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Science (New York, N.Y.)|April 2, 2016
Long-read sequence assembly of the gorilla genomeDavid Gordon, John Huddleston, Mark J P Chaisson, et al.Science (New York, N.Y.)|October 19, 2019
Adaptive archaic introgression of copy number variants and the discovery of previously unknown human genesPingHsun Hsieh, Mitchell R Vollger, Vy Dang, et al.Nature Communications|May 1, 2020
Haplotype-resolved genomes provide insights into structural variation and gene content in Angus and Brahman cattleWai Yee Low, Rick Tearle, Ruijie Liu, et al.Nature Communications|April 29, 2021
Extended haplotype-phasing of long-read de novo genome assemblies using Hi-CZev N Kronenberg, Arang Rhie, Sergey Koren, et al.Cell|February 9, 2019
Establishing Cerebral Organoids as Models of Human-Specific Brain EvolutionAlex A Pollen, Aparna Bhaduri, Madeline G Andrews, et al.Nature Communications|November 9, 2016
De novo genic mutations among a Chinese autism spectrum disorder cohortTianyun Wang, Hui Guo, Bo Xiong, et al.Science (New York, N.Y.)|June 9, 2018
High-resolution comparative analysis of great ape genomesZev N Kronenberg, Ian T Fiddes, David Gordon, et al.Biorxiv : the Preprint Server for Biology|August 16, 2024
A familial, telomere-to-telomere reference for human de novo mutation and recombination from a four-generation pedigreeDavid Porubsky, Harriet Dashnow, Thomas A Sasani, et al.Nature|April 24, 2025
Human de novo mutation rates from a four-generation pedigree referenceDavid Porubsky, Harriet Dashnow, Thomas A Sasani, et al.Nature Communications|April 18, 2019
Multi-platform discovery of haplotype-resolved structural variation in human genomesMark J P Chaisson, Ashley D Sanders, Xuefang Zhao, et al.Pageof 2