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Patrick Marks
Patrick Marks
10x Genomics
Verified email at 10xgenomics.com
Title
Cited by
Cited by
Year
Real-time DNA sequencing from single polymerase molecules
J Eid, A Fehr, J Gray, K Luong, J Lyle, G Otto, P Peluso, D Rank, ...
Science 323 (5910), 133-138, 2009
41882009
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
38442013
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
7052016
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
5752019
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
5272016
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
3372008
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
2752006
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
2402016
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
2372005
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
1772012
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
1612019
HLA typing for the next generation
NP Mayor, J Robinson, AJM McWhinnie, S Ranade, K Eng, W Midwinter, ...
PloS one 10 (5), e0127153, 2015
1602015
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
1212015
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
942015
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
812020
Algorithms for sequence determination
J Sorenson, S Tang, P Marks, C Chen-Shan
US Patent 8,370,079, 2013
772013
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
652019
Intermittent detection during analytical reactions
KM Maxham, J Sorenson, J Eid, P Marks, K Travers
US Patent 8,143,030, 2012
652012
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
642018
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
602021
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