Abstract
Summary: Quantification applications of short-tag sequencing data (such as CNVseq and RNAseq) depend on knowing the uniqueness of specific genomic regions at a given threshold of error. Here, we present the 'uniqueome', a genomic resource for understanding the uniquely mappable proportion of genomic sequences. Pre-computed data are available for human, mouse, fly and worm genomes in both color-space and nucletotide-space, and we demonstrate the utility of this resource as applied to the quantification of RNAseq data. © The Author(s) 2010. Published by Oxford University Press.
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CITATION STYLE
Koehler, R., Issac, H., Cloonan, N., & Grimmond, S. M. (2011). The uniqueome: A mappability resource for short-tag sequencing. Bioinformatics, 27(2), 272–274. https://doi.org/10.1093/bioinformatics/btq640
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