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Publications by Binghang Liu
BASE: A Practical De Novo Assembler for Large Genomes Using Long NGS Reads
BMC Genomics
Biotechnology
Genetics
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Assembler for De Novo Assembly of Large Genomes
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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
