Friday 7 September 2012

A Practical Approach to Microarray Data Analysis

A Practical Approach to Microarray Data Analysis

A Practical Approach to Microarray Data Analysis is for all life scientists, statisticians, computer experts, technology developers, managers, and other professionals tasked with developing, deploying, and using microarray technology including the necessary computational infrastructure and analytical tools. The book addresses the requirement of scientists and researchers to gain a basic understanding of microarray analysis methodologies and tools. It is intended for students, teachers, researchers, and research managers who want to understand the state of the art and of the presented methodologies and the areas in which gaps in our knowledge demand further research and development. The book is designed to be used by the practicing professional tasked with the design and analysis of microarray experiments or as a text for a senior undergraduate- or graduate level course in analytical genetics, biology, bioinformatics, computational biology, statistics and data mining, or applied computer science.
Key topics covered include:
-Format of result from data analysis, analytical modeling/experimentation;
-Validation of analytical results;
-Data analysis/Modeling task;
-Analysis/modeling tools;
-Scientific questions, goals, and tasks;
-Application;
-Data analysis methods;
-Criteria for assessing analysis methodologies, models, and tools

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Structure and Interpretation of Computer Programs (SICP)


Structure and Interpretation of Computer Programs (SICP) is a textbook published in 1984 about general computer programming concepts from MIT Press written by Massachusetts Institute of Technology (MIT) professors Harold Abelson and Gerald Jay Sussman, with Julie Sussman. It was formerly used as the textbook of MIT introductory programming class and at other schools.
Using a dialect of the Lisp programming language known as Scheme, the book explains core computer science concepts, including abstraction, recursion, interpreters and metalinguistic abstraction, and teaches modular programming.
The program also introduces a practical implementation of the register machine concept, defining and developing an assembler for such a construct, which is used as a virtual machine for the implementation of interpreters and compilers in the book, and as a testbed for illustrating the implementation and effect of modifications to the evaluation mechanism. Working Scheme systems based on the design described in this book are quite common student projects.

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Computational Biology: Genomes, Networks, Evolution


Lecture Slides

Lecture 1
Course Overview and Outline - Intro to Biology - Why Computational Biology - Regulatory Motif discovery

Lecture 2 - Sequence Alignment + Dynamic Programming
Fibonacci - Paths & Alignments - Bounded DP - Linear Space Alignment

Lecture 3 - Sequence Alignment II
Globa/Local/Semi-global alignment + Affine gaps + Alignment statistics

Lecture 4 - Exact string matching
Semi-numerical methods, prelude to hashing

Lecture 5 - Hashing + Blast
Database search - Hashing - Blast - Extensions - Combs - Suffix Trees

Lecture 6 - Modeling Biological Sequences with HMMs
Dishonest Casino, CpG islands, Markov Chains, HMMs, Viterbi

Lecture 7 - HMM decoding evaluation training
Viterbi+Decoding, Forward+Evaluation, Backward+Posterior Decoding, BaumWelch+Training


Lecture 9 - Clustering and Dimensionality Reduction
Running time analysis, feature selection, SVD, PCA

Lecture 10 - Regulatory Motif Discovery
Combinatorial/probabilistic formulation, weight matrices, gibbs sampling, EM

Lecture 11 - Graph algorithms
Connected components, spectral partitioning
Evolution, trees, distance-based methods, parsimony 

Lecture 13 - Phylogenetics
Jukes-Cantor, Kimura, ultrametric, additive, UPGMA, Neighbor-Joining, Dynamic programming parsimony

Lecture 15 - RNA folding
RNA folding - Nussinov's algorithm - Zucker's algorithm - context-free grammars - parsing

Lecture 16 - Stochastic Context-Free Grammars
CYK algorithm - Inside/Outside - HMM similarity - Posterior decoding

Lecture 17 - Genome Rearrangements
Evolution by rearrangements - Sorting by reversals - greedy algorithms - approximation algorithms - breakpoint graphs

Lecture 18 - Genome Duplication
Orthologs - Paralogs - Phylogenetic Tree Reconciliation - Genome Duplication - Duplicate gene divergence - Accelerated Evolution

Lecture 19: Genome assembly
Sequencing, assembly, whole genome shotgun, hierarchical approach

Lecture 22 - Biological Networks
Guest lecture by Laszlo Barabasi - Scale-free networks - Network growth - Robustness - Modularity - Hierarchical - Flux

Lecture 23 - Advanced Multiple Alignment and Assembly
Traditional assembly - String-graph assembly - Global and glocal alignment - Alignmnet with polymorphism

Lecture 24 - Whole-Genome Analysis
HMMs for Gene Finding - Classification based gene finding - Human Motif Finding - MicroRNA regulation

Recitation Notes







Problem Sets

Problem Set 1     

Problem Set 2     



Wednesday 5 September 2012

Listen about Bioinformatics....






One More is here

An Introduction to Genetic Algorithms- Melanie Mitchell

Science arises from the very human desire to understand and control the world. Over the course of history, we humans have gradually built up a grand edifice of knowledge that enables us to predict, to varying extents, the weather, the motions of the planets, solar and lunar eclipses, the courses of diseases, the rise and fall of economic growth, the stages of language development in children, and a vast panorama of other natural, social, and cultural phenomena. More recently we have even come to understand some fundamental limits to our abilities to predict. Over the eons we have developed increasingly complex means to control many aspects of our lives and our interactions with nature, and we have learned, often the hard way, the extent to which other aspects are uncontrollable.

The advent of electronic computers has arguably been the most revolutionary development in the history of science and technology. This ongoing revolution is profoundly increasing our ability to predict and control nature in ways that were barely conceived of even half a century ago. For many, the crowning achievements of this revolution will be the creation—in the form of computer programs—of new species of intelligent beings, and even of new forms of life.

The goals of creating artificial intelligence and artificial life can be traced back to the very beginnings of the computer age. The earliest computer scientists—Alan Turing, John von Neumann, Norbert Wiener, and others—were motivated in large part by visions of imbuing computer programs with intelligence, with the life−like ability to self−replicate, and with the adaptive capability to learn and to control their environments. These early pioneers of computer science were as much interested in biology and psychology as in electronics, and they looked to natural systems as guiding metaphors for how to achieve their visions. It  should be no surprise, then, that from the earliest days computers were applied not only to calculating missile trajectories and deciphering military codes but also to modeling the brain, mimicking human learning, and simulating biological evolution. These biologically motivated computing activities have waxed and waned over the years, but since the early 1980s they have all undergone a resurgence in the computation research community. The first has grown into the field of neural networks, the second into machine learning, and the third into what is now called "evolutionary computation," of which genetic algorithms are the most prominent example

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DNA Molecular Structure and Dynamics

Author: I.C. Baianu, editor with several contributors


Description

A concise overview with color image galleries of important DNA molecular dynamics applications to computing and quantum computations of DNA structure and dynamics.

Includes several image galleries with instrumentation, techniques and contributed brilliant images. 113-page textbook PDF of 24 Mb, May 25th, 2009.

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The Forbidden Combinations of Amino acids & Genetic Codes (codons)

The Forbidden Combinations of Amino acids & Genetic Codes (codons)



The proteogenic amino acids tryptophan, cysteine, and methionine have only a single codon for each in the table of universal genetic code. The relative frequency of each of these codons is 1.5625%. Strikingly, the relative distribution of these amino acids in enzymes is also invariably less than 3.0% irrespective of the class and  type of the reaction catalyzed.  The amino acids other than tryptophan, cysteine and methionine show variable distributions.  One would also find that the following genetic code combinations are  very rare  in nature. There are some hypothetical, predicted, or cloned sequences and proteins in the databases like NCBI. But, none of them are natural.The list of forbidden genetic code combinations:

1.  TGGTGTATG   corresponding to the amino acid combination WCM
2.  TGGATGTGT   corresponding to the amino acid combination WMC
3.  TGTATGTGG   corresponding to the amino acid combination CMW
4.  TGTTGGATG   corresponding to the amino acid combination CWM
5.  ATGTGTTGG  corresponding to the amino acid combination MCW
6.  ATGTGGTGT  corresponding to the amino acid combination MCW

Based on these observations, I conclude that nature does not allow all the genetic code combinations to occur with equal probability. If the combinations occur equally likely, then one should observe these combinations with the same relative frequency as those of other code combinations. Why nature forbids such combinations is yet to be answered. Is it biophysically restricted or is it a genetic restriction? These are unanswered questions. 
One could also make proteins, if possible, with these restricted combinations (either by site directed
mutagenesis or by solid state synthesis) and study their biophysical properties. The above observation is purely based on the data available from the NCBI and RCSB. 

To verify this claim:
1. Run blastp at http://blast.ncbi.nlm.nih.gov/Blast.cgi   for  wcmwmccmwcwmmcwmwc and check the output, check for the proteins, find whether they are hypothetical or biochemically characterized.
2. Run blastn at http://blast.ncbi.nlm.nih.gov/Blast.cgi   for  TGGTGTATGAAAAAAAAAAA, 
TGGATGTGTAAAAAAAAAAA, TGTATGTGGAAAAAAAAAAA, TGTTGGATGAAAAAAAAAAA,
ATGTGTTGGAAAAAAAAAAA, ATGTGGTGTAAAAAAAAAAA, and check each output. One would find similar sequences only, no exact match (except some clones).


Sivashanmugam. P., Lecturer, Biophysical Chemistry, 
Department of Bioinformatics, Jamal Mohamed College, Tiruchirappalli – 620020 – India
e-mail: soundaryanayaki@aol.com

RNA Processing

  • RNA Processing
RNA functions broadly as informational molecule, genome, enzyme and machinery for RNA processing. While these functions reflect ancient activities, they also remain vital components of contemporary biochemical pathways. In eukaryotic cells RNA processing impacts the biogenesis of RNA molecules of essentially every shape and function. The collection of articles in this volume describes the current state of understanding of the broad array of RNA processing events in animal and plant cells, key unanswered questions, and cutting edge approaches available to address these questions. Some questions discussed in this volume include, how viruses subvert the RNA processing machinery of the host cell, how the coordination of co-transcriptional RNA processing is regulated at the level of chromatin, the status of RNA processing in plant organelles, and how micro RNA machinery is biosynthesized and regulated.

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Protein Engineering

  • Protein Engineering
A broad range of topics are covered by providing a solid foundation in protein engineering and supplies readers with knowledge essential to the design and production of proteins. This volume presents in-depth discussions of various methods for protein engineering featuring contributions from leading experts from different counties. A broad series of articles covering significant aspects of methods and applications in the design of novel proteins with different functions are presented. These include the use of non-natural amino acids, bioinformatics, molecular evolution, protein folding and structure-functional insight to develop useful proteins with enhanced properties.

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Integrative Proteomics

  • Integrative Proteomics
Proteomics was thought to be a natural extension after the field of genomics has deposited significant amount of data. However, simply taking a straight verbatim approach to catalog all proteins in all tissues of different organisms is not viable. Researchers may need to focus on the perspectives of proteomics that are essential to the functional outcome of the cells. In Integrative Proteomics, expert researchers contribute both historical perspectives, new developments in sample preparation, gel-based and non-gel-based protein separation and identification using mass spectrometry. Substantial chapters are describing studies of the sub-proteomes such as phosphoproteome or glycoproteomes which are directly related to functional outcomes of the cells. Structural proteomics related to pharmaceutics development is also a perspective of the essence. Bioinformatics tools that can mine proteomics data and lead to pathway analyses become an integral part of proteomics. Integrative proteomics covers both look-backs and look-outs of proteomics. It is an ideal reference for students, new researchers, and experienced scientists who want to get an overview or insights into new development of the proteomics field.

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Molecular Interactions

  • Molecular Interactions
In a classical approach materials science is mainly dealing with interatomic interactions within molecules, without paying much interest on weak intermolecular interactions. However, the variety of structures actually is the result of weak ordering because of noncovalent interactions. Indeed, for self-assembly to be possible in soft materials, it is evident that forces between molecules must be much weaker than covalent bonds between the atoms of a molecule. The weak intermolecular interactions responsible for molecular ordering in soft materials include hydrogen bonds, coordination bonds in ligands and complexes, ionic and dipolar interactions, van der Waals forces, and hydrophobic interactions. Recent evolutions in nanosciences and nanotechnologies provide strong arguments to support the opportunity and importance of the topics approached in this book, the fundamental and applicative aspects related to molecular interactions being of large interest in both research and innovative environments. We expect this book to have a strong impact at various education and research training levels, for young and experienced researchers from both academia and industry.

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Protein-Protein Interactions - Computational and Experimental Tools

Protein-Protein Interactions - Computational and Experimental Tools 

Proteins are indispensable players in virtually all biological events. The functions of proteins are coordinated through intricate regulatory networks of transient protein-protein interactions (PPIs). To predict and/or study PPIs, a wide variety of techniques have been developed over the last several decades. Many in vitro and in vivo assays have been implemented to explore the mechanism of these ubiquitous interactions. However, despite significant advances in these experimental approaches, many limitations exist such as false-positives/false-negatives, difficulty in obtaining crystal structures of proteins, challenges in the detection of transient PPI, among others. To overcome these limitations, many computational approaches have been developed which are becoming increasingly widely used to facilitate the investigation of PPIs. This book has gathered an ensemble of experts in the field, in 22 chapters, which have been broadly categorized into Computational Approaches, Experimental Approaches, and Others.

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Molecular Dynamics - Studies of Synthetic and Biological Macromolecules

Molecular Dynamics is a two-volume compendium of the ever-growing applications of molecular dynamics simulations to solve a wider range of scientific and engineering challenges. The contents illustrate the rapid progress on molecular dynamics simulations in many fields of science and technology, such as nanotechnology, energy research, and biology, due to the advances of new dynamics theories and the extraordinary power of today's computers. This second book begins with an introduction of molecular dynamics simulations to macromolecules and then illustrates the computer experiments using molecular dynamics simulations in the studies of synthetic and biological macromolecules, plasmas, and nanomachines. Coverage of this book includes: Complex formation and dynamics of polymers Dynamics of lipid bilayers, peptides, DNA, RNA, and proteins Complex liquids and plasmas Dynamics of molecules on surfaces Nanofluidics and nanomachines

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Protein Structure

Since the dawn of recorded history, and probably even before, men and women have been grasping at the mechanisms by which they themselves exist. Only relatively recently, did this grasp yield anything of substance, and only within the last several decades did the proteins play a pivotal role in this existence. In this expose on the topic of protein structure some of the current issues in this scientific field are discussed. The aim is that a non-expert can gain some appreciation for the intricacies involved, and in the current state of affairs. The expert meanwhile, we hope, can gain a deeper understanding of the topic.

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Bioinformatics - Trends and Methodologies....project Ideas

Bioinformatics - Trends and Methodologies is a collection of different views on most recent topics and basic concepts in bioinformatics. This book suits young researchers who seek basic fundamentals of bioinformatic skills such as data mining, data integration, sequence analysis and gene expression analysis as well as scientists who are interested in current research in computational biology and bioinformatics including next generation sequencing, transcriptional analysis and drug design. Because of the rapid development of new technologies in molecular biology, new bioinformatic techniques emerge accordingly to keep the pace of in silico development of life science. This book focuses partly on such new techniques and their applications in biomedical science. These techniques maybe useful in identification of some diseases and cellular disorders and narrow down the number of experiments required for medical diagnostic.

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Easier Access to Bioinformatics Resources




The BioInformatics Resource Inventory (B.I.R.I.) is a public online searchable index of bioinformatics resources developed at the Biomedical Informatics Group. Information describing the resources has been automatically extracted from the literature and indexed using Natural Language and Text Mining techniques. The index is automatically updated by analyzing new papers describing existing resources (databases, tools, services…

The best part is that the team has made the new methodology available to everyone via a Web application called BioInformatics Resource Inventory (B.I.R.I.). BIRI allows the whole scientific community to search for bioinformatics resources by name, category, and domain.

Tuesday 7 August 2012

Protein sequence analysis A practical guide "A taste of bioinformatics"

Protein sequence analysis
A practical guide


"A taste of bioinformatics" 
 
This is an interactive exercise that aims to provide a taste of bioinformatics resources around the world. With hope to give a flavor of sequence analysis, by introducing a range of widely-used analysis tools and databases.
In this tutorial, brief instructions are given in the headers; their highlighted phrases control the contents of the left- and right- hand frames. 
There's plenty of time to complete the practical, so don't rush. 
 
 

how proteins really fold... (intresting way)


A short introduction to Bioinformatics..

What is Bioinformatics?

The genomic era

The genomic era has seen a massive explosion in the amount of biological information available due to huge advances in the fields of molecular biology and genomics.

Bioinformatics is the application of computer technology to the management and analysis of biological data. The result is that computers are being used to gather, store, analyse and merge biological data.

Bioinformatics is an interdisciplinary research area that is the interface between the biological and computational sciences. The ultimate goal of bioinformatics is to uncover the wealth of biological information hidden in the mass of data and obtain a clearer insight into the fundamental biology of organisms. This new knowledge could have profound impacts on fields as varied as human health, agriculture, the environment, energy and biotechnology.

Why is bioinformatics important?


The greatest challenge facing the molecular biology community today is to make sense of the wealth of data that has been produced by the genome sequencing projects. Traditionally, molecular biology research was carried out entirely at the experimental laboratory bench but the huge increase in the scale of data being produced in this genomic era has seen a need to incorporate computers into this research process.

Sequence generation, and its subsequent storage, interpretation and analysis are entirely computer dependent tasks. However, the molecular biology of an organism is a very complex issue with research being carried out at different levels including the genome, proteome, transcriptome and metabalome levels. Following on from the explosion in volume of genomic data, similar increase in data have been observed in the fields of proteomics, transcriptomics and metabalomics.

The first challenge facing the bioinformatics community today is the intelligent and efficient storage of this mass of data. It is then their responsibility to provide easy and reliable access to this data. The data itself is meaningless before analysis and the sheer volume present makes it impossible for even a trained biologist to begin to interpret it manually. Therefore, incisive computer tools must be developed to allow the extraction of meaningful biological information.

There are three central biological processes around which bioinformatics tools must be developed:
  • DNA sequence determines protein sequence
  • Protein sequence determines protein structure
  • Protein structure determines protein function
The integration of information learned about these key biological processes should allow us to achieve the long term goal of the complete understanding of the biology of organisms.




Biological databases


Biological databases are archives of consistent data that are stored in a uniform and efficient manner. These databases contain data from a broad spectrum of molecular biology areas. Primary or archived databases contain information and annotation of DNA and protein sequences, DNA and protein structures and DNA and protein expression profiles.

Secondary or derived databases are so called because they contain the results of analysis on the primary resources including information on sequence patterns or motifs, variants and mutations and evolutionary relationships. Information from the literature is contained in bibliographic databases, such as Medline.

It is essential that these databases are easily accessible and that an intuitive query system is provided to allow researchers to obtain very specific information on a particular biological subject. The data should be provided in a clear, consistent manner with some visualization tools to aid biological interpretation.

Specialist databases for particular subjects have been set-up for example EMBL database for nucleotide sequence data, UniProtKB/Swiss-Prot protein database and PDBe a 3D protein structure database.

Scientists also need to be able to integrate the information obtained from the underlying heterogeneous databases in a sensible manner in order to be able to get a clear overview of their biological subject. SRS (Sequence Retrieval System) is a powerful, querying tool provided by the EBI that links information from more than 150 heterogeneous resources. 

 Biological applications


Once all of the biological data is stored consistently and is easily available to the scientific community, the requirement is then to provide methods for extracting the meaningful information from the mass of data. Bioinformatic tools are software programs that are designed to carry out this analysis step.

Factors that must be taken into consideration when designing these tools are:
  • The end user (the biologist) may not be a frequent user of computer technology
  • These software tools must be made available over the internet given the global distribution of the scientific research community
The EBI provides a wide range of biological data analysis tools that fall into the following four major categories:


Similarity Searching Tools


Homologous sequences are sequences that are related by divergence from a common ancestor. Thus the degree of similarity between two sequences can be measured while their homology is a case of being either true of false. This set of tools can be used to identify similarities between novel query sequences of unknown structure and function and database sequences whose structure and function have been elucidated.

Protein Function Analysis


This group of programs allow you to compare your protein sequence to the secondary (or derived) protein databases that contain information on motifs, signatures and protein domains. Highly significant hits against these different pattern databases allow you to approximate the biochemical function of your query protein.

Structural Analysis


This set of tools allow you to compare structures with the known structure databases. The function of a protein is more directly a consequence of its structure rather than its sequence with structural homologs tending to share functions. The determination of a protein's 2D/3D structure is crucial in the study of its function.

Sequence Analysis


This set of tools allows you to carry out further, more detailed analysis on your query sequence including evolutionary analysis, identification of mutations, hydropathy regions, CpG islands and compositional biases. The identification of these and other biological properties are all clues that aid the search to elucidate the specific function of your sequence.


Real world applications of bioinformatics


The science of bioinformatics has many beneficial uses in the modern day world.

These include the following:




1. Molecular medicine

The human genome will have profound effects on the fields of biomedical research and clinical medicine. Every disease has a genetic component. This may be inherited (as is the case with an estimated 3000-4000 hereditary disease including Cystic Fibrosis and Huntingtons disease) or a result of the body's response to an environmental stress which causes alterations in the genome (eg. cancers, heart disease, diabetes..).

The completion of the human genome means that we can search for the genes directly associated with different diseases and begin to understand the molecular basis of these diseases more clearly. This new knowledge of the molecular mechanisms of disease will enable better treatments, cures and even preventative tests to be developed.





1.1 More drug targets


At present all drugs on the market target only about 500 proteins. With an improved understanding of disease mechanisms and using computational tools to identify and validate new drug targets, more specific medicines that act on the cause, not merely the symptoms, of the disease can be developed. These highly specific drugs promise to have fewer side effects than many of today's medicines.




1.2 Personalised medicine


Clinical medicine will become more personalised with the development of the field of pharmacogenomics. This is the study of how an individual's genetic inheritence affects the body's response to drugs. At present, some drugs fail to make it to the market because a small percentage of the clinical patient population show adverse affects to a drug due to sequence variants in their DNA.

As a result, potentially life saving drugs never make it to the marketplace. Today, doctors have to use trial and error to find the best drug to treat a particular patient as those with the same clinical symptoms can show a wide range of responses to the same treatment. In the future, doctors will be able to analyse a patient's genetic profile and prescribe the best available drug therapy and dosage from the beginning.


1.3 Preventative medicine


With the specific details of the genetic mechanisms of diseases being unravelled, the development of diagnostic tests to measure a persons susceptibility to different diseases may become a distinct reality. Preventative actions such as change of lifestyle or having treatment at the earliest possible stages when they are more likely to be successful, could result in huge advances in our struggle to conquer disease.



1.4 Gene therapy


In the not too distant future, the potential for using genes themselves to treat disease may become a reality. Gene therapy is the approach used to treat, cure or even prevent disease by changing the expression of a persons genes. Currently, this field is in its infantile stage with clinical trials for many different types of cancer and other diseases ongoing.

2. Microbial genome applications

Microorganisms are ubiquitous, that is they are found everywhere. They have been found surviving and thriving in extremes of heat, cold, radiation, salt, acidity and pressure. They are present in the environment, our bodies, the air, food and water.

Traditionally, use has been made of a variety of microbial properties in the baking, brewing and food industries. The arrival of the complete genome sequences and their potential to provide a greater insight into the microbial world and its capacities could have broad and far reaching implications for environment, health, energy and industrial applications. For these reasons, in 1994, the US Department of Energy (DOE) initiated the MGP (Microbial Genome Project) to sequence genomes of bacteria useful in energy production, environmental cleanup, industrial processing and toxic waste reduction.

By studying the genetic material of these organisms, scientists can begin to understand these microbes at a very fundamental level and isolate the genes that give them their unique abilities to survive under extreme conditions.




2.1 Waste cleanup


Deinococcus radiodurans is known as the world's toughest bacteria and it is the most radiation resistant organism known. Scientists are interested in this organism because of its potential usefulness in cleaning up waste sites that contain radiation and toxic chemicals.
 
Microbial Genome Program (MGP) scientists are determining the DNA sequence of the genome of C. crescentus, one of the organisms responsible for sewage treatment.



2.2 Climate change


Increasing levels of carbon dioxide emission, mainly through the expanding use of fossil fuels for energy, are thought to contribute to global climate change. Recently, the DOE (Department of Energy, USA) launched a program to decrease atmospheric carbon dioxide levels. One method of doing so is to study the genomes of microbes that use carbon dioxide as their sole carbon source.



2.3 Alternative energy sources


Scientists are studying the genome of the microbe Chlorobium tepidum which has an unusual capacity for generating energy from light.


2.4 Biotechnology


The archaeon Archaeoglobus fulgidus and the bacterium Thermotoga maritima have potential for practical applications in industry and government-funded environmental remediation. These microorganisms thrive in water temperatures above the boiling point and therefore may provide the DOE, the Department of Defence, and private companies with heat-stable enzymes suitable for use in industrial processes. Other industrially useful microbes include, Corynebacterium glutamicum which is of high industrial interest as a research object because it is used by the chemical industry for the biotechnological production of the amino acid lysine. The substance is employed as a source of protein in animal nutrition. Lysine is one of the essential amino acids in animal nutrition. Biotechnologically produced lysine is added to feed concentrates as a source of protein, and is an alternative to soybeans or meat and bonemeal.

Xanthomonas campestris pv. is grown commercially to produce the exopolysaccharide xanthan gum, which is used as a viscosifying and stabilising agent in many industries.

Lactococcus lactis is one of the most important micro-organisms involved in the dairy industry, it is a non-pathogenic rod-shaped bacterium that is critical for manufacturing dairy products like buttermilk, yogurt and cheese. This bacterium, Lactococcus lactis ssp., is also used to prepare pickled vegetables, beer, wine, some breads and sausages and other fermented foods. Researchers anticipate that understanding the physiology and genetic make-up of this bacterium will prove invaluable for food manufacturers as well as the pharmaceutical industry, which is exploring the capacity of L. lactis to serve as a vehicle for delivering drugs.





2.5 Antibiotic resistance


Scientists have been examining the genome of Enterococcus faecalis a leading cause of bacterial infection among hospital patients. They have discovered a virulence region made up of a number of antibiotic-resistant genes that may contribute to the bacterium's transformation from a harmless gut bacteria to a menacing invader. The discovery of the region, known as a pathogenicity island, could provide useful markers for detecting pathogenic strains and help to establish controls to prevent the spread of infection in wards.


2.6 Forensic analysis of microbes


Scientists used their genomic tools to help distinguish between the strain of Bacillus anthracis that was used in the summer of 2001 terrorist attack in Florida with that of closely related anthrax strains.



2.7 The reality of bioweapon creation


Scientists have recently built the virus poliomyelitis using entirely artificial means. They did this using genomic data available on the Internet and materials from a mail-order chemical supply. The research was financed by the US Department of Defence as part of a biowarfare response program to prove to the world the reality of bioweapons. The researchers also hope their work will discourage officials from ever relaxing programs of immunisation. This project has been met with very mixed feeelings, and more.



2.8 Evolutionary studies


The sequencing of genomes from all three domains of life, eukaryota, bacteria and archaea means that evolutionary studies can be performed in a quest to determine the tree of life and the last universal common ancestor. For more interesting stories, check the archive at the Genome News Network (GNN).

For information on structural, functional and comparative analysis of genomes and genes from a wide variety of organisms see The Institute of Genomic Research (TIGR).


3. Agriculture

The sequencing of the genomes of plants and animals should have enormous benefits for the agricultural community. Bioinformatic tools can be used to search for the genes within these genomes and to elucidate their functions. This specific genetic knowledge could then be used to produce stronger, more drought, disease and insect resistant crops and improve the quality of livestock making them healthier, more disease resistant and more productive.



3.1 Crops


Comparative genetics of the plant genomes has shown that the organisation of their genes has remained more conserved over evolutionary time than was previously believed. These findings suggest that information obtained from the model crop systems can be used to suggest improvements to other food crops. Arabidopsis thaliana (water cress) and Oryza sativa (rice) are examples of available complete plant genomes.


3.2 Insect resistance


Genes from Bacillus thuringiensis that can control a number of serious pests have been successfully transferred to cotton, maize and potatoes. This new ability of the plants to resist insect attack means that the amount of insecticides being used can be reduced and hence the nutritional quality of the crops is increased.



3.3 Improve nutritional quality


Scientists have recently succeeded in transferring genes into rice to increase levels of Vitamin A, iron and other micronutrients. This work could have a profound impact in reducing occurrences of blindness and anaemia caused by deficiencies in Vitamin A and iron respectively.

Scientists have inserted a gene from yeast into the tomato, and the result is a plant whose fruit stays longer on the vine and has an extended shelf life,and more.


3.4 Grow in poorer soils and drought resistant


Progress has been made in developing cereal varieties that have a greater tolerance for soil alkalinity, free aluminium and iron toxicities. These varieties will allow agriculture to succeed in poorer soil areas, thus adding more land to the global production base. Research is also in progress to produce crop varieties capable of tolerating reduced water conditions.


4. Animals


Sequencing projects of many farm animals including cows, pigs and sheep are now well under way in the hope that a better understanding of the biology of these organisms will have huge impacts for improving the production and health of livestock and ultimately have benefits for human nutrition.


5. Comparative studies


Analysing and comparing the genetic material of different species is an important method for studying the functions of genes, the mechanisms of inherited diseases and species evolution. Bioinformatics tools can be used to make comparisons between the numbers, locations and biochemical functions of genes in different organisms.

Organisms that are suitable for use in experimental research are termed model organisms. They have a number of properties that make them ideal for research purposes including short life spans, rapid reproduction, being easy to handle, inexpensive and they can be manipulated at the genetic level.

An example of a human model organism is the mouse. Mouse and human are very closely related (>98%) and for the most part we see a one to one correspondence between genes in the two species. Manipulation of the mouse at the molecular level and genome comparisons between the two species can and is revealing detailed information on the functions of human genes, the evolutionary relationship between the two species and the molecular mechanisms of many human diseases.

Thursday 31 May 2012

Perl Video Tutorial:125 PERL TUTORIAL VIDEOS by ScriptSocket

Excellent Video lectureshttp://www.scriptsocket.com/videos.php

Immunology :Complement System By Dr. Najeeb

Complement System 1/18:     http://www.youtube.com/watch?v=9IyufZf6QOM 

Complement System 2/18:     http://www.youtube.com/watch?v=QlZ6JP27noY&feature=relmfu

Complement System 3/18:     http://www.youtube.com/watch?v=H0zpC4HEEIU&feature=relmfu

Complement System 4/18:     http://www.youtube.com/watch?v=srDa-5fzF48&feature=relmfu

Complement System 5/18:     http://www.youtube.com/watch?v=m3FN1FcP8J4&feature=relmfu

Complement System 6/18:     http://www.youtube.com/watch?v=_d1p0php5jE&feature=relmfu

Complement System 718:     http://www.youtube.com/watch?v=3xgIQiSlnII&feature=relmfu

Complement System 8/18:     http://www.youtube.com/watch?v=tp7xqYyWJNg&feature=relmfu

Complement System 9/18:     http://www.youtube.com/watch?v=1wiQg_H1zAE&feature=relmfu

Complement System 10/18:     http://www.youtube.com/watch?v=kmc0VFTnvag&feature=relmfu

Complement System 11/18:     http://www.youtube.com/watch?v=IP78HTgy3x0&feature=relmfu

Complement System 12/18:     http://www.youtube.com/watch?v=4oTEDbMTohs&feature=relmfu

Complement System 13/18:     http://www.youtube.com/watch?v=drGPXWdoCSU&feature=relmfu

Complement System 14/18:     http://www.youtube.com/watch?v=IWFH3PLI9p8&feature=relmfu

Complement System 15/18:     http://www.youtube.com/watch?v=U7LH47juGdg&feature=relmfu

Complement System 16/18:     http://www.youtube.com/watch?v=QMgIRl8C4Xs&feature=relmfu

Complement System 1/718:     http://www.youtube.com/watch?v=s-swEsKBOR0&feature=relmfu

Complement System 18/18:     http://www.youtube.com/watch?v=Es1U6t5Jm2w&feature=relmfu

Wednesday 8 February 2012

Admission Notification for M.Phil/PhD/Pre-PhD Programme at various centres & Schools of JNU, New Delhi

JAWAHARLAL NEHRU UNIVERSITY
Admission Announcement : 2012-13

(Category-A) ADMISSION THROUGH ENTRANCE EXAMINATION
The University will hold Entrance Examination on May 22, 23, 24 and 25, 2012 for admission to various full-time programmes of study at the following 51 cities : Agartala, Ahmedabad, Aizawl, Allahabad, Amritsar, Bangalore, Bareilly, Bhubaneshwar, Calicut, Chandigarh, Chennai, Coimbatore, Dehradun, Delhi, Dimapur, Gangtok, Guwahati, Goa, Gorakhpur, Gwalior, Hyderabad, Imphal, Indore, Itanagar, Jaipur, Jammu, Katihar, Kolkata, Lucknow, Madurai, Mumbai, Nagpur, Noida, Pant Nagar, Patna, Pondicherry, Pune, Raipur, Ranchi, Sambalpur, Secunderabad, Shillong, Shimla, Silchar, Siliguri, Srinagar, Thiruvananthapuram, Udaipur, Varanasi, Vijayawada and Visakhapatnam. In addition, the University will hold entrance examination at Kathmandu (Nepal). (The University reserves the right to change/cancel any centre of examination without assigning any reason.)
SCHOOL OF LIFE SCIENCES :
(A) M.PHIL./PH.D. IN AREAS OF INTERDISCIPLINARY RESEARCH IN molecular biology, GENETIC ENGINEERING, PLANT Biotechnology, GENETICS, DEVELOPMENTAL BIOLOGY, Cell Biology, IMMUNOLOGY, NEUROBIOLOGY, Microbiology, RADIATION AND CANCER BIOLOGY, BIO-PHYSICS AND STRUCTURAL BIOLOGY.
ELIGIBILITY : Candidates with M.Sc. or equivalent degree, with at least 55% marks or equivalent grades, in Biological sciences, Bioinformatics or Physical Sciences, as well as those with M.B.B.S or M. Tech. or M.Sc. (Agriculture) or M. Sc. (Veterinary Sciences) degree with 55% marks are also eligible. Candidates having the M.Sc. or equivalent degree in allied subjects of Life Sciences, including Biochemistry, Biophysics, Biotechnology, Botany, Genetics, Microbiology, Pharmacology, Physiology, Zoology, or in Chemistry or Physics are also eligible. (B) M.Sc. in LIFE SCIENCES : An integrated interdisciplinary programme in Modern Biology.
ELIGIBILITY : Bachelor’s degree (B.Sc. or B.Tech or equivalent) in Biological, Physical or Agricultural Sciences under 10+2+3 pattern of education with at least 55% marks.
SCHOOL OF ENVIRONMENTAL SCIENCES :
(A) M.PHIL./PH.D. IN ENVIRONMENTAL SCIENCES INCLUDING INTERDISCIPLINARY AREAS OF BIOLOGY(ECOLOGY, Biotechnology, BIOPHYSICS, BIOREMEDIATION), CHEMISTRY (AIR, WATER, SOIL POLLUTION), GEOLOGY AND PHYSICS.
ELIGIBILITY :M.Sc. degree or equivalent in any branch of basic or applied science or MBBS or B.Tech./B.E. with minimum 55% marks.

(B) M.Sc. in ENVIRONMENTAL SCIENCES : AN INTERDISCIPLINARY COURSE WITH ENVIRONMENTAL ORIENTATION, DRAWN FROM RELEVANT AREAS OF BIOLOGICAL, CHEMICAL, EARTH AND PHYSICAL SCIENCES.

ELIGIBILITY :
Bachelor’s degree in any branch of basic or applied science under 10+2+3 pattern of education with at least 55% marks.
SCHOOL OF Biotechnology :
PRE-PH.D./PH.D. IN AREAS OF GENE TRANSFER AND EXPRESSION IN EUKARYOTIC SYSTEMS, TRANSCRIPTION CONTROL AND GENE REGULATION, PROTEIN ENGINEERING, molecular biology OF INFECTIOUS DISEASES, PROTEIN FOLDING AND STABILITY, OPTIMIZATION OF RECOMBINANT PROTEIN PRODUCTION, STRUCTURAL BIOLOGY & MOLECULAR Bioinformatics, AND BIOCHEMICAL ENGINEERING, MOLECULAR VIROLOGY, CANCER BIOLOGY, MOLECULAR Cell Biology.
ELIGIBILITY : Master’s Degree in Biotechnology, Biochemical Engineering, Biochemistry, Chemistry, Physics, Mathematics or any branch of Physical or Biological or Engineering Sciences with atleast 55% marks
CENTRE FOR MOLECULAR MEDICINE :
PRE-PH.D/PH.D IN AREAS OF METOBOLIC DISORDERS, INFECTIOUS AND NONINFECTIOUS DISEASES, DIAGNOSTICS AND MOLECULAR ENDOCRINOLOGY
ELIGIBILITY : Master’s degree or equivalent from recognized University/Institution in any branch of Biological sciences/MBBS/ BVSc./B.Pharm. with at least 55% marks.
(Category-B) DIRECT ADMISSION TO PH.D. PROGRAMME :
The University admits a limited number of candidates directly to Ph.D. programme either on the basis of viva-voce or written examination and viva-voce both as may be decided by each Centre/ School both in Monsoon and Winter Semesters in all Schools/Centres. In addition direct admission to Ph.D. is also offered in Centre for Comparative Politics and Political Theory, Adult Education, Women's Studies and Study of Discrimination and Exclusion. Candidates are required to check the availability of seats in each Centre/School before applying for admission in Winter Semester. Candidates are advised to refer to the admission announcement being notified separately.
(Category-C) ADMISSION OF JRF HOLDERS TO M.PHIL./PH.D. AND PRE-PH.D./
PH.D. PROGRAMME IN SCIENCE SCHOOLS :
The University admits a limited number of candidates to M.Phil./Ph.D. and Pre-Ph.D./Ph.D. programmes either on the basis of viva-voce or written examination and viva-voce both as may be decided by each School who have qualified a National Test entitling them to a JRF in Schools of Life Sciences, Physical Sciences, Environmental Sciences, Computer & Systems Sciences, Computational and Integrative Sciences and Biotechnology.
ELIGIBILITY: Only those candidates who fulfil the minimum eligibility requirements as prescribed for admission of candidates to M.Phil./Ph.D. and Pre-Ph.D. programmes through Entrance Examination under category A above in above Science Schools and have qualified a National Test entitling them to a JRF are eligible to apply.
HOW TO APPLY : A candidate can apply either “Online” or “Offline”. Online Application:
Candidates can apply Online on payment of prescribed fee if they have access to a computer, a printer and Internet by logging on to JNU website www.jnu.ac.in or www.jnuonline.in. The sites have been designed in a ‘user friendly’ way to help candidates for applying Online in a step-by-step fashion. Online application portal will remain open from 10:00 AM (IST) on 6th February, 2012 till 5:00 PM (IST) on 21st March, 2012. Offline Application : Set of
Application Form and Prospectus can be obtained through Post by sending crossed Bank Draft for Rs.300/- (Rs. Three Hundred only) drawn in favour of JAWAHARLAL NEHRU UNIVERSITY payble at NEW Delhi alongwith a self addressed (unstamped) envelope of the minimum size of 30 cms x 25 cms. clearly indicating the programme of study for which the Application Form is required on the self-addressed envelope to the SECTION OFFICER (ADMISSIONS), Room No.28, Administrative Block, Jawaharlal Nehru University, New Delhi 110067.
Candidates seeking a set of Application Form and Prospectus from Nepal are required to send a Demand Draft of Rs.400/- or equivalent in US Dollars. Money Orders and Cheques are not accepted. PLEASE DO NOT SEND YOUR REQUEST FOR SET OF APPLICATION FORM AND PROSPECTUS THROUGH COURIER. PLEASE NOTE THAT THERE WILL BE
NO CASH COUNTER FOR SALE OF SET OF APPLICATION FORM AND PROSPECTUS. BPL card holders will be issued a set of application form & prospectus free of cost on submissiion of a copy of the BPL card issued by the competent authority showing their name in the card.
Deadline : 21.03.12