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Machine learning identifies interacting genetic variants contributing to breast cancer risk: A case study in Finnish cases and controls

We propose an effective machine learning approach to identify group of interacting single nucleotide polymorphisms (SNPs), which contribute most to the breast cancer (BC) risk by assuming dependencies among BCAC iCOGS SNPs. We adopt a gradient tree boosting method followed by an adaptive iterative S...

詳細記述

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書誌詳細
出版年:Sci Rep
主要な著者: Behravan, Hamid, Hartikainen, Jaana M., Tengström, Maria, Pylkäs, Katri, Winqvist, Robert, Kosma, Veli–Matti, Mannermaa, Arto
フォーマット: Artigo
言語:Inglês
出版事項: Nature Publishing Group UK 2018
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC6120908/
https://ncbi.nlm.nih.gov/pubmed/30177847
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-018-31573-5
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