A Comprehensive Map of Mobile Element Insertion Polymorphisms in Humans
A Comprehensive Map of Mobile Element Insertion Polymorphisms in Humans
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Author / Creator
1000 Genomes Project , Stewart, Chip , Kural, Deniz , Strömberg, Michael P. , Walker, Jerilyn A. , Konkel, Miriam K. , Stütz, Adrian M. , Urban, Alexander E. , Grubert, Fabian , Lam, Hugo Y. K. , Lee, Wan-Ping , Busby, Michele , Indap, Amit R. , Garrison, Erik , Huff, Chad , Xing, Jinchuan , Snyder, Michael P. , Jorde, Lynn B. , Batzer, Mark A. , Korbel, Jan O. and Marth, Gabor T.
Publisher
United States: Public Library of Science
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Language
English
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Publisher
United States: Public Library of Science
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Contents
As a consequence of the accumulation of insertion events over evolutionary time, mobile elements now comprise nearly half of the human genome. The Alu, L1, and SVA mobile element families are still duplicating, generating variation between individual genomes. Mobile element insertions (MEI) have been identified as causes for genetic diseases, inclu...
Alternative Titles
Full title
A Comprehensive Map of Mobile Element Insertion Polymorphisms in Humans
Authors, Artists and Contributors
Author / Creator
Stewart, Chip
Kural, Deniz
Strömberg, Michael P.
Walker, Jerilyn A.
Konkel, Miriam K.
Stütz, Adrian M.
Urban, Alexander E.
Grubert, Fabian
Lam, Hugo Y. K.
Lee, Wan-Ping
Busby, Michele
Indap, Amit R.
Garrison, Erik
Huff, Chad
Xing, Jinchuan
Snyder, Michael P.
Jorde, Lynn B.
Batzer, Mark A.
Korbel, Jan O.
Marth, Gabor T.
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Primary Identifiers
Record Identifier
TN_cdi_plos_journals_1313539238
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1313539238
Other Identifiers
ISSN
1553-7404,1553-7390
E-ISSN
1553-7404
DOI
10.1371/journal.pgen.1002236