Recommended Global Healthcare Management Conferences
Molecular Biology & Genetics 2019
We are delighted to announce the commencement of the World Congress on Molecular Biology and Genetics, Slated to hold in Orlando, USA from March 27-28, 2019.
Global Conference on Molecular Biology and genetics aims to bring together leading academic scientists, researchers and research scholars and to exchange and share their experiences and research results on all aspects of Molecular Biology and Genetics. GCMBG 2019 a premier interdisciplinary platform for researchers, practitioners and educators to present and discuss the most recent innovations, trends, and concerns as well as practical challenges encountered and solutions adopted in the fields of Molecular Biology and Genetics.
In addition to the multidisciplinary talks, Keynote sessions, Poster Presentation and Workshops relevant to Molecular Biology and Genetics, Molecular Biology 2018 is a complete 2 day event , business meet, and exhibition with panel discussions, open Q & A to generate a prime learning knowledge between participants in the Orange Country in Orlando Florida.
Conference Series LLC Ltd is an open resource platform that conducts 3000+ global events including International Conferences, Workshops, Symposia, Trade Shows, Exhibitions and Science Congresses in all the major scientific disciplines, including Clinical, Medical, Pharmaceutical, Engineering, Technology, Business Management and Life Sciences across America, Europe, The Middle East, and Asia Pacific. It is reaching over 25 million researchers, scholars, students, professionals and corporate entities all over the globe.
- Academic Scientists
- Molecular & Genetics Biologists
- Biochemistry Researchers
- Big Data Analyst for Genomic Medicine
- Genomic Data Scientists
- Molecular Diagnosticians
- Pharmaceutical Leaders
- Health care Professionals
- Executives/Managers and Business Delegates
- Director of Laboratories, Universities
- Post-Doctoral Fellows
- Research & Diagnostic Laboratories
- Biomedical and Biotechnology Research organizations
- Structural Biology Societies and Associations
- Molecular Biology Societies and Associations
Why to Attend??
- Recent innovation & Researches in Molecular Biology & Genetics
- Sharpen your skills
- Meet experts and influencers face-to-face
- Certification, Remarkable Awards and Global Recognition to meritorious Researchers
- Global Business and Networking Opportunities with peers
- Absorb the energy of like-minded individuals
Being recognized as a world-renowned organization, Conference Series LLC Ltd takes pride to introduce the commencement of “World Congress on Molecular Biology and Genetics” from March 27-28, 2019 at Orlando, USA. Special interest and theme of this conference is “Molecular Biology and Genetics: Fostering Recent Innovation and Emerging Novel Research in Molecular Biology & genetics”.
Track 1: Molecular biology & biological sciences
Molecular Biology is the field of biology that studies the composition, structure and interactions of cellular molecules -such as nucleic acids and proteins -that carry out the biological processes essential for the cell’s functions and maintenance.The field of molecular biology overlaps with biology and chemistry and in particular, genetics and biochemistry. A key area of molecular biology concerns understanding how various cellular systems interact in terms of the way DNA, RNA and protein synthesis function.
The specific techniques used in molecular biology are native to the field but may also be combined with methods and concepts concerning genetics and biochemistry, so there is no big distinction made between these disciplines.
Biological sciences encompass all the divisions of natural sciences examining various aspects of vital processes. The concept includes anatomy, physiology, cell biology, biochemistry and biophysics, and covers all organisms from microorganisms, animals to plants.
Molecular signaling is an exponentially growing field that encompasses different molecular aspects of cell signaling underlying normal and pathological conditions. Specifically, the journal focuses on the normal or aberrant molecular mechanisms involving receptors, G-proteins, kinases, phosphatases, and transcription factors in regulating cell proliferation, differentiation, apoptosis, and oncogenesis in mammalian cells. This also includes the genetic and epigenetic changes that modulate the signaling properties of cells and the resultant physiological conditions.
Molecular evolution is the area of evolutionary biology that studies evolutionary change at the level of the DNA sequence. It includes the study of rates of sequence change, relative importance of adaptive and neutral changes, and changes in genome structure.
Track 2 : Molecular Diagnosis & Molecular Genetic Test
Molecular diagnostics is a collection of techniques used to analyses biological markers in the genome and proteome—the individual's genetic code and how their cells express their genes as proteins—by applying molecular biology to medical testing. The technique is used to diagnose and monitor disease, detect risk, and decide which therapies will work best for individual patients.By analyzing the specifics of the patient and their disease, molecular diagnostics offers the prospect of personalized medicine
Molecular Genetic testing is a type of medical test that identifies changes in chromosomes, genes, or proteins. The results of a genetic test can confirm or rule out a suspected genetic condition or help determine a person’s chance of developing or passing on a genetic disorder. More than 1,000 genetic tests are currently in use, and more are being developed.
Several methods can be used for genetic testing:
- Molecular genetic tests (or gene tests) study single genes or short lengths of DNA to identify variations or mutations that lead to a genetic disorder.
- Chromosomal genetic tests analyze whole chromosomes or long lengths of DNA to see if there are large genetic changes, such as an extra copy of a chromosome, that cause a genetic condition.
- Biochemical genetic tests study the amount or activity level of proteins; abnormalities in either can indicate changes to the DNA that result in a genetic disorder.
Track 3 : Molecular Medicine : Health & Medical Imaging
Molecular medicine is a broad field, where physical, chemical, biological, bioinformatics and medical techniques are used to describe molecular structures and mechanisms, identify fundamental molecular and genetic errors of disease, and to develop molecular interventions to correct them.The molecular medicine perspective emphasizes cellular and molecular phenomena and interventions rather than the previous conceptual and observational focus on patients and their organs.
Molecular Medicine strives to understand normal body functioning and disease pathogenesis at the molecular level, which may allow researchers and physician-scientists to use that knowledge in the design of specific molecular tools for disease diagnosis, treatment, prognosis, and prevention.
Medical imaging is the technique and process of creating visual representations of the interior of a body for clinical analysis and medical intervention, as well as visual representation of the function of some organs or tissues (physiology). Medical imaging seeks to reveal internal structures hidden by the skin and bones, as well as to diagnose and treat disease. Medical imaging also establishes a database of normal anatomy and physiology to make it possible to identify abnormalities. Although imaging of removed organs and tissues can be performed for medical reasons, such procedures are usually considered part of pathology instead of medical imaging.
Track 4 : Molecular Metabolomics
Metabolomics is the large-scale study of small molecules, commonly known as metabolites, within cells, biofluids, tissues or organisms. Collectively, these small molecules and their interactions within a biological system are known as the metabolome.Just as genomics is the study of DNA and genetic information within a cell, and transcriptomics is the study of RNA and differences in mRNA expression; metabolomics is the study of substrates and products of metabolism, which are influenced by both genetic and environmental factors.
Metabolomics is a powerful approach because metabolites and their concentrations, unlike other "omics" measures, directly reflect the underlying biochemical activity and state of cells / tissues. Thus metabolomics best represents the molecular phenotype.
Track 5 : Hormones Molecular Biology
Hormone Molecular Biology (HMB) is dedicated to the provision of basic data on molecular aspects of hormones in physiology and pathophysiology.
Track 6 : Technique of Molecular Biology
Molecular biology techniques are common methods used in molecular biology, biochemistry, genetics and biophysics which generally involve manipulation and analysis of DNA, RNA, protein, and lipid.
Molecular biology is an area of biology concerned with the process of gene transcription to yield RNA, the translation of RNA into proteins and the role those proteins play in cellular function. Since around 1960, molecular biologists have developed methods to identify, isolate, and manipulate molecular components in cells including DNA, RNA, and proteins.
Several techniques used in the field of molecular biology are described below.
- Polymerase chain reaction (PCR)
- Expression cloning
- Gel electrophoresis
- Macromolecule blotting and probing
Track 7 : DNA Forensics and Fingerprinting : Past, Present & Future
DNA fingerprinting, one of the great discoveries of the late 20th century, has revolutionized forensic investigations. This review briefly recapitulates 30 years of progress in forensic DNA analysis which helps to convict criminals, exonerate the wrongly accused, and identify victims of crime, disasters, and war. Current standard methods based on short tandem repeats (STRs) as well as lineage markers (Y chromosome, mitochondrial DNA) are covered and applications are illustrated by casework examples. Benefits and risks of expanding forensic DNA databases are discussed and we ask what the future holds for forensic DNA fingerprinting.
- DNA in a crime
- Molecular proofing
Track 8 : Pharmacogenomics
Pharmacogenomics is the study of how genes affect a person’s response to drugs. This relatively new field combines pharmacology (the science of drugs) and genomics (the study of genes and their functions) to develop effective, safe medications and doses that will be tailored to a person’s genetic makeup.Many drugs that are currently available are “one size fits all,” but they don't work the same way for everyone. It can be difficult to predict who will benefit from a medication, who will not respond at all, and who will experience negative side effects (called adverse drug reactions). Adverse drug reactions are a significant cause of hospitalizations and deaths in the United States. With the knowledge gained from the Human Genome Project, researchers are learning how inherited differences in genes affect the body’s response to medications. These genetic differences will be used to predict whether a medication will be effective for a particular person and to help prevent adverse drug reactions.
Track 9 : Human genetics & genetic disorders
Human genetics is the study of inheritance as it occurs in human beings. Human genetics encompasses a variety of overlapping fields including: classical genetics, cytogenetic, molecular genetics, biochemical genetics, genomics, population genetics, developmental genetics, clinical genetics, and genetic counseling.Genes can be the common factor of the qualities of most human-inherited traits. Study of human genetics can be useful as it can answer questions about human nature, understand the diseases and development of effective disease treatment, and understand genetics of human life. This article describes only basic features of human genetics; for the genetics of disorders please see: medical genetics.
A genetic disorder is a genetic problem caused by one or more abnormalities in the genome. Most genetic disorders are quite rare and affect one person in every several thousands or millions.Genetic disorders may be hereditary, passed down from the parents' genes. In other genetic disorders, defects may be caused by new mutations or changes to the DNA. In such cases, the defect will only be passed down if it occurs in the germ line.
Some types of recessive gene disorders confer an advantage in certain environments when only one copy of the gene is present.
Track 10 : Genetics And Genetic Engineering
Genetics is the branch of science concerned with genes, heredity, and variation in living organisms. It seeks to understand the process of trait inheritance from parents to offspring, including the molecular structure and function of genes, gene behaviour in the context of a cell or organism (e.g. dominance and epigenetics), gene distribution, and variation and change in populations.
Genetic engineering is the act of modifying the genetic makeup of an organism. Modifications can be generated by methods such as gene targeting, nuclear transplantation, transfection of synthetic chromosomes or viral insertion. Selective breeding is not considered a form of genetic engineering.
- Evolutionary Genetics
- Immunology & Immunogenetics
Track 11 : Plant Genetics & Human Genetics
Plant genetics is different from that of animals in a few ways. Like mitochondria, chloroplasts have their own DNA, complicating pedigrees somewhat. Like animals, plants have somatic mutations regularly, but these mutations can contribute to the germ line with ease, since flowers develop at the ends of branches composed of somatic cells. People have known of this for centuries, and mutant branches are called "sports". If the fruit on the sport is economically desirable, a new cultivar may be obtained.
Human genetics is the study of inheritance as it occurs in human beings. Human genetics encompasses a variety of overlapping fields including: classical genetics, cytogenetics, molecular genetics, biochemical genetics, genomics, population genetics, developmental genetics, clinical genetics, and genetic counseling.
Track 12 : Clinical Genetics
Clinical Genetics is the medical specialty which provides a diagnostic service and "genetic counselling" for individuals or families with, or at risk of, conditions which may have a genetic basis. Genetic disorders can affect any body system and any age group. The aim of Genetic Services is to help those affected by, or at risk of, a genetic disorder to live and reproduce as normally as possible. Genetic disorders include :
- Chromosomal abnormalities, which cause birth defects, mental retardation and/or reproductive problems.
- Single gene disorders such as cystic fibrosis, muscular dystrophy, Huntington's disease and sickle cell disease.
- Familial cancer and cancer-prone syndromes such as inherited breast or colorectal cancer and neurofibromatosis.
- Birth defects with a genetic component such as neural tube defects and cleft lip and palate.
Track 13 : Chromosomes & Genetic Conditions
Some genetic conditions are caused by mutations in a single gene. These conditions are usually inherited in one of several patterns, depending on the gene involved :
- Autosomal dominant
- Autosomal recessive
- X-linked dominant
- X-linked recessive
Track 14 : Global Market For Genetic Engineering & Molecular Biology
Genome Engineering represents the single largest technology in the global market for Synthetic Biology, demand for which is estimated at US$2.9 billion (45% share) in 2017 and is projected to reach US$9.4 billion by 2023. During period 2017-2023, the market for Biological Components and Integrated Systems is slated to record the fastest CAGR of 24.8%.
The major factors propelling growth of Synthetic Biology market include declining prices of DNA sequencing and synthesis, materialization of innovative technologies, increased funding from government and private bodies, growing demand for better-quality drugs and vaccines and advancements in the area of molecular biology, to name a few.
However, the factors responsible for hampering growth of Synthetic Biology include expensive research protocols, biological safety, bio security concerns, ethical issues and cuts in reimbursement leading to pricing pressure.
All honorable authors are kindly encouraged to contribute to and help shape the conference through submissions of their research abstracts, papers and e-posters. Also, high quality research contributions describing original and unpublished results of conceptual, constructive, empirical, experimental, or theoretical work in all areas of Molecular Biology & Genetics are cordially invited for presentation at the conference. The conference solicits contributions of abstracts, papers and e-posters that address themes and topics of the conference, including figures, tables and references of novel research materials.
A model abstract should contain the following elements:
- a statement of the purpose of your study
- the research methods/methodology used to arrive at your results and/or conclusions
- the results observed
- the conclusions drawn from your study and their significance
Past Conference Report
Journal of Molecular and Genetic Medicine
Journal of Molecular Biomarkers & Diagnosis
Journal of Molecular Imaging & Dynamics
All accepted abstracts will be published in respective Conference Series LLC LTD International Journals.
Abstracts will be provided with Digital Object Identifier by