Peluso, Paul
Pacific Biosciences (United States)
4 papers on CoChatORCID 0000-0002-9723-5185
Most cited papers
- Verified
Real-Time DNA Sequencing from Single Polymerase Molecules
Eid, J., Fehr, A., Gray, J., Luong, K., Lyle, J., Otto, G., Peluso, P., Rank, D., Baybayan, P., Bettman, B., et al. (2009) · Science
DNA and Nucleic Acid ChemistryAdvanced Fluorescence Microscopy Techniques
Cited by 3,732
- Verified
The complete sequence of a human genome
Nurk, S., Koren, S., Rhie, A., Rautiainen, M., Bzikadze, A. V., Mikheenko, A., Vollger, M. R., Altemose, N., Uralsky, L., Gershman, A., et al. (2022) · Science
Genomics and Phylogenetic StudiesGenomic variations and chromosomal abnormalities
Cited by 3,136
- Verified
Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genome
Wenger, A. M., Peluso, P., Rowell, W. J., Chang, P.-C., Hall, R. J., Concepcion, G. T., Ebler, J., Fungtammasan, A., Kolesnikov, A., Olson, N. D., et al. (2019) · Nature Biotechnology
Genomics and Phylogenetic StudiesGenomic variations and chromosomal abnormalities
Cited by 1,841
- Verified
Evaluation of GRCh38 and de novo haploid genome assemblies demonstrates the enduring quality of the reference assembly
Schneider, V. A., Graves-Lindsay, T., Howe, K., Bouk, N., Chen, H.-C., Kitts, P. A., Murphy, T. D., Pruitt, K. D., Thibaud-Nissen, F., Albracht, D., et al. (2017) · Genome Research
Genomics and Phylogenetic StudiesGenomic variations and chromosomal abnormalities
Cited by 1,193
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