PubMed Health⌕ Search

PubMed · 16859292

Supervised feature ranking using a genetic algorithm optimized artificial neural network.

Abstract

A genetic algorithm optimized artificial neural network GNW has been designed to rank features for two diversified multivariate data sets. The dimensions of these data sets are 85x24 and 62x25 for 24 or 25 molecular descriptors being computed for 85 matrix metalloproteinase-1 inhibitors or 62 hepatitis C virus NS3 protease inhibitors, respectively. Each molecular descriptor computed is treated as a feature and input into an input layer node of the artificial neural network. To optimize the artificial neural network by the genetic algorithm, each interconnected weight between input and hidden or between hidden and output layer nodes is binary encoded as a 16 bits string in a chromosome, and the chromosome is evolved by crossover and mutation operations. Each input layer node and its associated weights of the trained GNW are systematically omitted once (the self-depleted weights), and the corresponding weight adjustments due to the omission are computed to keep the overall network behavior unchanged. The primary feature ranking index defined as the sum of self-depleted weights and the corresponding weight adjustments computed is found capable of separating good from bad features for some artificial data sets of known feature rankings tested. The final feature indexes used to rank the data sets are computed as a sum of the weighted frequency of each feature being ranked in a particular rank for each data set being partitioned into numerous clusters. The two data sets are also clustered by a standard K-means method and trained by a support vector machine (SVM) for feature ranking using the computed F-scores as feature ranking index. It is found that GNW outperforms the SVM method on three artificial as well as the matrix metalloproteinase-1 inhibitor data sets studied. A clear-cut separation of good from bad features is offered by the GNW but not by the SVM method for a feature pool of known feature ranking.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Thy-Hou Lin, Shih-Hau Chiu, Keng-Chang Tsai. Supervised feature ranking using a genetic algorithm optimized artificial neural network.. https://doi.org/10.1021/ci0600354

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

A note on a generalized single step theory for any number of hierarchical genomic matrices.

BACKGROUND: The Single Step algorithm allows combining information from genotyped and un-genotyped individuals, provided they are connected by a pedigree. However, current single step theory is limited to a single list of markers. RESULTS: We present a generalized single step (GSS) method that can accommodate any number of hierarchical molecular datasets (e.g. sequence, high and low density arrays) and pedigree, avoiding imputation. We prove that a similar efficient inversion algorithm exists. The method is recursive, starting with the highest marker density scenario. We illustrate the method with simulation and show that GSS can increase predictive accuracy compared to standard single step. R code is provided so that custom scenarios can be easily compared, either with simulated or real data. CONCLUSION: The method developed generalizes extant single step theory to any number of hierarchical molecular relationship matrices, broadening the scenarios where single step can be applied. A topic of particular interest can be ecology field data or human populations where pedigree is not available, but where samples sequenced and genotyped at different densities can exist. GSS can also be a useful tool to optimize allocation of genotyping and / or sequencing resources.

Algorithms↗

cgDist: Nucleotide-level distance calculation from cgMLST allelic profiles.

Bacterial genomic surveillance requires balancing computational efficiency with genetic resolution for effective cluster investigation. cgMLST distance calculations treat all allelic differences as equivalent units, obscuring nucleotide-level variation. Furthermore, single nucleotide polymorphism-based pipelines provide finer resolution at substantially higher computational cost, which limits their routine deployment in surveillance laboratories. We present cgDist, an algorithm that calculates nucleotide-level distances directly from cgMLST allelic profiles, providing finer resolution than allele-count distances by leveraging within-allele nucleotide variation. The cache architecture stores alignment statistics, enabling distance calculation modes without computation and supporting both dataset-specific and schema-complete cache generation. This design enables incremental surveillance analysis, with performance benefits as laboratories accumulate alignment data. cgDist functions as a precision 'zoom lens' for the investigation of clusters identified through initial cgMLST screening. Rather than restructuring population relationships, this targeted approach concentrates enhanced resolution where it is most informative. The algorithm ensures that cgDist distances are greater than or equal to corresponding cgMLST distances, preserving epidemiological interpretability while adding genetic discrimination. By increasing resolution within identified clusters, cgDist may also support outbreak investigation, a potential application that remains to be evaluated on outbreak-derived data.

Algorithms↗

Theseus: fast and optimal affine-gap sequence-to-graph alignment.

MOTIVATION: Sequence-to-graph alignment is a central problem in bioinformatics, with applications in multiple sequence alignment (MSA) and pangenome analysis, among others. However, current algorithms for optimal affine-gap alignment impose high memory and computational requirements, limiting their scalability to aligning long sequences to complex graphs. Practical solutions partially address this problem using heuristic strategies that ultimately trade off optimality for speed. RESULTS: This work presents Theseus, a novel, fast, and optimal affine-gap sequence-to-graph alignment algorithm. Theseus leverages similarities between genomic sequences to accelerate the alignment computation and reduces the overall memory requirements without compromising optimality. To that end, Theseus processes only a subset of the dynamic programming cells, using a sparse-data strategy that enables efficient sequence-to-graph alignment. Moreover, our algorithm supports optimal affine-gap alignment on arbitrary directed graphs, including those with cycles. We evaluate Theseus on two key problems: MSA and pangenome read mapping. For MSA, we compare it against SPOA, abPOA, and POASTA. Theseus is 1.6× to 17.6× faster than POASTA, and 7.3× faster, on average, than SPOA, both optimal aligners. Compared with abPOA, Theseus ensures optimality and scales to the largest problems. For pangenome read mapping, we benchmark Theseus against the alignment stage of the mapping tool vg map, along with the alignment kernels of SPOA, abPOA, and POASTA. Theseus outperforms the other methods, showing a 1.9× to 16.9× speedup on short reads. Moreover, Theseus is 1.5× to 36.3× faster than vg when aligning against synthetic cyclic graphs. AVAILABILITY AND IMPLEMENTATION: Theseus code and documentation are publicly available at https://github.com/albertjimenezbl/theseus-lib.

Algorithms↗