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Biology subjects

Rami, B. R.

Publications and source records attributed to Rami, B. R..

3 recordsLinked to original sources

Machine learning based identification of candidate miRNA biomarkers for micro-invasive breast cancer diagnosis

Abstract PurposeEarly detection of cancer can be done by analyzing miRNA expression patterns. miRNAs play a significant role in biological processes, and they have been identified as one of the major biomarkers in cancer. miRNAs can also be detected in human blood (micro-invasive way of sample collection), which makes the diagnostic procedure much less stressful for the patients. In this article, we emphasize on identification of miRNAs as biomarkers (collected from blood sample) that are associated with breast cancer. MethodsIn this investigation we use three breast cancer data sets, obtained from blood samples. A combination of multiple feature selection and classification models is used to classify normal vs cancer samples. In the first stage, the significant miRNAs associated with cancer were selected by (a) classifier assigned weights and (b) feature selection algorithms. In the second stage, we apply multiple classifiers to observe the diagnostic capability of the selected miRNAs for consideration as potential biomarkers. ResultsOur miRNA selection stage identified ten miRNAs, which were subsequently analysed using multiple classifiers for their ability to distinguish between normal and cancerous cases. The performance is examined using a 5-fold cross validation technique using multiple measures such as precision, recall, F1-score, and accuracy. We also use a confusion matrix to evaluate the performance of the selected miRNAs. For two out of three datasets, we achieve satisfactory performance in terms of normal vs cancer classification. ConclusionWe observe that high expression levels of miRNA is relatively more important than the sample size, for effective blood-based diagnosis of breast cancer. The novelty of our investigation lies in combining three aspects viz., blood-based breast cancer diagnosis, use of multiple ML based feature selection algorithms to identify the miRNAs associated with breast cancer, evaluating them using various classifiers and the robustness of these ML models in feature selection and classification.

cancer biology↗

An in-silico comparative analysis of lncRNA expression and their role in the pathogenesis of representative fungal, bacterial and viral infections in rice

Long non-coding RNAs (lncRNAs) perform prominent role in the regulation of gene expression during plant development and stress response by directly interacting with DNA, RNA, proteins, and/or triggering production of small regulatory RNA molecules. The objective of our study is to understand the systems-level response of the same plant species to highly diverse pathogens across different kingdoms and evaluate the patterns of similarity vs differences, specifically in the context of lncRNAs. Towards this objective, we performed a comparative in silico analysis of lncRNAs of Rice that are differentially expressed in response to infection by bacteria (Xanthomonas oryzae), fungus (Magnaporthe oryzae) and virus (Rice black dwarf virus). Using a tailored lncRNA analysis pipeline, we successfully identified 1125, 719 and 240 lncRNAs in Xanthomonas oryzae infection susceptible cultivar CT9737-6-1-3P-M, Magnaporthe oryzae susceptible LTH accession, and Rice black streaked dwarf virus susceptible Wuyujing No. 7 rice cultivars respectively. The in-silico predicted Cis- and Trans-target genes of lncRNAs were subsequently used to identify the pathways modulated by these lncRNA and how they cluster into unique categories of plant responses to pathogen infections. To further substantiate the role of predicted lncRNAs in plant defence and immune response our analysis finds that many of the lncRNAs co-localize with the QTLs associated with Blast and Bacterial blight resistance in rice. Our in silico analysis provides a list of common and unique pathogen specific lncRNAs that can provide vital insights into the generic vs tailored mechanisms adopted by rice in different infection scenarios.

plant biology↗

Automated Navigation of the lncRNA Transcriptome: A comprehensive SnakeMake based computational Pipeline for robust Identification of lncRNAs and their putative targets

BackgroundLong non-coding RNAs (lncRNAs) have emerged as potent regulatory elements in cellular processes. The substantial increase in transcriptomic data resulting from high-throughput RNA sequencing necessitates effective approaches for the identification and functional annotation of lncRNAs. MethodTo address this need, we have developed a SnakeMake-based pipeline. Our pipeline automates and integrates several key steps: 1) RNA-seq analysis using Hisat2 and stringTie, (2) lncRNA identification using inhouse python scripts and tools CPC2 and BLASTX, (3) prediction of cis- and trans- gene targets of lncRNAs, and (4) KEGG pathway enrichment to obtain biological insights. Importantly, the pipeline allows users to customize parameters for each step through a user-friendly configuration file (config.yaml), enhancing flexibility and ease of use. One of the distinctive features of our approach is its single command execution, facilitating multiple runs without the need for extensive user intervention. This not only enhances user convenience but also ensures reproducibility of analyses across different studies. ResultWe applied our pipeline on rice, sorghum, and human RNA-seq data, to identify (1) List of all differentially expressed transcripts., (2) List of differentially expressed lncRNAs, (3) lncRNA target genes, (4) Enriched pathways to which target genes belong and (5) Obtain a visualization output in the form of a bubble plot that depicts the enriched pathways. Our approach can help researchers obtain valuable biological insights into how lncRNAs contribute to various biological functions. ConclusionThe distinctive features of our SnakeMake-based automation pipeline position it as a versatile asset for researchers seeking a user-friendly, adaptable, robust, and reproducible solution for pan species lncRNA analysis. By efficiently uncovering the regulatory roles of lncRNAs in cellular processes, this pipeline has the potential to shed light on various biological phenomena, such as developmental biology, disease progression, and cellular response to external stimuli. GRAPHICAL ABSTRACTThis study presents a SnakeMake-based pipeline for identifying and annotating long non-coding RNAs (IncRNAs) from RNA sequencing data. It integrates RNA-seq analysis, IncRNA identification, gene target prediction, and pathway enrichment, with customizable parameters through a user-friendly configuration file. The pipelines single command execution enhances convenience and reproducibility. (The bubble chart in the figure is a representative chart and provided as an example.) O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=96 SRC="FIGDIR/small/608522v1_ufig1.gif" ALT="Figure 1"> View larger version (26K): org.highwire.dtl.DTLVardef@9e2930org.highwire.dtl.DTLVardef@1a219e9org.highwire.dtl.DTLVardef@153462dorg.highwire.dtl.DTLVardef@243d3d_HPS_FORMAT_FIGEXP M_FIG C_FIG

bioinformatics↗