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Euro Genetic Disorders 2020

About Conference


Genetics and Genetic Disorders conferences, "13th International Conference on Genetics and Genetic Disorders" during September 23-24, 2020 in Milan, Italy. The theme of the conference will be “Innovations in Genetic Disorders Treatment”.

Euro Genetic Disorder 2020 aims to bring together leading academic scientists, researchers, specialists and research scholars to exchange and share their experiences and research results on all aspects of Genetic and Genetic Disorder. It conjointly provides a premier knowledge domain platform for researchers, practitioners and educators to present and discuss trends, the most recent innovations, and concerns as well as practical challenges encountered and solutions adopted in the fields of Genetics.

Euro Genetic Disorder 2020 aims are to engage new audiences to participate in activities on the day, Of course, we also want to reach existing followers of Genetic Disorder social media accounts, and to expand the global reach. Finally, this will be a great opportunity to explore as a new science communication tool.

Why to attend?

With members from around the world targeted on learning regarding healthful Plants and its advances; this can be your best chance to achieve the biggest assemblage of participants from the Genetic and Genetic Disorder. Conduct displays, distribute data, meet with current and potential scientists, build a splash with new advancements and developments, and receive name recognition at this 2-day event. World-renowned speakers, the foremost recent techniques, developments, and also the newest updates are hallmarks of this conference.

Benefits of Attending the Conference

  • The Career Guidance Workshops to the Graduates, Doctorates and Post-Doctoral Fellows, Certificate Accreditation from the Organizing Committee of presentation/ participation.
  • Accepted Abstracts will be published in the respective journals and will be labelled with a Digital Object Identification Number (DOI) provided by CrossRef (Free abstract publishing).
  • Speaker and Abstract pages created in Google on your name would get worldwide acknowledgement to your profile and Research.
  • Best Poster and Young Researcher Award.

Target Audience:

  • Genetics Students, Scientists, Faculty
  • Genetics Doctors, physicians
  • Genomics and Pharmacogenomics Researchers
  • Genomics and Pharmacogenomics Faculty
  • Genomics Scientists
  • Genomics Colleges
  • Human Genetics  Scientists
  • Pharmacology Health Professionals
  • Genetics Associations and Societies
  • Geneticists
  • Genetic Counsellors
  • Bio-pharmacists
  • Business Entrepreneurs
  • Genetic research Institutes
  • Human Genetics Doctor

 

 

Session / Tracks

Track 1 Genetics

Genetics could even be a branch of biology concerned with the study of genes, genetic variation, and heredity in organisms. Genetics study of heredity and varieties. Genomics and varieties are controlled by qualities—what they are, their specialty, and how they work. Genes inside the core of a cell are hung together so that the arrangement conveys data that data decide how living beings acquire different highlights (phenotypic attributes). For instance, posterity created by sexual multiplication normally appears to be like every one of their folks since they have acquired a portion of every one of their folk’s qualities. Genetics distinguishes which highlights are acquired, and clarifies how these highlights go from age to age. The Genetic code not just controls heritage. It likewise controls quality articulation, which happens when a segment of the twofold helix is uncoiled, uncovering a progression of the nucleotides, which are inside of the DNA to turn on the Gene. Closing the uncoiled segment turns off the gene

  • Genes and Chromosomes
  • Genetic Linkage and Chromosome Mapping
  • Regulation of Gene Activity
  • Quantitative Genetics and Multifactorial Inheritance
  • Genetic Engineering and Genome Analysis
  • Principles of Genetic Transmission

 Track 2 Genetic Disorders

A genetic ailment may be a genetic problem due to one or extra abnormalities formed within the genome. Most genetic issues are quite uncommon and have an effect on one individual in every several hundred or millions. The earliest recognized genetic situation during a hominid was in the fossil species Paranthropus robustus, with over a third of human beings displaying Amelogenesis imperfecta. Genetic illnesses could also be hereditary, exceeded down from the folks' genes. In other genetic sicknesses, defects could also be as a result of new mutations or modifications to the DNA. In that case, the illness will handiest be surpassed down if it occurs within the germline. The same disease like some styles of cancer may also be a result of an inherited genetic condition in some people, via new hereditary mutations in human beings, and particularly by way of the environmental reasons in different people. A genetic disease is a genetic problem because of one or more abnormalities within the genome, especially a circumstance that is a gift from delivery congenital. Most genetic sicknesses are pretty uncommon and have an effect on one individual in every several thousand or millions.

  • ADA Immnue Deficiency
  • Autosomal dominant disorders
  • Autosomal Recessive disorders
  • Down Syndrome
  • Breast cancer

 Track 3 Human Genetics

Human genetics is that the study of inheritance because it occurs in citizenry. Human genetics encompasses a spread of overlapping fields including: classical genetics, cytogenetics, molecular genetics, biochemical genetics, genomics, population genetics, developmental genetics, clinical genetics, and guidance .Human Genetics is the investigation of legacy as it occurs in individuals. Human Genetics joins an arrangement of covering fields including old style hereditary qualities, cytogenetic, sub-atomic hereditary qualities, biochemical hereditary qualities, genomics, populace hereditary qualities, formative hereditary qualities, clinical hereditary qualities, and hereditary advising. Qualities can be the standard factor of the attributes of most human obtained characteristics. Examination of human hereditary qualities can be useful as it can address questions with respect to human conduct, grasp the ailments and headway of effective illness treatment, and appreciate hereditary qualities of human life.

  • Human Genome mapping
  • Human Genome sequencing
  • Human genetic clustering
  • Human Genetics of Infectious Diseases
  • Gene Action: Developmental Genetics

 Track 4 Neurogenetics

Neurogenetics studies the role of genetics in nervous system development and function. This recognizes neural features like phenotypes (i.e., observable or non-measurable manifestations of an individual's genetic make-up) and is mainly based on the fact. Individuals ' nervous systems are belonging to the same species, may not be the same. As the name implies, it draws elements from both neuroscience and genetics research, concentrating especially on how its transmitted characteristics influence the ordering that an organism bears. Mutations can have a good range of effects on the individual's quality of life during this genetic sequence. In the context of neurogenetics, neurological diseases, behaviour, and personality are all studied. In the mid to late 1900s, the field of neurogenetics emerged with developments and closely following advances made in the technologies available.

  • Behavioral neurogenetics
  • Cross-species gene conservation
  • Neural development
  • Cognitive genomics
  • Computational Neurogenetic Modeling

Track 5 Immunology & Immunogenetics

Immunogenetics or immunogenetics is the branch of medical genetics that explores the connection between the device and genetics. Autoimmune diseases, such as type 1 diabetes, are complicated genetic tendencies that result from defects in the immune device. Identification of genes defining the immune defects may additionally pick out new goal genes for therapeutic approaches. Alternatively, genetic versions also can assist to outline the immunological pathway ensuing in disease.

Immunogenetics has a primary part in the assessment of unmarried features of characteristics and their part inside the way where attributes or situations are sat again then onto the accompanying. The assessment of the nuclear and cell elements that comprise the ensured structure, which includes their capability and affiliation transforms into the focal uniqueness of immunology. Resistant framework contaminations, for instance, type1 diabetes are mind-boggling hereditary attributes which end result from imperfections inside the invulnerable framework Distinguishing proof of traits describing the secure distortions might also perceive new goal traits for healing systems. On the other hand, hereditary types can in like manner depict the immunological pathway inciting disease.

  • Granulocyte Immunology
  • Genes and Immunity
  • Platelet Immunology
  • The immunogenetics of Neurological Disease
  • Immune-suppressive effects of interleukin-6

 Track 6 Cancer Genetics

Cancer may be a genetic problem where normal cell enhancement regulation is lost. Now, cancer biology is one among the fastest-growing cell differentiating abilities. At the nuclear level, a mutation(s) of DNA causes cancer, leading to the event of twisted cells. The increasing dimension of those changes is guarded and occurs in external cells. In any case, the germ line is secured by a couple of individuals. The mutation(s) occurs in two cell characteristics classes on cogenes and the characteristics of the tumour silencer. Tumour silencer characteristics monitor cell division and extension camouflage under standard conditions. Changes in these characteristics lead to unregulated cell replication which results in tumours with odd cell cycles and growth of tumours. The features of the tumour silencer contribute to the disease by inactivating limit BiogenesiCancer cytogenetics

  • The Genetic Basis of Cancer
  • Oncogenes
  • Cancer Genetics in the Clinic
  • Cancer cytogenetics
  • Cancer syndromes

 Track 7 Gene Therapy and Genetic Counselling

A variety of approaches for treating genetic disorders are under progress, including an inherited disease (e.g. monogenic / Mendelian) and acquired conditions such as cancer and infections. This topic reviews molecular techniques that can be used to change a gene's sequence or expression, including gene therapy, gene editing, and silencing of genes.

 Hereditary Counseling is the system by which the patients or relatives in danger of an obtained issue (or may pass on a child in danger) are instructed with the results and nature concerning the turmoil, the probability of making or transmitting it, and the decisions open to them in the executives and family arranging. These marvelous methodologies are often confined into characteristic (the genuine estimation of risk) and powerful angles.

  • Gene Polymorphism
  • Regenerative Medicine
  • Gene Editing and CRISPR Based Technologies
  • Viral Gene Therapy
  • Ethical Issues Related To Gene Therapy

 Track 8 Evolutionary and Population Genetics

Evolutionary genetics is that the broad discipline of research that resulted from the blending of genetics and Darwinian evolution, cited because the fashionable synthesis. The force of mutation is the final source of new genetic version inside populations. Although maximum mutations are independent with no effect on fitness or harmful, a few mutations have a small, positive effect on health and these versions are raw substances for gradualist adaptive evolution. Within finite populations, random genetic waft and natural desire affect the mutational version. Natural preference is that the most effective evolutionary force which could produce adaptation, the match between organism and environment, or preserve genetic states over very long durations of your time within the face of the dispersive forces of mutation and flow

Population genetics is that the study of genetic variation inner populace, and entails the exam and modeling of changes in the frequencies of genes and alleles in population over area and time. A sizeable variety of the genes discovered interior a populace may be polymorphic that is, they may arise in high-quality structures (or alleles). Numerical fashions are implemented to observe and are expecting the prevalence of specific alleles or mixture of alleles in populace, in view of advancements in the molecular information of genetics, Mendel's legal guidelines of inheritance and modern evolutionary theory. The focus is the population or the species not the person. Evolutionary Genetics are the investigation of ways hereditary range activates transformative exchange. It includes subjects, for example, evolution of genome structure, the genetic basis of speciation and adaptation, and genetic alternate in reaction to choice within populations.

  • Mutation and polymorphism
  • Admixture and ancestry analysis
  • Natural selection and adaptation
  • Hardy-Weinberg equilibrium
  • Microevolution

 Track 9 Forensic Genetics

Forensic genetics in the department of genetics that deals with the software of genetic know-how to criminal issues and felony proceedings. Forensic genetics is also a branch of forensic medication that offers greater extensively with the software of medical knowledge to prison matters.

Forensic genetics today has a tendency to conjure up DNA. However, even the term "DNA fingerprinting" is like older methods of police identification. Forensic genetics isn't a new field. Long earlier than the technology of DNA fingerprinting, blood grouping, HLA typing and other assessments of genetic markers in blood were finished to try to determine who did it (and, greater often, who did no longer do it).

  • DNA Fingerprinting
  • Evaluation and presentation of DNA evidence
  • Kinship testing
  • Lineage markers

 Track 10 Nutrigenetics 

Neurogenetics studies the role of genetics in nervous system development and function. This recognizes neural features like phenotypes (i.e., observable or non-measurable manifestations of an individual's genetic make-up) and is mainly based on the fact. Individuals ' nervous systems are belonging to the same species, may not be the same. As the name implies, it draws elements from both neuroscience and genetics research, concentrating especially on how its transmitted characteristics influence the ordering that an organism bears. Mutations can have a good range of effects on the individual's quality of life during this genetic sequence. In the context of neurogenetics, neurological diseases, behaviour and personality are all studied. In the mid to late 1900s, the field of neurogenetics emerged with developments and closely following advances made in the technologies available.    

  • Genetic therapies
  • Monogenic neurologic diseases
  • Polygenic diseases

Track 11 Reproductive Genetics/Prenatal Genetics

Part of the Division of Maternal-Foetal Medicine, the Reproductive Genetics Service changed into created to help girls with medical situations encountered or made worse by way of pregnancy or whose prenatal testing famous a birth defect or genetic condition in the foetus. Genetics in obstetrics can be complex due to the fact the genetic makeup of three people – the mother, the father of the toddler, and the unborn child – must be considered. Many women have a genetic condition this is unrecognized till they emerge as pregnant. Reproductive Genetics Service geneticists and seven board-certified counsellors help couples recognize how genetics can have an impact on their pregnancy, presenting counselling for those planning to possess an infant or women who are already pregnant.                                                               

  • Gene therapy products
  • Different vectors for gene therapy
  • Gene therapy for malignant melanoma
  • Gene therapy for sickle-cell disease
  • Development of regenerative treatment models

Track 12 Stem Cell research and Therapy

Immature microorganisms are undifferentiated regular cells that experience mitosis to convey more cells, which are found in multicellular living things. They are of two sorts, embryonic and grown up microorganisms. The undeveloped cell treatment was seen to be a lifesaving treatment for the patients with solid tumours and blood issue. Essential microorganisms are often obtained from the umbilical string after new-born’s first experience with the planet. Maybe they can moreover be gotten from periphery blood and bone marrow. As demonstrated by the reports, in US the availability of undifferentiated cell treatment was $15.2 million of each 2007 and $16.5 million of each 2008 and it is surveyed to reach $11 billion by 2020.

Undifferentiated creature treatment is the strategy for using undeveloped cells for with respect to and furthermore keeping any disease or strife. Bone marrow transplantation is the most by and large used youthful microorganism treatment, anyway some undeveloped cell treatment using umbilical string bloods are similarly for all intents and purposes.

  • Somatic Cell Reprogramming
  • Tissue Regeneration
  • Vascular Regeneration
  • Articular Cartilage Tissue 211 Engineering
  • Oral Bone Reconstruction

Track 13 Molecular Biology

Molecular biology is the have a look at of molecular underpinnings of the processes of replication, transcription, translation, and mobile function. Molecular biology worries the molecular foundation of biological interest among the biomolecules in diverse systems of a cellular, gene sequencing and this includes the interactions between the DNA, RNA and proteins and their biosynthesis. In molecular biology the researchers use specific strategies native to molecular biology, more and more combine these techniques and ideas from the genetics and biochemistry.

  • Macromolecule blotting and probing
  • Molecular cloning
  • Central dogma of molecular biology
  • Protein interaction prediction
  • Protein structure prediction

Track 14 Bioinformatics

Bioinformatics is an interdisciplinary location that develops strategies and software equipment for statistics organic facts. As an interdisciplinary subject of science, bioinformatics combines biology, laptop science, records engineering, mathematics, and facts to research and interpret organic records. Bioinformatics has been used for in silicon analyses of biological queries the usage of mathematical and statistical techniques.

Bioinformatics consists of organic studies that use computer programming as a part of their methodology, as well as a particular evaluation of "pipelines" which might be again and again used, particularly within the field of genomics. Common makes use of bioinformatics include the identification of candidates genes and unmarried nucleotide polymorphisms (SNPs). Often, such identity is made with the intention of higher information the genetic foundation of disease, specific adaptations, perfect properties (ESP. In agricultural species), or versions amongst populations. In a far less formal way, bioinformatics also attempts to understand the organizational standards within macromolecule and protein sequences, called proteomics.

  • Genome sequencing and assembly
  • Methods for data integration
  • Analysis of mutations in cancer
  • Computational biomodeling

Track 15 Cytogenetics

Cytogenetics is the study of cell structure, area, and ability of chromosomes. It involves studying the number and presence of chromosomes (karyotyping), the physical region of chromosomal properties, and chromosomal actions in procedures such as cell division. The ordinary human cell consists of 46 chromosomes: 22 autosomal pairs, numbered 1-22 by decreasing length query, 1 array of gonosomes, or sex chromosomes.

  • Chromosomes
  • Human mouse somatic cell hybrids
  • Chromosome abnormalities
  • Tumour Cytogenetics

Track 16 Molecular and Cellular Genetics

Molecular genetics can be a sub-field of genetics that applies an "investigative approach" to training sessions the structure and/or feature of genes in an organism’s genome using genetic screens. The subject of observing is primarily based on the merging of numerous sub-fields in biology: classical Mendelian inheritance, mobile biology, molecular biology, biochemistry, and biotechnology. Researchers search for mutations in a gene or result in mutations in a gene to hyperlink a gene sequence to a particular phenotype. Molecular genetics may be a powerful method for linking mutations to genetic situations in an effort to aid the search for treatments/remedies for diverse genetic diseases.

Atomic Genetics is the sector of technological know-how that surveys the shape and boundaries of characteristics at a sub-atomic degree and thusly uses a manner for both sub-atomic biology and hereditary qualities. The investigation of chromosomes and exceptional articulation of a residing being can give statistics into heredity, hereditary variety, and changes. The evaluation of Genetics at the degree of the essential structure squares of cells and on the DNA degree. Cells are as excellent as they may be close to nothing and lots are up till now cloud approximately the inward operations of those structure bits of life. In the event that you'll get a kick out of the chance to log hours in a lab and use pushed types of gear to help power the belief of the way cells work, contemplates in mobile and atomic technological know-how might be for you.

  • DNA Replication and its Control
  • Molecular Cloning
  • Transgenic Regulation in Laboratory Animals
  • The Polymerase Chain Reaction

Track 17 Epigenetics & Chromatin

Epigenetics is the investigation of heritable phenotype adjustments that do not include adjustments in the DNA arrangement. Epigenetics infers includes that are "over" or "notwithstanding" the normal hereditary reason for legacy. Epigenetics often means modifications that influence great motion and articulation, however, can likewise be utilized to depict any heritable phenotypic change. Such outcomes for cell and physiological phenotypic characteristics may end result from outside or ecological factors, or be a chunk of the normal formative program. The widespread which means of epigenetics requires these changes to be heritable either in the descendants of cells or of life forms. Epigenetic research makes use of a very good scope of atomic organic structures to further comprehension of epigenetic wonders, along with chromatin Immunoprecipitation (together with its large scale versions Chip-on-chip and Chip-Set), fluorescent in situ hybridization, methylation-delicate predicament compounds, DNA adenine methyltransferase distinguishing proof (Dam ID) and bisulphite sequencing. Besides, the utilization of bioinformatics techniques has a task in (computational epigenetics).

  • Histone modification
  • DNA methylation
  • Clinical Epigenetics
  • Translational epigenetics
  • Reproductive epigenetics

Track 18 Genome Integrity

Genomic Integrity is moreover known as genetic modification. It is the fast manipulate of residing creatures of the genome by using biotechnology. Qualities can be cleared, or "pounded out", the usage of a nuclease. Quality is targeting another approach that usages homologous recombination to change an endogenous excellent, and this may be used to erase first-class, get rid of exons, enlargement of pleasant, or to introduce inherited changes. It is a direction of action of advances used to change the genetic beautifying marketers of the mobile and such as the buying and selling of traits transversely over species factors of confinement to make upgraded novel residing things. Satisfactory planning doesn’t robotically join fashionable animal and plant raising, in vitro treatment, acknowledgment of polyploidy, mutagenesis and cell blend frameworks that do not use recombinant nucleic acids or an innately modified life shape at the identical time. The help of genome honesty is fundamental for residing being endurance and for the legacy of characteristics to posterity. Genomic flimsiness is resulting from DNA harm, unusual DNA replication or awkward cell division, which may prompt chromosomal distortions and great transformations.                                                   

  • Gene editing therapy
  • Genetic transformation
  • Nanotechnology in Genetics
  • Therapeutic Cloning

Track 19 Animal Genetics

An animal hereditary quality is a part of hereditary qualities that reviews heredity and variety mostly in livestock yet additionally in residential and wild creatures. It depends on general hereditary standards and ideas, and it is, for the most part, utilizes the crossbreed, cytological, populace, ontogenetic scientific measurable and twin strategies for general hereditary qualities.

  • Genetic Diversity and Inbreeding
  • Natural Selection in animals
  • Crossbreeding
  • Genetic Disorders in animals

Track 20 Plant Genetics And Molecular Pharming

Molecular Pharming utilizes plants to make substantial amounts of pharmaceutical substances like antibodies and vaccines. it's as same because the technique for creating Genetically Modified Crops, the synthetic introduction of genes into plants. Plant Genetics is that the study of genes, hereditary variety, and genetics, particularly in Plants. It is, for the foremost part, considered a field of biology and botany; however, it crosses much of the time with numerous other life sciences and is firmly connected with the investigation of knowledge frameworks. In agriculture, a plant's qualities impact the development of the plant, as they're parts of its chromosomes and are acquired through sexual propagation. There are two alternative ways by which qualities are often changed: the gene gun method strategy and therefore the agrobacterium technique. The gene gun method technique is especially helpful in changing monocot species like corn and rice and is otherwise called biolistic. The agrobacterium strategy has been effectively drilled in dicots, i.e. broadleaf plants, for instance, soybeans and tomatoes, for an extended time. It’s likewise viable in monocots like grasses, including corn and rice. This system is likewise favoured over the gene gun method strategy because it is a smaller amount demanding to screen due to a more prominent recurrence of single-site inclusions of out of doors DNA.

  • Molecular breeding
  • Marketing and societal issues in breeding
  • Plant cellular organization and genetic structure
  • Plant genetic resources

 

Market Analysis

Market Scenario : 

Genetics Conferences 2020 welcomes all the attendees, researchers, presenters, associations and exhibitors from everywhere the globe to Milan, Italy. We have a tendency to square measure delighted to ask you all to attend the "13th International Conference on Genetics and Genetic Disorders" that goes to be command on the month of September 23-24, 2020 in Milan, Italy. This Congress Committee is an exciting and informative conference program alongside comprehensive lectures, symposia, workshops on informative topics, poster shows and various programs for participants from everywhere the world. We invite you to Euro Genetic Disorder 2020 conferences, to share purposeful expertise with scholars from around the world. We look forward to seeing you in Milan, Italy.

Genetics is nothing but the study of genes, their capacities, and their impacts. Atomic genetics, formative genetics, populace genetics, and quantitative genetics, and human genetics are different sorts of hereditary investigations. It incorporates the investigation of quality articulation, quality structure, transformation examination, cytogenetic and genomic imaging, genome structure, and association, hereditary and physical mapping, malady affiliation contemplates atomic diagnostics, genetics of complex illnesses, epispastic collaborations, and different ideas. It additionally decides different hereditary components in charge of ailments. It offers different points of interest, for example, distinguishing proof and determination and treatment of different illnesses, for example, malignant growth, cardiovascular sicknesses, and other hereditary maladies.

The size of the Global Genetic Testing Market is expected to reach $16.9 billion by 2025, rising over the forecast period with market growth of 11.2 present CAGR. Genetic testing is the analysis of the gene-containing cells and tissues. Genetic testing is the study of the cells and tissues containing the gene

Key Market Trends: Molecular Testing Segment is predicted to Exhibit Fastest rate of growth over the Forecast Period.

To identify the mutations that lead to a genetic disorder, molecular genetic testing is the study of single genes or short lengths of DNA. The scope of the study discusses the use of gene testing for the development of personalized medicine, directed cancer therapy, and other genetic diseases. In addition to increasing performance and precision, new genetic testing techniques provide lucrative growth opportunities for the genetic testing industry. In addition, due to the growing patient ratio and awareness, the market is expected to witness exponential growth rates across emerging economies. One of the major trends in the genetic testing industry is the transfer in emphasis to bioinformatics on medical research.

Due to an increase in the incidence of genetic disorders & cancer and an increase in awareness and acceptance of personalized drugs, the global genetic testing market is expected to record significant development in the near future, the global genetic testing market is expected to record significant development.

The market for molecular testing is growing at a good pace. Currently, most of the molecular tests are either PCR or FISH. In addition, microarray technology has made it possible to evaluate thousands of loci that are widely used for expression analysis, targeted at specific cell signalling pathways, and also for metabolic pathways for pathological characterization of tumours.

Genetic Testing Market:

According to a study published by NCBI, about 75,000 genetic tests are available on the market as of August 217. These include nearly 10,000 separate exams. In addition, there have been more than 14,000 trials on the market since March 2014. With about 10 new tests increasing every day for more than four years, the market for genetic testing has gained momentum.

Importance & Scope: Genetic Testing Market size was valued at USD 10.6 billion in 2017 and is expected to witness more than 11.6% CAGR from 2018 to 2024.

U.S. Genetic Testing Market, By Test Type, 2013 – 2024

Increasing demand from patients for personalized medicines will fuel the demand for genetic testing during the forthcoming years. Personalized medicine offers tailored medical treatment to patients supported their molecular basis. Various developed economies such as Europe undergo genetic testing for the detection of various genetic and rare diseases. Detection of diseases at an early stage facilitates early treatment and helps reduce the severity of diseases. Growing adoption of personalized medicines including increasing awareness regarding early diagnosis of disease will boost the industry growth over the forecast period.

 

Technological advancement in genetic testing is expected to drive the genetic testing market during the coming years. The demand for genetic testing is increasing across the globe owing to the availability of new tests as well as advancement in genetic testing techniques. Innovations in tests that offer safer and efficient techniques of disease detection, surpassing the risk of miscarriage during early stages of pregnancy will serve to be a high impact rendering factor which will drive the genetic testing market growth during the forthcoming years. The dearth of experienced professionals and advanced infrastructure in developing as well as an underdeveloped economy is should hamper the market growth over the forecast period. Accessibility to quality healthcare in low resource areas is difficult to maintain owing to a lack of infrastructure. Moreover, the risk of false interpretations associated with the unavailability of experienced professionals will restrain industry growth noticeably.

Key Developments in the Market

September 2017: Myriad launched a risk score to enhance the hereditary cancer test my Risk. Risk Score determines the danger of girls to urge carcinoma by analysing their genome.

July 2017: Admiral Health Partners collaborates with Helix to Launch Genetic Tests to Assess the Risk of Inherited High Cholesterol, Sudden Cardiac Death, and Inherited Diabetes

 

Social and Ethical Implications of Genetic Testing

Insurance is an important asset to people. The fear of discrimination by insurance companies discourages people from undertaking genetic tests, which is a restraining factor for the market growth. The expensive nature of genetic tests affects the market, adversely. At times, the payments made by individuals are not reimbursed through insurance, thus, affecting the pockets of these patients. The high-import duty by the government on genetic test kits also acts as a barrier to market growth.

Past Conference Report

Human Genetics 2019

Conference series LLC hosted Joint Conference “8th International Conference on Human Genetics and Genetic Diseases &   13th International Conference on Genomics & Pharmacogenomics" November 25-26, 2019 in Madrid, Spain.
 
Conference Highlights
 
Human Genetics
Genetics Disorders
Molecular Genetics
Medical Genetics
Epigenetics
Gene Therapy
Stem Cell Research
Cytogenetic
Genetic Counselling
Biochemical Genetics
Genomics
Population Genetics
Clinical Genetics
Cancer Genetics
Pharmacogenomics
Immunogenetics
Pharmacogenomics
Genomics
Microbial Genomics
 
Active participation and generous response were received from the Organizing Committee Members, scientists, researchers, as well as experts from Non-government organizations, and students from diverse groups who made this conference as one of the most successful and productive events in 2019.

 

The conference was marked with multiple sessions, Keynote presentations, panel discussions, and Poster sessions. We received active participation from scientists, young and brilliant researchers, business delegates and talented student communities representing more than 35 countries, who have driven this event into the path of success.

The conference was initiated with a warm welcome note by Honourable guests and the Keynote forum. The proceedings went through interactive sessions and panel discussions headed by honourable Moderator Mr. Jallow Haruna, Gambia for the conference. 

 The conference proceedings were carried out through various Scientific-sessions and plenary lectures, of which the following Speakers were highlighted as Keynote speakers:

1: Personalized and Precision Medicine as a unique Healthcare Model to be Set Up via Genomics-based Innovations, Big Data Resources and Translational applications to secure the Human Wellness and Biosafety: Sergey Suchkov, Sechenov University and Moscow Engineering Physical Institute, Russia

 2: The Genetics of Common Diseases: Kari Stefansson, decode genetics, Iceland

Best Poster

Darta Pupola, University of Latvia, Latvia

Title: Long-term effect of Helicobacter Pylori Eradication therapy on Gastrointestinal Micro biome in a Latvian population

Conference has taken the privilege of felicitating Human Genetics & Genome 2019 Organizing Committee, Keynote Speakers who supported for the success of this event. On behalf of the Organizing Committee, congratulates the Best Poster awardees for their outstanding performance in the field of Human Genetics & Genome and appreciates all the participants who put their efforts in poster presentations and sincerely wishes them success in future endeavours.

We are also obliged to various delegate experts, company representatives and other eminent personalities who supported the conference by facilitating active discussion forums. We sincerely thank the Organizing Committee Members for their gracious presence, support, and assistance towards the success of Human Genetics & Genome 2019.

Now we are organizing: 13th International Conference on Genetics and Genetic Disorders Milan, Italy, Sep 23-24, 2020

For More details visit: https://geneticdisorders.geneticconferences.com/

 


Past Reports  Gallery  

To Collaborate Scientific Professionals around the World

Conference Date September 23-24, 2020

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