| PhISCS: a combinatorial approach for subperfect tumor phylogeny reconstruction via integrative use of single-cell and bulk sequencing data S Malikic, FR Mehrabadi, S Ciccolella, MK Rahman, C Ricketts, ... Genome research 29 (11), 1860-1877, 2019 | 94 | 2019 |
| CoLoRMap: correcting long reads by mapping short reads E Haghshenas, F Hach, SC Sahinalp, C Chauve Bioinformatics 32 (17), i545-i551, 2016 | 71 | 2016 |
| HASLR: fast hybrid assembly of long reads E Haghshenas, H Asghari, J Stoye, C Chauve, F Hach Iscience 23 (8), 2020 | 59 | 2020 |
| Creating discriminative models for time series classification and clustering by HMM ensembles N Asadi, A Mirzaei, E Haghshenas IEEE transactions on cybernetics 46 (12), 2899-2910, 2015 | 31 | 2015 |
| lordFAST: sensitive and fast alignment search tool for long noisy read sequencing data E Haghshenas, SC Sahinalp, F Hach Bioinformatics 35 (1), 20-27, 2019 | 24 | 2019 |
| Introducing a new intelligent adaptive learning content generation method E Haghshenas, A Mazaheri, A Gholipour, M Tavakoli, N Zandi, ... The Second International Conference on E-Learning and E-Teaching (ICELET …, 2010 | 20 | 2010 |
| CircMiner: accurate and rapid detection of circular RNA through splice-aware pseudo-alignment scheme H Asghari, YY Lin, Y Xu, E Haghshenas, CC Collins, F Hach Bioinformatics 36 (12), 3703-3711, 2020 | 15 | 2020 |
| Genotyping and copy number analysis of immunoglobin heavy chain variable genes using long reads M Ford, E Haghshenas, CT Watson, SC Sahinalp Iscience 23 (3), 2020 | 14 | 2020 |
| LRCstats, a tool for evaluating long reads correction methods S La, E Haghshenas, C Chauve Bioinformatics 33 (22), 3652-3654, 2017 | 11 | 2017 |
| Multiple Observations HMM Learning by Aggregating Ensemble Models N Asadi, A Mirzaei, E Haghshenas Signal Processing, IEEE Transactions on 61 (22), 5767-5776, 2013 | 6 | 2013 |
| Genotyping and copy number analysis of immunoglobulin heavy chain variable genes using long reads M Ford, E Haghshenas, CT Watson, SC Sahinalp Iscience 23 (9), 2020 | 4 | 2020 |
| SAGE2: parallel human genome assembly M Molnar, E Haghshenas, L Ilie Bioinformatics 34 (4), 678-680, 2018 | 4 | 2018 |
| An intelligent method for customizable adaptive learning content generation E Haghshenas, A Mazaheri, A Gholipour, M Tavakoli International Journal of Information and Communication Technology Research 3 …, 2011 | 2 | 2011 |
| Novel expression biomarkers via prediction of response to FOLFIRINOX (FFX) treatment for PDAC H Asghari, E Haghshenas, R Thomas, E Schultz, R Patro, S Skrzypczak, ... Cancer Research 83 (7_Supplement), 1400-1400, 2023 | 1 | 2023 |
| Development of a methylation-based, tissue-agnostic test for the detection of molecular residual disease by circulating tumor DNA. JPYC Shen, J Reiter, J Babiarz, P Srinivasan, F Lu, E Haghshenas, ... Journal of Clinical Oncology 43 (4_suppl), 266-266, 2025 | | 2025 |
| Performance of a blood-based screening test for the early detection of colorectal cancer. Y Nakamura, J Reiter, J Babiarz, P Srinivasan, E Haghshenas, TC Chen, ... Journal of Clinical Oncology 43 (4_suppl), 232-232, 2025 | | 2025 |
| Circulating differential methylation allele fraction (DMAF) strongly correlates with circulating tumor DNA (ctDNA) variant allele fraction (VAF) P Srinivasan, TC Chen, E Haghshenas, M Kordi, I Tunc, W Chan, ... Cancer Research 84 (6_Supplement), 2409-2409, 2024 | | 2024 |
| Computational methods for analysis of single molecule sequencing data E Haghshenas Simon Fraser University, 2020 | | 2020 |
| Accurate single individual haplotyping based on HuRef dataset using HapSAT algorithm E Haghshenas, N Barjaste, SR Mousavi International Journal of Functional Informatics and Personalised Medicine 4 …, 2014 | | 2014 |
| New algorithms for structural variation detection by de novo genome assembly E Haghshenas The University of Western Ontario, 2013 | | 2013 |
Faraz HachAssistant Professor at University of British ColumbiaПідтверджена електронна адреса в ubc.ca