Taylor-Weiner A, Stewart C, Giordano T, et al. DeTiN: overcoming tumor-in-normal contamination. Nat Methods. 2018;15(7):531-534. doi:10.1038/s41592-018-0036-9.

Yu L, Dawe RJ, Boyle PA, et al. Association Between Brain Gene Expression, DNA Methylation, and Alteration of Ex Vivo Magnetic Resonance Imaging Transverse Relaxation in Late-Life Cognitive Decline. JAMA Neurol. 2017;74(12):1473-1480. doi:10.1001/jamaneurol.2017.2807.

Dong Z, Ye L, Yang Z, et al. Balanced Chromosomal Rearrangement Detection by Low-Pass Whole-Genome Sequencing. Curr Protoc Hum Genet. 2018;96:8.18.1-8.18.16. doi:10.1002/cphg.51.

Reizel Y, Sabag O, Skversky Y, et al. Postnatal DNA demethylation and its role in tissue maturation. Nat Commun. 2018;9(1):2040. doi:10.1038/s41467-018-04456-6.

Chiu H-S, Martínez MR, Bansal M, et al. High-throughput validation of ceRNA regulatory networks. BMC Genomics. 2017;18(1):418. doi:10.1186/s12864-017-3790-7.

Lau JW, Kim Y-I, Murphy R, et al. Deep sequencing of RSV from an adult challenge study and from naturally infected infants reveals heterogeneous diversification dynamics. Virology. 2017;510:289-296. doi:10.1016/j.virol.2017.07.017.

Weiss ER, Lamers SL, Henderson JL, et al. Early Epstein-Barr Virus Genomic Diversity and Convergence toward the B95.8 Genome in Primary Infection. J Virol. 2018;92(2). doi:10.1128/JVI.01466-17.

Amamoto R, Zuccaro E, Curry NC, et al. FIN-Seq: transcriptional profiling of specific cell types from frozen archived tissue of the human central nervous system. Nucleic Acids Res. 2020;48(1):e4. doi:10.1093/nar/gkz968.

Marshall JL, Doughty BR, Subramanian V, et al. HyPR-seq: Single-cell quantification of chosen RNAs via hybridization and sequencing of DNA probes. Proc Natl Acad Sci U S A. 2020;117(52):33404-33413. doi:10.1073/pnas.2010738117.

Matranga CB, Gladden-Young A, Qu J, et al. Unbiased Deep Sequencing of RNA Viruses from Clinical Samples. J Vis Exp. 2016;(113). doi:10.3791/54117.