Conference series welcome all the participants globally to the upcoming conference “16th World Conference on Human Genomics and Genomic Medicine” scheduled on January 30-31, 2023 which is going to be held as an Barcelona, Spain. “HUMAN GENOME 2023 gives an Excellence Overview on the related topics and cordially invites all the participants from Genetic Experts, Genetic Counselors Professionals and Community Health Educators, Genetic Mutations Associations, Doctors, Healthcare Professionals to interact with Experienced and well qualified people to explore their excellence. This conference specially focuses on genetic stimulations, mutations and development activities in human body.

Benefits of the registration:

  • Collaborating & networking with global researchers
  • Access to all sessions
  • Coffee break, and lunch during the conference
  • Abstract book and conference material
  • Group registration discounts
  • Outstanding Young Researcher Award
  • Get your abstract published in the proceeding open access journal
  • International Speaker participation Ccrtificate
  • Global exposure of your research on the conference website which has 100000+ Page views.

Target Audience

  • Medical Geneticists
  • Clinical Geneticists
  • Genetic Counselors
  • Biopharmacists
  • Genetic Consultants
  • Genomic Students
  • Researchers
  • Associations and Societies
  • Genomics Faculty
  • Genomics Scientists
  • Genomics College Authorities
  • Pharmacology Scientists
  • Pharmacology Health Professionals
  • Genetics Associations and Societies
  • Business Entrepreneurs
  • Training Institutes
  • Business Entrepreneurs
  • Manufacturing Agricultural Devices Companies


Track 1: Genomics

Genomics is multidisciplinary field of biology that directing in the structure, function, evolution, mapping, and manage of genomes. A genome is an organism's complete set of deoxyribonucleic acid, as well as all of its genes in addition as its stratified, three-dimensional structural configuration. Genomics, the study of genes, is creating it attainable to predict, diagnose, and treat diseases a lot of exactly and in person than ever. An entire genomic sequence contains three billion base pairs of deoxyribonucleic acid.

  • Public health
  • Disinfection
  • Mendelian Phenotypes

Track 2: Genetically Modified Organisms

A genetically changed organism (GMO) is an animal, plant, or microorganism whose DNA has been altered exploitation gene-splicing techniques. For thousands of years, humans have used breeding ways to switch organisms. Corn, cattle, and even dogs are by selection bred over generations to own bound desired traits. The laboratories therefore on favour the expression of desired physiological traits or the generation of desired biological product


Track 3: Human Genetics

Human genetics is a branch of biology that deals how human traits are explained and passed down among generations. Genetics and genomics both play major roles in health and disease. Genetics refers to the study of genes and it explains how these traits or conditions are passed down from one generation to another. It well explained about all the genes. Since the genetic mutation is A - G, there are majorly three genome types exist - namely, AA, AG, and GG.

  • Health
  • Generation
  • Complex Traits

Track 4: Genomic Vaccination

Genomic vaccines take the shape of DNA or RNA that encodes desired proteins. On injection, the genes enter cells that then churn out the chosen proteins. Compared with producing proteins in cell cultures or eggs, manufacturing the genetic material ought to be easier and fewer costly. Standard vaccines to stop infectious diseases carries with it killed or weakened pathogens or proteins from those microorganisms. Vaccines that treat cancer conjointly place confidence in proteins. In distinction, a replacement quite immunizing agent that is poised to form major inroads in drugs consists of genes.

  • Genes
  • Genomic Medicine
  • Colorectal Cancers

Track 5: Epigenetics Biomarkers

Epigenetic biomarkers are trending as tools for the screening and early detection of assorted diseases, for prognostic and treatment observance, and for predicting future risk of infection development. Profound changes within the epigenetic landscape of cancer cells underlie the event of human malignancies. These changes embrace large-scale deoxyribonucleic acid methylation changes throughout the genome in addition as alterations within the compendium of post-translational body substance modifications. Epigenetic aberrations impact multiple steps throughout tumorigenesis, ultimately promoting the choice of growth cells with increasing pathogenic.


Track 6: Human Gene Therapy

The concept of sequence medical care is to fix a genetic problem at its supply. If for instance a mutation in an exceedingly bound sequence causes the assembly of a dysfunctional macromolecule ensuing (usually recessively) in a genetic disease, sequence medical care can be deliver to a replica of this sequence that doesn't contain the deleterious mutation and thereby produces a purposeful macromolecule. This strategy is brought up as sequence replacement medical care and is utilized to treat heritable retinal diseases.

Track 7: Infectious Diseases

Infectious diseases area disorders caused by organisms like microorganism, viruses, fungi or parasites. Many organisms sleep in our bodies. They're typically harmless or maybe helpful. But beneath certain conditions, some organisms would possibly cause unwellness. Some infectious diseases usually passed from one person to another person.

  • Infectious Mononucleosis
  • Giardiasis
  • Diphtheria


Track 8: Bioinformatics

Bioinformatics is outlined because the application of tools of a computation and an analysis to capture and an interpretation of biological knowledge. It is a multidisciplinary field that harnesses to applied science, arithmetic, physics, and biology. Bioinformatics uses pc programs for a spread of applications together with the determinative sequence and super molecule functions, establishing organic process relationships and predicting the three-dimensional shapes of proteins. Organism or between organisms staring at organic process relationships between organisms, and victimization the patterns that exist across DNA and macromolecule sequences to work out what their perform.

  • Polymers
  • Personalized Genetic Medicine

Track 9: Genome Mapping

The process of distribution or locating of specific a factor of a gene to particular space of a body that determines the situation of and relative distances between genes on the body. It helps to elaborate the genes and genetic markers along with the chromosomes as calculated by the frequency where they are inherited together.

Track 10: Preimplantation Genetic Diagnosis

Pre-implantation genetic diagnosis (PGD) is generally explained as the testing of pre-implantation of the stages of embryos or oocytes for genetic defects. This has been developed for couples whose potential offspring are at risk of severe Mendelian disorders, structural chromosome abnormalities or mitochondrial disorders. The past present and future of this development square measure energetically associated with the natural prevalence of body condition within the pre-implantation embryo. PGD should be enclosed in every procreative health care program. It is recognized as a very important and possible to pre-natal testing.

  • Clonal Cell lines
  • Heterogeneous Tumours
  • Cell Clusters

Track 11: Pharma Genomics & Pharma Informatics

Pharmacogenomics are that the study of how the genes has an effect on an individual's response to medicine. This relatively new field combines a pharmacology the science of medicine and biology the study of genes and their functions to develop effective, safe medications and doses which will be tailored to a personality's a genetic makeup.

  • Medication-Related Data
  • Electronic Medical Records
  • Telehealth


Track 12: Drug Detection & Development in Bioinformatics

Bioinformatics analysis cannot alone speed up the drug target identification and drug candidate screening and refinement however conjointly facilitate characterization of aspect effects and predict drug resistance. Drug discovery and development could be a complicated, high risk, time intense and doubtless extremely rewarding method. Pharmaceutical firms virtually burn variant greenback per drug to bring it to the market. The development of a new drug needs a technological expertise human resources and large capital investment.

  • Computational Algorithms
  • Microbial Genome
  • Bioinformatics

Track 13: Computational Biology

Computational Biology is a machine learning which expresses about the gene expression and its regulation. This is the branch which deals with the relationship between the computers and computer science to understand and create modeling of the structures and processes of life. It helps in underpinning of gene codes.

  • Gene Coding
  • Gene Mapping
  • Gene Computing
  • Gene Analytics

Track 14: Genomic Approach to Drug Discovery

Genomics, specifically high-throughput sequencing and a characterization of expressed human genes, has created new opportunities for a drug discovery. Information of all the human genes and their functions may allow effective preventive measures, and alter a drug analysis strategy and a drug discovery development processes.

  • Drug Delivery
  • Drug Usage
  • Precision Medicine

Track 15: Medicine Genomics

Genomic drugs is associated in nursing emerging medical discipline that involves victimization genomic data regarding a personal as a part of their clinical care e.g. for diagnostic or therapeutic decision-making and therefore the health outcomes and policy implications of that clinical use.

  • Simulation
  • Interactive learning
  • E-learning
  • Simulation-based learning       

Track 16: Personalized Medicine

A personalized medication is associate rising a follow of a medication that uses a person's a genetic profile to guide choices created in the respect to the bar, diagnosis, and treatment of sickness. Personalized the medication, as a result of it's to support every patient's a distinctive genetic makeup, and is commencing to overcome the constraints of an ancient medication. More and more it's permitting health care suppliers to: shift the stress in a medication from a reaction to a bar. Predict a condition to sickness.

  • Breast Cancer Cells
  • Health Biomarkers
  • Precision Medicine

Track 17: Cancer Genomics

The study of cancer genomes has revealed abnormalities in genes that drive the event and growth of the many styles of cancer. This data has improved our understanding of the biology of cancer and held the new ways of designation and treating the illness or disease.

Track 18: Cognitive Computing

The goal of a psychological feature computing is to simulate human thought processes in computerized processed model. The self-learning algorithms that use data processing, pattern recognition and a linguistic communication process the computer will mimic the method the human brain works.

  • Cognitive Models
  • Machine Learning
  • Artificial Intelligence

Track 19: Genomic Information in Medicine

Genomic medication is that the study of our genes and their interaction with our health. Genetic science investigates however a person’s biological data are accustomed improving their clinical care and health outcomes e.g. through an effective identification and personal treatment.

Track 20: Emergency Medicine

Emergency medicine is the branch of medicine that deals with illnesses or injuries that requires emergency medical intervention. Emergency physicians are always learning how to treat for patients of all ages who are unexpected and undifferentiated.



Importance and Scope

Genetic analysis is the study of genes or gene mutations done through different lab tests on the DNA or RNA that serves as the basis for all life. These tests are often carried out to determine whether a disease could develop or only to identify any programming flaws in the metabolic system. However, the most prevalent and well known of these are forensic tests done to confirm a person/suspect’s identity or to confirm genetic relation between multiple persons, the former being state judiciary’s responsibility (criminal cases) and the latter done majorly for private reasons (paternity tests, etc) (paternity tests, etc). In addition to these well-liked tests, genetic analysis is employed in a variety of scientific and academic studies. Since G.J. Mendel and Francis Crick revealed the basics of genetics, genetic analysis has advanced significantly. Today, it is the most diversified analytical research, making it an essential component of several diagnostic investigations.

The global market for genetic testing was estimated to be worth USD 10.6 billion in 2017 and is predicted to grow at a rate of around 11.6% between 2018 and 2024.

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

Increasing patient desire for tailored treatments will drive up demand for genetic testing in the coming years. Personalized medicine provides patients with medical therapy that is tailored to their molecular foundation. Various industrialized economies, including Europe, use genetic testing to diagnose hereditary and uncommon disorders. Early illness detection promotes early treatment and can lessen disease severity. Growing use of tailored medications, together with increased knowledge of illness early detection, will drive market growth throughout the projected period.

The development of cautious instrumentation has also been increasingly important over the past few years, as shown by a recent study that indicated the market for electrosurgical devices was valued at 740 million US dollars in 2015 and is predicted to reach a peak of 1.3 billion US dollars in 2024.



15th International Conference on Human Genomics and Genomic Medicine organized by ME Conferences in Singapore City, Singapore during June 08-08, 2022 and was based on the Theme-Exploring the Recent Advancements in Human Genomics and Genomic Medicine.

On behalf of our Organizing Committee, we would like to extend our appreciation for continued support and active participation of the Organizing Committee Member, Keynote Speakers and our Moderators for the successful completion of the Human genome 2022.

The researchers, surgeons, young researchers, students from different countries actively participated in the Conference, discussed the most important trends and issues in analytical sciences. Every Participant was having great reviews and had amazing experiences from the event.

Human genome 2022 was started by the opening ceremony which was followed by the Keynote speech and we are overwhelmed with their presence and generous response. 

We would like to take the privilege to felicitate our keynote Speakers and honourable guests for their prominent contribution towards the smooth functioning of this esteemed event.

The eminent personalities at the conference were

Carlo Staudacher | Vita-Salute San Raffaele University | Italy

Ergun Demirsoy | Kolan International Hospital | Turkey

Baris Cankaya | Marmara University Pendik Training Hospital | Turkey

Rani Kanthan | University of Saskatchewan | Canada

Elena Orsenigo | San Raffaele Hospital | Italy

In the last, we would also like to extend my ward regards to various delegate experts, Company representatives, eminent personalities who supported the Conference by facilitating active discussion forums. We would like to convey our sincere gratitude to all the supporters from Editorial Board Members of our Open Access Journals, Keynote Speakers, Honourable guests, Valuable Speakers, Students, delegates and special thank s to Media Partners  for their promotions to make this event a successful one.

With the unique feedbacks from the Conference Human genome 2022, we would like to announce the commencement of the 16th International Conference on Human Genomics and Genomic Medicine which is going to be held during January 30-31, 2023 Barcelona, Spain.

Let us meet again @ Human Genome 2023


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Conference Date October 26-27, 2023
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