This presentation provides the basic understanding of varous genomics and proteomics techniques.Systems biology studies life as a system .It includes the study of living system using various omic technologies .
Introduction
Overview
Reductionist approach
Holistic approach
What is systems biology?
○ Advantages of Systems Biology
Tools of holistic approach
○ Proteomics, Transcriptomics and Metabolomics
Conclusion
References
Systems biology is the computational and mathematical modeling of complex biological systems. It is a biology-based interdisciplinary field of study that focuses on complex interactions within biological systems, using a holistic approach (holism instead of the more traditional reductionism) to biological research.
Protein structure classification/domain prediction: SCOP and CATH (Bioinforma...SELF-EXPLANATORY
This pdf is about the protein structure classification/domain prediction: SCOP and CATH (Bioinformatics).
For more details visit on YouTube; @SELF-EXPLANATORY;
https://www.youtube.com/channel/UCAiarMZDNhe1A3Rnpr_WkzA/videos
Thanks...!
Introduction
Overview
Reductionist approach
Holistic approach
What is systems biology?
○ Advantages of Systems Biology
Tools of holistic approach
○ Proteomics, Transcriptomics and Metabolomics
Conclusion
References
Systems biology is the computational and mathematical modeling of complex biological systems. It is a biology-based interdisciplinary field of study that focuses on complex interactions within biological systems, using a holistic approach (holism instead of the more traditional reductionism) to biological research.
Protein structure classification/domain prediction: SCOP and CATH (Bioinforma...SELF-EXPLANATORY
This pdf is about the protein structure classification/domain prediction: SCOP and CATH (Bioinformatics).
For more details visit on YouTube; @SELF-EXPLANATORY;
https://www.youtube.com/channel/UCAiarMZDNhe1A3Rnpr_WkzA/videos
Thanks...!
Transcriptomics is the study of RNA, single-stranded nucleic acid, which was not separated from the DNA world until the central dogma was formulated by Francis Crick in 1958, i.e., the idea that genetic information is transcribed from DNA to RNA and then translated from RNA into protein.
Proteins play crucial roles in nearly all biological processes. These many functions of proteins are a result of the folding of proteins into many distinct 3D structures.
Protein analysis tries to explore how amino acid sequences specify the structure of proteins and how these proteins bind to substrates and other molecules to perform their functions.
Protein analysis allows us to understand the function of the protein based on its structure.
After sequencing of the genome has been done, the first thing that comes to mind is "Where are the genes?". Genome annotation is the process of attaching information to the biological sequences. It is an active area of research and it would help scientists a lot to undergo with their wet lab projects once they know the coding parts of a genome.
Genome annotation, NGS sequence data, decoding sequence information, The genome contains all the biological information required to build and maintain any given living organism.
Ab Initio Protein Structure Prediction is a method to determine the tertiary structure of protein in the absence of experimentally solved structure of a similar/homologous protein. This method builds protein structure guided by energy function.
I had prepared this presentation for an internal project during my masters degree course.
Systems Biology and Genomics of Microbial PathogensRamy K. Aziz
Talk at SCITA-BIOFANS (02 Feb 2016), entitled
"Systems Biology and Genomics of Microbial Pathogens:
From virulence gene discovery to vaccine development and therapeutic intervention"
Transcriptomics is the study of RNA, single-stranded nucleic acid, which was not separated from the DNA world until the central dogma was formulated by Francis Crick in 1958, i.e., the idea that genetic information is transcribed from DNA to RNA and then translated from RNA into protein.
Proteins play crucial roles in nearly all biological processes. These many functions of proteins are a result of the folding of proteins into many distinct 3D structures.
Protein analysis tries to explore how amino acid sequences specify the structure of proteins and how these proteins bind to substrates and other molecules to perform their functions.
Protein analysis allows us to understand the function of the protein based on its structure.
After sequencing of the genome has been done, the first thing that comes to mind is "Where are the genes?". Genome annotation is the process of attaching information to the biological sequences. It is an active area of research and it would help scientists a lot to undergo with their wet lab projects once they know the coding parts of a genome.
Genome annotation, NGS sequence data, decoding sequence information, The genome contains all the biological information required to build and maintain any given living organism.
Ab Initio Protein Structure Prediction is a method to determine the tertiary structure of protein in the absence of experimentally solved structure of a similar/homologous protein. This method builds protein structure guided by energy function.
I had prepared this presentation for an internal project during my masters degree course.
Systems Biology and Genomics of Microbial PathogensRamy K. Aziz
Talk at SCITA-BIOFANS (02 Feb 2016), entitled
"Systems Biology and Genomics of Microbial Pathogens:
From virulence gene discovery to vaccine development and therapeutic intervention"
A set of ideas on the use of artificial intelligence for data curation that has been presented at the Pharma-IT conference (London, 2017), in the artificial intelligence track.
It begins with some broad discussion about semantic web, knowledge representation, machine learning and artificial intelligence. It the focus on how a "data curation" problem can be framed and hints at some possible examples.
A (vintage) presentation about a database system for the study of gene expression data. Including distributed metadata annotation and some interactive analytics. Some ideas are still actual today.
I elaborated these slides for an introductory class on Network Medicine given at UPV (Valencia) in October 2017. The fundamental principle behind Network Medicine is that disease phenotypes emerge from genotypes via the network properties of interactions between the underlying biological components. These phenotypes are best conceptualized as consequences of perturbations to disease modules of the biological networks in the cell, whether at the node level (disease genes) or the link level (disease edgotypes). With the further analysis of drug-disease association and drug-target association data, one can investigate the effects - therapeutic and undesired - of the associated medication. Understanding the molecular level networks allows to understand the connections between different diseases and the effects of drugs designed to target them, paving the way for personalized treatments based on one's own interactome.
The Opera of Phantome - 2017 (presented at the 22nd Biennial Evergreen Phage ...Ramy K. Aziz
Tools and Methods developed under the SEED/RAST/PhAnToMe (http://www.phantome.org) project and sequels adopted in RASTtk and PATRIC. The tools and database rely on the Subsystems Technology, the SEED (http://theseed.org) environment, and RAST server (http://rast.nmpdr.org).
This is a part of the Phage Genomics Workshop at the 22nd Biennial Evergreen International Phage Meeting, Aug 6 2017.
Dr. Leroy Hood lectured to a group of Ohio State University College of Medicine students and faculty on May 13, 2010 in advance of an announcement of a partnership between the Ohio State University Medical Center and the Institute for Systems Biology. The partnership will be known as
GENOMICS
Genomics is the study of all genes in an organism, also known as its genome. Genomics includes identifying the specific building blocks of all the genes in a cell, mapping their location in relation to the rest of the DNA, and studying the function of those genes or combination of those genes.
Types of Genomics :
1. Structural Genomics
2. Comparative Genomics
3.Functional Genomics
4. Epigenomics
5. Metagenomics
6. Pharmacogenomics
7. Mutation Genomics.
PROTEOMICS : (PROTEin in complement to genOME)
Proteomics is the study of proteome [Proteome is a protein molecule that interacts to give the cell its individual character]. Proteomics is a subset of functional genomics.
The proteome of a cell is all the proteins expressed by its genome. The proteome is of intense interest to investigators because proteins are the major functional components of the cell.
Proteomics is the study of proteins in order to revolutionize the understanding of cell behaviour and disease.
1. It studies the translation of process of RNA into proteins as well as the overall process of DNA into proteins.
2. It studies the diseases through proteins because disease process manifest themselves at the level of protein activity.
3. Most drugs act by targeting proteins or protein receptors, so Proteomics is important in new generation of drugs.
4. Proteins are more complex than genes because they can be modified after formation.
5. Proteomics is the qualitative and quantitative comparison of proteomes under different conditions to further unravel biological processes.
6. Proteomics can use analysis techniques to determine all of the post translational modifications that proteins undergo and therefore determine what makes a diseased or mutant protein different from a normal protein.
Proteins are fundamental components of all living cells. Proteins help us digest our food, fight infections, control body chemistry, keep our bodies function smoothly. Identifying a proteins’ shape or structure is key to understanding its biological function and its role in health and disease.
Project report: Investigating the effect of cellular objectives on genome-sca...Jarle Pahr
Report from a half-semester master-level project carried out at the department of biotechnology, Norwegian University of Science and Technology. Describes a MATLAB-based framework for comparing experimental metabolic flux data with model predictions and evaluating objective functions.
Mass spectrometry is a powerful analytical technique used to quantify known materials, to identify unknown compounds within a sample, and to elucidate the structure and chemical properties of different molecules. The complete process involves the conversion of the sample into gaseous ions, with or without fragmentation, which are then characterized by their mass to charge ratios (m/z) and relative abundances.
This technique basically studies the effect of ionizing energy on molecules. It depends upon chemical reactions in the gas phase in which sample molecules are consumed during the formation of ionic and neutral species.
Interactomics, Integromics to Systems Biology: Next Animal Biotechnology Fron...Varij Nayan
“Organisms function in an integrated manner-our senses, our muscles, our metabolism and our minds work together seamlessly. But biologists have historically studied organisms part by part and celebrated the modern ability to study them molecule by molecule, gene by gene. Systems biology is critical science of future that seeks to understand the integration of the pieces to form biological
systems”
(David Baltimore, Nobel Laureate)
Genomics, Transcriptomics, Proteomics, Metabolomics - Basic concepts for clin...Prasenjit Mitra
This set of slides gives an overview regarding the various omics technologies available and how they can be used for improvement in clinical setting or research
Seminar of U.V. Spectroscopy by SAMIR PANDASAMIR PANDA
Spectroscopy is a branch of science dealing the study of interaction of electromagnetic radiation with matter.
Ultraviolet-visible spectroscopy refers to absorption spectroscopy or reflect spectroscopy in the UV-VIS spectral region.
Ultraviolet-visible spectroscopy is an analytical method that can measure the amount of light received by the analyte.
THE IMPORTANCE OF MARTIAN ATMOSPHERE SAMPLE RETURN.Sérgio Sacani
The return of a sample of near-surface atmosphere from Mars would facilitate answers to several first-order science questions surrounding the formation and evolution of the planet. One of the important aspects of terrestrial planet formation in general is the role that primary atmospheres played in influencing the chemistry and structure of the planets and their antecedents. Studies of the martian atmosphere can be used to investigate the role of a primary atmosphere in its history. Atmosphere samples would also inform our understanding of the near-surface chemistry of the planet, and ultimately the prospects for life. High-precision isotopic analyses of constituent gases are needed to address these questions, requiring that the analyses are made on returned samples rather than in situ.
Introduction:
RNA interference (RNAi) or Post-Transcriptional Gene Silencing (PTGS) is an important biological process for modulating eukaryotic gene expression.
It is highly conserved process of posttranscriptional gene silencing by which double stranded RNA (dsRNA) causes sequence-specific degradation of mRNA sequences.
dsRNA-induced gene silencing (RNAi) is reported in a wide range of eukaryotes ranging from worms, insects, mammals and plants.
This process mediates resistance to both endogenous parasitic and exogenous pathogenic nucleic acids, and regulates the expression of protein-coding genes.
What are small ncRNAs?
micro RNA (miRNA)
short interfering RNA (siRNA)
Properties of small non-coding RNA:
Involved in silencing mRNA transcripts.
Called “small” because they are usually only about 21-24 nucleotides long.
Synthesized by first cutting up longer precursor sequences (like the 61nt one that Lee discovered).
Silence an mRNA by base pairing with some sequence on the mRNA.
Discovery of siRNA?
The first small RNA:
In 1993 Rosalind Lee (Victor Ambros lab) was studying a non- coding gene in C. elegans, lin-4, that was involved in silencing of another gene, lin-14, at the appropriate time in the
development of the worm C. elegans.
Two small transcripts of lin-4 (22nt and 61nt) were found to be complementary to a sequence in the 3' UTR of lin-14.
Because lin-4 encoded no protein, she deduced that it must be these transcripts that are causing the silencing by RNA-RNA interactions.
Types of RNAi ( non coding RNA)
MiRNA
Length (23-25 nt)
Trans acting
Binds with target MRNA in mismatch
Translation inhibition
Si RNA
Length 21 nt.
Cis acting
Bind with target Mrna in perfect complementary sequence
Piwi-RNA
Length ; 25 to 36 nt.
Expressed in Germ Cells
Regulates trnasposomes activity
MECHANISM OF RNAI:
First the double-stranded RNA teams up with a protein complex named Dicer, which cuts the long RNA into short pieces.
Then another protein complex called RISC (RNA-induced silencing complex) discards one of the two RNA strands.
The RISC-docked, single-stranded RNA then pairs with the homologous mRNA and destroys it.
THE RISC COMPLEX:
RISC is large(>500kD) RNA multi- protein Binding complex which triggers MRNA degradation in response to MRNA
Unwinding of double stranded Si RNA by ATP independent Helicase
Active component of RISC is Ago proteins( ENDONUCLEASE) which cleave target MRNA.
DICER: endonuclease (RNase Family III)
Argonaute: Central Component of the RNA-Induced Silencing Complex (RISC)
One strand of the dsRNA produced by Dicer is retained in the RISC complex in association with Argonaute
ARGONAUTE PROTEIN :
1.PAZ(PIWI/Argonaute/ Zwille)- Recognition of target MRNA
2.PIWI (p-element induced wimpy Testis)- breaks Phosphodiester bond of mRNA.)RNAse H activity.
MiRNA:
The Double-stranded RNAs are naturally produced in eukaryotic cells during development, and they have a key role in regulating gene expression .
What is greenhouse gasses and how many gasses are there to affect the Earth.moosaasad1975
What are greenhouse gasses how they affect the earth and its environment what is the future of the environment and earth how the weather and the climate effects.
A brief information about the SCOP protein database used in bioinformatics.
The Structural Classification of Proteins (SCOP) database is a comprehensive and authoritative resource for the structural and evolutionary relationships of proteins. It provides a detailed and curated classification of protein structures, grouping them into families, superfamilies, and folds based on their structural and sequence similarities.
Cancer cell metabolism: special Reference to Lactate PathwayAADYARAJPANDEY1
Normal Cell Metabolism:
Cellular respiration describes the series of steps that cells use to break down sugar and other chemicals to get the energy we need to function.
Energy is stored in the bonds of glucose and when glucose is broken down, much of that energy is released.
Cell utilize energy in the form of ATP.
The first step of respiration is called glycolysis. In a series of steps, glycolysis breaks glucose into two smaller molecules - a chemical called pyruvate. A small amount of ATP is formed during this process.
Most healthy cells continue the breakdown in a second process, called the Kreb's cycle. The Kreb's cycle allows cells to “burn” the pyruvates made in glycolysis to get more ATP.
The last step in the breakdown of glucose is called oxidative phosphorylation (Ox-Phos).
It takes place in specialized cell structures called mitochondria. This process produces a large amount of ATP. Importantly, cells need oxygen to complete oxidative phosphorylation.
If a cell completes only glycolysis, only 2 molecules of ATP are made per glucose. However, if the cell completes the entire respiration process (glycolysis - Kreb's - oxidative phosphorylation), about 36 molecules of ATP are created, giving it much more energy to use.
IN CANCER CELL:
Unlike healthy cells that "burn" the entire molecule of sugar to capture a large amount of energy as ATP, cancer cells are wasteful.
Cancer cells only partially break down sugar molecules. They overuse the first step of respiration, glycolysis. They frequently do not complete the second step, oxidative phosphorylation.
This results in only 2 molecules of ATP per each glucose molecule instead of the 36 or so ATPs healthy cells gain. As a result, cancer cells need to use a lot more sugar molecules to get enough energy to survive.
Unlike healthy cells that "burn" the entire molecule of sugar to capture a large amount of energy as ATP, cancer cells are wasteful.
Cancer cells only partially break down sugar molecules. They overuse the first step of respiration, glycolysis. They frequently do not complete the second step, oxidative phosphorylation.
This results in only 2 molecules of ATP per each glucose molecule instead of the 36 or so ATPs healthy cells gain. As a result, cancer cells need to use a lot more sugar molecules to get enough energy to survive.
introduction to WARBERG PHENOMENA:
WARBURG EFFECT Usually, cancer cells are highly glycolytic (glucose addiction) and take up more glucose than do normal cells from outside.
Otto Heinrich Warburg (; 8 October 1883 – 1 August 1970) In 1931 was awarded the Nobel Prize in Physiology for his "discovery of the nature and mode of action of the respiratory enzyme.
WARNBURG EFFECT : cancer cells under aerobic (well-oxygenated) conditions to metabolize glucose to lactate (aerobic glycolysis) is known as the Warburg effect. Warburg made the observation that tumor slices consume glucose and secrete lactate at a higher rate than normal tissues.
Deep Behavioral Phenotyping in Systems Neuroscience for Functional Atlasing a...Ana Luísa Pinho
Functional Magnetic Resonance Imaging (fMRI) provides means to characterize brain activations in response to behavior. However, cognitive neuroscience has been limited to group-level effects referring to the performance of specific tasks. To obtain the functional profile of elementary cognitive mechanisms, the combination of brain responses to many tasks is required. Yet, to date, both structural atlases and parcellation-based activations do not fully account for cognitive function and still present several limitations. Further, they do not adapt overall to individual characteristics. In this talk, I will give an account of deep-behavioral phenotyping strategies, namely data-driven methods in large task-fMRI datasets, to optimize functional brain-data collection and improve inference of effects-of-interest related to mental processes. Key to this approach is the employment of fast multi-functional paradigms rich on features that can be well parametrized and, consequently, facilitate the creation of psycho-physiological constructs to be modelled with imaging data. Particular emphasis will be given to music stimuli when studying high-order cognitive mechanisms, due to their ecological nature and quality to enable complex behavior compounded by discrete entities. I will also discuss how deep-behavioral phenotyping and individualized models applied to neuroimaging data can better account for the subject-specific organization of domain-general cognitive systems in the human brain. Finally, the accumulation of functional brain signatures brings the possibility to clarify relationships among tasks and create a univocal link between brain systems and mental functions through: (1) the development of ontologies proposing an organization of cognitive processes; and (2) brain-network taxonomies describing functional specialization. To this end, tools to improve commensurability in cognitive science are necessary, such as public repositories, ontology-based platforms and automated meta-analysis tools. I will thus discuss some brain-atlasing resources currently under development, and their applicability in cognitive as well as clinical neuroscience.
This presentation explores a brief idea about the structural and functional attributes of nucleotides, the structure and function of genetic materials along with the impact of UV rays and pH upon them.
Professional air quality monitoring systems provide immediate, on-site data for analysis, compliance, and decision-making.
Monitor common gases, weather parameters, particulates.
Systems biology & Approaches of genomics and proteomics
1. Systems biology
(integrative biology)
Systems biology is the study of an
organism, viewed as an integrated and
interacting network of genes, proteins and
biochemical reactions which give rise to
life.o (Institute of Systems Biology).
Ultimate goal:to predict de novo biological
outcomes given the list of components
involved. (Genome Institute of Singapore).
2. Systemic perturbation of biological system
Monitoring the pathway responses
Integration of the data
Formulation of mathematical models that
describe the structure of the system &
its response to pertubations.
6. 09/04/15
Concepts in systems biology
• System
• Systems thinking
• Complexity theory
• Nonlinear dynamics
• Feedback control
• Robustness
• Emergent properties
• Network
8. A FRAMEWORK FOR SYSTEMS
BIOLOGY
Define all of the components of the system.
Systematically perturb and monitor the components.
Reconcile the experimentally observed responses with those
predicted by the model.
Design and perform new perturbation experiments to distinguish
between multiple or competing model hypotheses.
After choosing the set of new perturbations, repeat steps 2
through 4 and iterate.
9. Structure of systems :
Networks
APPROACHES:
1.Bottom up approach
•tries to construct a gene regulatory network
based on the compilation of independent
experimental data
2.Top down approach
•tries to make use of high throughput data
11. GENOMICS
• The branch of molecular biology concerned with the
structure, function, evolution, and mapping of
genomes i.e.study of genome.
• GENOME : the collection of genes contained within
a complete (haploid) set of chromosomes. The
genome is a static information resource with a
defined gene content.
15. In this process ,four reactin mixtures are set up; each one including:
1.DNA to be sequenced 2.DNA polymerase
3.A supply of nucleotides(A,G,C,T)
4.A small amount of labelled chain
terminating nucleotide :one in each of reaction mixture.
.
16. DNA polymerase synthesise the DNA but incorporation
of terminating nucleotide cause polymerization
to stop.
17.
18. Ending chain at every possible nucleotide position creates a no.
of DNA terminated at same nucleotide but different
positions(shown for 1 reaction mixture)
26. Proteomics
The term proteomics describes the study and
characterization of complete set of proteins
present in a cell, organ, or organism at a given
time .
28. Mass spectrometry (MS)
• Mass spectrometry (MS) is used to determine
the accurate masses of molecules.
• Mass spectrometry (MS) is an extremely
valuable analytical technique in which the
molecules in a test sample are converted to
gaseous ions that are subsequently separated
in a mass spectrometer according to their
mass-to-charge (m/z) ratio and detected.
40. Systems Biology vs. traditional
cell and molecular biology
• Experimental techniques in systems biology are high
throughput;but Intensive computation is involved from
the start in systems biology, in order to organize the data
into usable computable databases.
• Exploration in traditional biology proceeds by
successive cycles of hypothesis formation and testing;
data accumulates during these cycles;while Systems
biology initially gathers data without prior hypothesis
formation; hypothesis formation and testing comes
during post-experiment data analysis and modeling.
42. Understanding environment
•Understanding microbes interaction with
ecosystems
• Explain and predict consequences of complex
phenomena such as climate changes
•Recombine various mechanisms within these
diverse organisms to deal with some
extraordinary human problems
43. APPLICATIONS IN FIELD OF
MEDICINE
• In DRUG DISCOVERY
• Understanding complex situations such
as cancer
• Understanding developmental
neurotoxicology
44. CHALLENGES
1.MODELLING CHALLENGES
• Providing the means for checking the constraints and devising
modeling schemes with sound compositional mechanisms;
and
• managing models that may not be consistent with each other,
either across schemes or across scales
45. 2.CHALLENGES IN PROTEOMICS
• Membrane Proteome
• Serum Proteomics and Biomarker
Discovery
3.CHALLENGES IN HANDLING LARGE AMOUNT
OF DATA GENERATED AND COMBINING
THEM TO CREATE NETWORKS
4.SOME TIMES HYPOTHETICAL NETWORKS
GET CREATED