UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Enhancing the accuracy of next-generation sequencing for detecting rare and subclonal mutations

Nature reviews. Genetics, 2018-05, Vol.19 (5), p.269-285

2018

Volltextzugriff (PDF)

The influence of subclonal resistance mutations on targeted cancer therapy

Nature reviews. Clinical oncology, 2016-06, Vol.13 (6), p.335-347

2016

Volltextzugriff (PDF)

Detection of ultra-rare mutations by next-generation sequencing

Proceedings of the National Academy of Sciences - PNAS, 2012-09, Vol.109 (36), p.14508-14513

2012

Volltextzugriff (PDF)

Ultra-sensitive sequencing reveals an age-related increase in somatic mitochondrial mutations that are inconsistent with oxidative damage

PLoS genetics, 2013-09, Vol.9 (9), p.e1003794

2013

Volltextzugriff (PDF)

Direct quantification of in vivo mutagenesis and carcinogenesis using duplex sequencing

Proceedings of the National Academy of Sciences - PNAS, 2020-12, Vol.117 (52), p.33414-33425

2020

Volltextzugriff (PDF)

Duplex sequencing identifies genomic features that determine susceptibility to benzo(a)pyrene-induced in vivo mutations

BMC genomics, 2022-07, Vol.23 (1), p.542-15, Article 542

2022

Volltextzugriff (PDF)

Mutational heterogeneity in human cancers: origin and consequences

Annual review of pathology, 2010-01, Vol.5 (1), p.51-75

2010

Volltextzugriff (PDF)

Extensive subclonal mutational diversity in human colorectal cancer and its significance

Proceedings of the National Academy of Sciences - PNAS, 2019-12, Vol.116 (52), p.26863-26872

2019

Volltextzugriff (PDF)

Ultra-Sensitive TP53 Sequencing for Cancer Detection Reveals Progressive Clonal Selection in Normal Tissue over a Century of Human Lifespan

Cell reports (Cambridge), 2019-07, Vol.28 (1), p.132-144.e3

2019

Volltextzugriff (PDF)

Quantification of measurable residual disease using duplex sequencing in adults with acute myeloid leukemia

Haematologica (Roma), 2024-02, Vol.109 (2), p.401

2024

Volltextzugriff (PDF)

Optimization of DNA polymerase mutation rates during bacterial evolution

Proceedings of the National Academy of Sciences - PNAS, 2010-01, Vol.107 (3), p.1154-1159

2010

Volltextzugriff (PDF)

Decreased mitochondrial DNA mutagenesis in human colorectal cancer

PLoS genetics, 2012-06, Vol.8 (6), p.e1002689

2012

Volltextzugriff (PDF)

svCapture: efficient and specific detection of very low frequency structural variant junctions by error-minimized capture sequencing

NAR genomics and bioinformatics, 2023-06, Vol.5 (2)

2023

Volltextzugriff (PDF)

Hypermutable DNA chronicles the evolution of human colon cancer

Proceedings of the National Academy of Sciences - PNAS, 2014-05, Vol.111 (18), p.E1889-E1898

2014

Volltextzugriff (PDF)

Next‐Generation Genotoxicology: Using Modern Sequencing Technologies to Assess Somatic Mutagenesis and Cancer Risk

Environmental and molecular mutagenesis, 2020-01, Vol.61 (1), p.135-151

2020

Volltextzugriff (PDF)

Risks of double-counting in deep sequencing

Proceedings of the National Academy of Sciences - PNAS, 2014-04, Vol.111 (16), p.E1560-E1560

2014

Volltextzugriff (PDF)

Ultra-accurate Duplex Sequencing for the assessment of pretreatment ABL1 kinase domain mutations in Ph+ ALL

Blood cancer journal (New York), 2020-05, Vol.10 (5), p.61-61, Article 61

2020

Volltextzugriff (PDF)

Detecting ultralow-frequency mutations by Duplex Sequencing

Nature protocols, 2014-11, Vol.9 (11), p.2586-2606

2014

Volltextzugriff (PDF)

Clonal expansions in ulcerative colitis identify patients with neoplasia

Proceedings of the National Academy of Sciences - PNAS, 2009-12, Vol.106 (49), p.20871-20876

2009

Volltextzugriff (PDF)

Precancer in ulcerative colitis: the role of the field effect and its clinical implications

Carcinogenesis (New York), 2018-01, Vol.39 (1), p.11-20

2018

Volltextzugriff (PDF)

Targeted genome fragmentation with CRISPR/Cas9 enables fast and efficient enrichment of small genomic regions and ultra-accurate sequencing with low DNA input (CRISPR-DS)

Genome research, 2018-10, Vol.28 (10), p.1589-1599

2018

Volltextzugriff (PDF)

Error-corrected next-generation sequencing to advance nonclinical genotoxicity and carcinogenicity testing

Nature reviews. Drug discovery, 2023-03, Vol.22 (3), p.165-166

2023

Volltextzugriff (PDF)

Duplex sequencing provides detailed characterization of mutation frequencies and spectra in the bone marrow of MutaMouse males exposed to procarbazine hydrochloride

Archives of toxicology, 2023-08, Vol.97 (8), p.2245-2259

2023

Volltextzugriff (PDF)

Error-corrected next generation sequencing – Promises and challenges for genotoxicity and cancer risk assessment

Mutation research. Reviews in mutation research, 2023-07, Vol.792, p.108466, Article 108466

2023

Volltextzugriff (PDF)

Error-corrected duplex sequencing enables direct detection and quantification of mutations in human TK6 cells with strong inter-laboratory consistency

Mutation research. Genetic toxicology and environmental mutagenesis, 2023-07, Vol.889, p.503649-503649, Article 503649

2023

Volltextzugriff (PDF)

1 – 25 von 76

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(73)
Mit Volltextzugriff
(60)

Publikationsform

Artikel
(75)
Dissertationen
(1)

Sprache

Englisch
(76)

Erscheinungsjahr

n.n

Thema

Science & Technology
(40)
Humans
(32)
Life Sciences & Biomedicine
(31)
Mutation
(26)
Dna
(15)
Genetics & Heredity
(15)
Deoxyribonucleic Acid
(13)
Mutagenesis
(13)
Neoplasms - Genetics
(10)
Cancer
(9)
Genomes
(9)
Male
(9)
Multidisciplinary Sciences
(9)
Science & Technology - Other Topics
(9)
Toxicology
(9)
Biological Sciences
(8)
Biotechnology & Applied Microbiology
(8)
Dna Sequencing
(8)
Oncology
(8)
Animals
(7)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(3)

Menü

Weitere Dienste

Einstellungen

Enhancing the accuracy of next-generation sequencing for detecting rare and subclonal mutations

The influence of subclonal resistance mutations on targeted cancer therapy

Detection of ultra-rare mutations by next-generation sequencing

Ultra-sensitive sequencing reveals an age-related increase in somatic mitochondrial mutations that are inconsistent with oxidative damage

Direct quantification of in vivo mutagenesis and carcinogenesis using duplex sequencing

Duplex sequencing identifies genomic features that determine susceptibility to benzo(a)pyrene-induced in vivo mutations

Mutational heterogeneity in human cancers: origin and consequences

Extensive subclonal mutational diversity in human colorectal cancer and its significance

Ultra-Sensitive TP53 Sequencing for Cancer Detection Reveals Progressive Clonal Selection in Normal Tissue over a Century of Human Lifespan

Quantification of measurable residual disease using duplex sequencing in adults with acute myeloid leukemia

Optimization of DNA polymerase mutation rates during bacterial evolution

Decreased mitochondrial DNA mutagenesis in human colorectal cancer

svCapture: efficient and specific detection of very low frequency structural variant junctions by error-minimized capture sequencing

Hypermutable DNA chronicles the evolution of human colon cancer

Next‐Generation Genotoxicology: Using Modern Sequencing Technologies to Assess Somatic Mutagenesis and Cancer Risk

Risks of double-counting in deep sequencing

Ultra-accurate Duplex Sequencing for the assessment of pretreatment ABL1 kinase domain mutations in Ph+ ALL

Detecting ultralow-frequency mutations by Duplex Sequencing

Clonal expansions in ulcerative colitis identify patients with neoplasia

Precancer in ulcerative colitis: the role of the field effect and its clinical implications

Targeted genome fragmentation with CRISPR/Cas9 enables fast and efficient enrichment of small genomic regions and ultra-accurate sequencing with low DNA input (CRISPR-DS)

Error-corrected next-generation sequencing to advance nonclinical genotoxicity and carcinogenicity testing

Duplex sequencing provides detailed characterization of mutation frequencies and spectra in the bone marrow of MutaMouse males exposed to procarbazine hydrochloride

Error-corrected next generation sequencing – Promises and challenges for genotoxicity and cancer risk assessment

Error-corrected duplex sequencing enables direct detection and quantification of mutations in human TK6 cells with strong inter-laboratory consistency

Suchergebnisse filtern