Human Genetics 2021 will be the foremost conference for all eminent professionals dealing with vascular disease and research science to come together and enrich this event with their research findings and experiences. Human Genetis 2021 offers over 7 scientific sessions from different research areas in the field of gene therapy and gene editing research science in the form of keynote presentations, plenary sessions, oral sessions, panel discussions, posters presentations, workshops, symposia, and young researchers’ forum.

Human Genetis 2021 is going to be held in Rome, Italy Sep 29-30 2021. Human Genetis 2021 will address the succeeding research and development in the field of gene therapy and gene editing and this will provide a major opportunity for collaboration and interaction among all research scholars and industry personnel.

Sessions/Tracks

Session 1: Epigenetics

Epigenetics is the study of heritable phenotype changes that don't involve alterations within the DNA sequence. Unlike genetic changes, epigenetic changes are reversible and don't change your DNA sequence, but they will change how your body reads a DNA sequence. Types of epigenetic changes include: DNA methylation, histone modification, non-coding RNA.

Session 2: Evolutionary Genetics

Genetic variation leads to evolutionary changes. It includes topics such as the evolution of genome structure, the genetic basis of speciation and adaptation, and genetic change in response to selection within populations. Four evolutionary forces mutation, random genetic drift, natural selection, and gene flow acting within and among populations cause micro-evolutionary change and these processes are sufficient to account for macro-evolutionary patterns.

Session 3: Molecular and Cellular Genetics

Molecular Genetics is the field of science that reviews the structure and capacity of qualities at a molecular level and along these lines utilizes strategies for both biology and genetics. The study of chromosomes and organic phenomenon of an organism can give knowledge into heredity, genetic variation and transformations. The examination of genetics at the extent of the essential building squares of cells and at the DNA level. Cells are as amazing as they're little and far is so far obscure about the interior workings of those building pieces of life within the event that you'd get a kick out of the chance to log hours during a lab and use utilize propelled equipment’s to assist propel the comprehension of how cells function, cares in cell and nuclear science might be for you.

Session 4: Gene Therapy and Genetic Counselling

Genetic Counselling is the procedure by which the patients or relatives in danger of an acquired disorder are advised with the outcomes and nature of the disorder, the likelihood of making or transmitting it, and therefore the choices hospitable them in management and birth control. This mind-boggling procedure is often isolated into indicative and supportive aspects. The foremost surely understood kind of value transport is as DNA that encodes the common sense helpful quality to supplant the target changed quality. The polymer particles are packaged inside a vector which passes on the iotas inside and helps in their compromise. Gene Therapy is an exceptionally viable however simple to disprove kind of treatment of inherited issue dependent upon their level of sensibility and social and good affirmation.

Session 5: Genetic disorders

A genetic disease may be a disease caused in whole or partially by a change within the DNA sequence faraway from the traditional sequence. Genetic disorders are often caused by a mutation in one gene monogenic disorder, by mutations in multiple genes multifactorial inheritance disorder, by a mixture of gene mutations and environmental factors, or by damage to chromosomes changes within the number or structure of entire chromosomes, the structures that carry genes.

Session 6: Clinical Applications of Genetics

Genetic testing involves the analysis of chromosomes, deoxyribonucleic acid (DNA), RNA (RNA), or specific metabolites so as to detect variants that are related to human disease or a pharmacological response. Direct testing refers to gene-specific evaluation of a DNA and/or RNA sample. Genetic testing increasingly holds the potential to tell clinical practice and impact the outcomes of patients with the disorders that disrupt the structure, function, and/or developmental patterning of the glomerulus, tubules, and urogenital tract, and people that predispose to renal cell tumours.

Session 7: Cytogenetics and Neurogenetics

Cytogenetics is a branch of genetics that involves how the chromosomes relate to cell behaviour, particularly to their behaviour throughout cell division and meiosis. Techniques used include karyotyping, analysis of G-banded chromosomes, different cytogenetic band techniques, moreover as molecular cytogenetic like fluorescent in place hybridization (FISH) and comparative genomic hybridization (CGH). Neurogenetics is a part of genetics within the advancement and performance of the system nervosum . It considers about neural attributes as phenotypes is primarily in sight of the perception that the nervous systems of individuals, even of these having an area with similar animal types, might not be identical.

Market Analysis

The genetic testing market was valued at approximately USD 7,836 million in 2020, and it is expected to witness a revenue of USD 14,227 million in 2026, with a CAGR of 10.45% over the forecast period.The COVID-19 pandemic has left a significant impact on the growth of the genetic testing market over the crisis. According to the research article published in Genetics in Medicine 2020, all the clinical genetic testing was restricted and telemedicine-based consultations and counseling were adopted globally. As per this study, 112 prenatal and 156 clinical genetics/cancer patients were evaluated in a span of one month at the Columbia University Irving Medical Center (CUIMC). Most of the genetic testing services have adopted virtualization, along with home testing kit/home sample collection, to combat the transmission of the SARS-CoV2 virus. However, according to the research article published in the Journal of Medical Genetics 2020, there was hindrance reported in accessing genetic testing blood draws, as a result of which the genetic testing was tremendously impacted, wherein a reduction in genetic testing from 97.7% to 74.1% was observed during the virtual care period. Hence, COVID-19 is expected to have a direct and indirect impact on the genetic testing market over the ongoing crisis period.

Past Conferences Report

Human Genetics 2020

We gratefully thank all our wonderful speakers and delegates for making Human Genetics 2020 webinar successful.

International Webinar on Human Genetics and Genetic Disorder, hosted by the Longdom Conference was held during March 20, 2020 virtually based on the theme “Advancements in Genetics"