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World Congress on Molecular Biology & Genetics, will be organized around the theme Fostering Recent Innovation and Emerging Research in Molecular Biology & Genetics

Molecular Biology & Genetics 2019 is comprised of keynote and speakers sessions on latest cutting edge research designed to offer comprehensive global discussions that address current issues in Molecular Biology & Genetics 2019

Submit your abstract to any of the mentioned tracks.

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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 Signalling
  • Molecular Evolution

 

  • Track 1-1Cell Biology, Immunology, Cancer Research, neurobiological signaling pathway, Biochemistry, Biostatistics, Cellular Neurobiology, Bioinformatics

Regenerative medicine is the branch of medicine that develops methods to regrow, repair or replace damaged or diseased cells, organs or tissues. Regenerative medicine includes the generation and use of therapeutic stem cells, tissue engineering and the production of artificial organs.

  • Track 2-1Tissue Engineering and Biomaterials, Cellular Therapies, Medical Devices and Artificial Organs,

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 3-1Oncological, Regenerative Medicine, Molecular Basis of Disease Study Nutritional and Metabolic Mechanisms of Chronic Disease Study,Translational Pharmacology

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 : Small molecules, Single cells

 

  • Track 4-1 Metabolic Profiling,Therapeutic Metabolomics, Transcriptomics, Metabolic Modelling, Recent Advancements in Metabolomics, Analytical Metabolomics, Metabolomics & Pharmacology, Metabolic syndrome

Hormone Molecular Biology (HMB) is dedicated to the provision of basic data on molecular aspects of hormones in physiology and pathophysiology.

  • Track 5-1 Progesterone Safety, Progesterone and Breast Health, Progesterone and Menstrual Health/PMS, Infertility, Pregnancy, Progesterone and Bone Health, Progesterone and Bone Health, Progesterone and the Nervous System/Brain

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.

  • Track 6-1Molecular Cloning, Gene Delivery, DNA Sequencing, Microarrays, DNA Sequencing

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 7-1DNA and forensic science, DNA profiling , DNA analysis in forensic science – short tandem repeats, DNA analysis in forensic science – Y chromosome DNA

Pharmacogenomics, genomic information is used to study individual responses to drugs. When a gene variant is associated with a particular drug response in a patient, there is the potential for making clinical decisions based on genetics by adjusting the dosage or choosing a different drug, for example. Scientists assess gene variants affecting an individual's drug response the same way they assess gene variants associated with diseases: by identifying genetic loci associated with known drug responses, and then testing individuals whose response is unknown. Modern approaches include multigene analysis or whole-genome single nucleotide polymorphism (SNP) profiles, and these approaches are just coming into clinical use for drug discovery and development.

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.

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.

  • Track 9-1Genetic Epidemiology, Immunogenetics, Genetic Diseases, Medical genetics, DNA Sequencing, Human Evolutionary genetics, Cancer genetics, Pharmacogenomics and Pharmacogenetics, Bioinformatics and Computational Biology, Epigenetics
  • Track 9-2Single gene inheritance, Multifactorial inheritance, Chromosome abnormalities, Mitochondrial inheritance

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.

 

  • Track 10-1Academic Subtracks: Antibodies, Cloning, Congenital Disorders, Cytogenetics & Karyotyping, Drug treatments, Germ line mutations
  • Track 10-2Business subtracks : Cell biotechnology, Cloning, DNA technology, Gene expression, Gene isolation, Gene splicing, Genetic research

Plant genetics deals with heredity in plants, specifically mechanisms of hereditary transmission and variation of inherited characteristics. Plant genetics differs from animal genetics in a number of ways: somatic mutations can contribute to the germ line more easily as flowers develop at the end of branches composed of somatic cells; polyploidy is more common; and plants additionally contain chloroplastic DNA.

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 11-1Plant Biochemistry and Biosystem, Plant Molecular Biology, Plant & Environment, Plant Physiology
  • Track 11-2Human Genome Project, Gene structure and genome structure (DNA, chromatin, chromosomes, and nucleus), Genetic modification, Gene expression and control over it , Genetics of development processes, Population genetics, Application of genetics in medicine,

Bioorganic chemistry is a rapidly growing scientific discipline that combines organic chemistry and biochemistry. While biochemistry aims at understanding biological processes using chemistry, bioorganic chemistry attempts to expand organic-chemical researches (that is, structures, synthesis, and kinetics) toward biology. When investigating metalloenzymes and cofactors, bioorganic chemistry overlaps bioinorganic chemistry. Biophysical organic chemistry is a term used when attempting to describe intimate details of molecular recognition by bioorganic chemistry.

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
  • Y-linked
  • Codominant
  • Mitochondrial

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.

  • 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.