Recent advances in next-generation sequencing technologies have led to the successful insertion of video information into DNA using synthesized oligonucleotides. Several attempts have been made to embed larger data into living organisms. This process of embedding messages is called steganography and it is used for hiding and watermarking data to protect intellectual property. In contrast, steganalysis is a group of algorithms that serves to detect hidden information from covert media. Various methods have been developed to detect messages embedded in conventional covert channels. However, conventional steganalysis algorithms are mostly limited to common covert media. Most common detection approaches, such as frequency analysis-based methods, often overlook important signals when directly applied to DNA steganography and are easily bypassed by recently developed steganography techniques. To address the limitations of conventional approaches, a sequence-learning-based malicious DNA sequence analysis method based on neural networks has been proposed. The proposed method learns intrinsic distributions and identifies distribution variations using a classification score to predict whether a sequence is to be a coding or non-coding sequence. Based on our experiments and results, we have developed a framework to safeguard security against DNA steganography.
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http://dx.doi.org/10.1109/TCBB.2020.3017191 | DOI Listing |
Front Bioeng Biotechnol
July 2024
Applied Biosciences, Faculty of Science and Engineering, Macquarie University, Sydney, NSW, Australia.
DNA sequences of nearly any desired composition, length, and function can be synthesized to alter the biology of an organism for purposes ranging from the bioproduction of therapeutic compounds to invasive pest control. Yet despite offering many great benefits, engineered DNA poses a risk due to their possible misuse or abuse by malicious actors, or their unintentional introduction into the environment. Monitoring the presence of engineered DNA in biological or environmental systems is therefore crucial for routine and timely detection of emerging biological threats, and for improving public acceptance of genetic technologies.
View Article and Find Full Text PDFJMIR Bioinform Biotechnol
July 2023
Department of Electrical Engineering and Computer Science, University of Missouri, Columbia, MO, United States.
Background: While genomic variations can provide valuable information for health care and ancestry, the privacy of individual genomic data must be protected. Thus, a secure environment is desirable for a human DNA database such that the total data are queryable but not directly accessible to involved parties (eg, data hosts and hospitals) and that the query results are learned only by the user or authorized party.
Objective: In this study, we provide efficient and secure computations on panels of single nucleotide polymorphisms (SNPs) from genomic sequences as computed under the following set operations: union, intersection, set difference, and symmetric difference.
Int J Pharm
April 2024
Institute of Nano Science and Technology, Mohali, Punjab 140306, India. Electronic address:
Despite intense efforts at the bench, the development of successful brain-targeting therapeutics to relieve malicious neural diseases remains primitive. The brain, being a beautifully intricate organ, consists of heterogeneous arrays of neuronal and glial cells. Primarily acting as the support system for neuronal functioning and maturation, glial cells have been observed to be engaged more apparently in the progression and worsening of various neural pathologies.
View Article and Find Full Text PDFAnn Med Surg (Lond)
December 2023
ENT Head and Neck Surgery Department, Ibn Rochd University Hospital, Faculty of Medicine and Pharmacy, Hassan II University, Casablanca, Morocco.
Int J Environ Res Public Health
November 2022
Depatment of Nephrology and Kidney Transplantation, University Hospital Leuven, 3000 Leuven, Belgium.
The pathogenesis of systemic lupus erythematosus (SLE) remains elusive to this day; however, genetic, epigenetic, and environmental factors have been implicated to be involved in disease pathogenesis. Recently, it was demonstrated that in systemic lupus erythematosus (SLE) patients, interferon-regulated genes are hypomethylated in naïve CD4 T cells, CD19 B lymphocytes, and CD14 monocytes. This suggests that interferon-regulated genes may have been epigenetically poised in SLE patients for rapid expression upon stimulation by different environmental factors.
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