Open main menu
Home
Random
Recent changes
Special pages
Community portal
Preferences
About Wikipedia
Disclaimers
Incubator escapee wiki
Search
User menu
Talk
Dark mode
Contributions
Create account
Log in
Editing
DNA sequencing
(section)
Warning:
You are not logged in. Your IP address will be publicly visible if you make any edits. If you
log in
or
create an account
, your edits will be attributed to your username, along with other benefits.
Anti-spam check. Do
not
fill this in!
=== Sequencing of full genomes === [[File:Genome map of the bacteriophage Ξ¦X174 showing overlapping genes.svg|thumb|300px|right|The 5,386 bp genome of [[bacteriophage ΟX174]]. Each coloured block represents a gene.]]{{Main|Whole genome sequencing}} The first full DNA genome to be sequenced was that of [[bacteriophage ΟX174]] in 1977.<ref>{{cite journal | vauthors = Sanger F, Air GM, Barrell BG, Brown NL, Coulson AR, Fiddes CA, Hutchison CA, Slocombe PM, Smith M | title = Nucleotide sequence of bacteriophage phi X174 DNA | journal = Nature | volume = 265 | issue = 5596 | pages = 687β95 | date = February 1977 | pmid = 870828 | doi = 10.1038/265687a0 | bibcode = 1977Natur.265..687S | s2cid = 4206886 }}</ref> [[Medical Research Council (UK)|Medical Research Council]] scientists deciphered the complete DNA sequence of the [[Epstein-Barr virus]] in 1984, finding it contained 172,282 nucleotides. Completion of the sequence marked a significant turning point in DNA sequencing because it was achieved with no prior genetic profile knowledge of the virus.<ref>{{Cite web|title=The next frontier: Human viruses |url=https://www.whatisbiotechnology.org/index.php/exhibitions/sanger/sequencing|access-date=2023-06-27|website=What is Biotechnology?|language=en|first=L. |last=Marks}}</ref><ref name="Bambara Padmanabhan Wu 1974"/> A non-radioactive method for transferring the DNA molecules of sequencing reaction mixtures onto an immobilizing matrix during [[electrophoresis]] was developed by Herbert Pohl and co-workers in the early 1980s.<ref>{{cite journal | vauthors = Beck S, Pohl FM | title = DNA sequencing with direct blotting electrophoresis | journal = EMBO J | volume = 3 | issue = 12 | pages = 2905β09 | year = 1984 | pmid = 6396083 | pmc = 557787 | doi = 10.1002/j.1460-2075.1984.tb02230.x }}</ref><ref>United States Patent 4,631,122 (1986)</ref> Followed by the commercialization of the DNA sequencer "Direct-Blotting-Electrophoresis-System GATC 1500" by [[GATC Biotech]], which was intensively used in the framework of the EU genome-sequencing programme, the complete DNA sequence of the yeast ''[[Saccharomyces cerevisiae]]'' chromosome II.<ref name = "Feldmann_1994"/> [[Leroy E. Hood]]'s laboratory at the [[California Institute of Technology]] announced the first semi-automated DNA sequencing machine in 1986.<ref>{{cite journal | vauthors = Smith LM, Sanders JZ, Kaiser RJ, Hughes P, Dodd C, Connell CR, Heiner C, Kent SB, Hood LE | title = Fluorescence Detection in Automated DNA Sequence Analysis | journal = Nature | volume = 321 | issue = 6071 | pages = 674β79 | date = 12 June 1986 | pmid = 3713851 | doi = 10.1038/321674a0 | bibcode = 1986Natur.321..674S | s2cid = 27800972 }}</ref> This was followed by [[Applied Biosystems]]' marketing of the first fully automated sequencing machine, the ABI 370, in 1987 and by Dupont's Genesis 2000<ref>{{cite journal | vauthors = Prober JM, Trainor GL, Dam RJ, Hobbs FW, Robertson CW, Zagursky RJ, Cocuzza AJ, Jensen MA, Baumeister K | title = A system for rapid DNA sequencing with fluorescent chain-terminating dideoxynucleotides | journal = Science | volume = 238 | issue = 4825 | pages = 336β41 | date = 16 October 1987 | pmid = 2443975 | doi = 10.1126/science.2443975 | bibcode = 1987Sci...238..336P }}</ref> which used a novel fluorescent labeling technique enabling all four [[dideoxynucleotide]]s to be identified in a single lane. By 1990, the U.S. [[National Institutes of Health]] (NIH) had begun large-scale sequencing trials on ''[[Mycoplasma capricolum]]'', ''[[Escherichia coli]]'', ''[[Caenorhabditis elegans]]'', and ''[[Saccharomyces cerevisiae]]'' at a cost of US$0.75 per base. Meanwhile, sequencing of human [[cDNA]] sequences called [[expressed sequence tag]]s began in [[Craig Venter]]'s lab, an attempt to capture the coding fraction of the [[human genome]].<ref name="pmid2047873">{{cite journal | vauthors = Adams MD, Kelley JM, Gocayne JD, Dubnick M, Polymeropoulos MH, Xiao H, Merril CR, Wu A, Olde B, Moreno RF | title = Complementary DNA sequencing: expressed sequence tags and human genome project | journal = Science | volume = 252 | issue = 5013 | pages = 1651β56 | date = June 1991 | pmid = 2047873 | doi = 10.1126/science.2047873 | bibcode = 1991Sci...252.1651A | s2cid = 13436211 }}</ref> In 1995, Venter, [[Hamilton O. Smith|Hamilton Smith]], and colleagues at [[The Institute for Genomic Research]] (TIGR) published the first complete genome of a free-living organism, the bacterium ''[[Haemophilus influenzae]]''. The circular chromosome contains 1,830,137 bases and its publication in the journal Science<ref>{{cite journal | vauthors = Fleischmann RD, Adams MD, White O, Clayton RA, Kirkness EF, Kerlavage AR, Bult CJ, Tomb JF, Dougherty BA, Merrick JM | title = Whole-genome random sequencing and assembly of ''Haemophilus influenzae Rd'' | journal = Science | volume = 269 | issue = 5223 | pages = 496β512 | date = July 1995 | pmid = 7542800 | doi = 10.1126/science.7542800 | bibcode = 1995Sci...269..496F }}</ref> marked the first published use of whole-genome shotgun sequencing, eliminating the need for initial mapping efforts. By 2003, the Human Genome Project's shotgun sequencing methods had been used to produce a draft sequence of the human genome; it had a 92% accuracy.<ref name="Lander_2001"/><ref name="Venter_2001"/><ref>{{Cite web |date=2022-04-11 |title=First complete sequence of a human genome |url=https://www.nih.gov/news-events/nih-research-matters/first-complete-sequence-human-genome |access-date=2025-02-06 |website=National Institutes of Health (NIH) |language=EN}}</ref> In 2022, scientists successfully sequenced the last 8% of the human genome. The fully sequenced standard reference gene is called GRCh38.p14, and it contains 3.1 billion base pairs.<ref>{{Cite web |date=2022-04-11 |title=First complete sequence of a human genome |url=https://www.nih.gov/news-events/nih-research-matters/first-complete-sequence-human-genome |access-date=2025-02-06 |website=National Institutes of Health (NIH) |language=EN}}</ref><ref>{{Cite web |last=Hartley |first=Gabrielle |date=2022-03-31 |title=The Human Genome Project pieced together only 92% of the DNA β now scientists have finally filled in the remaining 8% |url=https://theconversation.com/the-human-genome-project-pieced-together-only-92-of-the-dna-now-scientists-have-finally-filled-in-the-remaining-8-176138 |access-date=2025-02-06 |website=The Conversation |language=en-US}}</ref>
Edit summary
(Briefly describe your changes)
By publishing changes, you agree to the
Terms of Use
, and you irrevocably agree to release your contribution under the
CC BY-SA 4.0 License
and the
GFDL
. You agree that a hyperlink or URL is sufficient attribution under the Creative Commons license.
Cancel
Editing help
(opens in new window)