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Patil P and Tonellato PJ. Individual whole genome mapping: from NGS reads to clinical variants. F1000Posters 2010, 1:375 (poster)

Individual whole genome mapping: from NGS reads to clinical variants

Prasad Patil1, Peter J Tonellato
Published 09 Aug 2010
Author Affiliations
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Published 09 Aug 2010

Individual whole genome mapping: from NGS reads to clinical variants

[version 1; not peer reviewed]

Prasad Patil1, Peter J Tonellato
Author Affiliations
1 Center for Biomedical Informatics, Harvard Medical School, USA
Presented at
2019 American Medical Informatics Association Summit on Clinical Research Informatics
Abstract
Competing Interests

No relevant conflicts of interest declared.

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