| Targeted sequencing reveals complex, phenotype-correlated genotypes in cystic fibrosis M Ivanov, A Matsvay, O Glazova, S Krasovskiy, M Usacheva, E Amelina, ... BMC medical genomics 11, 21-32, 2018 | 34 | 2018 |
| Sensitive alignment using paralogous sequence variants improves long-read mapping and variant calling in segmental duplications T Prodanov, V Bansal Nucleic acids research 48 (19), e114, 2020 | 15 | 2020 |
| Robust and accurate estimation of paralog-specific copy number for duplicated genes using whole-genome sequencing T Prodanov, V Bansal Nature Communications 13 (1), 3221, 2022 | 7 | 2022 |
| Long-read sequencing and structural variant characterization in 1,019 samples from the 1000 Genomes Project S Schloissnig, S Pani, B Rodriguez-Martin, J Ebler, C Hain, V Tsapalou, ... bioRxiv, 2024 | | 2024 |
| Structural and genetic diversity in the secreted mucins, MUC5AC and MUC5B EG Plender, T Prodanov, PH Hsieh, E Nizamis, WT Harvey, A Sulovari, ... bioRxiv, 2024.03. 18.585560, 2024 | | 2024 |
| A multilocus approach for accurate variant calling in low-copy repeats using whole-genome sequencing T Prodanov, V Bansal Bioinformatics 39 (Supplement_1), i279-i287, 2023 | | 2023 |
| Read Mapping, Variant Calling, and Copy Number Variation Detection in Segmental Duplications T Prodanov University of California, San Diego, 2022 | | 2022 |
| Haplotyping Long Reads Containing SNVs and Tandem Repeats M Bakhtiari, A Bzikadze, T Prodanov, I Mitra | | 2018 |
| Randomized algorithms with adaptive tuning of parameters for detecting communities in graphs N Amelina, O Granichin, O Granichina, I Kirianovskii, T Prodanov 2016 IEEE 55th Conference on Decision and Control (CDC), 6222-6227, 2016 | | 2016 |
