The uniqueome: a mappability resource for short-tag sequencing.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 21075741.
- Also identified by DOI 10.1093/bioinformatics/btq640 and PMC identifier 3018812.
- Licence recorded as CC BY-NC.
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Abstract
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. Files, scripts and supplementary data are available from http://grimmond.imb.uq.edu.au/uniqueome/; the ISAS uniqueome aligner is freely available from http://www.imagenix.com/.
Medical subject headings
- Chromosome Mapping
- Genomics
- Sequence Analysis, RNA