ABSTRACT
Gene sequencing technology has been playing an important role in many aspects, such as life science, disease medicine and health medicine, particularly in the extremely tough process of fighting against 2019-novel coronavirus. Drawing DNA restriction map is a particularly important technology in genetic biology. The simplified partial digestion method (SPDP), a biological method, has been widely used to cut DNA molecules into DNA fragments and obtain the biological information of each fragment. In this work, we propose an algorithm based on 0-1 planning for the location of restriction sites on a DNA molecule, which is able to solve the problem of DNA fragment reconstruction just based on data of fragments' length. Two specific examples are presented in detail. Furthermore, based on 1000 groups of original DNA sequences randomly generated, we define the coincidence rate and unique coincidence rate between the reconstructed DNA sequence and the original DNA sequence, and then analyze separately the effect of the number of fragments and the maximum length of DNA fragments on the coincidence rate and unique coincidence rate as defined. The effectiveness of the algorithm is proved. Besides, based on the existing optimization solution obtained, we simulate and discuss the influence of the error by computation method. It turns out that the error of position of one restriction site does not affect other restriction sites and errors of most restriction sites may lead to the failure of sequence reconstruction. Matlab 7.1 program is used to solve feasible solutions of the location of restriction sites, derive DNA fragment sequence and carry out the statistical analysis and error analysis. This paper focuses on basic computer algorithm implementation of rearrangement and sequencing rather than biochemical technology. The innovative application of the mathematical idea of 0-1 planning to DNA sequence mapping construction, to a certain extent, greatly simplifies the difficulty and complexity of calculation and accelerates the process of 'jigsaw' of DNA fragments.
Subject(s)
Algorithms , Sequence Analysis, DNA , Base Sequence , Models, Theoretical , Statistics as TopicABSTRACT
DNA sequence reconstruction is a challenging research problem in the computational biology field. The evolution of the DNA is too complex to be characterized by a few parameters. Therefore, there is a need for a modeling approach for analyzing DNA patterns. In this paper, we proposed a novel framework for DNA pattern analysis. The proposed framework consists of two main stages. The first stage is for analyzing the DNA sequences evolution, whereas the other stage is for the reconstruction process. We utilized cellular automata (CA) rules for analyzing and predicting the DNA sequence. Then, a modified procedure for the reconstruction process is introduced, which is based on the Probabilistic Cellular Automata (PCA) integrated with Particle Swarm Optimization (PSO) algorithm. This integration makes the proposed framework more efficient and achieves optimum transition rules. Our innovated model leans on the hypothesis that mutations are probabilistic events. As a result, their evolution can be simulated as a PCA model. The main objective of this paper is to analyze various DNA sequences to predict the changes that occur in DNA during evolution (mutations). We used a similarity score as a fitness measure to detect symmetry relations, which is appropriate for numerous extremely long sequences. Results are given for the CpG-methylation-deamination processes, which are regions of DNA where a guanine nucleotide follows a cytosine nucleotide in the linear sequence of bases. The DNA evolution is handled as the evolved colored paradigms. Therefore, incorporating probabilistic components help to produce a tool capable of foretelling the likelihood of specific mutations. Besides, it shows their capabilities in dealing with complex relations.