The uniqueome: A mappability resource for short-tag sequencing

52Citations
Citations of this article
196Readers
Mendeley users who have this article in their library.

This article is free to access.

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.

Cite

CITATION STYLE

APA

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

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free