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
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Human Genomics Conference Speakers
Recommended Sessions
- Animal cells & Microbial Interactions
- Calcium and Cell Function
- Cancer Genomics
- Cell and Immunology
- Cell Cycle and Cytogenetics
- Cell Physiology and Biochemistry
- Cellular Metabolism & Signalling
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- Human Genomics
- Membrane Processes
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- Molecular Cell Biology
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- Recombinant DNA Technology
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