Genomics is the study of an organism's entire genome, including all genes and their interactions. It involves sequencing genomes and analyzing genes at the DNA, mRNA, and protein levels. The goals of genomics include sequencing entire genomes and understanding gene expression. Key applications include medical diagnosis and treatment, agriculture, evolution studies, and forensic science. Genomics played an important role in understanding COVID-19 by providing insights into the virus's origins, transmission, and potential therapies.
High throughput next generation sequencing and robust transcriptome analysis help with gene expression profiling, gene annotation or discovery of non-coding RNA.
SNP (Single Nucleotide Polymorphic), SNP mapping, SNP profile, SNP types, SNP analysis by gel electropherosis and by mass spectrometry, SNP effects, single strand conformation polymorphism, SNP advantages and disadvantages and application of SNP profile in drug choice
description of functional genomics and structural genomics and the techniques involved in it and also decribing the models of forward genetics and techniques involved in it and reverse genetics and techniques involved in it
High throughput next generation sequencing and robust transcriptome analysis help with gene expression profiling, gene annotation or discovery of non-coding RNA.
SNP (Single Nucleotide Polymorphic), SNP mapping, SNP profile, SNP types, SNP analysis by gel electropherosis and by mass spectrometry, SNP effects, single strand conformation polymorphism, SNP advantages and disadvantages and application of SNP profile in drug choice
description of functional genomics and structural genomics and the techniques involved in it and also decribing the models of forward genetics and techniques involved in it and reverse genetics and techniques involved in it
It is a presentation showing the process of doing a prokaryotic genome annotation using RAST server. It is a basic work in bioinformatics field. Genome annotation is total genome analysis of an organism. We can easily do it using bioinformatics tool like RAST server.
complete Single Nucleotide Polymorphiitsm Detection methods with Advance techniques with its applications
Single nucleotide polymorphisms are single base variations between genomes within a species.
There are at least 10 million polymorphic sites in the human genome.
SNPs can distinguish individuals from one another
Denaturing Gradient Gel Electrophoresis
Chemical Cleavage Of Mismatch
Single-stranded Conformation Polymorphism (SSCP)
MutS Protein-binding Assays
Mismatch Repair Detection (MRD)
Heteroduplex Analysis (HA)
Denaturing High Performance Liquid Chromatography (DHPLC)
UNG-Mediated T-Sequencing
RNA-Mediated Finger printing with MALDI MS Detection
Sequencing by Hybridization
Direct DNA Sequencing
Single-feature polymorphism (SFP)
Invader probe
Allele-specific oligonucleotide probes
PCR-based methods
Allele specific primers
Sequence Polymorphism-Derived (SPD) markers
Targeting induced local lesions in genomes (TILLinG)
Minisequencing primers
Allele-specific ligation probes
Genomics is a discipline in genetics that applies recombinant DNA, DNA sequencing methods, and bioinformatics to sequence, assemble and analyze the function and structure of genomes
It is a presentation showing the process of doing a prokaryotic genome annotation using RAST server. It is a basic work in bioinformatics field. Genome annotation is total genome analysis of an organism. We can easily do it using bioinformatics tool like RAST server.
complete Single Nucleotide Polymorphiitsm Detection methods with Advance techniques with its applications
Single nucleotide polymorphisms are single base variations between genomes within a species.
There are at least 10 million polymorphic sites in the human genome.
SNPs can distinguish individuals from one another
Denaturing Gradient Gel Electrophoresis
Chemical Cleavage Of Mismatch
Single-stranded Conformation Polymorphism (SSCP)
MutS Protein-binding Assays
Mismatch Repair Detection (MRD)
Heteroduplex Analysis (HA)
Denaturing High Performance Liquid Chromatography (DHPLC)
UNG-Mediated T-Sequencing
RNA-Mediated Finger printing with MALDI MS Detection
Sequencing by Hybridization
Direct DNA Sequencing
Single-feature polymorphism (SFP)
Invader probe
Allele-specific oligonucleotide probes
PCR-based methods
Allele specific primers
Sequence Polymorphism-Derived (SPD) markers
Targeting induced local lesions in genomes (TILLinG)
Minisequencing primers
Allele-specific ligation probes
Genomics is a discipline in genetics that applies recombinant DNA, DNA sequencing methods, and bioinformatics to sequence, assemble and analyze the function and structure of genomes
this is done by me and my team mates of Wayamba University Sri Lanka for our project.From now we decided to allow download this file.I would be greatful if you could send your comments..
And I'm willing to help you in similar works.I'm in final year of my degree(.BSc Biotechnology)..
pubudu_gokarella@yahoo.com
The project was a great success, delivering the first rough draft human genome sequence in 2000 and the final high-quality version in April, 2003, ahead of schedule and under budget. For years, many considered the Human Genome Project to be biology's equivalent to "Man on the moon". This slide tends to explain the benefits of such project to medical diagnosis, treatment and management in India.
The Human Genome Project (HGP) was an international scientific research project with the goal of determining the base pairs that make up human DNA, and of identifying and mapping all of the genes of the human genome from both a physical and a functional standpoint.
What is bioinformatics?
About human genome
Human genome project
Aim of human genome project
History
Sequencing Strategy
Benefits of Human Genome Project research
Disadvantages of human genome project
Conclusion
References
HGP was conceived in 1984 & officially begun in earnest in October 1990.
HGP is a large multicentric, international collaborative venture, the main aim of which is to determine the nucleotide sequence of the entire human nuclear genome.
In 1997, United States established the National Human Genome Research Institute (NHGRI).
The HGP was an international research groups from six countries- USA, UK, France, Germany, Japan and China, & several laboratories and a large no. of scientists and technicians from various disciplines.
Conferencia de la Dra. Ana María Roa, Bióloga Molecular, sobre Epigenética, impartida en la Universidad Popular Carmen de Michelena de Tres Cantos el 1 de marzo de 2013.
Más información en:
http://www.universidadpopularc3c.es/index.php/actividades/conferencias/event/448-conferencia-una-revision-de-los-conocimientos-fundamentales-de-la-biologia-de-la-celula-la-epigenetica
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Feeding plate for a newborn with Cleft Palate.pptxSatvikaPrasad
A feeding plate is a prosthetic device used for newborns with a cleft palate to assist in feeding and improve nutrition intake. From a prosthodontic perspective, this plate acts as a barrier between the oral and nasal cavities, facilitating effective sucking and swallowing by providing a more normal anatomical structure. It helps to prevent milk from entering the nasal passage, thereby reducing the risk of aspiration and enhancing the infant's ability to feed efficiently. The feeding plate also aids in the development of the oral muscles and can contribute to better growth and weight gain. Its custom fabrication and proper fitting by a prosthodontist are crucial for ensuring comfort and functionality, as well as for minimizing potential complications. Early intervention with a feeding plate can significantly improve the quality of life for both the infant and the parents.
Deep Leg Vein Thrombosis (DVT): Meaning, Causes, Symptoms, Treatment, and Mor...The Lifesciences Magazine
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CHAPTER 1 SEMESTER V PREVENTIVE-PEDIATRICS.pdfSachin Sharma
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Cold Sores: Causes, Treatments, and Prevention Strategies | The Lifesciences ...The Lifesciences Magazine
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International Cancer Survivors Day is celebrated during June, placing the spotlight not only on cancer survivors, but also their caregivers.
CANSA has compiled a list of tips and guidelines of support:
https://cansa.org.za/who-cares-for-cancer-patients-caregivers/
PET CT beginners Guide covers some of the underrepresented topics in PET CTMiadAlsulami
This lecture briefly covers some of the underrepresented topics in Molecular imaging with cases , such as:
- Primary pleural tumors and pleural metastases.
- Distinguishing between MPM and Talc Pleurodesis.
- Urological tumors.
- The role of FDG PET in NET.
INFECTION OF THE BRAIN -ENCEPHALITIS ( PPT)blessyjannu21
Neurological system includes brain and spinal cord. It plays an important role in functioning of our body. Encephalitis is the inflammation of the brain. Causes include viral infections, infections from insect bites or an autoimmune reaction that affects the brain. It can be life-threatening or cause long-term complications. Treatment varies, but most people require hospitalization so they can receive intensive treatment, including life support.
Veterinary Diagnostics Market PPT 2024: Size, Growth, Demand and Forecast til...IMARC Group
The global veterinary diagnostics market size reached US$ 6.6 Billion in 2023. Looking forward, IMARC Group expects the market to reach US$ 12.6 Billion by 2032, exhibiting a growth rate (CAGR) of 7.3% during 2024-2032.
More Info:- https://www.imarcgroup.com/veterinary-diagnostics-market
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LGBTQ+ Adults: Unique Opportunities and Inclusive Approaches to CareVITASAuthor
This webinar helps clinicians understand the unique healthcare needs of the LGBTQ+ community, primarily in relation to end-of-life care. Topics include social and cultural background and challenges, healthcare disparities, advanced care planning, and strategies for reaching the community and improving quality of care.
The dimensions of healthcare quality refer to various attributes or aspects that define the standard of healthcare services. These dimensions are used to evaluate, measure, and improve the quality of care provided to patients. A comprehensive understanding of these dimensions ensures that healthcare systems can address various aspects of patient care effectively and holistically. Dimensions of Healthcare Quality and Performance of care include the following; Appropriateness, Availability, Competence, Continuity, Effectiveness, Efficiency, Efficacy, Prevention, Respect and Care, Safety as well as Timeliness.
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2. CONTENT
WHAT IS GENOMICS
GENOMES
HISTORY
GENETICS VS GENOMICS
SUBFIELDS OF GENOMICS
WHY TO SEQUENCE GENOMES
TECHNICAL FOUNDATIONS
STEPS IN GENOME SEQUENCING
HUMAN GENOME PROJECT, THE BASIC GOALS OF HGP
GENOMICS AND HEALTHCARE
ROLE OF GENOMICS IN COVID PANDEMIC
3. WHAT IS GENOMICS
Genomics is an area within genetics that concerns the
sequencing and analysis of an organism’s genome.
It involves the study of all genes at the DNA, mRNA, and
proteome level as well as the cellular or tissue level.
The term genomics was first coined in 1986 by Tom
Roderick, a geneticist at the Jackson Laboratory in Maine,
during a meeting about the mapping of the human genome
4. Genomics is the study of all genes present in an
organism.
By definition: it can be defined as “A discipline in
genetics that applies recombinant DNA,DNA
sequencing methods and bioinformatics to sequence,
assemble and analyze the structure and function of
genomes.”
It includes studies of intragenomic phenomena such
as heterosis, epistasis, pleiotropy and other
interactions between loci and alleles within the
genomes
5. Genomes
The term genome refers to the complete complement of
DNA for a given species
The human genome consists of 46 chromosomes.
Every cell (except sex cells and mature red blood cells)
contains the complete genome of an organism
6. HISTORY
Genomics is a concept that was first developed by Fred Sanger
in early 1970s, who first sequenced the complete genome of a
virus and of a mitochondrion.
In 1972, Walter Fiers and his research group became the first to
sequence a gene. They sequenced the gene of Bacteriophage
MS2.
In 1995, Hamilton O. Smith and his team became the first to
sequence a genome of a free living organism – that of
Haemophiles influenzae.
7. GENETICS VS. GENOMICS
GENETICS
Genetics is the study of
heredity.
“Gene" refers to a specific
sequence of DNA on a single
chromosome.
Genetics involves the study
of functions and composition
of the single gene.
GENOMICS
Genomics is the study of the
entirety of an organism’s
genes.
“Genome” refers to an
organism's entire genetic
makeup.
Genomics addresses all genes
and their inter relationships
8. SUBFIELDS OF GENOMICS
The different research areas of genomics can be as follows :
1. Structural Genomics- Aims to determine the structure
of every protein encoded by the genome.
2. Functional Genomics- Aims to collect and use data
from sequencing for describing gene and protein
functions.
3. Comparative Genomics- Aims to compare genomic
features between different species.
9. GOALS
The main goal of genomics is to :
Sequence the entire genome by cutting it into small,
manageable pieces (fragments).
Assemble the entire genome from the pieces (fragments).
Understand how gene expression takes place
10. WHY TO SEQUENCE GENOMES
Sequencing genomes helps understand how the genome as
a whole and how the genes work together to direct the
growth, development and maintenance of an entire
organism.
The genome sequence will represent a valuable shortcut,
thus helping to find genes much more easily and quickly
11. TECHNICAL FOUNDATIONS
The technical foundation of genomics involves :
Construction of Genomic and cDNA libraries
DNA Hybridization
Restriction-enzyme mapping
DNA sequencing
PCR amplification
12. STEPS IN GENOME SEQUENCING
Break genome into smaller fragments
Sequence those smaller pieces
Piece the sequences of the short fragments together
GENOME SEQUENCING APPROACHES
1. Hierarchical shotgun sequencing -Useful for sequencing genomes
of higher vertebrates that contain repetitive sequences.
2. Whole genome Shotgun Sequencing -Useful for smaller genomes.
13. HUMAN GENOME PROJECT
The Human Genome Project (HGP) is an international
scientific research project with the goal of determining the
sequence of chemical base pairs which make up human
DNA, and of identifying and mapping all of the genes of the
human genome from both a physical and functional
standpoint.
HGP was formally founded in 1990 by the US Department
of Energy and the National Institute of Health and was
declared completed on 14th April,2003.
14. THE BASIC GOALS OF HGP WERE :
To identify all the genes and their functions in a human
DNA.
To determine the sequences of 3 million base pairs the
makeup the human DNA.
To develop tools for data analysis.
To obtain physical map of human genome.
To store the information in public databases.
16. ROLE OF GENOMICS IN COVID PANDEMIC
The COVID-19 pandemic is due to infection caused by the novel SARS-
CoV-2 virus that impacts the lower respiratory tract. The spectrum of
symptoms ranges from asymptomatic infections to mild respiratory
symptoms to the lethal form of COVID-19 which is associated with severe
pneumonia, acute respiratory distress, and fatality.
To address this global crisis, up-to-date information on viral genomics
and transcriptomics is crucial for understanding the origins and global
dispersion of the virus, providing insights into viral pathogenicity,
transmission, and epidemiology, and enabling strategies for therapeutic
interventions, drug discovery, and vaccine development.
17. Animal genomics
Animal genomics has a wide range of applications
such as in drug development, generation of disease-
resistant transgenic animals, improved livestock
production, gene therapy, production of high-quality
fibers and hairs, biopharmaceuticals, animal health,
phylogenetic analysis, etc. to make the world healthy.
18. BENEFITS & APPLICATIONS
Genomics can be useful in following ways :
It can be used in the field of medicine for early detection of
genetic diseases and its diagnosis and treatment.
It is also useful in the field of agriculture.
To study evolution through mutation lineages.
In forensic science
Providing Nutritious Food for a Growing Human Population