Detecting genomic clustering of risk variants from sequence data: cases versus controls
Detecting genomic clustering of risk variants from sequence data: cases versus controls
About this item
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Author / Creator
Publisher
Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title
Language
English
Formats
Publication information
Publisher
Berlin/Heidelberg: Springer Berlin Heidelberg
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More information
Scope and Contents
Contents
As the ability to measure dense genetic markers approaches the limit of the DNA sequence itself, taking advantage of possible clustering of genetic variants in, and around, a gene would benefit genetic association analyses, and likely provide biological insights. The greatest benefit might be realized when multiple rare variants cluster in a functi...
Alternative Titles
Full title
Detecting genomic clustering of risk variants from sequence data: cases versus controls
Authors, Artists and Contributors
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Record Identifier
TN_cdi_proquest_miscellaneous_1448225019
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1448225019
Other Identifiers
ISSN
0340-6717
E-ISSN
1432-1203
DOI
10.1007/s00439-013-1335-y
