scholarly journals Histone Methyltransferases Useful in Gastric Cancer Research

2021 ◽  
Vol 20 ◽  
pp. 117693512110398
Author(s):  
Dafne Alejandra Reyes ◽  
Victor Manuel Saure Sarría ◽  
Marcela Salazar-Viedma ◽  
Vívian D’Afonseca
Keyword(s):  
Gastric Cancer ◽  
Cancer Control ◽  
Data Set ◽  
Histone Methyltransferases ◽  
Knowledge Based ◽  
Diagnosis And Prognosis ◽  
Genes Expression ◽  
Public Data ◽  
Stomach Adenocarcinoma ◽  
Somatic Copy Number Alteration

Gastric cancer (GC) is one of the most frequent tumors in the world. Stomach adenocarcinoma is a heterogeneous tumor, turning the prognosis prediction and patients’ clinical management difficult. Some diagnosis tests for GC are been development using knowledge based in polymorphisms, somatic copy number alteration (SCNA) and aberrant histone methylation. This last event, a posttranslational modification that occurs at the chromatin level, is an important epigenetic alteration seen in several tumors including stomach adenocarcinoma. Histone methyltransferases (HMT) are the proteins responsible for the methylation in specific amino acids residues of histones tails. Here, were presented several HMTs that could be relating to GC process. We use public data from 440 patients with stomach adenocarcinoma. We evaluated the alterations as SCNAs, mutations, and genes expression level of HMTs in these aforementioned samples. As results, it was identified the 10 HMTs most altered (up to 30%) in stomach adenocarcinoma samples, which are the PRDM14, PRDM9, SUV39H2, NSD2, SMYD5, SETDB1, PRDM12, SUV39H1, NSD3, and EHMT2 genes. The PRDM9 gene is among most mutated and amplified HMTs within the data set studied. PRDM14 is downregulated in 79% of the samples and the SUV39H2 gene is down expressed in patients with recurred/progressed disease. Several HMTs are altered in many cancers. It is important to generate a genetic atlas of alterations of cancer-related genes to improve the understanding of tumorigenesis events and to propose novel tools of diagnosis and prognosis for the cancer control.

No Silver Bullet

2012 ◽  
Vol 7 (4) ◽  
pp. 48-58 ◽  
Author(s):  
Nan Zhang ◽  
Liam O’Neill ◽  
Gautam Das ◽  
Xiuzhen Cheng ◽  
Heng Huang
Keyword(s):  
Domain Knowledge ◽  
Personal Information ◽  
Hospital Data ◽  
Data Set ◽  
Discharge Data ◽  
Knowledge Based ◽  
Privacy Leakage ◽  
Public Data ◽  
Related Group ◽  
Data Files

In accordance with HIPAA regulations, patients’ personal information is typically removed or generalized prior to being released as public data files. However, it is not known if the standard method of de-identification is sufficient to prevent re-identification by an intruder. The authors conducted analytical processing to identify security vulnerabilities in the protocols to de-identify hospital data. Their techniques for discovering privacy leakage utilized three disclosure channels: (1) data inter-dependency, (2) biomedical domain knowledge, and (3) suppression algorithms and partial suppression results. One state’s inpatient discharge data set was used to represent the current practice of de-identification of health care data, where a systematic approach had been employed to suppress certain elements of the patient’s record. Of the 1,098 records for which the hospital ID was suppressed, the original hospital ID was recovered for 616 records, leading to a nullification rate of 56.1%. Utilizing domain knowledge based on the patient’s Diagnosis Related Group (DRG) code, the authors recovered the real age of 64 patients, the gender of 83 male patients and 713 female patients. They also successfully identified the ZIP code of 1,219 patients. The procedure used to de-identify hospital records was found to be inadequate to prevent disclosure of patient information. As the masking procedure described was found to be reversible, this increases the risk that an intruder could use this information to re-identify individual patients.

Computer-Aided Diagnosis in Jaundice: Comparison of Knowledge-based and Probabilistic Approaches

1996 ◽  
Vol 35 (01) ◽  
pp. 41-51 ◽  
Author(s):  
F. Molino ◽  
D. Furia ◽  
F. Bar ◽  
S. Battista ◽  
N. Cappello ◽  
...  
Keyword(s):  
Clinical Presentation ◽  
Clinical Information ◽  
Diagnostic Value ◽  
Clinical Findings ◽  
Clinical Documentation ◽  
Data Set ◽  
Knowledge Based ◽  
Number Of Patients ◽  
Support Tools ◽  
Aided Diagnosis

AbstractThe study reported in this paper is aimed at evaluating the effectiveness of a knowledge-based expert system (ICTERUS) in diagnosing jaundiced patients, compared with a statistical system based on probabilistic concepts (TRIAL). The performances of both systems have been evaluated using the same set of data in the same number of patients. Both systems are spin-off products of the European project Euricterus, an EC-COMACBME Project designed to document the occurrence and diagnostic value of clinical findings in the clinical presentation of jaundice in Europe, and have been developed as decision-making tools for the identification of the cause of jaundice based only on clinical information and routine investigations. Two groups of jaundiced patients were studied, including 500 (retrospective sample) and 100 (prospective sample) subjects, respectively. All patients were independently submitted to both decision-support tools. The input of both systems was the data set agreed within the Euricterus Project. The performances of both systems were evaluated with respect to the reference diagnoses provided by experts on the basis of the full clinical documentation. Results indicate that both systems are clinically reliable, although the diagnostic prediction provided by the knowledge-based approach is slightly better.

scholarly journals A Benchmark and Evaluation of Non-Rigid Structure from Motion

2020 ◽  
Author(s):  
Sebastian Hoppe Nesgaard Jensen ◽  
Mads Emil Brix Doest ◽  
Henrik Aanæs ◽  
Alessio Del Bue
Keyword(s):  
Computer Vision ◽  
Structure From Motion ◽  
State Of The Art ◽  
The State ◽  
Quality Data ◽  
Data Set ◽  
Rigid Structure ◽  
Public Data ◽  
3D Information ◽  
Further Development

AbstractNon-rigid structure from motion (nrsfm), is a long standing and central problem in computer vision and its solution is necessary for obtaining 3D information from multiple images when the scene is dynamic. A main issue regarding the further development of this important computer vision topic, is the lack of high quality data sets. We here address this issue by presenting a data set created for this purpose, which is made publicly available, and considerably larger than the previous state of the art. To validate the applicability of this data set, and provide an investigation into the state of the art of nrsfm, including potential directions forward, we here present a benchmark and a scrupulous evaluation using this data set. This benchmark evaluates 18 different methods with available code that reasonably spans the state of the art in sparse nrsfm. This new public data set and evaluation protocol will provide benchmark tools for further development in this challenging field.

Exercise Performance in Adolescents with Fontan Physiology (From the Pediatric Heart Network Fontan Public Data Set)

2021 ◽  
Author(s):  
Michael D. Seckeler ◽  
Brent J. Barber ◽  
Jamie N. Colombo ◽  
Alyssa M. Bernardi ◽  
Andrew W. Hoyer ◽  
...  
Keyword(s):  
Exercise Performance ◽  
Data Set ◽  
Public Data ◽  
Fontan Physiology

scholarly journals Quality control in scRNA-Seq can discriminate pacemaker cells: the mtRNA bias

2021 ◽  
Author(s):  
Anne-Marie Galow ◽  
Sophie Kussauer ◽  
Markus Wolfien ◽  
Ronald M. Brunner ◽  
Tom Goldammer ◽  
...  
Keyword(s):  
Quality Control ◽  
Cardiac Tissue ◽  
High Energy ◽  
Tissue Type ◽  
Pacemaker Cells ◽  
Data Set ◽  
Public Data ◽  
Standard Quality ◽  
Mitochondrial Transcripts

AbstractSingle-cell RNA-sequencing (scRNA-seq) provides high-resolution insights into complex tissues. Cardiac tissue, however, poses a major challenge due to the delicate isolation process and the large size of mature cardiomyocytes. Regardless of the experimental technique, captured cells are often impaired and some capture sites may contain multiple or no cells at all. All this refers to “low quality” potentially leading to data misinterpretation. Common standard quality control parameters involve the number of detected genes, transcripts per cell, and the fraction of transcripts from mitochondrial genes. While cutoffs for transcripts and genes per cell are usually user-defined for each experiment or individually calculated, a fixed threshold of 5% mitochondrial transcripts is standard and often set as default in scRNA-seq software. However, this parameter is highly dependent on the tissue type. In the heart, mitochondrial transcripts comprise almost 30% of total mRNA due to high energy demands. Here, we demonstrate that a 5%-threshold not only causes an unacceptable exclusion of cardiomyocytes but also introduces a bias that particularly discriminates pacemaker cells. This effect is apparent for our in vitro generated induced-sinoatrial-bodies (iSABs; highly enriched physiologically functional pacemaker cells), and also evident in a public data set of cells isolated from embryonal murine sinoatrial node tissue (Goodyer William et al. in Circ Res 125:379–397, 2019). Taken together, we recommend omitting this filtering parameter for scRNA-seq in cardiovascular applications whenever possible.

Fast and accurate detection of surface defect based on improved YOLOv4

2021 ◽  
Vol ahead-of-print (ahead-of-print) ◽  
Author(s):  
Jiawei Lian ◽  
Junhong He ◽  
Yun Niu ◽  
Tianze Wang
Keyword(s):  
Feature Extraction ◽  
Real Time ◽  
Surface Defect ◽  
Steel Ingot ◽  
Industrial Applications ◽  
Data Sets ◽  
Data Set ◽  
Processing Technologies ◽  
Content Type ◽  
Public Data

Purpose The current popular image processing technologies based on convolutional neural network have the characteristics of large computation, high storage cost and low accuracy for tiny defect detection, which is contrary to the high real-time and accuracy, limited computing resources and storage required by industrial applications. Therefore, an improved YOLOv4 named as YOLOv4-Defect is proposed aim to solve the above problems. Design/methodology/approach On the one hand, this study performs multi-dimensional compression processing on the feature extraction network of YOLOv4 to simplify the model and improve the feature extraction ability of the model through knowledge distillation. On the other hand, a prediction scale with more detailed receptive field is added to optimize the model structure, which can improve the detection performance for tiny defects. Findings The effectiveness of the method is verified by public data sets NEU-CLS and DAGM 2007, and the steel ingot data set collected in the actual industrial field. The experimental results demonstrated that the proposed YOLOv4-Defect method can greatly improve the recognition efficiency and accuracy and reduce the size and computation consumption of the model. Originality/value This paper proposed an improved YOLOv4 named as YOLOv4-Defect for the detection of surface defect, which is conducive to application in various industrial scenarios with limited storage and computing resources, and meets the requirements of high real-time and precision.

A Novel ECG Automatic Detection Using LongShort-Term Memory Network and Internet of Things Technology

2021 ◽  
Vol 11 (6) ◽  
pp. 1592-1598
Author(s):  
Xufei Liu
Keyword(s):  
Machine Learning ◽  
Cardiovascular Diseases ◽  
Internet Of Things ◽  
Network Structure ◽  
Recognition Rate ◽  
Classification Model ◽  
Data Set ◽  
Public Data ◽  
Lstm Network ◽  
Internet Of Things Technology

The early detection of cardiovascular diseases based on electrocardiogram (ECG) is very important for the timely treatment of cardiovascular patients, which increases the survival rate of patients. ECG is a visual representation that describes changes in cardiac bioelectricity and is the basis for detecting heart health. With the rise of edge machine learning and Internet of Things (IoT) technologies, small machine learning models have received attention. This study proposes an ECG automatic classification method based on Internet of Things technology and LSTM network to achieve early monitoring and early prevention of cardiovascular diseases. Specifically, this paper first proposes a single-layer bidirectional LSTM network structure. Make full use of the timing-dependent features of the sampling points before and after to automatically extract features. The network structure is more lightweight and the calculation complexity is lower. In order to verify the effectiveness of the proposed classification model, the relevant comparison algorithm is used to verify on the MIT-BIH public data set. Secondly, the model is embedded in a wearable device to automatically classify the collected ECG. Finally, when an abnormality is detected, the user is alerted by an alarm. The experimental results show that the proposed model has a simple structure and a high classification and recognition rate, which can meet the needs of wearable devices for monitoring ECG of patients.

scholarly journals SHI7 Is a Self-Learning Pipeline for Multipurpose Short-Read DNA Quality Control

mSystems ◽  
2018 ◽  
Vol 3 (3) ◽  
Author(s):  
Gabriel A. Al-Ghalith ◽  
Benjamin Hillmann ◽  
Kaiwei Ang ◽  
Robin Shields-Cutler ◽  
Dan Knights
Keyword(s):  
Quality Control ◽  
Dna Sequences ◽  
Sequence Data ◽  
Background Knowledge ◽  
Sequencing Technology ◽  
Data Set ◽  
Short Read ◽  
Dna Quality ◽  
Public Data ◽  
User Friendly

ABSTRACT Next-generation sequencing technology is of great importance for many biological disciplines; however, due to technical and biological limitations, the short DNA sequences produced by modern sequencers require numerous quality control (QC) measures to reduce errors, remove technical contaminants, or merge paired-end reads together into longer or higher-quality contigs. Many tools for each step exist, but choosing the appropriate methods and usage parameters can be challenging because the parameterization of each step depends on the particularities of the sequencing technology used, the type of samples being analyzed, and the stochasticity of the instrumentation and sample preparation. Furthermore, end users may not know all of the relevant information about how their data were generated, such as the expected overlap for paired-end sequences or type of adaptors used to make informed choices. This increasing complexity and nuance demand a pipeline that combines existing steps together in a user-friendly way and, when possible, learns reasonable quality parameters from the data automatically. We propose a user-friendly quality control pipeline called SHI7 (canonically pronounced “shizen”), which aims to simplify quality control of short-read data for the end user by predicting presence and/or type of common sequencing adaptors, what quality scores to trim, whether the data set is shotgun or amplicon sequencing, whether reads are paired end or single end, and whether pairs are stitchable, including the expected amount of pair overlap. We hope that SHI7 will make it easier for all researchers, expert and novice alike, to follow reasonable practices for short-read data quality control. IMPORTANCE Quality control of high-throughput DNA sequencing data is an important but sometimes laborious task requiring background knowledge of the sequencing protocol used (such as adaptor type, sequencing technology, insert size/stitchability, paired-endedness, etc.). Quality control protocols typically require applying this background knowledge to selecting and executing numerous quality control steps with the appropriate parameters, which is especially difficult when working with public data or data from collaborators who use different protocols. We have created a streamlined quality control pipeline intended to substantially simplify the process of DNA quality control from raw machine output files to actionable sequence data. In contrast to other methods, our proposed pipeline is easy to install and use and attempts to learn the necessary parameters from the data automatically with a single command.

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