Bioinformatics · 2012 · 146 citations · 12 references
Life SciencesBioinformaticsBiologyGenome AssemblyGenomicsPlant GenomicsContig ConstructionDe Novo Genome AssemblyDna SequencingGenome SequencingSequence AssemblyShort-read AssemblyOverlap AssemblyOverlap DetectionPaired-end Read AssemblyPaired-end Read LinkingPaired-end SequencingRead BridgingRead Overlap AnalysisRead Pairing
MOTIVATION: The boost of next-generation sequencing technologies provides us with an unprecedented opportunity for elucidating genetic mysteries, yet the short-read length hinders us from better assembling the genome from scratch. New protocols now exist that can generate overlapping pair-end reads. By joining the 3' ends of each read pair, one is able to construct longer reads for assembling. However, effectively joining two overlapped pair-end reads remains a challenging task. RESULT: In this article, we present an efficient tool called Connecting Overlapped Pair-End (COPE) reads, to connect overlapping pair-end reads using k-mer frequencies. We evaluated our tool on 30× simulated pair-end reads from Arabidopsis thaliana with 1% base error. COPE connected over 99% of reads with 98.8% accuracy, which is, respectively, 10 and 2% higher than the recently published tool FLASH. When COPE is applied to real reads for genome assembly, the resulting contigs are found to have fewer errors and give a 14-fold improvement in the N50 measurement when compared with the contigs produced using unconnected reads. AVAILABILITY AND IMPLEMENTATION: COPE is implemented in C++ and is freely available as open-source code at ftp://ftp.genomics.org.cn/pub/cope. CONTACT: twlam@cs.hku.hk or luoruibang@genomics.org.cn
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FLASH: fast length adjustment of short reads to improve genome assemblies
Tanja Magoč, Steven L. Salzberg · Bioinformatics · 2011 · 15.7K citations · Full text
De novo assembly of human genomes with massively parallel short read sequencing
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PANDAseq: paired-end assembler for illumina sequences
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Adaptive seeds tame genomic sequence comparison
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Life Sciences, Biology, Genetics +11