Fabricio Martins Lopes

arXiv2024

GRAMEP: an alignment-free method based on the Maximum Entropy Principle for identifying SNPs

Background: Advances in high throughput sequencing technologies provide a huge number of genomes to be analyzed. Thus, computational methods play a crucial role in analyzing and extracting knowledge from the data generated. Investigating genomic mutations is critical because of their impact on chromosomal evolution, genetic disorders, and diseases. It is common to adopt aligning sequences for analyzing genomic variations. However, this approach can be computationally expensive and restrictive in scenarios with large datasets. Results: We present a novel method for identifying single nucleotide polymorphisms (SNPs) in DNA sequences from assembled genomes. This study proposes GRAMEP, an alignment-free approach that adopts the principle of maximum entropy to discover the most informative k-mers specific to a genome or set of sequences under investigation. The informative k-mers enable the detection of variant-specific mutations in comparison to a reference genome or other set of sequences. In addition, our method offers the possibility of classifying novel sequences with no need for organism-specific information. GRAMEP demonstrated high accuracy in both in silico simulations and analyses of viral genomes, including Dengue, HIV, and SARS-CoV-2. Our approach maintained accurate SARS-CoV-2 variant identification while demonstrating a lower computational cost compared to methods with the same purpose. Conclusions: GRAMEP is an open and user-friendly software based on maximum entropy that provides an efficient alignment-free approach to identifying and classifying unique genomic subsequences and SNPs with high accuracy, offering advantages over comparative methods. The instructions for use, applicability, and usability of GRAMEP are open access at https://github.com/omatheuspimenta/GRAMEP

q-bio.GN↗

arXiv2011

DimReduction - Interactive Graphic Environment for Dimensionality Reduction

Feature selection is a pattern recognition approach to choose important variables according to some criteria to distinguish or explain certain phenomena. There are many genomic and proteomic applications which rely on feature selection to answer questions such as: selecting signature genes which are informative about some biological state, e.g. normal tissues and several types of cancer; or defining a network of prediction or inference among elements such as genes, proteins, external stimuli and other elements of interest. In these applications, a recurrent problem is the lack of samples to perform an adequate estimate of the joint probabilities between element states. A myriad of feature selection algorithms and criterion functions are proposed, although it is difficult to point the best solution in general. The intent of this work is to provide an open-source multiplataform graphical environment to apply, test and compare many feature selection approaches suitable to be used in bioinformatics problems.

cs.CV↗