A quantification method of somatic mutations in normal tissues and their accumulation in pediatric patients with chemotherapy
Published 2022 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
A quantification method of somatic mutations in normal tissues and their accumulation in pediatric patients with chemotherapy
Authors
Keywords
-
Journal
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Volume 119, Issue 31, Pages -
Publisher
Proceedings of the National Academy of Sciences
Online
2022-07-28
DOI
10.1073/pnas.2123241119
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Somatic mutation landscapes at single-molecule resolution
- (2021) Federico Abascal et al. NATURE
- Mapping genomic and epigenomic evolution in cancer ecosystems
- (2021) Toshikazu Ushijima et al. SCIENCE
- The evolution of hematopoietic cells under cancer therapy
- (2021) Oriol Pich et al. Nature Communications
- Tobacco smoking and somatic mutations in human bronchial epithelium
- (2020) Kenichi Yoshida et al. NATURE
- Macroscopic somatic clonal expansion in morphologically normal human urothelium
- (2020) Ruoyan Li et al. SCIENCE
- A Compendium of Mutational Signatures of Environmental Agents
- (2019) Jill E. Kucab et al. CELL
- Genome-wide somatic mutation analysis via Hawk-Seq™ reveals mutation profiles associated with chemical mutagens
- (2019) Shoji Matsumura et al. ARCHIVES OF TOXICOLOGY
- Enhancing the accuracy of next-generation sequencing for detecting rare and subclonal mutations
- (2018) Jesse J. Salk et al. NATURE REVIEWS GENETICS
- Detecting Rare Mutations and DNA Damage with Sequencing-Based Methods
- (2018) Daniel B. Sloan et al. TRENDS IN BIOTECHNOLOGY
- Somatic mutagenesis in satellite cells associates with human skeletal muscle aging
- (2018) Irene Franco et al. Nature Communications
- Duplex Proximity Sequencing (Pro-Seq): A method to improve DNA sequencing accuracy without the cost of molecular barcoding redundancy
- (2018) Joel Pel et al. PLoS One
- Age-related remodelling of oesophageal epithelia by mutated cancer drivers
- (2018) Akira Yokoyama et al. NATURE
- COSMIC: the Catalogue Of Somatic Mutations In Cancer
- (2018) John G Tate et al. NUCLEIC ACIDS RESEARCH
- Somatic mutant clones colonize the human esophagus with age
- (2018) Iñigo Martincorena et al. SCIENCE
- Tissue-specific mutation accumulation in human adult stem cells during life
- (2016) Francis Blokzijl et al. NATURE
- Genome-wide quantification of rare somatic mutations in normal human tissues using massively parallel sequencing
- (2016) Margaret L. Hoang et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- High burden and pervasive positive selection of somatic mutations in normal human skin
- (2015) I. Martincorena et al. SCIENCE
- Pre-leukemic evolution of hematopoietic stem cells: the importance of early mutations in leukemogenesis
- (2014) M R Corces-Zimmerman et al. LEUKEMIA
- Detecting ultralow-frequency mutations by Duplex Sequencing
- (2014) Scott R Kennedy et al. Nature Protocols
- Characterization of the Mutagenic Spectrum of 4-Nitroquinoline 1-Oxide (4-NQO) in Aspergillus nidulans by Whole Genome Sequencing
- (2014) Damien J. Downes et al. G3-Genes Genomes Genetics
- Mutational heterogeneity in cancer and the search for new cancer-associated genes
- (2013) Michael S. Lawrence et al. NATURE
- Signatures of mutational processes in human cancer
- (2013) Ludmil B. Alexandrov et al. NATURE
- Therapy-Related Myelodysplasia and Acute Myeloid Leukemia
- (2013) Smita Bhatia SEMINARS IN ONCOLOGY
- Detection of ultra-rare mutations by next-generation sequencing
- (2012) M. W. Schmitt et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- A reduced representation approach to population genetic analyses and applications to human evolution
- (2011) F. Luca et al. GENOME RESEARCH
- Long-term Risks of Subsequent Primary Neoplasms Among Survivors of Childhood Cancer
- (2011) Raoul C. Reulen JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
- SNP discovery and allele frequency estimation by deep sequencing of reduced representation libraries
- (2008) Curtis P Van Tassell et al. NATURE METHODS
Discover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversationAdd your recorded webinar
Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.
Upload Now