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The biochemistry of RNA-Seq library preparation results in cDNA fragments that are not uniformly distributed within the transcripts they represent. This non-uniformity must be accounted for when estimating expression levels, and we show how to perform the needed corrections using a likelihood based approach. We find improvements in expression estimates as measured by correlation with independently performed qRT-PCR and show that correction of bias leads to improved replicability of results across libraries and sequencing technologies.
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Adam Roberts
University of York
Cole Trapnell
University of Washington
Julie Donaghey
Aastrom Biosciences (United States)
Genome biology
Harvard University
University of California, Berkeley
Broad Institute
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Roberts et al. (Wed,) studied this question.
synapsesocial.com/papers/69d75bc4b4cef8fedc48f7d3 — DOI: https://doi.org/10.1186/gb-2011-12-3-r22
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