Cheng, Haoyu
Harvard University · Dana-Farber Cancer Institute
9 papers on CoChatORCID 0000-0002-9209-5793
Most cited papers
- Verified
Haplotype-resolved de novo assembly using phased assembly graphs with hifiasm
Cheng, H., Concepcion, G. T., Feng, X., Zhang, H., & Li, H. (2021) · Nature Methods
Genomics and Phylogenetic StudiesGenomic variations and chromosomal abnormalities
Cited by 5,859
- 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
A draft human pangenome reference.
Liao, W.-W., Asri, M., Ebler, J., Doerr, D., Haukness, M., Hickey, G., Lu, S., Lucas, J. K., Monlong, J., Abel, H. J., et al. (2023) · Nature
Genomics and Phylogenetic StudiesGenomic variations and chromosomal abnormalities
Cited by 1,129
- Verified
Pangenome graph construction from genome alignments with Minigraph-Cactus
Hickey, G., Monlong, J., Ebler, J., Novak, A. M., Eizenga, J. M., Gao, Y., Human Pangenome Reference Consortium, Abel, H. J., Antonacci-Fulton, L. L., Asri, M., et al. (2024) · Nature Biotechnology
Genomics and Phylogenetic StudiesGenomic variations and chromosomal abnormalities
Cited by 343
- Verified
Curated variation benchmarks for challenging medically relevant autosomal genes
Wagner, J., Olson, N. D., Harris, L., McDaniel, J., Cheng, H., Fungtammasan, A., Hwang, Y.-C., Gupta, R., Wenger, A. M., Rowell, W. J., et al. (2022) · Nature Biotechnology
Genomics and Phylogenetic StudiesGenomics and Rare Diseases
Cited by 241
- Verified
Scalable telomere-to-telomere assembly for diploid and polyploid genomes with double graph
Cheng, H., Asri, M., Lucas, J., Koren, S., & Li, H. (2024) · Nature Methods
Genomics and Phylogenetic StudiesChromosomal and Genetic Variations
Cited by 222
- Verified
Semi-automated assembly of high-quality diploid human reference genomes
Jarvis, E. D., Formenti, G., Rhie, A., Guarracino, A., Yang, C., Wood, J., Tracey, A., Thibaud-Nissen, F., Vollger, M. R., Porubsky, D., et al. (2022) · Nature
Genomics and Phylogenetic StudiesGenomic variations and chromosomal abnormalities
Cited by 209
- Verified
Recombination between heterologous human acrocentric chromosomes
Guarracino, A., Buonaiuto, S., de Lima, L. G., Potapova, T., Rhie, A., Koren, S., Rubinstein, B., Fischer, C., Human Pangenome Reference Consortium, Abel, H. J., et al. (2023) · Nature
Chromosomal and Genetic VariationsGenomic variations and chromosomal abnormalities
Cited by 134
- Verified
Increased mutation and gene conversion within human segmental duplications
Vollger, M. R., Dishuck, P. C., Harvey, W. T., DeWitt, W. S., Guitart, X., Goldberg, M. E., Rozanski, A. N., Lucas, J., Asri, M., Human Pangenome Reference Consortium, et al. (2023) · Nature
Genomic variations and chromosomal abnormalitiesChromosomal and Genetic Variations
Cited by 104
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