Add DNA sequencing history
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@@ -284,3 +284,61 @@
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eprint = {https://www.pnas.org/content/74/12/5463.full.pdf},
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journal = {Proceedings of the National Academy of Sciences}
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}
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@Article{InternationalHumanGenomeSequencingConsortium2004,
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author = {Consortium, International Human Genome Sequencing},
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title = {Finishing the euchromatic sequence of the human genome},
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journal = {Nature},
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year = 2004,
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month = {Oct},
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day = 01,
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volume = 431,
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number = 7011,
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pages = {931-945},
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abstract = {The sequence of the human genome encodes the genetic
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instructions for human physiology, as well as rich information
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about human evolution. In 2001, the International Human Genome
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Sequencing Consortium reported a draft sequence of the
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euchromatic portion of the human genome. Since then, the
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international collaboration has worked to convert this draft
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into a genome sequence with high accuracy and nearly complete
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coverage. Here, we report the result of this finishing
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process. The current genome sequence (Build 35) contains 2.85
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billion nucleotides interrupted by only 341 gaps. It covers
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∼99{\%} of the euchromatic genome and is accurate to an error
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rate of ∼1 event per 100,000 bases. Many of the remaining
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euchromatic gaps are associated with segmental duplications
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and will require focused work with new methods. The
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near-complete sequence, the first for a vertebrate, greatly
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improves the precision of biological analyses of the human
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genome including studies of gene number, birth and death.
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Notably, the human genome seems to encode only 20,000--25,000
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protein-coding genes. The genome sequence reported here should
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serve as a firm foundation for biomedical research in the
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decades ahead.},
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issn = {1476-4687},
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doi = {10.1038/nature03001},
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url = {https://doi.org/10.1038/nature03001}
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}
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@Article{Schloss2008,
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author = {Schloss, Jeffery A.},
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title = {How to get genomes at one ten-thousandth the cost},
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journal = {Nature Biotechnology},
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year = 2008,
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month = {Oct},
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day = 01,
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volume = 26,
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number = 10,
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pages = {1113-1115},
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abstract = {The NHGRI's Advanced DNA Sequencing Technology program is
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spearheading the development of platforms that will bring
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routine whole-genome sequencing closer to reality.},
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issn = {1546-1696},
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doi = {10.1038/nbt1008-1113},
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url = {https://doi.org/10.1038/nbt1008-1113}
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}
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