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Riyazuddin Mohammed

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2 published item(s)

preprint2026arXiv

Beyond the Wrapper: Identifying Artifact Reliance in Static Malware Classifiers using TRUSTEE

Modern cybersecurity relies heavily on static machine-learning-based malware classifiers. However, transformations such as packing and other non-semantic modifications applied to executable files limit their reliability. Malware classifiers often learn these unnecessary artifacts rather than the true binary behavior because of the high association between maliciousness and packing. Moreover, these malware classifiers are black boxes, making it difficult to understand what they learn. To address this issue, we proposed a two-part framework using the post-hoc interpretability XAI tool TRUSTEE, followed by a manual analysis of the top features. We conducted several controlled experiments by varying the dataset composition ratios to understand their impact on the results. The top-ranked features across all experiments, identified by TRUSTEE, were predominantly packing artifacts, portable executable(PE) metadata, and n-grams at the string level, rather than malicious semantics. These results suggest that these malware classifiers are highly sensitive to dataset composition and can misinterpret packing as malicious behavior. Our proposed framework allows for the reproducible diagnosis of such biases and forms a guideline for building more robust and semantically meaningful malware detection models

preprint2010arXiv

Information Analysis of DNA Sequences

The problem of differentiating the informational content of coding (exons) and non-coding (introns) regions of a DNA sequence is one of the central problems of genomics. The introns are estimated to be nearly 95% of the DNA and since they do not seem to participate in the process of transcription of amino-acids, they have been termed "junk DNA." Although it is believed that the non-coding regions in genomes have no role in cell growth and evolution, demonstration that these regions carry useful information would tend to falsify this belief. In this paper, we consider entropy as a measure of information by modifying the entropy expression to take into account the varying length of these sequences. Exons are usually much shorter in length than introns; therefore the comparison of the entropy values needs to be normalized. A length correction strategy was employed using randomly generated nucleonic base strings built out of the alphabet of the same size as the exons under question. Our analysis shows that introns carry nearly as much of information as exons, disproving the notion that they do not carry any information. The entropy findings of this paper are likely to be of use in further study of other challenging works like the analysis of symmetry models of the genetic code.