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Publications by Dinghua Li

BASE: A Practical De Novo Assembler for Large Genomes Using Long NGS Reads

BMC Genomics
BiotechnologyGenetics
2016English

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A Distributed Framework for Aligning Short Reads to Genomes

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FastUniq: A Fast De Novo Duplicates Removal Tool for Paired Short Reads

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PGcloser: Fast Parallel Gap-Closing Tool Using Long-Reads or Contigs to Fill Gaps in Genomes

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A Combined Approach for De Novo DNA Sequence Assembly of Very Short Reads

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NGSReadsTreatment – A Cuckoo Filter-Based Tool for Removing Duplicate Reads in NGS Data

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An Enrichment Method for Mapping Ambiguous Reads to Reference Genome for NGS Analysis

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