213 results on '"Salk Jesse J"'
Search Results
2. Two-temperature LATE-PCR endpoint genotyping
3. Error-corrected next generation sequencing – Promises and challenges for genotoxicity and cancer risk assessment
4. Error-corrected duplex sequencing enables direct detection and quantification of mutations in human TK6 cells with strong inter-laboratory consistency
5. Adopting Duplex Sequencing Technology for Genetic Toxicity Testing: A Proof-of-Concept Mutagenesis Experiment with N-Ethyl-N-Nitrosourea (ENU)-Exposed Rats
6. PolyG-DS : An ultrasensitive polyguanine tract–profiling method to detect clonal expansions and trace cell lineage
7. Duplex sequencing identifies genomic features that determine susceptibility to benzo(a)pyrene-induced in vivo mutations
8. Error-corrected next-generation sequencing to advance nonclinical genotoxicity and carcinogenicity testing
9. Direct quantification of in vivo mutagenesis and carcinogenesis using duplex sequencing
10. Extensive subclonal mutational diversity in human colorectal cancer and its significance
11. Measurable Residual FLT3 Internal Tandem Duplication Before Allogeneic Transplant for Acute Myeloid Leukemia
12. An AML Targeted Duplex Sequencing Assay That Can Detect Measurable Residual Disease (MRD) at a Sensitivity Better Than 0.01% Variant Allele Frequency
13. Quantification of measurable residual disease using duplex sequencing in adults with acute myeloid leukemia
14. Next Generation Sequencing Workshop at the Royal Society of Medicine (London, May 2022): how genomics is on the path to modernizing genetic toxicology
15. Ultra-accurate Duplex Sequencing for the assessment of pretreatment ABL1 kinase domain mutations in Ph+ ALL
16. Adopting Duplex Sequencing Technology for Genetic Toxicity Testing: A Proof-of-Concept Mutagenesis Experiment with N-Ethyl-N-Nitrosourea (ENU)-Exposed Rats
17. Abstract LB254: Accurate detection of low frequency AML-associated mutations in vitro using Duplex Sequencing with enzymatic fragmentation
18. Duplex Sequencing Provides Detailed Characterization of Mutation Frequencies and Spectra in the Bone Marrow of MutaMouse Males Exposed to Procarbazine Hydrochloride
19. Error-corrected Duplex Sequencing enables direct detection and quantification of mutations in human TK6 cells with remarkable inter-laboratory consistency
20. Umbrella Trial in Myeloid Malignancies: The Myelomatch National Clinical Trials Network Precision Medicine Initiative
21. Precancer in ulcerative colitis: the role of the field effect and its clinical implications
22. Hypermutable DNA chronicles the evolution of human colon cancer
23. svCapture: Efficient and specific detection of very low frequency structural variant junctions by error-minimized capture sequencing
24. Abstract LB063: Duplex Sequencing reveals ubiquitous clonal hematopoiesis and complex donor-recipient clonal dynamics following HSCT
25. Detection of ultra-rare mutations by next-generation sequencing
26. Abstract A009: Longitudinal monitoring of pediatric acute myeloid leukemia using duplex sequencing of patient-specific panels reveals ultra-low frequency MRD that marks persistent carcinogenesis and complex clonal evolution
27. Additional file 1 of Duplex sequencing identifies genomic features that determine susceptibility to benzo(a)pyrene-induced in vivo mutations
28. Optimization of DNA Polymerase Mutation Rates during Bacterial Evolution
29. Clonal Expansions in Ulcerative Colitis Identify Patients with Neoplasia
30. Detecting ultralow-frequency mutations by Duplex Sequencing
31. The influence of subclonal resistance mutations on targeted cancer therapy
32. Response
33. Duplex Sequencing for Ultra-Low Frequency Measurable Residual Disease Detection in Adult Acute Myeloid Leukemia
34. Genetic toxicity testing using human in vitro organotypic airway cultures: Assessing DNA damage with the CometChip and mutagenesis by Duplex Sequencing
35. Analytical Validation of a Duplex Sequencing AML Assay with a Limit of Detection Below 0.01% VAF for SNVs and Indels
36. Response to: ‘when man got his mtDNA deletions?’
37. Direct amplification of single-stranded DNA for pyrosequencing using linear-after-the-exponential (LATE)–PCR
38. Duplex Sequencing with Patient-Specific Hybrid Capture Panels Reveals Ultra-Low Frequency Measurable Residual Disease in Pediatric Acute Myeloid Leukemia
39. Direct Quantification of in vivo Mutagenesis and Carcinogenesis Using Duplex Sequencing
40. Abstract PR04: Clonal landscapes of hematologic malignancies redefined by ultrasensitive duplex sequencing
41. Generation, Function, and Prognostic Utility of Somatic Mitochondrial DNA Mutations in Cancer
42. PolyG-DS: An ultrasensitive polyguanine tract-profiling method to detect clonal expansions and trace cell lineage.
43. Redefining "Gold Standard": Ultra-Sensitive Characterization of Commercial DNA Standards with Duplex Sequencing
44. Characterization of Clonal Dynamics after Hematopoietic Cell Transplantation Using Ultra-Sensitive Duplex Sequencing
45. Ultra-Accurate Assessment of Pretreatment ABL1 Kinase Domain (KD) Mutations in Patients (pts) with Newly Diagnosed Philadelphia Chromosome-Positive Acute Lymphoblastic Leukemia (Ph+ ALL) Using Duplex Sequencing (DS)
46. Next‐Generation Genotoxicology: Using Modern Sequencing Technologies to Assess Somatic Mutagenesis and Cancer Risk
47. Abstract 422: Duplex sequencing for MRD detection in acute myeloid leukemia
48. Ultra-Sensitive TP53 Sequencing for Cancer Detection Reveals Progressive Clonal Selection in Normal Tissue over a Century of Human Lifespan
49. Unexpectedly High Subclonal Mutational Diversity in Human Colorectal Cancer and Its Significance
50. Next‐Generation Genotoxicology: Using Modern Sequencing Technologies to Assess Somatic Mutagenesis and Cancer Risk.
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