Detecting ultralow-frequency mutations by Duplex Sequencing

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Items 201–300 of 462

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2. Assessing the genotoxicity of N‐nitrosodiethylamine with three in vivo endpoints in male Big Blue® transgenic and wild‐type C57BL/6N mice
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3. A high-resolution landscape of mutations in the BCL6 super-enhancer in normal human B cells
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4. Detection of Low-Frequency Mutations and Identification of Heat-Induced Artifactual Mutations Using Duplex Sequencing
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5. Clinical impact of circulating tumor DNA to track minimal residual disease in colorectal cancer patients. Hopes and limitations
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6. Effects of urban-induced mutations on ecology, evolution and health
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7. Mitochondrial mutations in Caenorhabditis elegans show signatures of oxidative damage and an AT-bias
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8. Decreased mitochondrial mutagenesis during transformation of breast stem cells into tumorigenic cells
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9. Origins of Second Malignancies in Children and Mutational Footprint of Chemotherapy in Normal Tissues
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10. Moving toward a conceptualization of measurable residual disease in myelodysplastic syndromes
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11. A quantification method of somatic mutations in normal tissues and their accumulation in pediatric patients with chemotherapy
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13. The promise of toxicogenomics for genetic toxicology: past, present and future
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14. The stochastic nature of errors in next-generation sequencing of circulating cell-free DNA
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15. Extracellular vesicles and ctDNA in lung cancer: biomarker sources and therapeutic applications
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16. Bioinformatics Analysis for Cell-Free Tumor DNA Sequencing Data.
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17. Circulating tumor DNA determinants of response and outcome in relapsed/refractory mantle cell lymphoma
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18. Alignment between Duplex Sequencing and transgenic rodent mutation assay data in the assessment of in vivo NDMA-induced mutagenesis
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19. Genome-wide direct quantification of in vivo mutagenesis using high-accuracy paired-end and complementary consensus sequencing
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20. Adopting Duplex Sequencing Technology for Genetic Toxicity Testing: A Proof-of-Concept Mutagenesis Experiment with N-Ethyl-N-Nitrosourea (ENU)-Exposed Rats
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21. Adopting Duplex Sequencing™ Technology for Genetic Toxicity Testing: A Proof-of-Concept Mutagenesis Experiment with N-Ethyl-N-Nitrosourea (ENU)-Exposed Rats
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22. An update on advances in new developing DNA conjugation diagnostics and ultra-resolution imaging technologies: Possible applications in medical and biotechnological utilities.
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23. Impact of preleukemic mutations and their persistence on hematologic recovery after induction chemotherapy for AML
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24. On statistical modeling of sequencing noise in high depth data to assess tumor evolution
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25. Integration of intra-sample contextual error modeling for improved detection of somatic mutations from deep sequencing
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26. Rare haplotype load as marker for lethal mutagenesis
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27. Implementing circulating tumor DNA analysis in a clinical laboratory: A user manual
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28. Precision medicine in cutaneous melanoma—A comprehensive review
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29. Allele frequency selection and no age-related increase in human oocyte mitochondrial mutations
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30. Measurable residual disease (MRD) as a surrogate end point for clinical drug approval in acute myeloid leukemia (AML): Perspectives from the MRD Partnership and Alliance in AML Clinical Treatment Consortium
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31. Hawk-Seq™ differentiates between various mutations in Salmonella typhimurium TA100 strain caused by exposure to Ames test-positive mutagens
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32. Quantification of cancer driver mutations in human breast and lung DNA using targeted, error‐corrected CarcSeq
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33. Low-level parental mosaicism affects the recurrence risk of holoprosencephaly
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34. Mapping single-cell diploid chromatin fiber architectures using DAF-seq
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35. The human brain through the lens of somatic mosaicism
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36. Duplex Sequencing Uncovers Recurrent Low-frequency Cancer-associated Mutations in Infant and Childhood KMT2A-rearranged Acute Leukemia
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37. Uterine Lavage Identifies Cancer Mutations and Increased TP53 Somatic Mutation Burden in Individuals with Ovarian Cancer
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38. Single-strand specific nuclease enhances accuracy of error-corrected sequencing and improves rare mutation-detection sensitivity
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39. Pathways and signatures of mutagenesis at targeted DNA nicks
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40. The Feasibility of Patient-Specific Circulating Tumor DNA Monitoring throughout Multi-Modality Therapy for Locally Advanced Esophageal and Rectal Cancer: A Potential Biomarker for Early Detection of Subclinical Disease
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41. Targeted Next Generation Sequencing to study insert stability in genetically modified plants
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45. DNA mutagenesis driven by transcription factor competition with mismatch repair
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46. Somatic mutation and selection at epidemiological scale
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47. Frequencies and spectra of aflatoxin B1-induced mutations in liver genomes of NEIL1-deficient mice as revealed by duplex sequencing
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49. Peritoneal cell-free DNA as a sensitive biomarker for detection of peritoneal metastasis in colorectal cancer: a prospective diagnostic study
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50. Applications of molecular barcode sequencing for the detection of low‐frequency variants in circulating tumour DNA from hepatocellular carcinoma
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52. Detecting Ultralow Frequency Mutation in Circulating Cell‐Free DNA of Early‐Stage Nonsmall Cell Lung Cancer Patients with Unique Molecular Identifiers
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54. Charting single-cell lineages with synthetic and natural barcodes
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55. Long Term Exposure to Benzo[b]fluoranthene Does Not Induce Mutations in MutaMouse Male Germ Cells.
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58. Clinical applications of circulating tumor DNA in central nervous system lymphoma.
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59. In silico error correction improves cfDNA mutation calling
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60. MUTE‐Seq: An Ultrasensitive Method for Detecting Low‐Frequency Mutations in cfDNA With Engineered Advanced‐Fidelity FnCas9
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