The diploid genome sequence of an individual human S Levy, G Sutton, PC Ng, L Feuk, AL Halpern, BP Walenz, N Axelrod, ... PLoS biology 5 (10), e254, 2007 | 2340 | 2007 |
Origins and functional impact of copy number variation in the human genome DF Conrad, D Pinto, R Redon, L Feuk, O Gokcumen, Y Zhang, J Aerts, ... Nature 464 (7289), 704-712, 2010 | 2296 | 2010 |
Multi-platform discovery of haplotype-resolved structural variation in human genomes Nature Communications, 2019 | 828 | 2019 |
The axolotl genome and the evolution of key tissue formation regulators S Nowoshilow, S Schloissnig, JF Fei, A Dahl, AWC Pang, M Pippel, ... Nature 554 (7690), 50-55, 2018 | 564 | 2018 |
Assembly and diploid architecture of an individual human genome via single-molecule technologies Nature Methods 12 (8), 780-786, 2015 | 541 | 2015 |
Towards a comprehensive structural variation map of an individual human genome AW Pang, JR MacDonald, D Pinto, J Wei, MA Rafiq, DF Conrad, H Park, ... | 406 | 2010 |
High-resolution comparative analysis of great ape genomes ZN Kronenberg, IT Fiddes, D Gordon, S Murali, S Cantsilieris, ... Science 360 (6393), 2018 | 385 | 2018 |
Genome-Wide Structural Variation Detection by Genome Mapping on Nanochannel Arrays Genetics 202 (1), 351362, 2016 | 153* | 2016 |
Whole Genome Mutational Burden Analysis of Three Pluripotency Induction Methods K Bhutani, K Nazor, R Williams, H Tran, H Dai, Z Dzakula, E Cho, ... Nature Communications, 2016 | 131 | 2016 |
Haplotype-resolved genomes provide insights into structural variation and gene content in Angus and Brahman cattle WY Low, R Tearle, R Liu, S Koren, A Rhie, DM Bickhart, BD Rosen, ... Nature communications 11 (1), 2071, 2020 | 118 | 2020 |
Human-specific tandem repeat expansion and differential gene expression during primate evolution A Sulovari, R Li, PA Audano, D Porubsky, MR Vollger, GA Logsdon, ... Proceedings of the National Academy of Sciences 116 (46), 23243-23253, 2019 | 104 | 2019 |
Combination of short-read, long-read, and optical mapping assemblies reveals large-scale tandem repeat arrays with population genetic implications MH Weissensteiner, AWC Pang, I Bunikis, I Höijer, O Vinnere-Petterson, ... Genome research 27 (5), 697-708, 2017 | 101 | 2017 |
A high-quality bonobo genome refines the analysis of hominid evolution Y Mao, CR Catacchio, LDW Hillier, D Porubsky, R Li, A Sulovari, ... Nature 594 (7861), 77-81, 2021 | 66 | 2021 |
SIMPROT: using an empirically determined indel distribution in simulations of protein evolution A Pang, AD Smith, PAS Nuin, ERM Tillier BMC bioinformatics 6, 1-7, 2005 | 58 | 2005 |
Mechanisms of formation of structural variation in a fully sequenced human genome AWC Pang, O Migita, JR MacDonald, L Feuk, SW Scherer Human mutation 34 (2), 345-354, 2013 | 49 | 2013 |
Performance of high-throughput sequencing for the discovery of genetic variation across the complete size spectrum AWC Pang, JR MacDonald, RKC Yuen, VM Hayes, SW Scherer G3: Genes, Genomes, Genetics 4 (1), 63-65, 2014 | 38 | 2014 |
Rapid automated large structural variation detection in a diploid genome by nanochannel based next-generation mapping AR Hastie, ET Lam, AWC Pang, LX Zhang, W Andrews, J Lee, TY Liang, ... BioRxiv, 102764, 2017 | 36 | 2017 |
Identification of somatic structural variants in solid tumors by optical genome mapping DY Goldrich, B LaBarge, S Chartrand, L Zhang, HB Sadowski, Y Zhang, ... Journal of Personalized Medicine 11 (2), 142, 2021 | 29 | 2021 |
A multi-platform reference for somatic structural variation detection JE Valle-Inclan, NJM Besselink, E de Bruijn, DL Cameron, J Ebler, ... Cell Genomics 2 (6), 2022 | 26 | 2022 |
Genomic inversions and GOLGA core duplicons underlie disease instability at the 15q25 locus FAM Maggiolini, S Cantsilieris, P D’Addabbo, M Manganelli, BP Coe, ... PLoS Genetics 15 (3), e1008075, 2019 | 24 | 2019 |