Human Genomics

Human genomics is the study of provision as it occurs in human beings. The Human genome is the total set of nucleic acid sequences for humans, encoded as DNA within the 23 chromosome couple in cell nuclei and in a small DNA molecule found within own  mitochondria. Human genomes involve both protein-coding DNA genes and noncoding DNA. Human genetics encompasses a differently of overlapping fields including classical genetics , cytogenetic, molecular genetics, biochemical genetics, genomics, developmental genetics,  genetic counselling and  clinical Ethic genetics. Human genetic variation is the genetic differences in whole populations, there may be multiple variants of any given gene in the human population, a situation called polymorphism. No two humans are genetically identical, even monozygotic twins having infrequent genetic differences due to mutations occurring during improvement and gene copy-number variation.

 

 

 

  • Molecular organization and gene content
  • Coding sequences (protein-coding genes)
  • Coding vs. Noncoding DNA
  • Genomic variation in humans
  • Human genetic disorders
  • Human mitochondrial DNA Haplogroups
  • Genetic Recombination
  • Genetic Interaction

Related Conference of Human Genomics

October 21-22, 2019

23rd European Biotechnology Congress

Zurich, Switzerland
November 26-27, 2019

International Conference On Genomics and Molecular Biology

Lisbon | Portugal
November 26-27, 2019

International Conference on Cell and Gene Therapy

| Lisbon, Portugal
February 24-25, 2020

24th Global Congress on Biotechnology

London, UK
March 16-17, 2020 |

12th World Congress and Expo on Cell & Stem Cell Research

Chicago, Illinois, USA

Human Genomics Conference Speakers

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