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High-coverage nanopore sequencing of samples from the 1000 Genomes Project to build a comprehensive catalog of human genetic variation

  • First Published October 2, 2024
Resource

SOAPindel: Efficient identification of indels from short paired reads

  • First Published September 12, 2012
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Assemblathon 1: A competitive assessment of de novo short read assembly methods

  • First Published September 16, 2011
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De novo assembly of human genomes with massively parallel short read sequencing

  • First Published December 17, 2009
Resource

SNP detection for massively parallel whole-genome resequencing

  • First Published May 6, 2009
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