Maxime Vallée

Employment

• Sophia Genetics (Switzerland) Senior Bioinformatics Customer Services Specialist
  2022 - Present
• Hospices Civils de Lyon Bioinformatician
  2019 - 2022
• International Agency for Research on Cancer Bioinformatician
  2018 - 2019
• Centre de Recherche du CHU de Québec Bioinformatician
  2014 - 2018
• International Agency for Research on Cancer Bioinformatician
  2012 - 2014

Education

• Université Lyon 1 Bioinformatics PhD
  2008 - 2012
• INSA Lyon Engineer
  2005 - 2008

Projects & Funding

Projects & funding information is unavailable.

Publications (35)

• Identification of rare genetic variants in familial forms and unrelated cases of bisphosphonates-associated atypical femur fracture
  Joint Bone Spine 2025 DOI: 10.1016/j.jbspin.2025.105994
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• Putative multiple myeloma susceptibility genes identified by exome sequencing of 347 familial and early-onset cases
  Leukemia 2025 DOI: 10.1038/s41375-025-02802-4
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• Place of concordance-discordance model in evaluating NGS performance.
  Human heredity 2024 DOI: 10.1159/000538401
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• Development, Evaluation, and Implementation of a House-Made Targeted Next-Generation Sequencing Spoligotyping in a French Laboratory
  International Journal of Molecular Sciences 2022 DOI: 10.3390/ijms231911302
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• Uncovering the Contribution of Moderate-Penetrance Susceptibility Genes to Breast Cancer by Whole-Exome Sequencing and Targeted Enrichment Sequencing of Candidate Genes in Women of European Ancestry
  Cancers 2022 DOI: 10.3390/cancers14143363
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• Consistency of Mycobacterium tuberculosis Complex Spoligotyping between the Membrane-Based Method and In Silico Approach
  Microbiology Spectrum 2022 DOI: 10.1128/spectrum.00223-22
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• Autophagy and Mitophagy-Related Pathways at the Crossroads of Genetic Pathways Involved in Familial Sarcoidosis and Host-Pathogen Interactions Induced by Coronaviruses
  Cells 2021 DOI: 10.3390/cells10081995
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• The PI3K/mTOR Pathway Is Targeted by Rare Germline Variants in Patients with Both Melanoma and Renal Cell Carcinoma
  Cancers 2021 DOI: 10.3390/cancers13092243
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• Performances of Targeted RNA Sequencing for the Analysis of Fusion Transcripts, Gene Mutation, and Expression in Hematological Malignancies
  HemaSphere 2021 DOI: 10.1097/hs9.0000000000000522
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• Needlestack: an ultra-sensitive variant caller for multi-sample next generation sequencing data.
  NAR genomics and bioinformatics 2020 DOI: 10.1093/nargab/lqaa021
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