Call for Abstract

9th World Congress on Human Genetics and Genetic Diseases, will be organized around the theme “Theme: "Arising New Innovations and Learning the Latest Trends in Genetics"”

HUMAN GENETICS MEET 2022 is comprised of 16 tracks and 3 sessions designed to offer comprehensive sessions that address current issues in HUMAN GENETICS MEET 2022.

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.

Human Genetics is study for Analysis of the parent's progression of attributes. Human legacy in no crucial manner varies from that in different creatures. Human heredity research possesses a critical hereditary job. A lot of this interest gets from a profound longing to know who and why individuals are as they are. In a more reasonable manner, Understanding human legacy is basic in the expectation, analysis and treatment of hereditary infections. The journey to build up human wellbeing's hereditary premise has led to the clinical hereditary qualities industry. Medication has commonly given accentuation and reason to human hereditary qualities, so it is frequently viewed as exchangeable with the provisions of clinical hereditary qualities and human hereditary qualities.

  • 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

Developmental hereditary qualities are the wide field of studies that came about because of the reconciliation of hereditary qualities and Darwinian advancement, called the cutting edge blend. The power of change is a definitive wellspring of new hereditary variety inside populaces. Albeit most changes are unbiased with no impact on wellness or hurtful, a few transformations have a little, beneficial outcome on wellness and these variations are unrefined components for gradualist versatile development. Inside limited populaces, irregular hereditary float and regular determination influence the mutational variety. Regular choice is the main transformative power which can create variation, the fit among creature and climate, or ration hereditary states throughout extremely extensive stretches of time notwithstanding the dispersive powers of change and float.

  • Track 2-1Mutation and polymorphism
  • Track 2-2Admixture and ancestry analysis
  • Track 2-3Natural selection and adaptation
  • Track 2-4Origin of life in a digital microcosm
  • Track 2-5Genetic diversity and phylogenetic study of Humans

Bioinformatics is both an umbrella term for the collection of organic investigations that utilization PC programming as a component of their technique, just as a source of perspective to explicit examination "pipelines" that are more than once utilized, especially in the field of genomics. Normal employments of bioinformatics incorporate the distinguishing proof of up-and-comer qualities and single nucleotide polymorphisms. Frequently, such distinguishing proof is made with the point of better understanding the hereditary sickness, interesting transformations, and helpful properties in rural species, or contrasts between populaces. In a less conventional manner, bioinformatics additionally attempts to comprehend the authoritative standards inside nucleic corrosive and protein successions, called proteomics.


  • Track 3-1Methods/tools for variant calling in human genomes
  • Track 3-2Genome sequencing and assembly
  • Track 3-3Methods for data integration
  • Track 3-4Novel bioinformatics/computational tools and methods
  • Track 3-5Analysis of mutations in cancer
  • Track 3-6Computational biomodeling

DNA sequencing is the most common way of deciding the exact request of nucleotides inside a DNA particle. It incorporates any technique or innovation that is utilized to decide the request for the four bases is: adenine, guanine, cytosine, and thymine, in a strand of DNA. The coming of quick DNA sequencing techniques has extraordinarily sped up natural and clinical exploration and disclosure. Information on DNA arrangements has become crucial for fundamental natural examination, and in various applied fields like clinical finding, biotechnology, scientific science, virology and Primate Systematics. The quick speed of sequencing achieved with current DNA sequencing innovation has been instrumental in the sequencing of complete DNA successions, or genomes of various kinds and types of life, including the human genome and other complete DNA groupings of numerous creature, plants, and microbial species

  • Track 4-1Next-Generation Gene Sequencing
  • Track 4-2The Impact of Hereditary Cancer Gene panels on Clinical Care
  • Track 4-3gene and protein expression across multiple studies and organisms
  • Track 4-4Evaluation of whole genome sequencing
  • Track 4-5Computational Challenges of gene Sequencing

Hereditary sicknesses might be innate, passed down from the guardians qualities. In other hereditary sicknesses, deformities might be brought about by new transformations or changes to the DNA. All things considered, the deformity may be passed down assuming it happens in the microbe line. A similar illness, for example, a few types of disease might be brought about by an acquired hereditary condition in certain individuals, by new hereditary changes in others, and mostly by the natural causes in others. A hereditary infection is a hereditary issue brought about by at least one anomaly in the genome, particularly a condition that is available from birth intrinsic. Most hereditary illnesses are very uncommon and influence one individual in each few thousands or millions.

  • Track 5-1Gene therapy
  • Track 5-2Enzyme replacement therapy
  • Track 5-3Drug treatments
  • Track 5-4RNA therapies
  • Track 5-5Treatment of Allergies and Autoimmune Diseases

Sickle-cell problem happens when somebody acquires two peculiar duplicates of the hemoglobin quality, one from each parent. This quality happens in chromosome eleven. A few subtypes exist, depending on the specific change in each hemoglobin quality. An attack might be actuating by utilizing temperature alterations, strain, drying out, and high height. A person with an unmarried unprecedented generation doesn't regularly have side effects and is expressed to have sickle-cell quality.


  • Track 6-1Signs and symptoms
  • Track 6-2Genetics of sickle Cell Anaemia
  • Track 6-3Pathophysiology of sickle-cell disease.
  • Track 6-4Diagnosis of Sickle Cell Diseases

Thalassemia is a hereditary issue which is caused because of unusual haemoglobin creation. Thalassemia is hereditary sickness acquired from an individual's father and mother. There are most significant sort, alpha thalassemia and beta thalassemia. The seriousness of alpha and beta thalassemia depends upon on how among the four qualities for alpha globin or two qualities for beta globin is inadequate.

  • Track 7-1Signs and symptoms
  • Track 7-2Pathophysiology
  • Track 7-3Management of thalassemia

Molecular biology is the study of molecular underpinnings of the processes of replication, transcription, translation, and cell function. Molecular biology concerns the molecular basis of biological activity between the biomolecules in various systems of a cell, gene sequencing and this includes the interactions between the DNA, RNA and proteins and their biosynthesis. In molecular biology the researchers use specific techniques native to molecular biology, increasingly combine these techniques and ideas from the genetics and biochemistry.

  • Track 8-1Macromolecule blotting and probing
  • Track 8-2Role of Molecular Biology in Cancer Treatment
  • Track 8-3Molecular cloning
  • Track 8-4Central dogma of molecular biology
  • Track 8-5Protein interaction prediction
  • Track 8-6Protein structure prediction

In science, a change is the long-lasting adjustment of the nucleotide arrangement of the genome of a creature, infection, or extra chromosomal DNA or other hereditary components. Transformations result from blunders during DNA replication or different kinds of harm to DNA, which then, at that point, may go through mistake inclined fix or cause a mistake during different types of fix, or, more than likely may cause a blunder during replication interpretation amalgamation. Changes may likewise result from addition or erasure of portions of DNA because of versatile hereditary components. Transformations might create recognizable changes in the perceptible qualities aggregate of a living being. Transformations have an influence in both ordinary and unusual organic cycles including: advancement, disease, and the improvement of the invulnerable framework, including utilitarian variety. The genomes of RNA infections depend on RNA rather than DNA. The RNA viral genome can be twofold abandoned DNA or single abandoned. In a portion of these infections, for example, the single abandoned human immunodeficiency infection replication happens rapidly and there are no components to really look at the genome for precision.

  • Track 9-1Induced Mutations
  • Track 9-2Site-directed mutagenesis
  • Track 9-3Next generation panel sequencing
  • Track 9-4Are There Different Kinds of Aging
  • Track 9-5Auto inflammatory disease genes in gene mutation

Molecular genetics is the sector of biology that researches the structure and characteristic of genes at a molecular stage and hence employs strategies of each molecular biology and genetics. The study of chromosomes and gene expression of an organism can give insight into heredity, genetic variant, and mutations. This is useful in the observe of Developmental Biology and in expertise and treating genetic illnesses.

  • Track 10-1DNA replication stress and cancer chemotherapy
  • Track 10-2Gene therapy
  • Track 10-3Human Genome Project
  • Track 10-4Viral Infection and Apoptosis
  • Track 10-5Role of Non-Coding RNAs in the Etiology of Bladder Cancer

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 modelling of any reasonably sized system. The common feature of molecular modelling methods is the atomistic level description of the molecular systems.

  • Track 11-1Differential processing in modality-specific Mauthner cell dendrites.
  • Track 11-2Molecular docking
  • Track 11-3Molecular Modelling of Peptide-Based Materials for Biomedical Applications
  • Track 11-4Cheminformatics
  • Track 11-5Formal Models of Biological Systems

Immunogenetics is the part of clinical examination that investigates the connection between the safe framework and hereditary qualities. Immune system illnesses, like sort diabetes, are complicated hereditary attributes which result from surrenders in the insusceptible framework. Distinguishing proof of qualities characterizing the insusceptible imperfections might recognize new objective qualities for remedial methodologies. Then again, hereditary varieties can likewise assist with characterizing the immunological pathway prompting sickness.

  • Track 12-1immunogenetics of Neurological Disease
  • Track 12-2Immune-suppressive effects of interleukin-6
  • Track 12-3Bone involvement in monogenic auto inflammatory syndromes
  • Track 12-4Immunoglobulin genotypes and cognitive functions
  • Track 12-5Mechanisms behind TB, HBV, and HIV chronic infections

Pharmacogenetics is the investigation of microbe line transformations, the single-nucleotide polymorphisms influencing qualities coding for liver proteins liable for drug testimony and pharmacokinetics, though pharmacogenomics alludes to physical changes in tumoral DNA prompting modification in drug reaction KRAS changes in patients treated with hostile to Her1 biologics. Pharmacogenetics is an acquired hereditary contrast in drug metabolic pathways which can influence individual reactions to drugs, both as far as helpful impact just as antagonistic impacts. The term Pharmacogenetics is frequently utilized reciprocally with the term pharmacogenomics which additionally explores the job of gained and acquired hereditary contrasts according to medicate reaction and medication conduct through a precise assessment of qualities, quality items, and between and intra-individual variety in quality articulation and capacity.

  • Track 13-1Functional studies of associated variants or loci
  • Track 13-2Genome-wide association studies
  • Track 13-3Candidate genes/regions and fine mapping
  • Track 13-4Clinical Pharmacogenetics
  • Track 13-5pharmacogenetics and drug-drug interactions
  • Track 13-6Pharmacogenetics in Cardiovascular Medicine
  • Track 13-7Pharmacoepigenetics and Toxic epigenetics

Epigenetics are stable heritable traits that cannot be explained by changes in DNA sequence. Epigenetics often refers to changes in a chromosome that affect gene activity and expression, but can also be used to describe any heritable phenotypic change that does not derive from a modification of the genome, such as prions. Such effects on cellular and physiological phenotypic traits may result from external or environmental factors, or be part of normal developmental program. Gene expression can be controlled through the action of repressor proteins that attach to silencer regions of the DNA. These epigenetic changes may last through cell divisions for the duration of the cell's life, and may also last for multiple generations even though they do not involve changes in the underlying DNA sequence of the organism; instead, non-genetic factors cause the organism's genes to behave or "express themselves" differently.

  • 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

Hematopoietic foundational microorganism transplantation is the transplantation of multipotent hematopoietic undeveloped cells, typically got from bone marrow, fringe blood, or umbilical string blood. It could be autologous the patient's own immature microorganisms are utilized, allogeneic the undeveloped cells come from a giver or syngeneic from an indistinguishable twin. It is an operation in the area of hematology, most frequently performed for patients with specific malignant growths of the blood or bone marrow, like different myeloma or leukemia. In these cases, the beneficiary's resistant framework is generally obliterated with radiation or chemotherapy before the transplantation. Contamination and unite versus-have illness are significant complexities of allogeneic.

Hematopoietic undifferentiated cell transplantation stays a hazardous system with numerous potential entanglements; it is saved for patients with dangerous sicknesses. As endurance following the system has expanded, its utilization has extended past malignant growth, like immune system sicknesses and inherited skeletal dysplasia's quite dangerous puerile osteoporosis and mucopolysaccharidosis.

  • Track 15-1What is the role of apheresis technology in stem cell transplantation
  • Track 15-2Linking Race, Cancer Outcomes and Tissue Repair
  • Track 15-3Expanding transplantation of patients with a liver cancer without harming allocation

Translational medication is a quickly developing discipline in biomedical examination and plans to speed up the disclosure of new indicative devices and therapies by utilizing a multi-disciplinary, profoundly cooperative; "seat to-bedside" approach. Inside general wellbeing, translational medication is centred on guaranteeing that demonstrated techniques for illness treatment and counteraction are really executed inside the local area. One predominant depiction of translational medication, first presented by the Institute of Medicine's Clinical Research Roundtable, features two barricades that is unmistakable regions needing improvement the primary translational square (T1) keeps fundamental examination discoveries from being tried in a clinical setting; the second translational square (T2) keeps demonstrated mediations from becoming standard practice. The National Centre for Advancing Translational Science (NCATS) was set up inside the NIH to "change the translational science process with the goal that new medicines and remedies for illness can be conveyed to patients quicker.

  • Track 16-1Xenotransplantation
  • Track 16-2Allogeneic hematopoietic cell transplantation
  • Track 16-3Translational Genomics