Journal article
GAT: a simulation framework for testing the association of genomic intervals
- Abstract:
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Motivation: A common question in genomic analysis is whether two sets of genomic intervals overlap significantly. This question arises, for example, when interpreting ChIP-Seq or RNA-Seq data in functional terms. Because genome organization is complex, answering this question is non-trivial.
Summary: We present Genomic Association Test (GAT), a tool for estimating the significance of overlap between multiple sets of genomic intervals. GAT implements a null model that the two sets of intervals are placed independently of one another, but allows each set’s density to depend on external variables, for example, isochore structure or chromosome identity. GAT estimates statistical significance based on simulation and controls for multiple tests using the false discovery rate.
Availability: GAT’s source code, documentation and tutorials are available at http://code.google.com/p/genomic-association-tester.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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- Files:
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(Preview, Version of record, pdf, 103.8KB, Terms of use)
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- Publisher copy:
- 10.1093/bioinformatics/btt343
- Publisher:
- Oxford University Press
- Journal:
- Bioinformatics More from this journal
- Volume:
- 29
- Issue:
- 16
- Pages:
- 2046-2048
- Publication date:
- 2013-08-01
- Edition:
- Publisher's version
- DOI:
- EISSN:
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1460-2059
- ISSN:
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1367-4803
- Language:
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English
- Keywords:
- Subjects:
- UUID:
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uuid:2d59dfc1-13fe-45f4-ac5c-4d08a559654c
- Local pid:
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ora:7772
- Deposit date:
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2014-02-03
Terms of use
- Copyright holder:
- Heger et al
- Copyright date:
- 2013
- Notes:
- Copyright The Author 2013. Published by Oxford University Press. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
- Licence:
- CC Attribution (CC BY)
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