The complete sequence of a human genome S Nurk, S Koren, A Rhie, M Rautiainen, AV Bzikadze, A Mikheenko, ... Science 376 (6588), 44-53, 2022 | 2378 | 2022 |
Major impacts of widespread structural variation on gene expression and crop improvement in tomato M Alonge, X Wang, M Benoit, S Soyk, L Pereira, L Zhang, H Suresh, ... Cell 182 (1), 145-161. e23, 2020 | 603 | 2020 |
Automated assembly scaffolding using RagTag elevates a new tomato system for high-throughput genome editing M Alonge, L Lebeigle, M Kirsche, K Jenike, S Ou, S Aganezov, X Wang, ... Genome biology 23 (1), 258, 2022 | 310 | 2022 |
A complete reference genome improves analysis of human genetic variation S Aganezov, SM Yan, DC Soto, M Kirsche, S Zarate, P Avdeyev, ... Science 376 (6588), eabl3533, 2022 | 284 | 2022 |
Paragraph: a graph-based structural variant genotyper for short-read sequence data S Chen, P Krusche, E Dolzhenko, RM Sherman, R Petrovski, ... Genome biology 20, 1-13, 2019 | 151 | 2019 |
Semi-automated assembly of high-quality diploid human reference genomes ED Jarvis, G Formenti, A Rhie, A Guarracino, C Yang, J Wood, A Tracey, ... Nature 611 (7936), 519-531, 2022 | 148 | 2022 |
Benchmarking challenging small variants with linked and long reads J Wagner, ND Olson, L Harris, Z Khan, J Farek, M Mahmoud, A Stankovic, ... Cell genomics 2 (5), 2022 | 142 | 2022 |
Comprehensive analysis of structural variants in breast cancer genomes using single-molecule sequencing S Aganezov, S Goodwin, RM Sherman, FJ Sedlazeck, G Arun, S Bhatia, ... Genome research 30 (9), 1258-1273, 2020 | 98 | 2020 |
Automated assembly scaffolding elevates a new tomato system for high-throughput genome editing M Alonge, L Lebeigle, M Kirsche, S Aganezov, X Wang, ZB Lippman, ... BioRxiv, 2021.11. 18.469135, 2021 | 96 | 2021 |
A diploid assembly-based benchmark for variants in the major histocompatibility complex CS Chin, J Wagner, Q Zeng, E Garrison, S Garg, A Fungtammasan, ... Nature communications 11 (1), 4794, 2020 | 62 | 2020 |
Jasmine and Iris: population-scale structural variant comparison and analysis M Kirsche, G Prabhu, R Sherman, B Ni, A Battle, S Aganezov, MC Schatz Nature methods 20 (3), 408-417, 2023 | 51 | 2023 |
Genomic diversity of SARS-CoV-2 during early introduction into the Baltimore–Washington metropolitan area PM Thielen, S Wohl, T Mehoke, S Ramakrishnan, M Kirsche, ... JCI insight 6 (6), 2021 | 33 | 2021 |
The EN-TEx resource of multi-tissue personal epigenomes & variant-impact models J Rozowsky, J Gao, B Borsari, YT Yang, T Galeev, G Gürsoy, CB Epstein, ... Cell 186 (7), 1493-1511. e40, 2023 | 31 | 2023 |
Jasmine: Population-scale structural variant comparison and analysis M Kirsche, G Prabhu, R Sherman, B Ni, S Aganezov, MC Schatz BioRxiv, 2021.05. 27.445886, 2021 | 27 | 2021 |
Sapling: accelerating suffix array queries with learned data models M Kirsche, A Das, MC Schatz Bioinformatics 37 (6), 744-749, 2021 | 23 | 2021 |
Genomic diversity of SARS-CoV-2 during early introduction into the United States National Capital Region PM Thielen, S Wohl, T Mehoke, S Ramakrishnan, M Kirsche, ... MedRxiv, 2020 | 14 | 2020 |
Multi-tissue integrative analysis of personal epigenomes J Rozowsky, J Drenkow, Y Yang, G Gursoy, T Galeev, B Borsari, ... BioRxiv, 2021 | 7 | 2021 |
A complete human reference genome improves variant calling for population and clinical genomics S Aganezov, SM Yan, DC Soto, M Kirsche, S Zarate, P Avdeyev, ... bioRxiv (to appear), 2021 | 4 | 2021 |
Democratizing long-read genome assembly M Kirsche, MC Schatz Cell Systems 12 (10), 945-947, 2021 | 3 | 2021 |
The human reference genome is finally complete DC Soto, M Kirsche, SM Yan, S Zarate TheScienceBreaker 9 (3), 2023 | | 2023 |