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An Active Learning Framework Improves Tumor Variant Interpretation

delete2022-06-10
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OA
AI
A
Alexandra M. Blee
B
Bian Li
T
Turner Pecen
J
Jens Meiler
Z
Zachary D. Nagel
J
John A. Capra *
W
Walter Chazin *
DOI:10.1158/0008-5472.CAN-21-3798delete
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Abstract

Abstract

En 中文
For precision medicine to reach its full potential for treatment of cancer and other diseases, protein variant effect prediction tools are needed to characterize variants of unknown significance (VUS) in a patient's genome with respect to their likelihood to influence treatment response and outcomes. However, the performance of most variant prediction tools is limited by the difficulty of acquiring sufficient training and validation data. To overcome these limitations, we applied an iterative active learning approach starting from available biochemical, evolutionary, and functional annotations. With active learning, VUS that are most challenging to classify by an initial machine learning model are functionally evaluated and then reincorporated with the phenotype information in subsequent iterations of algorithm training. The potential of active learning to improve variant interpretation was first demonstrated by applying it to synthetic and deep mutational scanning datasets for four cancer-relevant
Keywords:
NUCLEOTIDE EXCISION-REPAIR
COMPLEMENTATION GROUP-A
XERODERMA-PIGMENTOSUM
STRUCTURAL BASIS
MOLECULAR-BASIS
DNA-BINDING
XPA
PROTEIN
RECOGNITION
MUTATIONS

Journal

Cancer Research cover
Cancer Research
IF:
16.6
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10.9W
Citations:
11.9W

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Harvard University
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vanderbilt university
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University of California System cover
University of California System
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