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BASE: a practical de novo assembler for large genomes using long NGS reads.

BMC genomics | 2016

De novo genome assembly using NGS data remains a computation-intensive task especially for large genomes. In practice, efficiency is often a primary concern and favors using a more efficient assembler like SOAPdenovo2. Yet SOAPdenovo2, based on de Bruijn graph, fails to take full advantage of longer NGS reads (say, 150 bp to 250 bp from Illumina HiSeq and MiSeq). Assemblers that are based on string graphs (e.g., SGA), though less popular and also very slow, are more favorable for longer reads.

Pubmed ID: 27586129 RIS Download

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BASE (tool)

RRID:SCR_010937

A comprehensive management application for information, data, and analysis of microarray experiments, available as free open source software.

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