The Human Genome Project was one of the great scientific achievements in history—an international research effort to sequence and map the human genome.
The Human Genome Project was completed in April 2003. This week, BCM is celebrating the 10-year anniversary of its completion, commemorating all of the successes of BCM researchers and all of the key players in this triumph.
In 1998, the Baylor College of Medicine Human Genome Sequencing Center was chosen by the National Human Research Institute as one of the three centers to finish the sequencing of the human genome.
Take a look at major milestones that led up to the completion of the Human Genome Project, and exciting happenings since then. Make sure to check back with BCM Momentum as we take time this week to celebrate this major scientific accomplishment.
Human Genome Project timeline
1985: Institute of Molecular and Human Genetics is created.
1990: The International Human Genome Project officially begins.
1991: Major gene discoveries at Baylor College of Medicine begin.
1994: Institute of Molecular and Human Genetics renamed Department of Molecular and Human Genetics.
1994: Dr. Caskey departs, and Dr. Beaudet is named chair.
1996: Human Genome Sequencing Center at BCM is established.
1998: Baylor College of Medicine Human Genome Sequencing Center chosen by National Human Genome Research Institute as one of the three centers to finish the sequencing of human genome.
2000: Human Genome Project leaders and President Clinton announce the completion of a working draft DNA sequence of the human genome.
2000: Fruit fly genome sequenced.
2003: Human Genome Project declared complete, with BCM Sequencing Center taking a major role.
2006: Dr. James Lupski and colleagues begin to lay out the case for copy number variation.
2008: Genomes of common form of lung cancer and glioblastoma sequenced in effort led by Baylor College of Medicine Human Genome Sequencing Center.
2008: International research consortium announces 1000 Genomes Project, an effort to sequence the genomes of at least 1000 people from around the world to create the most detailed illustration of human genetic variation.
2010: Dr. Lupski and Dr. Gibbs sequence Dr. Lupski’s genome to find the form of Charcot-Marie-Tooth disease that affects him and his family.
2011: A report in Science Translational Medicine describes how the sequencing of twins Noah and Alexis Beery’s genome helped treat their disorder.
Do you remember any of these notable happenings? Share your stories here, and check out more important dates and highlights on the National Human Genome Research Institute’s timeline.