The Nobel Prize awarded to Watson & Crick for their discovery of the double helix structure of DNA using X –ray diffraction and the mathematics of a helix transform published in Nature in the 50s turned the world on its side and paved the way for understanding our most precious code for life. Since those days the entire world has made enormous advances in the complex arena of genetics, especially in humans. In 1984, the English scientist Alec Jeffreys invented Restriction Fragment Length Polymorphism (RFLP) initially used to find genes related to Huntington Disease and Cystic Fibrosis and even Alcoholism. However, RFLP has been replaced with less expensive DNA profiling techniques such as polymerase chain reaction (PCR). In 1993 Kary Mullis shared the Nobel Prize in Chemistry with Michael Smith for the invention of PCR. Started in 1984 and the mosaic completed in 2003, The Human Genome Project (HGP) was an international scientific research project with the goal of determining the sequence of nucleotide base pairs that make up human DNA, and identifying and mapping all of the genes of the human genome from a physical and functional standpoint, remains the world’s largest collaborative biological project. Certainly, we have come a long way since Patrick O. Brown published his seminal work in 1981 on macro-arrays and now micro-arrays. Today using measurement of fluorescent intensity across the array of transcribed and spliced genes to produce mRNA transcripts and the subsequent development of DNA chip or biochip to enable scientists to measure the expression levels of large number of genes simultaneously or to genotype multiple regions of a genome, has revolutionized our exploration and journey to identifying the genetic basis of disease. While we have a long way to go, one could only imagine what the world will look like in 100 years from today.
For the conference we have selected evidence-based scientifically sound abstracts pertaining to all aspects of genetics and methodology and disease. These abstracts selected for presentation represent both animal and human studies and novel methods relevant to all aspects involving current issues worldwide. While I will present a novel genetically based solution to Americas worst drug-epidemic (opioids) involving Genetic Addiction Risk Score (GARS) coupled with precision pro-dopamine regulation (Precision Behavioral Management [PBM), it constitutes just the tip of the iceberg. Particularly, the areas covered in this conference involve genomics, epigenetics, pharmacogenomics, neuroimaging, nutrigenomics, molecular neurobiology, pharmacology, neurogenetics, and clinical trials. A number of abstracts involve genome-wide DNA methylation mapping and gene expression including histone replacement, messenger RNA interference (miRNA) as well any other epigenetic studies.
The conference will promote an open discussion of novel hypotheses to provide attendees with a global understanding of the interdisciplinary nature of gene based research, treatment and novel ways of enhancing the quality of human life on earth.
The conferences’ mission is to propagate knowledge that would allow every individual to enjoy the reward of our human legacy, the experience of pleasure and the ability to cope with life's stressors free from disease. So join us in this new adventure linking genes, epigenetics and therapeutic interventions to promote both tertiary treatment and prevention of disease across our universe. Our message is to “Lick our Pups “as espoused by the epigenetic arena, “love Needs Care” and through new discoveries as presented herein is there a future Nobel Prize amongst the presentations, especially at the home of this prestigious prize, and even not. I am sure everyone in attendance will be invigorated by the discourse and network interaction of the greatest minds having a unique mission as espoused by those involved in the genetic medicine arena and “Redeem Joy” in victims of simple molecular gene polymorphic rearrangements and development of new therapeutic targets.
Thank you for attending this special conference, we know you will have a wonderful experience!
Kenneth Blum PhD, DHL, Professor Western University Health Sciences
In continuation to 1st successful past scientific meetings, 2nd World Congress on Genetics & Genetic Disorders will be held on May 13-14, 2019 on Stockholm, Sweden.
EuroSciCon suggests every single person to attend "Genetics 2019” in the midst of May 13-14, 2019 at Stockholm, Sweden which merges brief keynote introductions, speaker talks, Poster Presentations , Exhibitions, Symposia, Workshops.
Genetics 2019 will gather world-class educators, researchers, analysts, Molecular Biologist Geneticist, Gene Therapist and Young Researchers working in the related fields to consider, exchange views and their experiences before an extensive worldwide social occasion of individuals. The social gathering warmly welcomes Presidents, CEO's, Delegates and present day experts from the field of Genetics & Genetic Disorders and Public wellbeing and other pertinent organization positions to take an interest in these sessions, B2B get together and board talks. The assembly of this event will be revolving around the topic “Innovation and Discoveries in field of Genetics will lead to better future”.
EuroSciCon is the longest running independent life science events company with a predominantly academic client base. Our multi professional and multi-specialty approach creates a unique experience that cannot be found with a specialist society or commercially. EuroSciCon are corporate members of the following organizations: Royal Society of Biology, IBMS Company.
This global meeting gives the chance to Molecular Biologist, Geneticist, Gene Therapist and Young researchers, specialists and analysts throughout the world to assemble and take in the most recent advances in the field of Genetics & Genetics Disorders and to trade innovative thoughts and encounters.
- 2 days of scientific exchange
- 100+ abstracts submitted
- 20+ scientific sessions
- 50+ worldwide professionals
- 80+ healthcare experts
Genetics 2019 is the yearly gathering directed with the help of the Organizing Committee Members and individuals from the Editorial Board of the supporting Genetics & Molecular Biology related journals.
Reason to attend?
Genetics 2019 is relied upon to give young researchers and scientists a platform to present their revolutions in the field of Genetics and Molecular Biology. This conference invites Presidents, CEO's, Delegates and present day specialists from the field of Genetics and Public wellbeing and other pertinent organization positions to take an interest in this sessions, B2B get together and board talks.
Scope of Genetics:-
The global market for Genetic Testing is forecast to reach US$2.2 billion by 2017. Increasing knowledge about the potential benefits of genetic testing is one of the prime reasons for the growth of the genetic testing market.Advancements in the genetic testing space, aging population and a subsequent rise in the number of chronic diseases, and increasing incidence of cancer cases are the other factors propelling growth in the genetic testing market.
EuroSciCon are corporate members of the following organizations
- Royal Society of Biology
Opportunities for Conference Attendees
For Researchers &Faculty:
- Speaker Presentations
- Poster Display
- Symposium hosting
- Workshop organizing
For Universities, Associations & Societies:
- Association Partnering
- Collaboration proposals
- Academic Partnering
- Group Participation
For Students & Research Scholars:
- Poster Competition (Winner will get Best Poster Award)
- Young Researcher Forum (YRF Award to the best presenter)
- Student Attendee
- Group registrations
For Business Delegates:
- Speaker Presentations
- Symposium hosting
- Book Launch event
- Networking opportunities
- Audience participation
- Exhibitor and Vendor booths
- Sponsorships opportunities
Sessions & Tracks
Track 1 Genetics
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 decides how living beings acquire different highlights (phenotypic attributes). For instance, posterity created by sexual multiplication normally appear to be like every one of their folks since they have acquired a portion of every one of their folks' 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
Genetic disorders are a hereditary problem, meaning that they are passed down from the parent’s genes or caused by one or more abnormalities in the genome. In such cases, the defect will only be passed down if it occurs in the germline and most genetic disorders are quite rare and affect one person in every several thousands or millions. Genetic disorders may likewise be complex, multifactorial, or polygenic, which means they are likely connected with the impacts of numerous genes lifestyles and environmental factors. Multifactorial disorders incorporate coronary illness and diabetes. Although complex issue frequently group in families, they don't have an obvious example of legacy. This makes it hard to decide a man's danger of acquiring or passing on these disarranges. Complex issue are likewise hard to study and treat, on the grounds that the particular factors that reason the vast majority of these clutters have not yet been recognized.
- Congenital Disorders
- Cystic fibrosis
- Polycystic kidney disease
- Down’s syndrome
- Diabetes and Obesity
- Neurodevelopmental disorders
- Multifactorial diseases
- Autosomal dominant disorders
- Autosomal Recessive disorders
- Huntington Disease
- Maternal transmission, heteroplasty
- Complex Parent of origin effects due to genomic imprinting.
- Autosomal recessive characterized by variable expressivity, and genetic heterogeneity
- Turner Syndrome
- Polycystic Kidney Disease
- Osteogenesis Imperfect
Track 3 Animal Genetics
Animal genetics is a branch of genetics that studies heredity and variation chiefly in farm animals but also in domestic and wild animals. It is based on general genetic principles and concepts, and it mainly uses the hybrid, cytological, population, ontogenetic, mathematical-statistical, and twin methods of general genetics.
- Genetic Diversity and Inbreeding
- Natural Selection in animals
- Genetic Disorders in animals
Track 4 Cancer Genetics
Cancer Genetics is an inherited issue in which the normal control of cell change is lost. Malignant inherited characteristics are by and by one of the speediest stretching out restorative qualities. The influenced qualities are partitioned into two general classifications. Oncogenes are qualities that advance cell development and propagation. Tumor suppressor genes are genes that restrain cell division and survival. Harmful change can happen through the arrangement of novel oncogenes, the unseemly finished articulation of ordinary oncogenes, or by the under-articulation or crippling of tumor silencer genes. Regularly, changes in various genes are required to change an ordinary cell into a tumor cell. Hereditary changes can happen at various levels and by various components.
- The Genetic Basis of Cancer
- Cancer Genetics in the Clinic
- Genetic Alternations in Common Cancers
- Cancer Genomes
- Genetics of common cancers
Track 5 Human Genetics
Human Genetics is the study of inheritance as it happens in people. Human Genetics incorporates an assortment of covering fields including: classical genetics, cytogenetics, molecular genetics, biochemical genetics, genomics, population genetics, developmental genetics, clinical genetics, and genetic counselling. Genes can be the normal factor of the characteristics of most human-acquired attributes. Investigation of human genetics can be helpful as it can answer questions regarding human behaviour, comprehend the sicknesses and advancement of successful malady treatment, and comprehend genetics of human life.
- Human Genome Sequence and Variation
- From Genes to Genomics to Proteomics
- Oligogenic Disease
- Formal Genetics of Humans: Multifactorial Inheritance and Common Diseases
- Human Genetics of Infectious Diseases
- Gene Action: Developmental Genetics
- Consanguinity, Genetic Drift, and Genetic Diseases in Populations with Reduced Numbers of Founders
- Cloning in Research and Treatment of Human Genetic Disease
Molecular Pharming utilizes plants to create substantial amounts of pharmaceutical substances like antibodies and vaccines. It is as same as the technique for creating Genetically Modified Crops, the artificial introduction of genes into plants. Plant Genetics is the study of genes, hereditary variety, and genetics particularly in Plants. It is for the most part thought about a field of biology and botany, however crosses much of the time with numerous other life sciences and is firmly connected with the investigation of data frameworks. In agriculture, a plant's qualities impact the improvement of the plant, as they are parts of its chromosomes and are acquired through sexual propagation. There are two different ways by which qualities can be changed: the gene gun method strategy and the agrobacterium technique. The gene gun method technique is particularly 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 example, soybeans and tomatoes, for a long time. It is likewise viable in monocots like grasses, including corn and rice. This technique is likewise favoured over the gene gun method strategy as it is less demanding to screen because of a more prominent recurrence of single-site inclusions of outside DNA.
- Germplasm for breeding
- Molecular breeding
- Molecular genetic modifications and genome-wide genetics
- Marketing and societal issues in breeding
- Plant cellular organization and genetic structure
- Clonal propagation and in vitro culture
- Plant genetic resources
Track 7 Molecular and Cellular Genetics
Molecular Genetics is the field of science that reviews the structure and capacity of qualities at a molecular level and along these lines utilizes strategies for both molecular biology and genetics. The study of chromosomes and gene expression of an organism can give knowledge into heredity, genetic variation and transformations. The examination of Genetics at the level of the basic building squares of cells and at the DNA level. Cells are as mind boggling as they are little and much is as yet obscure about the internal workings of these building pieces of life. In the event that you'd get a kick out of the opportunity to log hours in a lab and use utilize propelled equipments to help propel the comprehension of how cells function, thinks about in cell and nuclear science could be for you.
- Role of Histones and their Acetylation in Control of Gene Expression
- DNA Replication and its Control
- Molecular Cloning
- Transgenic Regulation in Laboratory Animals
- The Polymerase Chain Reaction
Track 8 Medicinal Genetics
Medicinal Genetics is the branch of medication that includes the analysis and management of genetic issue. Medicinal Genetics varies from human genetics in that human genetics is a field of scientific research that might apply to drug, while medicinal Genetics research to the application of genetics to medical care. For instance, look into on the causes and inheritance of genetic disorders would be considered within both human genetics and medicinal genetics, while the diagnosis, management, and counselling people with hereditary disarranges would be considered part of medicinal genetics. Genetic Medicine is a newer term for medicinal genetics and incorporates areas such as gene therapy, personalized medicine, and the rapidly emerging new medical specialty, predictive medicine. Medicinal genetics incorporate a wide range of genetic counsellors, and nutritionists, clinical diagnostic laboratory activities, and research into the causes and inheritance of genetic disorders. Examples of conditions that fall inside the extent of therapeutic hereditary qualities incorporate birth surrenders and dysmorphology, mental hindrance, extreme introvertedness, mitochondrial clutters, skeletal dysplasia, connective tissue issue, disease hereditary qualities, teratogens, and pre-birth finding. Medicinal genetics is progressively getting to be important to numerous normal infections. Overlaps with other therapeutic claims to fame are starting to rise, as on-going advances in genetics are revealing etiologies for neurologic, endocrine, cardiovascular, aspiratory, ophthalmologic, renal, mental, and dermatologic conditions.
- Chromosome disorders
- MathematicaI and population genetics
- Patterns of in heritance
- Drug Metabolism
- Genetic Variations revealed solely by effects of drugs
- Genetic factors in common diseases
Population genetics is the study of genetic variation within population, and involves the examination and modelling of changes in the frequencies of genes and alleles in population over space and time. A significant number of the genes found within a population will be polymorphic - that is, they will occur in different structures (or alleles). Numerical models are utilized to examine and predict the occurrence of specific alleles or combination of alleles in population, in view of advancements in the molecular understanding of genetics, Mendel's laws of inheritance and modern evolutionary theory. The focus is the populace or the species not the person. Evolutionary Genetics are the investigation of how hereditary variety prompts transformative change. It incorporates subjects, for example, evolution of genome structure, the genetic basis of speciation and adaptation, and genetic change in response to selection within populations.
- Hardy-Weinberg equilibrium
- Non-random mating
- Natural selection
- Gene pool
- New developments
- Genetic drift, bottlenecks & founder effects
- Genetic diversity
Track 10 Cytogenetics
Cytogenetics is a branch of genetics that is concerned with how the chromosomes relate to cell behaviour, particularly to their behaviour during mitosis and meiosis. Techniques used include karyotyping, analysis of G-banded chromosomes, other cytogenetic banding techniques, as well as molecular cytogenetic such as fluorescent in situ hybridization (FISH) and comparative genomic hybridization (CGH).Their conduct in creature (lizard) cells was depicted by Walther Flemingdization (CGH). Chromosomes were first seen in plant cells by Karl Wil, the pioneer of mitosis, in 1882. The name was begat by another German anatomist, von Waldeyer in 1888.
- Chromosome banding techniques and staining
- International System for human Cytogenetic Nomenclature (ISCN)
- Chromosome abnormalities
- Tumor Cytogenetics
- Cancer Cytogenetics
Track 11 Genome Integrity
The Genomic Integrity is additionally called as hereditary alteration. It is the immediate control of living beings of the genome by utilizing biotechnology. Genes might be evacuated, or "thumped out", utilizing a nuclease. Gene is focusing on an alternate method that utilizations homologous recombination to change an endogenous quality, and this can be utilized to delete gene, expel exons, addition of gene, or to present hereditary transformations. It is an arrangement of advances used to change the hereditary cosmetics of the cell and including the exchange of qualities crosswise over species limits to create enhanced novel life forms. Genes designing does not regularly incorporate customary creature and plant rearing, in vitro treatment, acceptance of polyploidy, mutagenesis and cell combination systems that don't utilize recombinant nucleic acids or a hereditarily altered life form all the while. The maintenance of genome integrity is essential for organism survival and for the inheritance of traits to offspring. Genomic instability is caused by DNA damage, aberrant DNA replication or uncoordinated cell division, which can lead to chromosomal aberrations and gene mutations.
- Gene editing therapy
- Genetic transformation
- Bio fabrication & 3 D-Bio printing in Life Science
- Nanotechnology in Genetics
- Therapeutic Cloning
Track 12 Bioinformatics in Genetics
Bioinformatics in Genetics is the utilization of programming building, bits of knowledge, and number juggling to issues in science. Bioinformatics in Genetics crosses a broad assortment of fields inside science, including genomics/innate characteristics, biophysics, cell science, natural science, and improvement. In like way, it makes use of instruments and techniques from an extensive variety of quantitative fields, including figuring design, machine learning, Bayesian and visit estimations, and real material science.
A great deal of computational science is stressed over the examination of sub-nuclear data, for instance, bio groupings (DNA, RNA, or protein courses of action), three-dimensional protein structures, quality enunciation data, or sub-nuclear natural frameworks (metabolic pathways, protein-protein joint effort frameworks, or quality managerial frameworks). A wide combination of issues can be had a tendency to using this data, for instance, the distinctive evidence of affliction causing characteristics, the diversion of the Transformative narratives of species, and the opening of the complex regulatory codes that turn characteristics on and off. Bioinformatics in Genetics can in like manner be stressed over non-sub-nuclear data, for instance, clinical or natural data.
- Computational biomodeling
- Computational neuroscience
- Computational pharmacology
- Computational evolutionary biology
- Computational Entomology
- Next generation sequencing
- Expression profiling, gene targeting, tissue-specific and inducible gene ablation
Track 13 Neurogenetics
Neurogenetics is the part of genetics in the advancement and function of the nervous system. It consider about neural attributes as phenotypes (i.e. appearances, measurable or not, of the genetic make-up of an individual), is primarily in view of the perception that the nervous systems of people, even of those having a place with similar animal types, may not be identical. As the name infers, it draws perspectives from both the studies of neuroscience and hereditary qualities, focusing specifically how the hereditary code a life form conveys influences its communicated attributes. Transformations in this hereditary succession can have an extensive variety of impacts on the personal satisfaction of the person. Neurological sicknesses, conduct and identity are altogether examined with regards to neurogenetics. The field of neurogenetics developed in the mid to late 1900s with progresses firmly following headways made in accessible technology. Currently, neurogenetics is the focal point of much research using cutting edge techniques. The field of neurogenetics emerged from advances made in molecular biology, genetics and a desire to understand the link between genes, behaviour, the brain, and neurological disorders and diseases.
- Behavioral neurogenetics
- Cross-species gene conservation
- Neural development
- Cognitive genomics
- Computational Neurogenetic Modeling
Periodontitis is a multifactorial disease that causes tooth loss. The intricate pathogenesis of periodontitis infers the involvement of a susceptible host and a bacterial challenge. Numerous studies provided a valuable contribution to understanding the genetic basis of periodontal disease, but the specific candidate genes of susceptibility are still unknown. Truly, huge examinations and screening of single-nucleotide polymorphisms have yielded new innate information without a total response for the organization of periodontal disorder. In this unique duplicate, we give a survey of the most relevant written work, showing the standard thoughts and bits of learning of the philosophies that have been creating to all the more likely break down and treat periodontal infection in view of biomarker examination and host regulation.
- Gene Polymorphisms in Chronic Periodontitis
- Genetics and Susceptibility to Periodontists
- Effect of gene polymorphisms on periodontal diseases
- Epigenetics in periodontics
- Periodontitis is a multifactorial disease
- Inherited periodontitis
Track 15 Epigenetics & Chromatin
Epigenetics is the study of heritable phenotype changes that do not involve alterations in the DNA sequence. Epigenetics implies features that are "on top of" or "in addition to" the traditional genetic basis for inheritance. Epigenetics most often denotes changes that affect gene activity and expression, but can also be used to describe any heritable phenotypic change. Such effects on cellular and physiological phenotypic traits may result from external or environmental factors, or be part of normal developmental program. The standard definition of epigenetics requires these alterations to be heritable either in the progeny of cells or of organisms. Epigenetic research uses a wide range of molecular biological techniques to further understanding of epigenetic phenomena, including chromatin immunoprecipitation (together with its large-scale variants ChIP-on-chip and ChIP-Seq), fluorescent in situ hybridization, methylation-sensitive restriction enzymes, DNA adenine methyltransferase identification (DamID) and bisulfite sequencing. Furthermore, the use of bioinformatics methods has a role in (computational epigenetics).
- Histone modification
- DNA methylation
- Clinical Epigenetics
- Translational epigenetics
- Reproductive epigenetics
Track 16 Immunology & Immunogenetics
Immunogenetics has a critical part in the examination of single characteristics of genes and their part in the manner in which traits or conditions are passed beginning with one time then onto the following. The examination of the atomic and cell parts that include the protected structure, including their ability and association turns into the central craft of immunology. Immune system infections, for example, type 1 diabetes, are complex genetic characteristics which result from defects in the immune system Distinguishing proof of qualities characterizing the insusceptible deformities may recognize new target qualities for remedial methodologies. Then again; genetic assortments can in like manner describe the immunological pathway provoking illness.
- Granulocyte Immunology
- Genes and Immunity
- Immunogenetics and Pharmacogenetics
- Vasculitis and Autoimmune Disease
- Platelet Immunology
- Genetic Research
- Genetics of Allo Antigens
- Genetic control of immune cell activation
- Chronic Inflammation
Track 17 Gene Therapy and Genetic Counselling
Genetic Counselling is the procedure by which the patients or relatives at risk of an acquired disorder (or might convey a kid at risk) are advised with the outcomes and nature of the disorder, the likelihood of creating or transmitting it, and the choices open to them in management and family planning. This mind boggling procedure can be isolated into indicative (the real estimation of hazard) and supportive aspects.
Gene Therapy is a preliminary strategy that uses characteristics or basically nucleic destructive polymers to treat or hinder ailment into a patient's cell as a pharmaceutical for disease treatment. Later on, this strategy may empower authorities to treat disarray by implanting's a gene into a patient's cells rather than using solutions or medical procedure. Gene Therapy is a way to deal with settle an innate issue at its inside or source. The polymers are either changed over into proteins which meddle with the target quality articulation or else they could amend inherited changes.
The most surely understood sort of value transport is as DNA that encodes the common sense helpful quality to supplant the target changed quality. The polymer particles are packaged inside a vector which passes on the iotas inside and helps in their compromise. Gene Therapy is an exceptionally viable however simple to disprove sort of treatment of inherited issue dependent upon their level of sensibility and social and good affirmation.
- Gene Polymorphism
- Regenerative Medicine
- Gene Editing and CRISPR Based Technologies
- Viral Gene Therapy
- Ethical Issues Related To Gene Therapy
- Advanced Therapy Production
Track 18 Chaemogenetics and Optogenetics
Optogenetics and chemo genetics are the recent and well known strategies used to study this relationship. Both of these strategies target particular mind circuits and cell populace to impact cell movement. Be that as it may, they utilize distinctive strategies to achieve this undertaking. Optogenetics utilizes light-delicate channels and pumps that are virally introduced into neurons. Cells' movement, having these channels, would then be able to be controlled by light. Chemo genetics, then again, utilizes synthetically designed receptors and exogenous atoms particular for those receptors, to influence the movement of those cells.
DREADDs are the most widely recognized GPCRs utilized in chemo genetics. These receptors exclusively get initiated by the medication of intrigue (inert molecule) and impact physiological and neural procedures that occur inside and outside of the central nervous system.
Chemo genetics has been favoured over Optogenetics, and it maintains a strategic distance from a portion of the difficulties of Optogenetics. Chemo genetics does not require the costly light equipment, and in this way, is more available. The goals in Optogenetic decreases because of light scrambling and illuminance declined levels as the separation between the subject and the light source increases. These factors, in this manner, don't take into consideration all cells to be influenced by light and prompt lower spatial goals. Chemo genetics, be that as it may, does not require light utilization and accordingly can accomplish higher spatial goals.
- Mapping of the brain and behaviour
- Cell culture, Network analysis
- Improvement of appropriate light sources
- Transfection methods
- Parkinson disease, Epilepsy
- Forward chemogenomics
- Reverse chemogenomics
- Personalized medicine
- Phenotypic screening
Track 19 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 can be obtained from the umbilical string after new-born’s first experience with the world. 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 20 Microbial Genetics
Microbial Genetics is a subject area inside microbiology and genetic engineering. It examines the genetics of small (micro) life forms; microscopic organisms, archaea, infections and some protozoa and parasites. This includes the investigation of the genotype of microbial species and furthermore the articulation framework as phenotypes.
For instance: Microorganisms' quick development rates and short age times are utilized by researchers to think about advancement. Microbial hereditary qualities additionally has applications in having the capacity to examine forms and pathways that are like those found in people, for example, drug metabolism. Microorganisms are in a perfect world suited for biochemical and hereditary qualities examines and have made huge contributions to these fields of science, for example, demonstration that DNA is the hereditary material. Utilizing organisms, conventions were created to embed qualities into bacterial plasmids, exploiting their quick generation, to make bio factories for the gene of interest. Such hereditarily built microorganisms can deliver pharmaceuticals, for example, insulin, human development hormone; interferon’s and blood clotting factors.
- Gene fusions
- Eukaryotic Genomes
- Prokaryotic Genomes
- Genetic Recombination
- Transposons and Transposition
- Mechanisms of Gene Transfer
Track 21 Structural Genomics
Structural genomics seeks to depict the 3-dimensional structure of each protein encoded by a given genome. This genome-based approach takes into consideration a high-throughput technique for structure assurance by a combination of experimental and modelling approaches. The important contrast between structural genomics and traditional structure prediction is that structural genomics endeavors to decide the structure of each protein encoded by the genome, instead of concentrating on one specific protein. With full-genome arrangements accessible, structure prediction should be possible all the more rapidly through a combination of experimental and modelling approaches, particularly in light of the fact that the accessibility of expansive number of sequenced genomes and beforehand explained protein structures enables researchers to display protein structure on the structures of previously solved homologs.
- Modelling Threading
- Structure databases
- Traditional structural prediction
- Structural homology
- Structural bioinformatics
Track 22 Forensic Genetics
Forensic genetics: The branch of genetics that deals with the application of genetic knowledge to legal problems and legal proceedings. Forensic genetics is also a branch of forensic medicine which deals more broadly with the application of medical knowledge to legal matters.
Forensic genetics today tends to conjure up DNA. However, even the term "DNA fingerprinting" is reminiscent of older methods of police identification. Forensic genetics is not a new field. Long before the era of DNA fingerprinting, blood grouping, HLA typing and other tests of genetic markers in blood were done to try to determine who did it (and, more often, who did not do it).
- DNA Fingerprinting
- Evaluation and presentation of DNA evidence
- Kinship testing
- Lineage markers
- Single nucleotide polymorphisms
- Statistical interpretation of STR profiles
- PCR amplification
- Anthropological studies
Track 23 Nutrigenetics
Nutrigenetics intends to recognize how genetic variation affects response to nutrients. This data can be applied to improve health and prevent or treat diseases. The ultimate aim of nutrigenetics is to offer individuals customized nourishment in light based on their genetic makeup.
A major goal for nutrigenetic scientists is to identify genes that make certain people more susceptible to obesity and obesity related diseases. The thrifty gene hypothesis is a example of a nutrigenetic factor in obesity. Future progressions in nutrigenetics research may conceivably demonstrate the presence of thrifty genes and in addition discover counter-impacts keeping in mind the end goal to prevent obesity and obesity-related diseases.
- Nutrition Market
- Clinical Trials
- Genetic variations affecting the nutritional environment
- Dietary bioactives with genome
The Global Genetic testing market is anticipated to grow at a CAGR of 13.56% between 2018 and 2026. Genetic testing includes observing the DNA, a chemical databank that transports directives for the body’s utilities. Genetic testing can reveal changes or alterations in the genes that may cause illness or disease. The Genetic testing market is primarily driven by the following factors:
Geographically, the global genetic testing’s market has been segmented on the basis of four major regions, which include:
- Genetic Testing
- Digital Genome Market
- Global genetic disorder diagnosis market
- Pharmacogenetic testing
- Inherited disorder testing
GENETICS UNIVERSITIES IN USA
Harvard University || Massachusetts Institute of Technology || University of California--San Francisco University of Washington || Johns Hopkins University || Yale University || University of California--San Diego || University of Pennsylvania || Washington University in St. Louis || University of California, Berkeley || Cornell University || University of Albama
GENETICS UNIVERSITIES IN EUROPE
University of Vienna || Vienna University of Technology || Universität Innsbruck || Technische Universität Graz || Johannes Kepler University Linz || KU Leuven || Ghent University || Université Catholique de Louvain (UCL) || Paris Sciences et Lettres Research University (PSL) || Ruprecht-Karls-Universität Heidelberg || Trinity College Dublin || National University of Ireland || Delft University of Technology || University of Groningen || Technical University of Denmark || Cambridge University University of Amsterdam || Oxford University
GENETICS UNIVERSITIES IN ASIA
University of Tokyo || National University of Singapore || Kyoto University || Peking University || Weizmann Institute of Science || Proteomics Conferences || Osaka University || Seoul National University || Shanghai Jiao Tong University || Fudan University || Zhejiang University || Tel Aviv University || Pohang University of Science and Technology || Indian Institute of Science || Nankai University || Tongji University || King Saud University || Nanjing University || Harbin Institute of Technology | Kyung Hee University || Sichuan University || Xiamen University || Chonnam National University || Jilin University || Central South University || University of Tehran || Aligarh Muslim University || Chinese University Hong Kong || University of Delhi || South China University of Technology || Waseda University || Okayama University || Southeast University || Soochow University || Mahidol University || Hiroshima University || Tianjin Medical University || Kanazawa University || Tehran University of Medical Sciences || Kumamoto University || Kyungpook National University || National Yang-Ming University || China Medical University Taiwan
GENETICS AND MOLECULAR BIOLOGY COMPANIES
Gene Works || Fusion Genomics || Ambry Genetics || Illumina || Singlera Genomics || Blueprint Genetics || Helix || Encoded Genomics || Med Genome || Gen Script || Genomics PLC || iGenomX || Cellecta || Bio cytogen || Edi Gene || Neo Genomics || Xcelris Genomics || GenoSpace || GenePeeks || Lineagen || Blue Heron Biotech || Global Genomics Group || Congenica || Congenica || Diffinity Genomics || Sema4 Genomics || Sciomics || Dovetail Genomics || Genapsys || Synbal
JOURNALS OF GENETICS
Advancements in Genetic Engineering || Advances in Molecular Diagnostics || Cell & Developmental Biology || Cell Biology: Research & Therapy || Hybrid Cellular & Molecular Medicine || Cellular and Molecular Biology Cloning & Transgenesis || Epigenetics Research || Fungal Genomics & Biology || Gene Technology Hereditary Genetics : Current Research || Human Genetics & Embryology || Insights in Stem Cells || Journal of Aging Science || Journal of Cell Science & Therapy || Journal of Clinical & Medical Genomics || Journal of Clinical Developmental Biology || Journal of Clinical Epigenetics Journal of Cytology & Histology || Journal of Down Syndrome & Chromosome Abnormalities || Journal of Fertilization: In Vitro - IVF-Worldwide, Reproductive Medicine, Genetics & Stem Cell Biology Journal of Genetic Disorders || Journal of Genetic Disorders & Genetic Reports || Hybrid Journal of Genetic Syndromes & Gene Therapy || Journal of European Biotechnology Thematic Network Association || Journal of Genetics and DNA Research || Journal of Genetics and Genomes || Journal of Molecular and Genetic Medicine || Journal of Molecular Biology and Biotechnology || Journal of Molecular Biomarkers & Diagnosis || Journal of Molecular Imaging & Dynamics || Journal of Plant Genetics and Breeding || Journal of Stem Cell Research & Therapy || Journal of Tissue Science & Engineering Molecular Biology
GENETICS SOCIETY IN USA
Genetics Society of America || Clinical Genetics Society || Cancer Genetics society || American Genetic Association || American Society of Human Genetics || Genetic inheritance and evolution Genetic determinism in science and society || Frontiers in epigenetic chemical biology || Maternal Nutrition and Epigenetics - American Society for Nutrition
GENETICS SOCIETY IN EUROPE
European Society of Human Genetics || The Genetics Society || Epigenetics, society, and bio-objects || Cancer Genetics || European Society of Gene and Cell Therapy || Clinical Genetics || Behaviour Genetics Association| International Behavioural and Neural Genetics Society || DNA methylation and epigenetics || Estonian Society of Human Genetics
GENETICS SOCIETY IN ASIA
Medical genetics || Asia Pacific Society of Human Genetics || Human Genetics Society of Australasia Epigenetics in Society - Scholarship at U Windsor || Cancer Genetics Society || UICC || Trends in Recent Research of Epigenetics || Professionals Society of Genetic Counsellors in Asia
GENETICS CONFERENCES IN USA
International Genetics and Genomics Conferences, San Francisco, USA, June 7 - 8, 2020 || International Genetics and Genomics Conferences, San Francisco, USA, November 5 - 6, 2019 || International Genetics and Genomics Conferences, San Francisco, USA, June 6 - 7, 2019 || International Experimental Genetics and Applications Conferences, New York, USA, January 30 - 31, 2019 || International Genetics of Mood Disorders Conferences , New York, USA, June 4 - 5, 2020 || International Computational Evolutionary Genetics Conferences, San Francisco, USA, November 5 - 6, 2019 || International Human and Statistical Genetics Conferences, Los Angeles, USA, October 30 - 31, 2019 || International Molecular Pathology and Genetics Conferences, New York, USA, August 8 - 9, 2019 || International Computational Evolutionary Genetics Conferences, San Francisco, USA, November 26 - 27, 2018
GENETICS CONFERENCES IN EUROPE
International Cell and Gene Therapy Conferences, Vienna Austria, October 15-17, 2018 || International Fungal Genetics Conferences, Venice, Italy, June 21 - 22, 2020 || International Speciation and Genetics Conferences Paris, France, November 20 - 21, 2019 || International Experimental Genetics and Biology Conferences Paris, France July 18 - 19, 2019 || International Advances in Experimental Genetics Conferences Paris, France July 18 - 19, 2019 || International Evolutionary and Quantitative Genetics Conferences, Paris, France July 18 - 19, 2019 || International Speciation and Genetics Conferences Paris, France, November 8 - 9, 2018 || International Genetics and Molecular Biology Conferences, Amsterdam, The Netherlands, July 14 - 15, 2020
GENETICS CONFERENCES IN ASIA
International Genetics, Singapore Conferences, SG , November 18 - 19, 2019 || International Genetics Conferences, Singapore, SG, November 22 - 23, 2018 || International Clinical Genetics Conferences, Singapore, SG, January 8 - 9, 2020 || International Genetics and Genomics Conferences, Singapore, SG, September 10 - 11, 2018 || International Human Genetics Conferences, Bangkok, Thailand, December 17 - 18, 2019 || International Computational Genetics Conferences, Bangkok, Thailand, November 28 - 29, 2019 || International Computational Genetics and Bioinformatics Conferences, Kyoto, Japan, November 13 - 14, 2019 || International Prediabetes and Genetics of Diabetes Conferences, Singapore, SG, July 4 - 5, 2019 || International Ethology and Behavioural Genetics Conferences, Osaka, Japan, May 29 - 30, 2019 || International Genetics and Molecular Biology Conferences Singapore, SG, November 22 - 23, 2018
JOB OPPORTUNITIES FOR GENETICISTS IN USA
Statistical Geneticist || Research Geneticist (Plants) Research Associate || Crop Scientist/Geneticist || Research Geneticist Plants || Research Geneticist Plants (Postdoctoral Research Associate) || Clinical Geneticist || Director of Statistical Genetics || Pediatric Geneticist - Assistant/Associate Professor || Genetic Counsellor - Medical Genetics| Research Geneticist Plants Research Associate || Director, Molecular Genetics & Cytogenetics or Biochemical Genetics || Genetics Counsellor || Research Associate I - Human Molecular Genetics || Research Fellow - Statistical Genetics || Human Genetics - Research Assistant III (Stottmann Lab) || Post-Doctoral Scientist - Human Genetics || Genetic Counsellor-Genetics Clinic || Corn Specialist || Clinical Genetics Counsellor
JOB OPPORTUNITIES FOR GENETICISTS IN EUROPE
Professor, Molecular and Cell Biology and Chief Scientific Director, Innovative Genomics Institute || Clinical Genetics Supervisor || Sr. Manager of Cytogenetics || Scientist - Genome Analysis Unit (Computational Biology) || Senior Scientist, Genetics Research || PhD Position - Genetic and Epigenetic Control of Mouse Organ Development || Postdoc and PhD positions in archaeogenomics, population genetics, bioarchaeology, and archaeologic || Application Scientist - Genetics/Molecular - Cambridge, UK || Staff Scientist - Mouse Genome Engineering || Senior Scientist, Computational and Statistical Genetics || Post-Doctoral Research Fellow, Statistical Genetics || Clinical Genetics Technologist || Senior Scientist, Genetics Research || Wanted Molecular and Genetics Biology Graduates || Genomics Project Manager || Part-time Research Technician - Cell Biology and Genetics Senior Bioinformatician - Genomics England || Senior Medical Advisor, Genetic Diseases - National Scope || Certified Genetic Counsellor San Francisco Perinatal
JOB OPPORTUNITIES FOR GENETICISTS IN ASIA
Full Professor in Plant Evolutionary Genomics and Development || Editing Technology Developments in molecular biology and In Vitro Biology || Faculty Positions at Westlake University || Full Professor in Plant Evolutionary Genomics and Development || Faculty Search for Zheizhang University || Job Opening in China Pharmaceutical University: Professor and Dean, tenured || Xinyu University
Genetics Analysis is the investigation of qualities or quality transformations done by directing different research facility probes the essential code of life i.e. DNA or RNA. These tests are generally performed to test either the likelihood of the event of an infection or essentially to comprehend the blunders in the metabolic framework programming. Be that as it may, the most common and surely understood of these are scientific tests done to affirm a man/suspect's personality or to affirm Genetics connection between various people, the previous being state legal's duty (criminal cases) and the last done significantly for private reasons (paternity tests, and so forth). Close to these well known tests, Genetics examination is utilized for various logical and scholarly research purposes. Genetics examination has made some amazing progress since GJ Mendel and Watson-Crick presented the basics of Genetics qualities, today it is the most assorted logical investigation making it an endless piece of different demonstrative investigations.
Genetics Testing Market measure was esteemed at USD 10.6 billion out of 2017 and is relied upon to see over 11.6% CAGR from 2018 to 2024.
U.S. Genetics Testing Market, By Test Type, 2013 – 2024
Expanding request from patients for customized prescriptions will fuel the interest for Genetics testing amid the inevitable years. Customized solution offers custom-made medicinal treatment to patients in light of their atomic premise. Different created economies, for example, Europe experience Genetics testing for discovery of different Genetics and uncommon ailments. Discovery of sicknesses at a beginning period encourages early treatment and diminishes seriousness of infections. Developing reception of customized solutions combined with expanding mindfulness in regards to early analysis of ailment will support the business development over the gauge time frame.
Mechanical headway in Genetics testing is relied upon to drive the Genetics testing market amid the coming years. The interest for Genetics testing is expanding over the globe attributable to the accessibility of new tests and additionally progression in the Genetics testing strategies. Developments in tests that offer more secure and proficient strategies of infection recognition, outperforming the danger of premature delivery amid beginning times of pregnancy will serve to be a high effect rendering factor that will drive the Genetics testing market development amid the expected years.
Lack of experienced experts and propelled foundation in creating and immature economies is should hamper the market development over the gauge time frame. Openness to quality medicinal services in low asset zones is hard to keep up attributable to absence of foundation. In addition, danger of false translations related with inaccessibility of experienced experts will control industry development observably.
Genetics Testing Market, By Test Type
Analytic testing portion represented the most elevated piece of the overall industry with an income offer of USD 5690.6 million and is relied upon to develop at a noteworthy rate over the gauge time allotment inferable from its wide applications in different ailments. Location of sicknesses at beginning period enables patients to experience helpful treatment at a beginning period and limits the seriousness of ailments prompting diminished death rate. Expanding commonness of perpetual sicknesses worldwide will enlarge the section development over the figure time frame.
Pre-birth and new conceived testing section is assessed to observe lucrative development with a CAGR of 11.6% amid the gauge period.Increasing pervasiveness of chromosomal variations from the norm and Genetics issue in the new borns worldwide is one of the main source of baby dismalness and mortality. As indicated by Centers for Disease Control and Prevention (CDC), around 3% of all infants conceived in the U.S. are influenced by birth surrenders prompting baby demise. Previously mentioned variables will fuel the interest for pre-birth and new-conceived Genetics testing amid are the coming years.
Genetics Testing Market, By Application
Cardiovascular malady determination portion of Genetics testing business sector will develop at the speediest CAGR of nearly12.8% inferable from rising commonness of heart sicknesses over the globe. Genetics testing permits testing for an extensive variety of cardiovascular infections (CVDs) enveloping inborn heart mutations. Auspicious analysis of heart issue helps spare lives and lessen the quantity of CVD passings. Medicinal services framework's endeavors towards decreasing CVD frequencies should fuel business development over the conjecture time frame.
Growth finding fragment commanded the Genetics testing market with an income of USD 5562.8 million out of 2017. As indicated by, The Institute for Health Metrics and Evaluation (IHME), around 8.9 million malignancy passings were recorded in 2016, of which around 5%-10% were caused by acquiring Genetics transformation. Rising predominance of different sorts of disease, for example, prostate malignancy, bosom tumor and lung tumor combined with expanding mindfulness relating to early location of malignancy will empower the market development all through the forecastperiod.
Genetics Testing Market, By Region
North America overwhelmed the Genetics testing market with an income of USD 6382.1 million of every 2017 and is anticipated to develop at a critical rate over the gauge time frame. This is owing to expanding occurrences Genetics maladies, for example, malignancy, Turner disorder, neurofibromatosis, and spinal strong decay. Accessibility of new tests attributable to innovative progressions will fuel the interest for Genetics testing. Propelled foundation combined with high medicinal services consumption and administrative help for coordinate to-buyer Genetics testing will additionally enlarge the market development in the coming years.
Latin America Genetic Testing Market is anticipated to develop at a hearty CAGR of around 13.3% amid the conjecture time frame inferable from expanding commonness of different sorts of disease, for example, prostate malignancy, bosom tumor and lung growth. Bosom tumor is the most widely recognized growth among ladies in Latin America. As per the Pan American Health Organization (PAHO), around 4,08,200 ladies were determined to have bosom growth and the number is evaluated to develop by 46% by 2030. Subsequently, appropriation of Genetics testing for early discovery and avoidance of tumor and other Genetics illnesses will quicken the local development over the forecastperiod.
Aggressive Market Share
A portion of the prominent business players working in worldwide Genetics testing market are 23andMe, Abbott Molecular, Bayer Diagnostics, Biocartis, BioHelix, BioMerieux, BGI, Celera Genomics, Cepheid, Counsyl, deCODEme, Genentech, Genomictree, Genomic Health, HTG Molecular Diagnostics, IntegraGen, LabCorp Diagnostics, Luminex, MolecularMD, Myriad, Natera, PacBio, Pathway Genomics, Qiagen, Roche Diagnostics, Sequenom and Siemens. Industry players are concentrating on key extension through acquisitions, mergers and joint efforts assist the players with strengthening and upgrade the item portfolio. For example, in December 2017, Roche obtained Ariosa Diagnostics, an atomic indicative testing administrations supplier, to enter the non-obtrusive pre-birth test (NIPT) and without cell DNA testing administrations showcase.
Genetics Testing Industry Background
Rising commonness of sicknesses, for example, tumor, cystic fibrosis, Alzheimer's and other Genetics ailments will drive worldwide Genetics testing industry. Expanding selection of Genetics testing for early recognition of ailments and recognizable proof of Genetics change before its indication will additionally increase industry development over the figure time frame. The business is relied upon to see quick development later on inferable from rising doctor appropriation of Genetics testing into clinical care. Accessibility of administrative help for direct to buyer (DTC) testing and continuous progressions in innovation empower industry players to keep up their market position.
Developing Demand for Personalized Medicine
Customized solution, where custom-made treatment is made accessible to patients with a comprehension of the sub-atomic premise of sicknesses, has turned out to be famous over the ongoing years. Genetics testing and genome sequencing are two of the most vital instruments that are utilized to comprehend the atomic premise of a sickness. European nations are screened for a few Genetics infections, as an early discovery of these sicknesses can keep the beginning of indications, or limit the seriousness of the illness. Genetics testing for growth conclusion can show the inclination of the ailment in the quality, before its real sign. This sort of symptomatic system empowers a man to make prudent strides, and keep away from conceivable dangers later on.
Social and Ethical Implications of Genetic Testing
Protection is an essential resource for individuals. The dread of segregation by insurance agencies disheartens individuals from undertaking Genetics tests, which is a controlling variable for the market development. The costly idea of Genetics tests influences the market, unfavourably. Now and again, the instalments made by people are not repaid through protection, in this way, influencing the pockets of these patients. The high-import obligation by the administration on Genetics tests units additionally goes about as a hindrance to the market development.
North America to Dominate the Market
The Genetics testing market is portioned by treatment compose, sicknesses, innovation, and geology. By topography, the market has been divided into North America, Europe, Asia-Pacific, the Middle East and Africa, and South America.
Attributable to the nearness of entrenched medicinal services offices and new disclosures in the field of Genetics markers, North America overwhelms the Genetics testing market. The Asia-Pacific market is relied upon to enlist the most noteworthy CAGR, as government and private firms are making huge interests in the human services industry. In the course of the most recent few years, to put resources into the Japanese market, a few mergers, acquisitions, and coordinated efforts between organizations have occurred.
Enter Developments in the Market
September 2017: Myriad Launched risk Score to upgrade
July 2017: Admera Health Partners collaborates with Helix to Launch Genetic Tests to Assess the Risk of Inherited High Cholesterol, Sudden Cardiac Death, and Inherited Diabetes
Major Players: Illumina, Inc, Abbott Molecular Inc, 23 And Me, Roche Diagnostics, Qagen, Blueprint Genetics, BJI Tech, Eurofins Scientific, Centogene AG, Thermo Fisher Scientific, Elitech Group, amongst others.
Reasons to Purchase This Report
- Market analysis for the global genetic testing market, with region-specific assessments and competition analysis on the global and regional scale
- Analyzing various market perspectives, with the help of Porter’s five forces analysis
- The treatment type that is expected to dominate the market
- Regions that are expected to witness fastest growth during the forecast period
- Identify the latest developments, market shares, and strategies employed by the major market players
- 3 months analyst support, along with the Market Estimate sheet (in excel)
Customization of the Report
- This report can be customized to meet your requirements. Please connect with our analyst, who will ensure you get a report that suits your needs.
Past Conference Report (Genetics 2018)
The World Congress of Genetics & Genetic Engineering (Genetics2018) hosted by Euroscicon took place at Hyatt Place, Amsterdam, Netherlands during August 20-21, 2018. It was organized by Euroscicon and generous response was received from the Editorial Board Members of Euroscicon Journals as well as from eminent scientists, talented researchers and young student community. Researchers and students who attended from different parts of the world made the conference one of the most successful and productive events in 2018 from Euroscicon. The program witnessed thought provoking keynote and plenary presentations from experts in the field of Genetics, Genetic Engineering and Molecular Biology, highlighting the theme, "Review the ideas of latest technology development in Genetics & Genetic Engineering".
The meeting was carried out through various sessions, in which the discussions were held on the following major scientific tracks:
- Genetics & Genetic Engineering
- Human Genetics & Genetic Disorders
- Gene Mutation and Cloning
- Immunology & Immunogenetics
- Plant Genetics
- Bioinformatics in Genetics
- Next Generation Sequencing
- Stem Cell Therapy
- Regenerative Medicine
The highlights of the meeting were form the eminent keynote lectures from
- Richard Harbottle, German Cancer Research Centre, Germany
- Jan Lukas Robertus, Imperial College London, United Kingdom
- Magnus S. Magnusson, University of Iceland, Iceland
Genetics 2018 played an important role in promoting multidisciplinary interactions between science and technology to enhance research in Genetics & Genetic Engineering. The program covered current and emerging research innovations in the field of Genetics.We would specially thank the Moderator of the event Dr. Ewelina Kawecka, Warsaw University of Life Sciences, Poland for her contribution for the conference.
We are obliged to the various delegates from companies and institutes who actively took part in the discussions. We sincerely thank the Organizing Committee Members and Editorial board of Genetics 2018 for their gracious presence and continuous support throughout the proceedings of this event with the valuable feedback and generous response received from the participants of the event,Euroscicon would like to announce the commencement of "2nd World Congress on Genetics & Genetic Disorders" during May 13-14, 2019, Stockholm, Sweden.