| The complete sequence of a human genome S Nurk, S Koren, A Rhie, M Rautiainen, AV Bzikadze, A Mikheenko, ... bioRxiv, 2021 | 49 | 2021 |
| Parliament2: Fast Structural Variant Calling Using Optimized Combinations of Callers S Zarate, A Carroll, O Krasheninina, FJ Sedlazeck, G Jun, W Salerno, ... bioRxiv, 424267, 2018 | 21 | 2018 |
| 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), 1-9, 2020 | 19 | 2020 |
| Benchmarking challenging small variants with linked and long reads J Wagner, ND Olson, L Harris, Z Khan, J Farek, M Mahmoud, A Stankovic, ... BioRxiv, 2020 | 16 | 2020 |
| Parliament2: Accurate structural variant calling at scale S Zarate, A Carroll, M Mahmoud, O Krasheninina, G Jun, WJ Salerno, ... GigaScience 9 (12), giaa145, 2020 | 13 | 2020 |
| Multiethnic catalog of structural variants and their translational impact for disease phenotypes across 19,652 genomes FJ Sedlazeck, B Yu, AJ Mansfield, H Chen, O Krasheninina, A Tin, Q Qi, ... bioRxiv, 2020 | 1 | 2020 |
| Hidden biases in germline structural variant detection MM Khayat, SME Sahraeian, S Zarate, A Carroll, H Hong, B Pan, L Shi, ... Genome biology 22 (1), 1-15, 2021 | | 2021 |
| A complete reference genome improves analysis of human genetic variation S Aganezov, SM Yan, DC Soto, M Kirsche, S Zarate, P Avdeyev, ... bioRxiv, 2021 | | 2021 |
Fritz J SedlazeckHuman Genome Sequencing Center, Baylor College of Medicine, One Baylor Plaza, Houston TX 77030Verified email at bcm.edu
