DiscoverInference for Change-Point and Related ProcessesDetecting copy number variants for rare genetic disorders and non-invasive pre-natal diagnosis
Detecting copy number variants for rare genetic disorders and non-invasive pre-natal diagnosis

Detecting copy number variants for rare genetic disorders and non-invasive pre-natal diagnosis

Update: 2014-02-12
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Plagnol, V (University College London)
Tuesday 04 February 2014, 11:30-12:30
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Detecting copy number variants for rare genetic disorders and non-invasive pre-natal diagnosis

Detecting copy number variants for rare genetic disorders and non-invasive pre-natal diagnosis

Vincenzo Abete