High-throughput sequencing reveals extensive variation in human-specific L1 content in individual human genomes

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ID: 273619
2010
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Abstract
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 ...
Reference Key
jr2010genomehigh-throughput Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Adam D. Ewing, Haig H. Kazazian, Jr;Adam D. Ewing;Haig H. Kazazian, Jr;
Journal genome research
Year 2010
DOI
10.1101/gr.106419.110
URL
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2928504/
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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