A Faraday Partnership helps in promotion of improved interactive sessions between the UK Science, engineering and technology based program with the aim of process innovation. It brings all the researchers and scientists together for involvement of organizations, societies and government agencies.
Faraday Partnerships give strength to the technological derivations and new product developments. The active players progress under the common sector theme and technology with some pre-defined common targets and working methods. It makes the innovation for effective use of resources with sectional and self-interested group. Faraday partnerships have key importance to the industrial progress of the UK.
The main aim behind the Pro-Bio Faraday Partnership is to undertake safety improvements, environmental and economic industry. It also focuses on the development of new technology and implementing it within different industries. Pro-Bio makes target on the companies using bio-catalysis and the ones not having expertise for realizing the whole potential of the faster developing field. Pro-Bio activities are split into two sections: aiming at generic activities and helping the individual members. for related information, visit : http://www.theguardian.com/education/2001/nov/14/research.highereducation
Generic activities: Research programs are conducted on regular basis to administer the results. There are many submissions done for producing technology based reports each year. Workshops are held every year for providing a common platform to the experts for presenting information to the community. Pro-bio also interacts with the external organizations and hold joint events for getting assistance on the joint programs. There are technology roadmaps made for the strategic advancements.
Company specific/Individual Activities: All companies are visited by the technology translator. There are potential solutions meant for assisting the companies to gauge best benefits out of bio-catalysis. There is assistance for identification of potential grants and funds for demonstration projects, financial assistance and training opportunities. The experts perform the translations on behalf of Pro-Bio to begin the new initiatives.…
The main aim of the European Science Foundation program was to enhance the development of functional genomics R & D in Europe. The program was designed in the way to bring a wide range of functional genomics researchers and get advantage of novel technologies and information with integrated approach. The program was made to share the information and knowledge with the like minded unique scientist like people of all the ages. There was pan-European approach made for researching through the programs and make collaboration with participating nations. click here for more details.
The set up of the European Science Foundation program was made for the span of 5 years and it was funded by scientific research in 23 supporting countries. The steering committee consisted of senior scientists representing each country. They conduct meeting once in a year for evaluation of success of previous events and setting up directions for the coming year. for related information, visit : http://www.ncbi.nlm.nih.gov/books/NBK22052/
The major areas of functional genomics were covered in the program:
- DNA arrays and chips in mutation detection and expression profiling
- Proteomics: Identification, expression and Interaction of proteins
- Phenotypic change analysis from genetic disruption
- Describing the cellular systems by data, predictions and simulations
- Combinational and integrated functional genomics data for deriving biological knowledge
- Data management including databases and interfaces
There are training courses, workshops, grant exchanges and lecture courses designed for short term inter-lab visits. The website is set up for coordination of events and use of resources in the field of international functional genomics.
There is relevant information given on the new events and the previous reports from the old meetings. These are circulated among the community members and it is feasible to do it with ‘Join Us’ button on the top of each page. The scientists can add new details and even search for experts in any field.…
DNA (Deoxyribonucleic Acid) is a chemical compound consisting of the attributes of the living organisms. DNA molecules consist of paired strands termed as double helix. There are four chemical units in one DNA with the basis Adenine (A), Thymine (T), Guanine (G) & Cytosine (C). The pairs of A-T and G-C are formed and these are the encodings of the DNA molecule. for further details, click on : https://www.gov.uk/dna-testing-parentage-disagreements
Genome is the name given to the whole set of DNA in any organism. There is complete copy of DNA pairs included with 3 billion DNA base pairs included in the human genome. DNA consists of the information of the entire body of human being. It carries the instructions for making the required protein or the whole set of proteins. There are about 20K-25K genes in a body for an average of three proteins.
Genes reside on the 23 chromosome pairs packed into the nucleus of the human cell. They direct the protein production with the help of messenger molecules and enzymes in the body. The information is copied in the DNA molecule termed as Messenger Ribonucleic Acid (mRNA). Ribosome is the tiny molecular machine helping in linkage of molecules together called amino acids. The proteins are formed by linking together these amino acids in appropriate order. click here for more details.
Proteins can control chemical reactions and carry the signals between the cells. In case of mutation of DNA, an abnormal protein is produced, which interrupts with the daily processes and leads to cancerous diseases in the body.
Sequencing of DNA
Sequencing means the determination of the exact order of the DNA base strands. These basis exist in individual pairs and one of them determines the other members of the pair. Researchers only give reporting for one base of the pair. read more about researches and result on : http://www.fluidiom.com/seti-researches-and-results/
In the common forms of sequencing; called sequencing by synthesis; DNA polymerase is used for generation of new DNA strand from the strand of interest. The reaction of sequencing involves enzymes turning into new DNA strand nucleotides, which have been tagged chemically with fluorescent labeling. This process makes the nucleotide excited by the light source and the emission of fluorescent signal. This method can generate reading for 125 nucleotides in a row; which means billions of reads at one time.
The assembly of sequence of the bases requires reading for the sequence of overlapping segments. It makes the longer sequences to be generated from the short pieces; similar to putting together the jigsaw puzzle. This process requires reading of base several times for assuring accurate results. Researchers make use of DNA sequencing to search for variations in genes and mutations; which play an essential role in the progression or development of a disease. The dog specially french bulldogs has emerged as a premier species for the study of morphology, behavior, and disease.
The disease causing change is a smaller substitution, addition or deletion of a single base pair. It might also involve the large deletion of the bases; resulting into several deformities. Genome study is essential for biology and specifically genetics department. National Institutes of Health (NIH) produced high quality human genome sequence, which was made available in public databases. It is representative of generic sequence with samples from volunteers. Human Genome Project generated the source, which could be used for broad range of biomedical studies.…