Call for Abstract
4th World Congress on Human Genetics and Genetic Diseases, will be organized around the theme “New insights into the Human Genetics and Genome Biology”
Human Genetics Meet 2018 is comprised of 16 tracks and 79 sessions designed to offer comprehensive sessions that address current issues in Human Genetics Meet 2018.
Submit your abstract to any of the mentioned tracks. All related abstracts are accepted.
Register now for the conference by choosing an appropriate package suitable to you.
- Track 1-1Human Genome mapping
- Track 1-2Human Genome sequencing
- Track 1-3The genetics of human personality.
- Track 1-4Medical Genetics
- Track 1-5Human genetic clustering
- Track 1-6Genetic differences and inheritance patterns
- Track 1-7Spatial population genomics
- Track 2-1Gene therapy
- Track 2-2Enzyme replacement therapy
- Track 2-3Drug treatments
- Track 2-4RNAi therapies
- Track 2-5Treatment of Allergies and Autoimmune Diseases.
Sickle-cell disorder takes place when someone inherits two bizarre copies of the haemoglobin gene, one from each parent. This gene takes place in chromosome eleven. Several subtypes exist, relying on the exact mutation in every haemoglobin gene. An assault may be activate by using temperature modifications, strain, dehydration, and high altitude. A individual with a unmarried extraordinary reproduction does not commonly have symptoms and is stated to have sickle-cell trait.
- Track 3-1Signs and symptoms
- Track 3-2 Genetics
- Track 3-3Pathophysiology of sickle-cell disease.
- Track 3-4Diagnosis of Sickle Cell Diseases
Thalassemia is a genetic disorder which is caused as a result of abnormal haemoglobin production. Thalassemia are genetic disease inherited from a person's dad and mom. There are most important type, alpha thalassemia and beta thalassemia. The severity of alpha and beta thalassemia relies upon on how among the four genes for alpha globin or two genes for beta globin are lacking.
- Track 4-1Signs and symptoms
- Track 4-2Pathophysiology
- Track 4-3Management of thalassemia
- Track 5-1Mutation and polymorphism
- Track 5-2Admixture and ancestry analysis
- Track 5-3Natural selection and adaptation
- Track 5-4Origin of life in a digital microcosm.
- Track 5-5Genetic diversity and phylogenetic study of Humans
- Track 6-1Macromolecule blotting and probing
- Track 6-2Role of Molecular Biology in Cancer Treatment
- Track 6-3Molecular cloning
- Track 6-4Central dogma of molecular biology
- Track 6-5Protein interaction prediction
- Track 6-6Protein structure prediction
- Track 7-1Induced Mutations
- Track 7-2Site-directed mutagenesis
- Track 7-3Next generation panel sequencing
- Track 7-4Are There Different Kinds of Aging?
- Track 7-5autoinflammatory disease genes in gene mutation
- Track 8-1DNA replication stress and cancer chemotherapy.
- Track 8-2Gene therapy
- Track 8-3The Human Genome Project
- Track 8-4Viral Infection and Apoptosis.
- Track 8-5Role of Non-Coding RNAs in the Etiology of Bladder Cancer.
- Track 9-1Methods/tools for variant calling in human genomes
- Track 9-2 Genome sequencing and assembly
- Track 9-3Methods for data integration
- Track 9-4Novel bioinformatics/computational tools and methods
- Track 9-5Analysis of mutations in cancer
- Track 9-6Computational biomodeling
Molecular modeling encompasses all methods, theoretical and computational, used to model or mimic the behavior of molecules. The methods are used in the fields of computational chemistry, drug design, computational biology and materials science to study molecular systems ranging from small chemical systems to large biological molecules and material assemblies. The simplest calculations can be performed by hand, but inevitably computers are required to perform molecular modeling of any reasonably sized system. The common feature of molecular modeling methods is the atomistic level description of the molecular systems.
- Track 10-1Differential processing in modality-specific Mauthner cell dendrites.
- Track 10-2Molecular docking
- Track 10-3Molecular Modelling of Peptide-Based Materials for Biomedical Applications.
- Track 10-4Cheminformatics
- Track 10-5Formal Models of Biological Systems.
- Track 11-1Next-Generation Gene Sequencing
- Track 11-2The impact of hereditary cancer gene panels on clinical care
- Track 11-3gene and protein expression across multiple studies and organisms.
- Track 11-4Evaluation of whole genome sequencing
- Track 11-5Computational challenges of gene sequencing
- Track 12-1Functional studies of associated variants or loci
- Track 12-2Genome-wide association studies
- Track 12-3Candidate genes/regions and fine mapping
- Track 12-4Clinical Pharmacogenetics
- Track 12-5pharmacogenetics and drug-drug interactions.
- Track 12-6Pharmacogenetics in Cardiovascular Medicine.
- Track 12-7Pharmacoepigenetics and Toxicoepigenetics
- Track 13-1The immunogenetics of Neurological Disease.
- Track 13-2Immune-suppressive effects of interleukin-6
- Track 13-3Bone involvement in monogenic autoinflammatory syndromes.
- Track 13-4Immunoglobulin genotypes and cognitive functions
- Track 13-5Mechanisms behind TB, HBV, and HIV chronic infections.
- Track 14-1Structure and Epigenetic Regulation of Chromatin Fibers.
- Track 14-2DNA methylation
- Track 14-3X-inactivation
- Track 14-4Histone modification
- Track 14-5Basics of Epigenetic Control.-Primer in Genetics and Genomics
- Track 15-1Xenotransplantation.
- Track 15-2Allogeneic hematopoietic cell transplantation
- Track 15-3Translational Genomics
- Track 16-1What is the role of apheresis technology in stem cell transplantation
- Track 16-2Linking Race, Cancer Outcomes and Tissue Repair.
- Track 16-3Expanding transplantation of patients with a liver cancer without harming allocation