High-throughput sequencing reveals extensive variation in human-specific L1 content in individual human genomes
Clicks: 174
ID: 273654
2010
Using high-throughput sequencing, we devised a technique to determine the insertion sites of virtually all members of the human-specific L1 retrotransposon family in any human genome. Using diagnostic nucleotides, we were able to locate the approximately 800 L1Hs copies corresponding specifically to …
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ad2010genomehigh-throughput
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| Authors | Ewing AD;Kazazian HH;; |
| Journal | genome research |
| Year | 2010 |
| DOI | DOI not found |
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| Keywords |
National Center for Biotechnology Information
NCBI
NLM
MEDLINE
humans
pubmed abstract
nih
national institutes of health
national library of medicine
research support
non-u.s. gov't
N.I.H.
Extramural
DNA
Sequence Analysis
genome
human / genetics*
retroelements
genetic variation / genetics*
pmid:20488934
pmc2928504
doi:10.1101/gr.106419.110
adam d ewing
haig h kazazian
long interspersed nucleotide elements / genetics*
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