Citation Export
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Jeon, Hyeonseong | - |
dc.contributor.author | Ahn, Junhak | - |
dc.contributor.author | Na, Byunggook | - |
dc.contributor.author | Hong, Soona | - |
dc.contributor.author | Sael, Lee | - |
dc.contributor.author | Kim, Sun | - |
dc.contributor.author | Yoon, Sungroh | - |
dc.contributor.author | Baek, Daehyun | - |
dc.date.issued | 2023-08-01 | - |
dc.identifier.uri | https://dspace.ajou.ac.kr/dev/handle/2018.oak/33561 | - |
dc.description.abstract | The detection of somatic DNA variants in tumor samples with low tumor purity or sequencing depth remains a daunting challenge despite numerous attempts to address this problem. In this study, we constructed a substantially extended set of actual positive variants originating from a wide range of tumor purities and sequencing depths, as well as actual negative variants derived from sequencer-specific sequencing errors. A deep learning model named AIVariant, trained on this extended dataset, outperforms previously reported methods when tested under various tumor purities and sequencing depths, especially low tumor purity and sequencing depth. | - |
dc.description.sponsorship | We express our gratitude to Sangho Park from Genome4me Inc. for valuable advice and fruitful discussions regarding software development and optimization for AIVariant. This study was supported by the National Research Foundation of Korea (NRF), funded by the Ministry of Science and ICT, Republic of Korea (NRF-2014M3C9A3063541, NRF-2019M3E5D3073104, NRF-2020R1A2C3007032, NRF-2020R1A5A1018081, and NRF-2022M3A9I2082294), by the Korea Health Industry Development Institute (KHIDI), funded by the Ministry of Health and Welfare, Republic of Korea (HI15C3224), and by KREONET (Korea Research Environment Open NETwork), managed and operated by KISTI (Korea Institute of Science and Technology Information). | - |
dc.language.iso | eng | - |
dc.publisher | Springer Nature | - |
dc.subject.mesh | Algorithms | - |
dc.subject.mesh | Computational Biology | - |
dc.subject.mesh | Deep Learning | - |
dc.subject.mesh | Gene Frequency | - |
dc.subject.mesh | Humans | - |
dc.subject.mesh | Mutation | - |
dc.subject.mesh | Neoplasms | - |
dc.title | AIVariant: a deep learning-based somatic variant detector for highly contaminated tumor samples | - |
dc.type | Article | - |
dc.citation.endPage | 1742 | - |
dc.citation.startPage | 1734 | - |
dc.citation.title | Experimental and Molecular Medicine | - |
dc.citation.volume | 55 | - |
dc.identifier.bibliographicCitation | Experimental and Molecular Medicine, Vol.55, pp.1734-1742 | - |
dc.identifier.doi | 10.1038/s12276-023-01049-2 | - |
dc.identifier.pmid | 37524869 | - |
dc.identifier.scopusid | 2-s2.0-85166178399 | - |
dc.identifier.url | https://www.nature.com/emm/ | - |
dc.description.isoa | true | - |
dc.subject.subarea | Biochemistry | - |
dc.subject.subarea | Molecular Medicine | - |
dc.subject.subarea | Molecular Biology | - |
dc.subject.subarea | Clinical Biochemistry | - |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.