Cell Biology and Genomics

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.