14^th International Conference on Human Genetics and Genetic Diseases March 25-26, 2024 Montreal, Canada

Genomic Medicine is a branch of genomics which allows the next generation genomic techniques to be used by the clinicians, biomedical researchers and the heathcare institutions to deliver healthcare with modern human genetics and genomics to the people. The  genomic medicine reasearch  branches out to cover many disciplines of biology including oncology, cardiology, pediatrics, endocrinology and respiratory medicine.

The delivery of proper modernized healthcare is insured by the field of molecular diagnostics, which makes use of a collection of techniques used to analyze biological markers in the genome and proteome- the individual's genetic code and how their cells express their genes as proteins by applying molecular biology methods to medical testing.

Stem cell research and therapy hold immense promise in the field of medicine. Stem cells have the unique ability to transform into various cell types in the body, making them a valuable resource for regenerative medicine. This research area explores the potential to repair or replace damaged tissues and organs, offering hope for patients with conditions such as Parkinson's disease, spinal cord injuries, and heart disease. Stem cell therapy has already demonstrated significant success in treating some diseases and injuries, marking a significant breakthrough in modern healthcare. However, ethical and regulatory challenges continue to be important considerations in the advancement of this revolutionary field.

Nutritional genomics, also known as nutrigenomics, is a science studying the relationship between human genome, human nutrition and health. People in the field work toward developing an understanding of how the whole body responds to a food via systems biology, as well as single gene/single food compound relationships.

Gene therapy is an experimental technique that uses genes or simply nucleic acid polymers to treat or prevent disease into a patient's cell as a drug for disease treatment.  In the future, this technique may allow doctors to treat a disorder by inserting a gene into a patient's cells instead of using drugs or surgery. Gene therapy is a way to fix a genetic problem at its core or source. The polymers are either translated into proteins which interfere with the target gene expression or else they could possibly correct genetic mutations.

The most common form of gene delivery is in the form of DNA that encodes the functional therapeutic gene to replace the target mutated gene. the polymer molecules are packaged inside a vector which  carries the molecules inside and helps in their integration. Gene therapy is a very effective but debatable form of treatment of genetic disorders depending upon their extent of viability and social and ethical acceptance.

Genetic counseling is the process by whixch an individual or individuals at risk of any inherited disorders are advised and made aware of the consequences and nature of the disorder , as well as te probability of developing or transmitting it.

Human Genetics Engineering  is one aspect of study of the overall field of Human Biotechnology. It involves the direct manipulation of the human genome using molecular engineering tools. Recently developed methods of modification is known as gene editing. There are two types of modification : Somatic Genetic Modification and Germline Genetic Modification.

Somatic genetic modifications is about addition, cutting or changing the genes in some of the cells of an existing person, to typically alleviate any medical condition. this form of gene therapy techniques are approaching clinical practice but only for few conditions and at a high cost. This track deals with the methods and procedures and ideas regarding the modification of the human genome.

Immunogenetics or immungenetics is the part of therapeutic research that examines the association between the insusceptible structure and genetic characteristics. Invulnerable framework diseases, for instance, sort 1 diabetes, are eccentric genetic traits which result from surrenders in the safe system. Recognizing evidence of characteristics describing the safe flaws may perceive new target characteristics for accommodating techniques. Then again, inherited assortments can in like manner describe the immunological pathway inciting disease. The term Immunogenetics relies upon the two words immunology and genetic characteristics and is portrayed as "a sub-class of innate characteristics focusing on the inherited reason of the sheltered reaction" as shown by Work. Inherited characteristics are the science asking about the trading of qualities beginning with one age then onto the following. The characteristics of a living being (strands of DNA) and the trading of characteristics from the parent to the child age of an actual existence structure in the degree of possible assortments are the premises of genetic characteristics.

Pharmacogenetics is the investigation of acquired hereditary contrasts in medication metabolic pathways which can impact particular responses to drugs, both with respect to the remedial effect and furthermore negative effects. Metabolic pathways can influence singular reactions to drugs, both as far as restorative impact just as unfavorable impacts. The term Pharmacogenetics is routinely used correspondingly with the term pharmacogenomics which moreover investigates the piece of obtained and gained inherited complexities in association with cure response and drug direct through a productive examination of characteristics, quality things, and between and intra-particular assortment in quality verbalization and limit. In oncology, Pharmacogenetics really is the examination of germline changes (for example single-nucleotide polymorphisms affecting characteristics coding for liver impetuses responsible for drug declaration and pharmacokinetics), however pharmacogenomics implies physical changes in tumoral DNA inciting alteration in sedating response.

Developmental genetics is the investigation of the manner by which qualities control the development and advancement of a living being for a mind-blowing duration cycle. A recently prepared egg cell or zygote contains a remarkable gathering of qualities that will control its improvement from a solitary cell into a fetus through examples of differential quality articulation during the time spent embryogenesis.

Genomics is an interdisciplinary field of science focusing on the structure, work, headway, mapping, and modifying of genomes. A genome is a life structure's whole plan of DNA, including most of its characteristics. As opposed to innate characteristics, which insinuates the examination of individual characteristics and their parts in inheritance, genomics goes for the total depiction and assessment of characteristics, which arrange the age of proteins with the assistance of mixes and minister particles. In this manner, proteins make up body structures, for instance, organs and tissues and also control mixture reactions and pass on movements between cells. Genomics in like manner incorporates the sequencing and examination of genomes through businesses of high throughput DNA sequencing and bioinformatics to gather and separate the limit and structure of entire genomes.

Biochemical genetics includes diagnosing and treating metabolic sicknesses. These are issues with how the body makes, separates or uses proteins, fats or starches. They are brought about by qualities that are not typical and can't make the compounds the body needs. These sicknesses are called intrinsic mistakes of digestion.

Genetic counseling is a correspondence procedure, which intends to support people, couples and families comprehend and adjust to the restorative, mental, familial and regenerative ramifications of the genetic commitment to explicit wellbeing conditions.

Genetic counseling includes discussing a genetic condition with a wellbeing proficient that has capabilities in both genetics and counseling. Genetic conditions are brought about by changes or mix-ups in qualities. These conditions might be acquired from one or the two guardians. Genetic counseling expects to help individuals comprehend and adjust to the effect that a genetic condition may have on their lives.

Cancer is a genetic issue in which the typical control of cell improvement is lost. Cancer genetics is presently one of the quickest stretching out restorative distinguishing strengths. At the nuclear dimension, the tumor is brought about by a mutation(s) in DNA, which result in twisted cell development. An expansive part of these changes is secured and occur in physical cells. In any case, a couple of individuals secure mutation(s) in the germ line. The mutation(s) occur in two classes of cell characteristics: oncogenes and tumor silencer characteristics. Under standard conditions, tumor silencer characteristics oversee cell division and camouflage of extension. Changes in these characteristics result in unchecked cell duplication realizing tumors with strange cell cycles and tumor development. The tumor silencer characteristics add to malady by the inactivating of loss of limit change.

Clinical Genetics is the restorative claim to fame which gives an indicative administration and "hereditary guiding" for people or families with, or in danger of, conditions which may have a hereditary premise. Hereditary scatters can influence anyone framework and any age gathering. The point of Hereditary Administrations is to help those influenced by, or in danger of, a hereditary issue to live and duplicate as regularly as could reasonably be expected. What's more, an extensive number of people with birth surrenders as well as learning inabilities are alluded to and researched for hereditary components. People distinguished through youth or pregnancy screening programs additionally require hereditary administrations. Later on, as the hereditary commitments to a regular later-beginning issue, for example, diabetes and coronary illness are recognized; hereditary administrations might be required for those at high hazard. Testing for hereditary components that influence sedate endorsing will likewise progressively become a significant action.

Cytogenetics is the investigation of chromosomal structure, area, and capacity in cells. It incorporates the investigation of chromosome number and appearance (karyotyping), the physical area of qualities on chromosomes, and chromosomal conduct in procedures, for example, cell division. The ordinary human cell is comprised of 46 chromosomes: 22 sets of autosomes, numbered 1-22 by request of diminishing length, 1 set of gonosomes, or sex chromosomes.

Stem cells are undifferentiated natural cells that experience mitosis to deliver more cells, which are found in multicellular living beings. They are of two sorts, embryonic and grown-up stem cells. The stem cell treatment was observed to be a lifesaving treatment for patients with strong tumors and blood issue. Stem cells can be acquired from the umbilical string after a child's introduction to the world. Conceivably they can likewise be gotten from fringe blood and bone marrow. As indicated by the reports, in US the accessibility of stem cell treatment was $15.2 million out of 2007 and $16.5 million of every 2008 and it is evaluated to reach $11 billion by 2020.

Stem cell treatment is the method for utilizing stem cells for treating just as averting any malady or confusion. Bone marrow transplantation is the most broadly utilized stem cell therapy, but some stem cell treatment using umbilical cord bloods are also in practice.

The word “epigenetic” literally means “in addition to changes in genetic sequence.” The term has evolved to include any process that alters gene activity without changing the DNA sequence, and leads to modifications that can be transmitted to daughter cells (although experiments show that some epigenetic changes can be reversed). There likely will continue to be debate over exactly what the term means and what it covers.

Many types of epigenetic processes have been identified—they include methylation, acetylation, phosphorylation, ubiquitylation and sumolyation. Other epigenetic mechanisms and considerations are likely to surface as work proceeds. Epigenetic processes are natural and essential to many organism functions, but if they occur improperly, there can be major adverse health and behavioral effects.

Genes are the structure squares of heredity. They are passed from parent to tyke. They hold DNA, the directions for making proteins. Proteins do the vast majority of the work in cells. They move particles starting with one spot then onto the next, form structures, separate poisons, and do numerous other support employments.

At times there is a transformation, an adjustment in a quality or genes. The transformation changes the quality's guidelines for making a protein, so the protein does not work appropriately or is missing totally. This can cause an ailment called a hereditary issue.

You can acquire a quality change from one or the two guardians. A transformation can likewise occur amid your lifetime.

There are a number of different types of genetic disorders (inherited), including the following:

• Single gene inheritance
• Multifactorial inheritance
• Chromosome abnormalities
• Mitochondrial inheritance

Medical genetics is the part of a prescription that includes the determination and the board of inherited issue. Medical genetics varies from human genetics in that human genetics is a field of logical research that might apply to a drug, while medical genetics alludes to the utilization of genetics to medical consideration. For instance, inquire about on the causes and legacy of a hereditary issue would be considered inside both human genetics and medical genetics, while the determination, the board, and advising individuals with hereditary scatters would be viewed as a feature of medical genetics.

Conversely, the investigation of normally non-medical phenotypes, for example, the genetics of eye shading would be viewed as a feature of human genetics, however not really important to medical. The hereditary drug is a more up to date term for medical genetics and joins zones, for example, quality treatment, customized prescription, and the quickly developing new medical claim to fame, predictive medication.

Gene therapy includes the introduction of one or more foreign genes into an organism to treat hereditary or acquired genetic defects. In gene therapy, DNA encoding a remedial protein is bundled inside a "vector", which transports the DNA inside cells inside the body.

There are two unique sorts of gene therapy relying upon which kinds of cells are dealt with: Substantial gene therapy: exchange of a segment of DNA to any cell of the body that doesn't create sperm or eggs. Germ line gene therapy: exchange of a segment of DNA to cells that produce eggs or sperm.

Human genetics is both a basic and connected science. As a key science, it is a piece of hereditary qualities the part of science that analyzes the laws of capacity, transmission, and acknowledgment of data for improvement and capacity of living beings. Inside this system, Human genetics qualities worry about the most fascinating life form the person. This worry with our very own species influences us to investigate logical outcomes in human hereditary qualities for their hypothetical noteworthiness as well as for their down to earth and incentive for human welfare. Consequently, Human genetics qualities are additionally a connected science. Its incentive for human welfare will undoubtedly have repercussions for hypothetical research too since it impacts the choice of issues by human geneticists, their preparation, and the financing of their exploration. In view of its proceeded with hypothetical and functional intrigue, human hereditary qualities offer interest and human satisfaction unparalleled by work in fields that are either fundamentally hypothetical or completely viable in the subject matter.

Population genetics is a branch of biology that explores the genetic composition and changes within populations of organisms. It seeks to understand how genes and alleles are distributed, inherited, and evolve within a group of interbreeding individuals. By studying factors like mutation, migration, genetic drift, and natural selection, population genetics provides crucial insights into the mechanisms behind evolution and the diversity of life on Earth. This field plays a pivotal role in fields such as ecology, conservation biology, and epidemiology, helping us comprehend the intricate dynamics that shape the genetic makeup of species and their ability to adapt to changing environments.

Oncogenomics is a field of medical research that focuses on understanding the genetic basis of cancer. It delves deep into the genomic alterations and mutations that drive the development and progression of cancer. By analyzing the genetic makeup of cancer cells, oncogenomics aims to identify specific genes, known as oncogenes, that play a critical role in promoting tumor growth. This knowledge has paved the way for targeted therapies that can specifically target these genetic abnormalities, offering more precise and effective treatments for cancer patients.

Gene editing technologies like CRISPR-Cas9 offer tremendous promise in advancing medical science, agriculture, and biotechnology. However, they also raise significant ethical and social concerns. The ability to manipulate genes opens the door to potential misuse, including designer babies, genetic discrimination, and unintended ecological consequences. Ethical questions surround the alteration of the human germline, as it could have far-reaching and unpredictable effects on future generations. Additionally, issues of equitable access to gene editing therapies and the potential for genetic enhancement exacerbate existing societal inequalities. Striking a balance between the benefits of gene editing and the need for responsible, equitable, and transparent governance is crucial in navigating this rapidly advancing field.