The application of next-generation sequencing to validate D12S391 microvariation
Objective: In a paternity case, the D12S391 locus was reported as a mismatch. To confirm the existence of mutations and mutations come from father or mother. Methods: STR and next-generation sequencing technology were used to validate the sequence. Results: NGS showed the loss of one adenine between...
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Main Authors: | , , , , , , , , |
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Format: | Book |
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Wolters Kluwer Medknow Publications,
2018-01-01T00:00:00Z.
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Internet
Connect to this object online.3rd Floor Main Library
Call Number: |
A1234.567 |
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Copy 1 | Available |