subSeq: determining appropriate sequencing depth through efficient read subsampling.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 25189781.
- Also identified by DOI 10.1093/bioinformatics/btu552 and PMC identifier 4296149.
- Licence recorded as CC BY-NC.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
Next-generation sequencing experiments, such as RNA-Seq, play an increasingly important role in biological research. One complication is that the power and accuracy of such experiments depend substantially on the number of reads sequenced, so it is important and challenging to determine the optimal read depth for an experiment or to verify whether one has adequate depth in an existing experiment. By randomly sampling lower depths from a sequencing experiment and determining where the saturation of power and accuracy occurs, one can determine what the most useful depth should be for future experiments, and furthermore, confirm whether an existing experiment had sufficient depth to justify its conclusions. We introduce the subSeq R package, which uses a novel efficient approach to perform this subsampling and to calculate informative metrics at each depth. The subSeq R package is available at http://github.com/StoreyLab/subSeq/.
Medical subject headings
- High-Throughput Nucleotide Sequencing
- Sequence Analysis, RNA
- Software