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| Nonhybrid, finished microbial genome assemblies from long-read SMRT sequencing data CS Chin, DH Alexander, P Marks, AA Klammer, J Drake, C Heiner, ... Nature methods 10 (6), 563-569, 2013 | 4255 | 2013 |
| Haplotyping germline and cancer genomes with high-throughput linked-read sequencing GXY Zheng, BT Lau, M Schnall-Levin, M Jarosz, JM Bell, CM Hindson, ... Nature biotechnology 34 (3), 303-311, 2016 | 815 | 2016 |
| Multi-platform discovery of haplotype-resolved structural variation in human genomes MJP Chaisson, AD Sanders, X Zhao, A Malhotra, D Porubsky, T Rausch, ... Nature communications 10 (1), 1784, 2019 | 750 | 2019 |
| Extensive sequencing of seven human genomes to characterize benchmark reference materials JM Zook, D Catoe, J McDaniel, L Vang, N Spies, A Sidow, Z Weng, Y Liu, ... Scientific data 3 (1), 1-26, 2016 | 663 | 2016 |
| Selective aluminum passivation for targeted immobilization of single DNA polymerase molecules in zero-mode waveguide nanostructures J Korlach, PJ Marks, RL Cicero, JJ Gray, DL Murphy, DB Roitman, ... Proceedings of the National Academy of Sciences 105 (4), 1176-1181, 2008 | 361 | 2008 |
| The electromechanics of DNA in a synthetic nanopore JB Heng, A Aksimentiev, C Ho, P Marks, YV Grinkova, S Sligar, ... Biophysical journal 90 (3), 1098-1106, 2006 | 279 | 2006 |
| A hybrid approach for de novo human genome sequence assembly and phasing Y Mostovoy, M Levy-Sakin, J Lam, ET Lam, AR Hastie, P Marks, J Lee, ... Nature methods 13 (7), 587-590, 2016 | 250 | 2016 |
| Stretching DNA using the electric field in a synthetic nanopore JB Heng, A Aksimentiev, C Ho, P Marks, YV Grinkova, S Sligar, ... Nano letters 5 (10), 1883-1888, 2005 | 241 | 2005 |
| Resolving the full spectrum of human genome variation using Linked-Reads P Marks, S Garcia, AM Barrio, K Belhocine, J Bernate, R Bharadwaj, ... Genome research 29 (4), 635-645, 2019 | 205 | 2019 |
| Methods and processes for calling bases in sequence by incorporation methods AB Tomaney, KM Maxham, D Holden, K Hester, D Murphy, P Marks US Patent 8,182,993, 2012 | 205 | 2012 |
| HLA typing for the next generation NP Mayor, J Robinson, AJM McWhinnie, S Ranade, K Eng, W Midwinter, ... PloS one 10 (5), e0127153, 2015 | 184 | 2015 |
| Analysis of nucleic acid sequences M Schnall-Levin, M Jarosz, C Hindson, K Ness, S Saxonov, B Hindson, ... US Patent App. 14/752,589, 2015 | 163 | 2015 |
| Systems and methods for determining structural variation and phasing using variant call data S Kyriazopoulou-Panagiotopoulou, P Marks, M Schnall-Levin, X Zheng, ... US Patent 10,854,315, 2020 | 126 | 2020 |
| Methods for identifying nucleic acid modifications B Flusberg, J Korlach, J Wegener, TA Clark, I Vilfan, A Kislyuk, S Turner, ... US Patent 9,175,338, 2015 | 109 | 2015 |
| 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 | 93 | 2019 |
| Algorithms for sequence determination J Sorenson, S Tang, P Marks, C Chen-Shan US Patent 8,370,079, 2013 | 92 | 2013 |
| Systems, methods, and media for de novo assembly of whole genome sequence data D Jaffe, P Marks, M Schnall-Levin, N Weisenfeld US Patent 11,081,208, 2021 | 87 | 2021 |
| Analysis of nucleic acid sequences M Schnall-Levin, M Jarosz, C Hindson, K Ness, S Saxonov, B Hindson, ... US Patent App. 15/985,388, 2018 | 74 | 2018 |
| Intermittent detection during analytical reactions KM Maxham, J Sorenson, J Eid, P Marks, K Travers US Patent 8,143,030, 2012 | 70 | 2012 |
