICOM SR TID1500: measurements + characterizations
● TID 1500 “Measurement report”
● General-purpose template
● Reuses existing templates
● Planar or volumetric region definition
● Qualitative characterizations
19
Example from Fedorov et al. DICOM for quantitative imaging biomarker
development: a standards based approach to sharing clinical data and
structured PET/CT analysis results in head and neck cancer research.
PeerJ 4, e2057 (2016).
20. DICOM SR approach to coded content
● Qualitative assessment reporting
○ Coded concept
○ Coded value
● Coded = (Code Value, Coding Scheme Designator, Code Meaning) tuple
○ E.g., ("CodeMeaning": "Lung","CodingSchemeDesignator": "SRT","CodeValue": "T-28000")
● Sources of codes
○ Standard dictionaries: SNOMED, NCIt, RadLex, UCUM, …
○ “Private” dictionaries: when standard dictionaries do not contian suitable terms, indicated
by “99” prefix of the Coding Scheme Designator
20
21. Harmonization of LIDC with existing terminologies
● Review existing lexicons: NCI Thesaurus, RadLex, SNOMED (only those
terms included in the DICOM standard)
○ BioPortal http://bioportal.bioontology.org/
○ Ontology Lookup Service https://www.ebi.ac.uk/ols
● Imaging Biomarker Standardization Initiative (IBSI) lexicon
● “99LIDCQIICR” coding scheme for codes not located in existing lexicons
21
Zwanenburg, A., Leger, S., Vallières, M., Löck, S. & for the Image Biomarker Standardisation Initiative. Image
biomarker standardisation initiative. arXiv [cs.CV] (2016). at http://arxiv.org/abs/1612.07003
23. Coding concept values
● Some concept values are categorical (e.g., “Internal structure”)
● Others are ordinal scores
○ With or without specific assignment of meaning
23
24. Results of mapping
● Concepts (9 total):
○ 6 mapped to NCIt
○ 1 to RadLex
○ 1 to IBSI
○ 1 not mapped (99LIDCQIICR)
● Values (45 total):
○ 29 not mapped (99LIDCQIICR)
○ 12 to RadLex
○ 4 to NCIt
24
Coordinated with the Opulencia et al. work after v1!
25. DICOM SR conversion process
● One nodule characterization per DICOM Segmentation object
● Use pylidc to get characterizations for each nodule
○ Also use pylidc to get nodule volume, surface area, 2D diameter
● Populate metadata JSON
● Use dcmqi to write DICOM SR object
● Conversion process includes pointer to the source CT series and DICOM
Segmentation object
○ Propagate composite context
○ Establish references to the source series analyzed
○ Establish references to the segmentation associated with the characterizations
25
28. Status
● Conversion results available on TCIA since RSNA 2018 (Google Drive folder)
● Conversion pipeline script is available on GitHub
● Details in preprint (v1, will be updated!) - feedback is welcomed!
28
https://doi.org/10.7287/peerj.preprints.27378
29. ● DICOM Segmentation object: supported in multiple tools (see
https://dicom4qi.readthedocs.io/)
○ Open source: 3D Slicer, ePAD, MITK, MeVisLab, OHIF Viewer + dcmjs
○ Commercial: Brainlab, Siemens syngo.via, Terarecon (more in development)
● DICOM TID1500 SR:
○ 3D Slicer, ePAD can read and write
○ Pixelmed tools
○ Used in RSNA Crowds Cure Cancer for planar annotations+measurements
○ General-purpose DCMTK tools can be used to convert to XML representation (both
atribute-level and SR tree level)
● Conversion of measurements into tabulated form
○ https://github.com/QIICR/dcm2tables
LIDC DICOM in context: Support in tools
29
31. LIDC DICOM in context: harmonization of TCIA derived data
● Numerous other collections follow “the DICOM
approach” for derived data
○ QIN-HEADNECK: head and neck cancer, PET/CT, SUV,
segmentations, SUV quantification
○ QIN-PROSTATE-Repeatability: prostate cancer,
multiparametric MRI, segmentations, measurements
○ TCIA-LGG and TCIA-GBM: glioblastoma, multiparametric
MRI, segmentations
● Extensible with other types of derived data
○ Framework for analysis from multiple groups/tools to be
combined
○ pyradiomics supports output of radiomics features as
DICOM SR TID1500
○ IBSI lexicon of radiomics features is being integrated with
the DICOM Standard 31
https://peerj.com/articles/2057/
https://www.nature.com/articles/sdata2018281
32. Queries like this become possible:
Find all subjects that have a
neoplasm segmented using
automatic method at the base of
tongue larger than 5 cc that show
Glycolysis Within First Quarter
of Intensity Range above 10
grams
32
33. Acknowledgments
This project has been funded in part with federal funds from the National Cancer Institute,
National Institutes of Health under Contract No. HHSN261200800001E, and by the NIH grants
U24 CA180918, U24 CA199460 and U01 CA190234. Under this contract the University of
Arkansas for Medical Sciences is funded by Leidos Biomedical Research subcontract 16X011.
The content of this presentation does not necessarily reflect the views or policies of the
Department of Health and Human Services, nor does mention of trade names, commercial
products, or organizations imply endorsement by the U.S. Government.
We acknowledge NCI-led Informatics Technology for Cancer Research (ITCR) and Quantitative
Imaging Network (QIN). This project would not be possible without those network efforts and
support!
We are grateful to the NCI and LIDC project for making valuable dataset publicly available in the
TCIA LIDC-IDRI collection, and to Sam Armato and the LIDC team for responding to our
questions that came up in the process of conversion.
33
http://qiicr.org