What are the best co-expression tools in plant biology?5 answersIn plant biology, several valuable co-expression tools have been developed to analyze gene interactions. One prominent tool is CoExpNetViz, available as a Cytoscape plug-in and web tool, facilitating comparative transcriptomics analysis for plant researchers without specialized bioinformatics knowledge. Additionally, PlantNexus offers global and tissue-specific gene co-expression networks for barley and sorghum, aiding in functional genomics research for these important cereal crops. Furthermore, the review highlights various gene co-expression network databases that store correlation values, gene descriptions, and expression profiles, supporting functional genomics advancements in crops and enabling robust interpretation of biologically relevant information. Overall, these tools play a crucial role in understanding gene regulatory networks and functional connectivity in plants.
Can transcriptomics be used to predict protein expression?4 answersTranscriptomics can be used to predict protein expression levels. Machine learning models combined with appropriate feature selection methods have shown excellent predictive performance in inferring protein expression levels using RNA expression profiles. The incorporation of additional trans-locus transcript abundance data as input features has been found to improve the ability to predict sample protein abundance. Furthermore, the predictive models have revealed that the abundance of a protein is not solely explained by its own cognate transcript level, but also by the transcript levels of its interaction partners. This suggests that protein-protein interactions exert post-transcriptional influence on proteome compositions, indicating the utility of mRNA and protein co-expression analysis in predicting expression changes in biological systems.
How to analysis gene data?5 answersGene data analysis involves several methods and platforms. One approach is to use genetic algorithms (GA) to select a subset of genes from microarray data for cancer classification. Another method involves using a heterogeneous scheduling platform to perform assembly line management on gene data analysis tasks, improving load balancing and resource allocation. The spark platform can be utilized to achieve gene data analysis through the execution of comparison with reference genes on an elastic distributed data set RDD, enhancing efficiency and flexibility. Additionally, gene data analysis can be performed using tools like SVM, KNN, and the R program, which can generate differentially expressed genes, gene clusters, and classify observed data. Furthermore, a gene analysis annotation method involves capturing gene data from existing databases, constructing an annotation gene database, and carrying out retrieval and annotation on the standard file to generate analysis reports.
What is the the database used?3 answersDatabases are used in various clinical and administrative settings for capturing patient data. They are valuable research options for studies of aetiology and prognosis, or when conducting trials is not feasible. High-quality databases can capture outcome data without the need for additional trial-related follow-up. They can also be used in hybrid models that combine randomization with outcome ascertainment using existing databases. Databases are also widely used in clinical research for data management automation. They play an important role in clinical research practice and have advancements such as reanalysis of randomized controlled trials (RCTs) and cloud computing techniques. Additionally, databases are used in the investigation of the possibility of wide deployment of floating wind power plants, specifically in the ocean around Japan.
What is the importance of clean omics datasets in the field of genomics?5 answersClean omics datasets are crucial in the field of genomics for accurate and meaningful analysis. Technical artefacts present in most omics datasets can introduce variations that hinder useful analyses. Batch effects, variations in sample preparation, platform settings, and other experimental procedures need to be adjusted for prior to analysis. The tunable median polish of ratio (TAMPOR) approach has been developed for batch effect correction and agglomeration of multi-batch datasets, resulting in a single analyte abundance data matrix suitable for systems biology analyses. Additionally, the generation of functional genomics datasets is increasing, providing insights into gene regulation and phenotypes. However, privacy concerns arise due to the use of next-generation sequencing. A data-sanitization procedure has been developed to share raw functional genomics reads while minimizing privacy leakage. Clean omics datasets are essential for personalized medicine, discovering cures for diseases, and understanding population diversity. The field of genomics is expanding rapidly, and the availability of inexpensive genome sequencing technology is driving this growth. However, the large amount of data produced requires efficient cleaning and harmonization methods.
Is RNA seq Big Data?10 answers