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Error correction of high-throughput sequencing datasets with non-uniform coverage

Motivation: The continuing improvements to high-throughput sequencing (HTS) platforms have begun to unfold a myriad of new applications. As a result, error correction of sequencing reads remains an important problem. Though several tools do an excellent job of correcting datasets where the reads are...

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Detalles Bibliográficos
Autores principales: Medvedev, Paul, Scott, Eric, Kakaradov, Boyko, Pevzner, Pavel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3117386/
https://www.ncbi.nlm.nih.gov/pubmed/21685062
http://dx.doi.org/10.1093/bioinformatics/btr208
Descripción
Sumario:Motivation: The continuing improvements to high-throughput sequencing (HTS) platforms have begun to unfold a myriad of new applications. As a result, error correction of sequencing reads remains an important problem. Though several tools do an excellent job of correcting datasets where the reads are sampled close to uniformly, the problem of correcting reads coming from drastically non-uniform datasets, such as those from single-cell sequencing, remains open. Results: In this article, we develop the method Hammer for error correction without any uniformity assumptions. Hammer is based on a combination of a Hamming graph and a simple probabilistic model for sequencing errors. It is a simple and adaptable algorithm that improves on other tools on non-uniform single-cell data, while achieving comparable results on normal multi-cell data. Availability: http://www.cs.toronto.edu/~pashadag. Contact: pmedvedev@cs.ucsd.edu