genomics is the study of an entire sequence of an organism's DNA, while bioinformatics is the use of computers and data bases to organize and analyze DNA. bioinformatics makes genomics a bit easier.
Proteome: an organism's complete set of proteins Bioinformatics: combines biological science, computer science, and information technology to enable the discovery of new biological insights and unifying principles
The difference between them is that : In genomic imprinting : one of the alleles in the two chromosomes ( for example the color of the eyes ) are tend to be heavily methylated, in contrast to the nonimpringting copy of the allele which typically is not methylated. In X-chromosome in activation : As you know in female there are two X chromosomes, so one of the two X xhromosomes is methylated which mean one of the two chromosomes become inactivation.
Methylation is a process where methyl groups are added to DNA, which can affect gene expression. Genomic imprinting is a phenomenon where certain genes are expressed based on whether they are inherited from the mother or father. Methylation plays a key role in genomic imprinting by regulating which parent's gene is expressed.
Genomic library
The purpose of using the Basic Local Alignment Search Tool (BLAST) in bioinformatics research is to compare biological sequences, such as DNA or protein sequences, to identify similarities and relationships between them. This helps researchers understand the function and evolutionary history of these sequences.
Bioinformatics is basically using computers to organize and analyze biological data, like comparing genomes between organisms or species.
what is the eligibility for bioinformatics? what is the eligibility for bioinformatics?
Genomic research involves the study of an organism's complete set of DNA, including its genes and their functions. This field encompasses various techniques, such as sequencing, bioinformatics, and genetic analysis, to understand genetic variation, disease mechanisms, and evolutionary processes. By exploring the genome, researchers aim to uncover insights that can lead to advancements in medicine, agriculture, and biotechnology. Ultimately, genomic research plays a crucial role in personalized medicine, helping tailor treatments based on individual genetic profiles.
Proteome: an organism's complete set of proteins Bioinformatics: combines biological science, computer science, and information technology to enable the discovery of new biological insights and unifying principles
DUP-SCAN ARTL FLO is a tool designed for the detection of duplications in genomic sequences, particularly focusing on structural variations that may contribute to diseases. It utilizes advanced algorithms to analyze and visualize genomic data, allowing researchers to identify and characterize duplications effectively. This tool is part of the broader field of bioinformatics, which leverages computational methods to understand biological data.
Plasmic DNA is extrachromosomal DNA found in prokaryotes that replicates independently of the chromosomal DNA. Genomic DNA refers to the complete set of genetic material within the nucleus of eukaryotic cells or the nucleoid region of prokaryotic cells.
Evolutionary Bioinformatics was created in 2005.
Briefings in Bioinformatics was created in 2000.
Key events that have significantly advanced bioinformatics include the completion of the Human Genome Project in 2003, which provided a comprehensive map of human DNA and highlighted the need for computational tools to analyze large genomic datasets. The rapid development of high-throughput sequencing technologies has also generated vast amounts of biological data, necessitating sophisticated algorithms and databases for efficient analysis. Additionally, the rise of interdisciplinary collaborations between biologists, computer scientists, and statisticians has fostered the growth of bioinformatics as a distinct field, enabling better understanding of biological processes through computational modeling and data integration.
The difference between them is that : In genomic imprinting : one of the alleles in the two chromosomes ( for example the color of the eyes ) are tend to be heavily methylated, in contrast to the nonimpringting copy of the allele which typically is not methylated. In X-chromosome in activation : As you know in female there are two X chromosomes, so one of the two X xhromosomes is methylated which mean one of the two chromosomes become inactivation.
EBI is the European Bioinformatics Institute, an outstation of the European Molecular Biology Laboratory, based near Cambridge, UK. It is a site of bioinformatics research and development, and also hosts bioinformatics services.
Swiss Institute of Bioinformatics was created in 1998.