In 1953, James D. Watson and Frances Crick discovered the double helix structure of DNA.
In 1956, Jo Hin Tjio and Albert Levan determined that there are 46 human chromosomes.
In 1966, Marshall Niremberg, Heinrich Mathaei and Severo Ochoa cracked the human genetic code, opening the door for the explosion of genetic engineering studies and achievements beginning in the late 1970s. The genetic code is the set of rules by which information encoded in genetic material (DNA or RNA sequences) is translated into proteins (amino acid sequences) by living cells.
In 1972, scientists Stanley Cohen and Herbert Boyer developed recombinant DNA (rDNA) technology, an artificial DNA sequencing process that “recombines” the DNA of two different organisms.
In 1977, molecular geneticists Walter Gilbert and Allan Maxam pioneered a new DNA sequencing method.
In 1981, population geneticist Luigi Luca Cavalli-Sforza established the dual inheritance theory with Marcus Feldman which suggests that human variation is the result of both biological and cultural evolution.
In 1983, scientists successfully mapped the first human disease gene—the gene for Huntington's disease—with DNA markers.
In 1989, Francis Collins and Lap-Chee Tsui sequenced the first human gene. It encoded the CFTR protein, the defective gene that causes cystic fibrosis.
In 2001, the Human Genome Project and Celera Genomics released the first draft sequences of the human genome.
The Human Genome Project was successfully completed with 99% of the human genome sequenced to within 99.99% accuracy.
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