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Published November 7, 2023 | Version v1
Software Open

A method to comprehensively identify germline SNVs, INDELs and CNVs from whole exome sequencing data of BRCA1/2 negative breast cancer patients

Authors/Creators

  • Andrea Bianchi (Contact person)1 ORCID icon
  • 1. ROR icon University of L'Aquila

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IntegratedSNVINDELSandCNV-main.zip

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DOI
10.5281/zenodo.10078336
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DOI

10.5281/zenodo.10078336

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cc-by-4.0 icon Creative Commons Attribution 4.0 International
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Created
November 7, 2023
Modified
November 7, 2023

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