Audano, Peter A.
University of Washington
7 papers on CoChatORCID 0000-0002-5187-0415
Most cited papers
- Verified
Multi-platform discovery of haplotype-resolved structural variation in human genomes
Chaisson, M. J. P., Sanders, A. D., Zhao, X., Malhotra, A., Porubsky, D., Rausch, T., Gardner, E. J., Rodriguez, O. L., Guo, L., Collins, R. L., et al. (2019) · Nature Communications
Genomic variations and chromosomal abnormalitiesGenomics and Phylogenetic Studies
Cited by 891
- Verified
Haplotype-resolved diverse human genomes and integrated analysis of structural variation
Ebert, P., Audano, P. A., Zhu, Q., Rodriguez-Martin, B., Porubsky, D., Bonder, M. J., Sulovari, A., Ebler, J., Zhou, W., Serra Mari, R., et al. (2021) · Science
Genomic variations and chromosomal abnormalitiesGenomics and Phylogenetic Studies
Cited by 702
- Verified
Characterizing the Major Structural Variant Alleles of the Human Genome
Audano, P. A., Sulovari, A., Graves-Lindsay, T. A., Cantsilieris, S., Sorensen, M., Welch, A. E., Dougherty, M. L., Nelson, B. J., Shah, A., Dutcher, S. K., et al. (2019) · Cell
Genomic variations and chromosomal abnormalitiesGenome Rearrangement Algorithms
Cited by 492
- Verified
Pangenome-based genome inference allows efficient and accurate genotyping across a wide spectrum of variant classes
Ebler, J., Ebert, P., Clarke, W. E., Rausch, T., Audano, P. A., Houwaart, T., Mao, Y., Korbel, J. O., Eichler, E. E., Zody, M. C., et al. (2022) · Nature Genetics
Genomics and Phylogenetic StudiesGenomic variations and chromosomal abnormalities
Cited by 277
- Verified
Fully phased human genome assembly without parental data using single-cell strand sequencing and long reads
Human Genome Structural Variation Consortium, Porubsky, D., Ebert, P., Audano, P. A., Vollger, M. R., Harvey, W. T., Marijon, P., Ebler, J., Munson, K. M., Sorensen, M., et al. (2021) · Nature Biotechnology
Genomics and Phylogenetic StudiesGenomic variations and chromosomal abnormalities
Cited by 203
- Verified
Expectations and blind spots for structural variation detection from long-read assemblies and short-read genome sequencing technologies
Zhao, X., Collins, R. L., Lee, W.-P., Weber, A. M., Jun, Y., Zhu, Q., Weisburd, B., Huang, Y., Audano, P. A., Wang, H., et al. (2021) · The American Journal of Human Genetics
Genomic variations and chromosomal abnormalitiesGenomics and Rare Diseases
Cited by 132
- Verified
Structurally divergent and recurrently mutated regions of primate genomes
Mao, Y., Harvey, W. T., Porubsky, D., Munson, K. M., Hoekzema, K., Lewis, A. P., Audano, P. A., Rozanski, A., Yang, X., Zhang, S., et al. (2023) · Cell
Genomic variations and chromosomal abnormalitiesChromosomal and Genetic Variations
Cited by 73
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