Publication | Open Access
Error correction of high-throughput sequencing datasets with non-uniform coverage
123
Citations
26
References
2011
Year
Abstract MotivationEngineeringGeneticsGenomicsHigh Throughput SequencingData ScienceSingle Cell SequencingBiostatisticsError CorrectionSingle-cell GenomicsUniformity AssumptionsOmicsFunctional GenomicsSequencingBioinformaticsLong-read SequencingNext-generation SequencingComputational BiologySystems BiologyMedicineGenome EditingSequence Assembly
Abstract 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
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