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Amrita Chattopadhyay
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2020 – today
- 2024
- [j9]Han-Ching Chan, Amrita Chattopadhyay, Tzu-Pin Lu:
Cross-population enhancement of PrediXcan predictions with a gnomAD-based east Asian reference framework. Briefings Bioinform. 25(6) (2024) - 2023
- [j8]Amrita Chattopadhyay, Chien-Yueh Lee, Ying-Cheng Shen, Kuan-Chen Lu, Tzu-Hung Hsiao, Ching-Heng Lin, Liang-Chuan Lai, Mong-Hsun Tsai, Tzu-Pin Lu, Eric Y. Chuang:
Multi-ethnic Imputation System (MI-System): A genotype imputation server for high-dimensional data. J. Biomed. Informatics 143: 104423 (2023) - 2022
- [j7]Untari Novia Wisesty, Ayu Purwarianti, Adi Pancoro, Amrita Chattopadhyay, Nam Nhut Phan, Eric Y. Chuang, Tati Rajab Mengko:
Join Classifier of Type and Index Mutation on Lung Cancer DNA Using Sequential Labeling Model. IEEE Access 10: 9004-9021 (2022) - [j6]Amrita Chattopadhyay, Ching-Yu Shih, Yu-Chen Hsu, Jyh-Ming Jimmy Juang, Eric Y. Chuang, Tzu-Pin Lu:
CLIN_SKAT: an R package to conduct association analysis using functionally relevant variants. BMC Bioinform. 23(1): 441 (2022) - 2021
- [j5]Nam Nhut Phan, Amrita Chattopadhyay, Tsui-Ting Lee, Hsiang-I Yin, Tzu-Pin Lu, Liang-Chuan Lai, Hsiao-Lin Hwa, Mong-Hsun Tsai, Eric Y. Chuang:
High-performance deep learning pipeline predicts individuals in mixtures of DNA using sequencing data. Briefings Bioinform. 22(6) (2021) - [j4]Amrita Chattopadhyay, Zi Han Teoh, Chi-Yun Wu, Jyh-Ming Jimmy Juang, Liang-Chuan Lai, Mong-Hsun Tsai, Chia-Hsin Wu, Tzu-Pin Lu, Eric Y. Chuang:
CNVIntegrate: the first multi-ethnic database for identifying copy number variations associated with cancer. Database J. Biol. Databases Curation 2021 (2021) - [j3]Ching-Yu Shih, Amrita Chattopadhyay, Chien-Hui Wu, Yu-Wen Tien, Tzu-Pin Lu:
Transcript annotation tool (TransAT): an R package for retrieving annotations for transcript-specific genetic variants. BMC Bioinform. 22(1): 350 (2021)
2010 – 2019
- 2019
- [j2]Chien-Yueh Lee, Amrita Chattopadhyay, Li-Mei Chiang, Jyh-Ming Jimmy Juang, Liang-Chuan Lai, Mong-Hsun Tsai, Tzu-Pin Lu, Eric Y. Chuang:
VariED: the first integrated database of gene annotation and expression profiles for variants related to human diseases. Database J. Biol. Databases Curation 2019: baz075 (2019) - 2016
- [j1]Amrita Sengupta Chattopadhyay, Ying-Chao Lin, Ai-Ru Hsieh, Chien-Ching Chang, Ie-Bin Lian, Cathy S. J. Fann:
Using propensity score adjustment method in genetic association studies. Comput. Biol. Chem. 62: 1-11 (2016)
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