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Universal Count Correction for High-Throughput Sequencing

Overview of attention for article published in PLoS Computational Biology, March 2014
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47 X users
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194 Mendeley
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Title
Universal Count Correction for High-Throughput Sequencing
Published in
PLoS Computational Biology, March 2014
DOI 10.1371/journal.pcbi.1003494
Pubmed ID
Authors

Tatsunori B. Hashimoto, Matthew D. Edwards, David K. Gifford

Abstract

We show that existing RNA-seq, DNase-seq, and ChIP-seq data exhibit overdispersed per-base read count distributions that are not matched to existing computational method assumptions. To compensate for this overdispersion we introduce a nonparametric and universal method for processing per-base sequencing read count data called FIXSEQ. We demonstrate that FIXSEQ substantially improves the performance of existing RNA-seq, DNase-seq, and ChIP-seq analysis tools when compared with existing alternatives.

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X Demographics

The data shown below were collected from the profiles of 47 X users who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 194 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 13 7%
Germany 3 2%
Canada 3 2%
Spain 2 1%
Denmark 2 1%
Norway 2 1%
Austria 1 <1%
Sweden 1 <1%
Finland 1 <1%
Other 9 5%
Unknown 157 81%

Demographic breakdown

Readers by professional status Count As %
Researcher 62 32%
Student > Ph. D. Student 59 30%
Professor > Associate Professor 11 6%
Student > Master 11 6%
Professor 10 5%
Other 28 14%
Unknown 13 7%
Readers by discipline Count As %
Agricultural and Biological Sciences 100 52%
Biochemistry, Genetics and Molecular Biology 46 24%
Computer Science 12 6%
Mathematics 5 3%
Environmental Science 3 2%
Other 12 6%
Unknown 16 8%