Armand Garot
1PUBLICATIONS
3CO-AUTHORS

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Publications (1)
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|Jun 15, 2018
Detecting Rare AID-Induced Mutations in B-Lineage Oncogenes from High-Throughput Sequencing Data Using the Detection of Minor Variants by Error Correction Method.Ophélie Alyssa Martin, Armand Garot, Sandrine Le Noir
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