McGarrity S, Ziehr DR, Austin-Tse CA, Wein MN, Chivukula RR, Oldham WM. Exercise Intolerance and Low Cardiac Filling Pressures in a Woman With a Novel eNOS Mutation. Circulation. Genomic and precision medicine. 2024:e004741. doi:10.1161/CIRCGEN.124.004741DOIGoogle ScholarPubMed
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.aas9824DOIGoogle ScholarPubMed
Schloss PD, Gevers D, Westcott SL. Reducing the effects of PCR amplification and sequencing artifacts on 16S rRNA-based studies. PLoS One. 2011;6(12):e27310. doi:10.1371/journal.pone.0027310DOIGoogle ScholarPubMed
Costello M, Pugh TJ, Fennell TJ, et al. Discovery and characterization of artifactual mutations in deep coverage targeted capture sequencing data due to oxidative DNA damage during sample preparation. Nucleic Acids Res. 2013;41(6):e67. doi:10.1093/nar/gks1443DOIGoogle ScholarPubMed
Adiconis X, Borges-Rivera D, Satija R, et al. Comparative analysis of RNA sequencing methods for degraded or low-input samples. Nat Methods. 2013;10(7):623-9. doi:10.1038/nmeth.2483DOIGoogle ScholarPubMed
Lawrence MS, Stojanov P, Polak P, et al. Mutational heterogeneity in cancer and the search for new cancer-associated genes. Nature. 2013;499(7457):214-218. doi:10.1038/nature12213DOIGoogle ScholarPubMed
Li H. Toward better understanding of artifacts in variant calling from high-coverage samples. Bioinformatics. 2014;30(20):2843-51. doi:10.1093/bioinformatics/btu356DOIGoogle ScholarPubMed
Uhlmann V, Singh S, Carpenter AE. CP-CHARM: segmentation-free image classification made accessible. BMC Bioinformatics. 2016;17:51. doi:10.1186/s12859-016-0895-yDOIGoogle ScholarPubMed
Moses AM, Chiang DY, Kellis M, Lander ES, Eisen MB. Position specific variation in the rate of evolution in transcription factor binding sites. BMC Evol Biol. 2003;3:19. doi:10.1186/1471-2148-3-19DOIGoogle ScholarPubMed