Human Genomics and Proteomics

Identifying and characterizing all common sequence variants in the human genome has changed our understanding of segregating diversity, population genetics and vulnerability to disease. Single Nucleotidepolymorphisms, (SNPs) historically thought to be the dominant source of sequence variation while certain sequence variants, such as microscopically recognized sequence duplication and deletion, is identified.

  • Genome Sequencing
  • Genome Engineering
  • Proteogenomics
  • Protein Interactions
  • Next Generation Sequencing

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Human Genomics and Proteomics Conference Speakers

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