Threshold-seq: a tool for determining the threshold in short RNA-seq datasets.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 28203700.
- Also identified by DOI 10.1093/bioinformatics/btx073 and PMC identifier 5870860.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
We present 'Threshold-seq,' a new approach for determining thresholds in deep-sequencing datasets of short RNA transcripts. Threshold-seq addresses the critical question of how many reads need to support a short RNA molecule in a given dataset before it can be considered different from 'background.' The proposed scheme is easy to implement and incorporate into existing pipelines. Source code of Threshold-seq is freely available as an R package at: http://cm.jefferson.edu/threshold-seq/. isidore.rigoutsos@jefferson.edu. Supplementary data are available at Bioinformatics online.
Medical subject headings
- High-Throughput Nucleotide Sequencing
- Sequence Analysis, RNA
- Software