16th International Conference on Genomics and Molecular Biology

About Conference

Conference Series llc LTD invites all the participants from all over the world to attend 15^th International Conference on Genomics & Molecular Biology' during March 28-29, 2022 Berlin, Germany with theme of "Genomic Strategies for Global Health" which includes prompt keynote presentations, Oral talks, Poster presentations and Exhibitions.

Genomics-2022 Genomics is an area within genetics that concerns the sequencing and analysis of an organism’s genome. Genomics also involves the study of intragenomic processes such as epistasis, heterosis and pleiotropy as well as the interactions between loci and alleles within the genome. The fields of molecular biology and genetics are mainly concerned with the study of the role and function of single genes, a major topic in today’s biomedical research. By contrast, genomics does not involve single gene research unless the purpose is to understand a single gene’s effects in context of the entire genome.

ConferenceSeries Ltd organizes a conference series of 1000+ Global Events inclusive of 300+ Conferences, 500+ Upcoming and Previous Symposiums and Workshops in USA, Europe & Asia with support from 1000 more scientific societies and publishes 700+ Open access journals which contains over 30000 eminent personalities, reputed scientists as editorial board members.

Young Researchers Forum - Young Scientist Awards Genomics 2022

Young Research’s Awards at Genomics 2022 for the Nomination: Young Researcher Forum - Outstanding Masters/Ph.D./Post Doctorate thesis work Presentation.

Young Scientist Benefits

Our conferences provide best Platform for your research through oral presentations.
Share the ideas with both eminent researchers and mentors.
Young Scientist Award reorganization certificate and memento to the winners
Young Scientists will get appropriate and timely information by this Forum.
Platform for collaboration among young researchers for better development
Award should motivate participants to strive to realize their full potential which could in turn be beneficial to the field as whole.

Why to attend???

With members from around the world focused on learning about Genomics & Molecular Biology and its advances; this is your best opportunity to reach the largest assemblage of participants from the Genomics and its allied areas. Conduct presentations, distribute information, meet with current and potential scientists, make a splash with new drug developments, and receive name recognition at this 2-day event. World-renowned speakers, the most recent techniques, developments, and the newest updates in Genomics & Pharmacogenomics are hallmarks of this conference.

Target Audience:

Genomic Students
Genomics Researchers
Genomics Faculty
Genomics Scientists
Genomics Colleges
Pharmacology Scientists
Pharmacology Health Professionals
Genetics Associations and Societies
Geneticists
Genetic Counselors
Biopharmacists
Business Entrepreneurs
Training Institutes
Software developing companies
Data Management Companies

Conference Highlights

Track 1: Genomics

Genomics is an interdisciplinary field of science concentrating on the structure, work, advancement, mapping, and altering of genomes. A genome is a life form's entire arrangement of DNA, including the greater part of its qualities. Rather than hereditary qualities, which alludes to the investigation of individual qualities and their parts in legacy, genomics goes for the aggregate portrayal and evaluation of qualities, which coordinate the generation of proteins with the help of compounds and ambassador particles. Thus, proteins make up body structures, for example, organs and tissues and additionally control concoction responses and convey motions between cells. Genomics likewise includes the sequencing and examination of genomes through employments of high throughput DNA sequencing and bioinformatics to collect and break down the capacity and structure of whole genomes.

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Europe:

Association of French Speaking Cytogeneticists, Association des Cytogénéticiens de langue Française, German Society for Human Genetics, German Society of Neurogenetics, Hellenic Society of Human Genetics, Hungarian Society of Human Genetics, Irish Society of Human Genetics, Italian Society of Human Genetics, Latvian Medical Genetics Society, Lithuanian Society of Human Genetics, Netherlands Society of Human Genetics, Norwegian Society of Medical Genetics, Polish Society of Human Genetics.

United States:

Council of Medical Genetics Organizations, Association of Professors of Human or Medical Genetics, American Society of Gene Therapy, Ibero-American Society of Human Genetics of North America, American Human Geneticists of Indian Subcontinent Origin, Canadian College of Medical Geneticists, Canadian Association of Genetic Counsellors, Canadian Collaborative Group for Cancer Genetics, Mexican Association of Human Genetics, Canadian Association of Genetic Counsellors, National Society of Genetic Counsellors, College of Medical Geneticists, American College of Medical Genetics and Genomics.

Asia:

Indian Society of Human Genetics, Human Genetics Society of Australasia, Australian Society of Genetic Counsellors, Genetic Society of Australia, Southern African Society for Human Genetics, Biochemistry Moroccan Society and Molecular Biology, Federation of African societies of Biochemistry & Molecular Biology, South African Stem Cell Transplantation Society, Human Variome Project, International Federation of Human Genetics Societies, Human Genetics Society of Australasia, Asia Pacific Society of Human Genetics.

Track 2: Cancer Genomics

Cancer Genomics is the study of genetic mutations responsible for cancer, using genome sequencing and bioinformatics. Clinical genomics is to improve cancer treatment and outcomes lies in determining which sets of genes and gene interactions affect different subsets of cancers. International Cancer Genome Consortium (ICGC) is a voluntary scientific organization that provides a forum for collaboration among the world's leading cancer and genomic researchers.

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Europe:

European Society of Human Genetics, European Genetics Foundation, European Cytogeneticist Association, European Society of Gene Therapy, Clinical Molecular Genetics Society, Association of Genetic Nurses and Counsellors, Association of Clinical Cytogeneticists, British Society for Human Genetics, Clinical Genetics Society, Clinical Molecular Genetics Society, Genetics Society, Human Genetics Commission, The United Kingdom Genetical Society, Austrian Society for Human Genetics, Belgian Society for Human Genetics, Czech Society of Medical Genetics, Danish Society of Medical Genetics, Dutch Association of Clinical Genetics, Finnish Society of Medical Genetics, French Society of Human Genetics.

United States:

American Society of Human Genetics, National Society of Genetic Counselors, American College of Medical Genetics, American Board of Genetic Counseling, American Board of Medical Genetics, Natioan Coalition for Health Education in Genetics, International Society of Nurses in Genetics, Council of Regional Networks, Association of Genetic Technologists, Genetic Society of America

Asia:

East Asian Union of Human Genetics Societies, Association of Chinese Geneticists in America, Hong Kong Society of Medical Genetics, Japan Society of Human Genetics, Genetics Society of Korea, Korean Society of Human Genetics, Genetics Society of Vietnam, Turkish Association of Medical Genetics, Japan Society of Gene Therapy, American Human Geneticists of Indian Subcontinent Origin

Track 2: Molecular Biology

Molecular biology concerns the molecular basis of biological activity between the various systems of a cell, including the interactions between the different types of DNA, RNA and proteins and their biosynthesis, and studies how these interactions are regulated. It has many applications like in gene finding, molecular mechanisms of diseases and its therapeutic approaches by cloning, expression and regulation of gene. Research area includes gene expression, epigenetics and chromatin structure and function, RNA processing, functions of non-coding RNAs, transcription. Nowadays, Most advaced researches are going on these topics: Molecular biology, DNA replication, repair and recombination, Transcription, RNA processing, Post-translational modification, proteomics, Mutation, Site-directed mutagenesis, Epigenetics, chromatin structure and function, Molecular mechanisms of diseases.

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Track 4: Plant Genomics and Molecular Plant Sciences

Plant Genomics is the part of molecular biology working with the structure, function, evolution, and mapping of genomes in plants. Genomics is a branch of genetics that is concerned with the sequencing and analysis of organism's genome.

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Europe:

Hellenic Society of Human Genetics, Romanian Society of Human Geneticsm, Russian Society of Human Genetics, Spanish Association of Human Genetics, Swedish Society of Human Genetics, Swiss Society of Medical Genetics, Human Genome Organisation, German Society of Human Genetics, Association of French Speaking Cytogeneticists.

United States:

American Society of Gene Therapy, Association of Genetic Counsellors, Council of Medical Genetics Organizations, Association of Professors of Human, National International Society of Nurses in Genetics, Council of Regional Networks.

Asia:

Genetics Society of Korea, Turkish Association of Medical Genetics, Japan Society of Gene Therapy, Genetic Society of Australia, Federation of African societies of Biochemistry & Molecular Biology, East Asian Union of Human Genetics Societies, Human Variome Project.

Track 5: Structural Biology

Structural biology seeks to provide a complete and coherent picture of biological phenomena at the molecular and atomic level. The goals of structural biology include developing a comprehensive understanding of the molecular shapes and forms embraced by biological macromolecules and extending this knowledge to understand how different molecular architectures are used to perform the chemical reactions that are central to life.Most recent topics related to structural biology are:Structural Biochemistry, Structure and Function Determination, Hybrid Approaches for Structure Prediction, Structural Biology In Cancer Research, Computational Approaches in Structural Biology, Strucutural Biology Databases.

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Europe:

Clinical Genetics Society, The United Kingdom Genetical Society, Hellenic Society of Human Genetics, Hungarian Society of Human Genetics, Irish Society of Human Genetics, Russian Society of Human Genetics, Turkish Association of Medical Genetics, European Cytogeneticists Association Europe.

United States:

Canadian Collaborative Group for Cancer Genetics, Mexican Association of Human Genetics, Canadian Association of Genetic Counsellors, National Society of Genetic Counsellors, College of Medical Geneticists, American College of Medical Genetics and Genomics.

Asia:

Track 6: Stem Cell Biology

Stem cells are cells originate in all multi-cellular organisms. They were isolated in mice in 1981 and in humans in 1998. In humans there are several types of stem cells, each with variable levels of potency. Stem cell treatments are a type of cell therapy that introduces new cells into adult bodies for possible treatment of cancer, diabetes, neurological disorders and other medical conditions. Stem cells have been used to repair tissue damaged by disease or age. In a developing embryo, stem cells can differentiate into all the specialized cells—ectoderm, endoderm and mesoderm, but also maintain the normal turnover of regenerative organs, such as blood, skin, or intestinal tissues.

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Track 7; Human Genomics

The human genome is the entire arrangement of nucleic corrosive successions for people, encoded as DNA inside the 23 chromosome combines in cell cores and in a little DNA particle found inside individual mitochondria. Human genomes incorporate both protein-coding DNA qualities and noncoding DNA.

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Track 8; Clinical Genomics

Clinical Genomics is the utilization of genome sequencing to educate understanding analysis and care. Genome sequencing is relied upon to have the most effect in: portraying and diagnosing hereditary infection; stratifying patients for fitting malignancy treatment; and giving data around an individual's imaginable reaction to treatment to lessen antagonistic medication responses.

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Track 9: Bioinformatics in Genomics

Bioinformatics is the exploration of gathering and breaking down complex organic information, for example, hereditary codes. Sub-atomic solution requires the joining and examination of genomic, sub-atomic, cell, and additionally clinical information and it in this way offers a momentous arrangement of difficulties to bioinformatics.

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Track 10: Cell Biology

The investigation of cells is called cell science. Cells comprise of cytoplasm encased inside a layer, which contains numerous biomolecules, for example, proteins and nucleic acids. Life forms can be named unicellular (comprising of a solitary cell; including microscopic organisms) or multicellular (counting plants and creatures).

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Netherlands Society of Human Genetics, Norwegian Society of Medical Genetics, Polish Society of Human Genetics, Portuguese Society of Human Genetics, Romanian Society of Human Geneticsm, Russian Society of Human Genetics, Serbian Society for Human Genetics, Spanish Association of Human Genetics, Swedish Society of Human Genetics, Swiss Society of Medical Genetics, Turkish Association of Medical Genetics, European Cytogeneticists Association Europe, Human Genome Organisation, German Society of Human Genetics.

United States:

Asia:

South African Stem Cell Transplantation Society, Human Variome Project, International Federation of Human Genetics Societies, Human Genetics Society of Australasia, Asia Pacific Society of Human Genetics, American Human Geneticists of Indian Subcontinent Origin.

Track 11: Next Generation Sequencing

Cutting edge sequencing (NGS) is regularly alluded to as greatly parallel sequencing, which implies that a large number of little parts of DNA can be sequenced in the meantime, making a gigantic pool of information. Cutting edge sequencing (NGS), hugely parallel or profound sequencing is connected terms that portray a DNA sequencing innovation which has upset genomic research.

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Track 12; Micro RNA

MicroRNAs comprise a novel class of small, non-coding endogenous RNAs that regulate gene expression by directing their target mRNAs for degradation or translational repression. miRNAs represent small RNA molecules encoded in the genomes of plants and animals. These highly conserved 22 nucleotides long RNA sequences regulate the expression of genes by binding to the 3'-untranslated regions (3'-UTR) of specific mRNAs. A growing body of evidence shows that mRNAs are one of the key players in cell differentiation and growth, mobility and apoptosis.

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Track 13: Comparative Genomics

Similar Genomics and genomic medicine new field of natural examination in which the genome groupins of various species-human, mouse and a wide assortment of different life forms from yeast to chimpanzees-are looked at. The assessment of likenesses and contrasts between genomes of various life forms; can uncover contrasts in the middle of people and species and also transformative connections.

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Track 14: Functional Genomics

Utilitarian Genomics use incomprehensible abundance of information created by genomic transcriptomic tasks to portray quality capacities and cooperation’s. Patterns in Functional Genomics are Affymetrix developed as an early trend-setter around there by imagining a common sense approach to examine quality capacity as a framework.

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Track 15: Pharmacogenomics

Pharmacogenomics is a piece of a field called customized solution that means to tweak human services, with choices and medications custom-made to every individual patient inside and out conceivable. Pharmacogenomics and pharmacogenomics manage new developments in the field of customized meds and advancements in modified medication revelation utilizing proteome innovation.

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Track 16: Gene Editing

Genome editing (also called gene editing) is a group of technologies that give scientists the ability to change an organism's DNA. These technologies allow genetic material to be added, removed, or altered at particular locations in the genome.

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Track 17: Genome Medicine

Genomic Medicine "as an emerging medical discipline that involves using genomic information about an individual as part of their clinical care (e.g., for diagnostic or therapeutic decision-making) and the health outcomes and policy implications of that clinical use." Already, genomic medicine is making an impact in the fields of oncology, pharmacology, rare and undiagnosed diseases, and infectious disease.

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Track 18: Biomarkers

Biomarkers can be trademark organic properties or particles that can be distinguished and measured in parts of the body such as the blood or tissue. Biomarkers can be particular cells, atoms, or qualities, quality items, chemicals, or hormones. Atomic marker is a section of DNA that is connected with a specific area inside of the genome. Atomic markers are utilized as a part of sub-atomic science and biotechnology to distinguish a specific grouping of DNA in a pool of obscure DNA.

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Track 19: Microbial Genomics

Microbial Genomics applies recombinant DNA, DNA sequencing routines, and bioinformatics to succession, gather, and dissect the capacity and structure of genomes in organisms. Amid the previous 10 years, genomics-based methodologies have profoundly affected the field of microbiology and our comprehension of microbial species. In view of their bigger genome sizes, genome sequencing endeavor on growths and unicellular eukaryotes were slower to begin than ventures concentrated on prokaryotes.

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Track 20: Proteomics

Proteomics is the vast scale investigation of proteins. Proteins are imperative parts of living life forms, with numerous capacities. The term proteomics was begat in 1997 in relationship with genomics, the investigation of the genome.

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Track 21: Genome Engineering

Genome engineering refers to the strategies and techniques developed in recent years for the targeted, specific modification of the genetic information or genome of living organisms. The CRISPR-cas9 system makes gene editing in many organisms and cells like our own egg, sperm or embryo — more efficient, accessible and simple than ever before. These ground-breaking capabilities have spawned discussions surrounding the ethics and applications of the new system, and have garnered significant attention around the world to ensure ethically correct usage.

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Track 22; Future Trends in Genomics

Genomics research holds the key to meeting many of the challenges of the coming years. At the moment, the biggest challenge is in data analysis. We can generate large amounts of data very inexpensively, but that overwhelms our capacity to understand it. The major challenge of the Genome Research is we need to infuse genomic information into medical practice, which is really hard. There are issues around confidentiality, education, electronic medical records, how to carry genomic information throughout lifespan and make it available to physicians.

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Track 23: Genomics Market

Genomics is the study of the genetic material or genomes of an organism. Analysts forecast the Global Genomics market will grow at a CAGR of 11.21% over the period 2013-2021. According to the report, the most important driver of the market is an increase in the demand for consumables. The growing adoption of genetic testing for various applications, especially in regions such as the APAC, and an increase in genetic testing volumes in North America and Western Europe is increasing the demand for consumables.

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Cellular and Molecular Biology

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16^thInternational Conference on Genomics and Molecular Biology

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Sunday, 24 October 2021

Genomics 2023

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