Initial sequencing and Initial sequencing and analysis of the human analysis of the human
genomegenome
Averya JohnsonNick Patrick
Aaron LernerJoel Burrill
Computer Science 4GOctober 18, 2005
How and why the human genome project was started
There was a dynamic interplay of goals and aspirations that initially drove scientists to
undertake the monumental task of sequencing the human genome.
Planning the project
• Early 1980s: realizations about what a global genome project would require and could accomplish: could accelerate biomedical research but would require global cooperation
• 1984-1986: first discussions about the idea of sequencing the entire human genome
• 1988: U.S. endorses the idea, but realizes that project must encompass several things: creation of genetic, physical, and sequence maps of genome, development of new genetic technology to support the program, research into ethical, legal, and social issues
Progress of the project
• Early 1990s: groups began to collaborate and sequence, pilot projects to determine if the overall project was feasible
• 1995: construction of genetic and physical map of the human and mouse genomes, sequencing of the yeast and worm genomes
• Late 1990s: Human Genome Organization created to coordinate efforts
• October 7, 2000: human genome draft sequence released J. Craig Venter, head of
Celera, and Francis Collins, head of the
Human Genome Project
How the human genome was sequenced and technologies
involvedMany important technologies were vital in sequencing human
genetic data on a large scale during the Human Genome Project. These technologies, as well as group collaboration
and effective execution of their applications, were essential to making the project a success.
Technologies• Whole genome shotgun
sequencing vs. hierarchical shotgun sequencing: decided to use hierarchical technique (Celera, however, used both techniques)
• Technologies for gathering and improving the quality of data: fluorescence-based sequence detection, specially designed polymerases, gel electrophoresis
• Automated sequencing techniques: automatic, faster, standardized sequencing algorithms
Generating sequence data
1. Cloning selected genome sequences
2. Sequencing the clones using hierarchical shotgun sequencing
3. Assembling sequenced clones into an overall, finished sequence1. Filtering – eliminate contaminated segments
2. Layout – associate sequences with locations on a physical genomic map
3. Merging – ordering, orienting, and connecting overlapping sequences using computer algorithms
Group collaboration
• Important principles related to data sharing1. Global effort: collaboration open to any sequencing center
from any nation2. Public, rapidly released data: all data will be released
rapidly into public databases accessible by all groups involved in the project
• Collaboration extremely important and efficient• Sequence data developed all around the world at different
rates using different techniques• However, data could be directly integrated because of
standardized analysis procedures and rapidly released, readily available data
The result: a draft sequence
• Integrated draft sequence of the human genome released on October 7, 2000
• Important to note that this is a draft sequence: errors and gaps in data
• A work in progress: data still being added, improvements being made to the physical genomic map, new clones are being sequenced to close the gaps and reduce errors
What scientists learned from the Human Genome Project
Scientists have been able to draw many conclusions from the genetic sequence data gathered by the Human Genome
Project. They have been able to draw direct conclusions about how different aspects of the sequence directly influence
genes and human development.
Patterns in the human genome sequence
Variation in GC content: why do some regions of the genome have higher CG ratios while others may have lower?
CpG islands: similar to GC content in that there are regions where the CpG dinucleotide occurs much more frequently
Repeat content of the human genome
Transposon-derived repeats: 45% of the human genome is composed of various transposable elements
Age distribution: transposable elements can be analyzed to determine, with relative accuracy, their age
Comparison with other organisms: three distinct differences were found when comparing the transposable elements from those genomes to those of the human genome
Distribution of transposable elements: transposable elements are like GC content in that they occur more frequently in some portions of the genome
Repeat content of the human genome
Gene content of the human genome
Non-coding RNAs: there are four major groups of non-coding RNAs
Protein-coding genes: one of the more difficult parts of the project, but also one of the most important
Applications in medicine and the future of human
genome researchThe Human Genome Project was not just about coming up with a nucleotide sequence, as there are many applications for the data in real life. And though the human genome has basically
been sequenced, scientists still have a long way to go in terms of understanding and finalizing the draft sequence.
Applications in medicine and biology
• Identifying disease genes: will allow a more rapid identification of susceptibility to a disease
• Finding drug targets: will help us to understand how diseases work within the body, develop personalized medicine, better treatment
• Applications to basic biology: will allow us to more fully understand how body processes work
The future of human genome research
What is still left to do?
• Finish the sequence: gaps and errors in the data• Identify all genes and proteins: much is still unknown
about the genes in the human genome and the proteins they produce
• Sequence other genomes: conclusions about the human genome can be drawn from comparing it to other organisms
• Understand the function of sequences: scientists still have much to figure out about what sequences code for and how they work