History Paulien Hogeweg coined the term "Bioinformatics" in 1970 to refer to the study of information processes in biotic systems.[4][5][6] This definition placed bioinformatics as a field parallel to biophysics (the study of physical processes in biological systems) or biochemistry (the study of chemical processes in biological systems).[4] Sequences. Computers became essential in molecular biology when protein sequences became available after Frederick Sanger determined the sequence of insulin in the early 1950s. Comparing multiple sequences manually turned out to be impractical. A pioneer in the field was Margaret Oakley Dayhoff, who has been hailed by David Lipman, director of the National Center for Biotechnology Information, as the "mother and father of bioinformatics."[7] Dayhoff compiled one of the first protein sequence databases, initially published as books[8] and pioneered methods of sequence alignment and molecular evolution.[9] Another early contributor to bioinformatics was Elvin A. Kabat, who pioneered biological sequence analysis in 1970 with his comprehensive volumes of antibody sequences released with Tai Te Wu between 1980 and 1991.[10] Genomes. As whole genome sequences became available, again with the pioneering work of Frederick Sanger,[11] the term bioinformatics was re-discovered to refer to the creation of databases such as GenBank in 1982. With the public availability of data tools for their analysis were quickly developed and described in journals such as Nucleic Acids Research which published specialized issues on bioinformatics tools as early as 1982. Goals In order to study how normal cellular activities are altered in different disease states, the biological data must be combined to form a comprehensive picture of these activities. Therefore, the field of bioinformatics has evolved such that the most pressing task now involves the analysis and interpretation of various types of data. This includes nucleotide and amino acid sequences, protein domains, and protein structures.[12] The actual process of analyzing and interpreting data is referred to as computational biology. Important sub-disciplines within bioinformatics and computational biology include: the development and implementation of tools that enable efficient access to, use and management of, various types of information. the development of new algorithms (mathematical formulas) and statistics with which to assess relationships among members of large data sets. For example, methods to locate a gene within a sequence, predict protein structure and/or function, and cluster protein sequences into families of related sequences. The primary goal of bioinformatics is to increase the understanding of biological processes. What sets it apart from other approaches, however, is its focus on developing and applying computationally intensive techniques to achieve this goal. Examples include: pattern recognition, data mining, machine learning algorithms, and visualization. Major research efforts in the field include sequence alignment, gene finding, genome assembly, drug design, drug discovery, protein structure alignment, protein structure prediction, prediction of gene expression and protein–protein interactions, genome-wide association studies, and the modeling of evolution. Bioinformatics now entails the creation and advancement of databases, algorithms, computational and statistical techniques, and theory to solve formal and practical problems arising from the management and analysis of biological data. Over the past few decades rapid developments in genomic and other molecular research technologies and developments in information technologies have combined to produce a tremendous amount of information related to molecular biology. Bioinformatics is the name given to these mathematical and computing approaches used to glean understanding of biological processes. Approaches Common activities in bioinformatics include mapping and analyzing DNA and protein sequences, aligning different DNA and protein sequences to compare them, and creating and viewing 3-D models of protein structures. There are two fundamental ways of modelling a Biological system (e.g., living cell) both coming under Bioinformatic approaches. Static Sequences – Proteins, Nucleic acids and Peptides Interaction data among the above entities including microarray data and Networks of proteins, metabolites Dynamic Structures – Proteins, Nucleic acids, Ligands (including metabolites and drugs) and Peptides (structures studied with bioinformatics tools are not considered static anymore and their dynamics is often the core of the structural studies) Systems Biology comes under this category including reaction fluxes and variable concentrations of metabolites Multi-Agent Based modelling approaches capturing cellular events such as signalling, transcription and reaction dynamics A broad sub-category under bioinformatics is structural bioinformatics.
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