Detecting copy number variants for rare genetic disorders and non-invasive pre-natal diagnosis
59 mins 42 secs,
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About this item
Description: |
Plagnol, V (University College London)
Tuesday 04 February 2014, 11:30-12:30 |
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Created: | 2014-02-12 15:56 |
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Collection: | Inference for Change-Point and Related Processes |
Publisher: | Isaac Newton Institute |
Copyright: | Plagnol, V |
Language: | eng (English) |
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