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State of the art de novoassembly of human genomes from massively parallel sequencing data

Overview of attention for article published in Human Genomics, April 2010
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Title
State of the art de novoassembly of human genomes from massively parallel sequencing data
Published in
Human Genomics, April 2010
DOI 10.1186/1479-7364-4-4-271
Pubmed ID
Authors

Yingrui Li, Yujie Hu, Lars Bolund, Jun Wang

Abstract

Recent studies in human genomes have demonstrated the use of de novo assemblies to identify genetic variations that are difficult for mapping-based approaches. Construction of multiple human genome assemblies is enabled by massively parallel sequencing, but a conventional bioinformatics solution is costly and slow, creating bottlenecks in the process. This review describes two public short-read de novo assembly applications that can handle human genomes, ABySS and SOAPdenovo. It also discusses the technical aspects and future challenges of human genome de novo assembly by short reads.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 107 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Germany 3 3%
France 2 2%
United Kingdom 2 2%
United States 2 2%
Hong Kong 1 <1%
Brazil 1 <1%
New Zealand 1 <1%
Italy 1 <1%
Russia 1 <1%
Other 1 <1%
Unknown 92 86%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 27 25%
Researcher 27 25%
Student > Master 14 13%
Student > Bachelor 7 7%
Student > Doctoral Student 6 6%
Other 19 18%
Unknown 7 7%
Readers by discipline Count As %
Agricultural and Biological Sciences 62 58%
Computer Science 16 15%
Biochemistry, Genetics and Molecular Biology 13 12%
Environmental Science 3 3%
Chemistry 2 2%
Other 3 3%
Unknown 8 7%