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Threshold-seq: a tool for determining the threshold in short RNA-seq datasets

SUMMARY: 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 ‘bac...

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Detalles Bibliográficos
Autores principales: Magee, Rogan, Loher, Phillipe, Londin, Eric, Rigoutsos, Isidore
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5870860/
https://www.ncbi.nlm.nih.gov/pubmed/28203700
http://dx.doi.org/10.1093/bioinformatics/btx073
Descripción
Sumario:SUMMARY: 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. AVAILABILITY AND IMPLEMENTATION: Source code of Threshold-seq is freely available as an R package at: http://cm.jefferson.edu/threshold-seq/ SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.