Byrska-Bishop M, Evani US, Zhao X, et al. High-coverage whole-genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios. Cell. 2022;185(18):3426-3440.e19. doi:10.1016/j.cell.2022.08.004.
Currall BB, Antolik CW, Collins RL, Talkowski ME. Next Generation Sequencing of Prenatal Structural Chromosomal Rearrangements Using Large-Insert Libraries. Methods Mol Biol. 2019;1885:251-265. doi:10.1007/978-1-4939-8889-1_17.
Brody Y, Kimmerling RJ, Maruvka YE, et al. Quantification of somatic mutation flow across individual cell division events by lineage sequencing. Genome Res. 2018;28(12):1901-1918. doi:10.1101/gr.238543.118.
Li B, Gould J, Yang Y, et al. Cumulus provides cloud-based data analysis for large-scale single-cell and single-nucleus RNA-seq. Nat Methods. 2020;17(8):793-798. doi:10.1038/s41592-020-0905-x.
D'Gama AM, Walsh CA. Somatic mosaicism and neurodevelopmental disease. Nat Neurosci. 2018;21(11):1504-1514. doi:10.1038/s41593-018-0257-3.
Salmén F, Ståhl PL, Mollbrink A, et al. Barcoded solid-phase RNA capture for Spatial Transcriptomics profiling in mammalian tissue sections. Nat Protoc. 2018;13(11):2501-2534. doi:10.1038/s41596-018-0045-2.
Ranu N, Villani A-C, Hacohen N, Blainey PC. Targeting individual cells by barcode in pooled sequence libraries. Nucleic Acids Res. 2019;47(1):e4. doi:10.1093/nar/gky856.
Chung M, Bruno VM, Rasko DA, et al. Best practices on the differential expression analysis of multi-species RNA-seq. Genome Biol. 2021;22(1):121. doi:10.1186/s13059-021-02337-8.
Stewart C, Leshchiner I, Hess J, Getz G. Comment on "DNA damage is a pervasive cause of sequencing errors, directly confounding variant identification". Science. 2018;361(6409). doi:10.1126/science.aas9824.
Hart R, Biesecker BB, Blout CL, et al. Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study. Genet Med. 2019;21(5):1100-1110. doi:10.1038/s41436-018-0308-x.