(Q33673752)

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Circulating Tumor DNA Mutation Profiling by Targeted Next Generation Sequencing Provides Guidance for Personalized Treatments in Multiple Cancer Types

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28373672%20AND%20SRC:MED&resulttype=core&format=json

15 March 2020

Circulating Tumor DNA Mutation Profiling by Targeted Next Generation Sequencing Provides Guidance for Personalized Treatments in Multiple Cancer Types (English)

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15 March 2020

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15 March 2020

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Yongqian Shu

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15 March 2020

Xiaoling Tong

3

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15 March 2020

Xiaonan Wang

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15 March 2020

Zhili Chang

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15 March 2020

Yu Mao

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15 March 2020

Xiaofeng Chen

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15 March 2020

Jing Sun

8

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15 March 2020

Zhenxin Wang

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15 March 2020

Zhuan Hong

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15 March 2020

Liangjun Zhu

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15 March 2020

Chunrong Zhu

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15 March 2020

Jun Chen

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15 March 2020

Ying Liang

14

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15 March 2020

Huawu Shao

15

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15 March 2020

Yang W Shao

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15 March 2020

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3 April 2017

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15 March 2020

Scientific Reports

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15 March 2020

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15 March 2020

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15 March 2020

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15 March 2020

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3 April 2017

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https://scigraph.springernature.com/pub.10.1038/s41598-017-00520-1

0 references

Integrated digital error suppression for improved detection of circulating tumor DNA

1 reference

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Cell-free DNA Comprises an In Vivo Nucleosome Footprint that Informs Its Tissues-Of-Origin

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21 June 2018

Analytical and Clinical Validation of a Digital Sequencing Panel for Quantitative, Highly Accurate Evaluation of Cell-Free Circulating Tumor DNA

1 reference

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21 June 2018

TP53 Mutational Status and Prediction of Benefit from Adjuvant 5-Fluorouracil in Stage III Colon Cancer Patients

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21 June 2018

Epidemiology of lung cancer in China

1 reference

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21 June 2018

Circulating tumor DNA outperforms circulating tumor cells for KRAS mutation detection in thoracic malignancies

1 reference

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21 June 2018

Acquired EGFR C797S mutation mediates resistance to AZD9291 in non-small cell lung cancer harboring EGFR T790M.

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Lengthening and shortening of plasma DNA in hepatocellular carcinoma patients

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Inferring copy number and genotype in tumour exome data

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FACTERA: a practical method for the discovery of genomic rearrangements at breakpoint resolution

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21 June 2018

Coexistence of EGFR with KRAS, or BRAF, or PIK3CA somatic mutations in lung cancer: a comprehensive mutation profiling from 5125 Chinese cohorts

1 reference

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21 June 2018

An ultrasensitive method for quantitating circulating tumor DNA with broad patient coverage.

1 reference

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Trimmomatic: a flexible trimmer for Illumina sequence data

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21 June 2018

Clinical validation of the detection of KRAS and BRAF mutations from circulating tumor DNA.

1 reference

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21 June 2018

Computational tools for copy number variation (CNV) detection using next-generation sequencing data: features and perspectives

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21 June 2018

Detection of circulating tumor DNA in early- and late-stage human malignancies

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21 June 2018

A prospective, molecular epidemiology study of EGFR mutations in Asian patients with advanced non-small-cell lung cancer of adenocarcinoma histology (PIONEER)

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21 June 2018

Tumour heterogeneity and cancer cell plasticity

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21 June 2018

Crizotinib versus chemotherapy in advanced ALK-positive lung cancer.

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21 June 2018

High-resolution profiling of fetal DNA clearance from maternal plasma by massively parallel sequencing.

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21 June 2018

Non-invasive analysis of acquired resistance to cancer therapy by sequencing of plasma DNA

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21 June 2018

Detection of chromosomal alterations in the circulation of cancer patients with whole-genome sequencing

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21 June 2018

Genome and transcriptome sequencing in prospective metastatic triple-negative breast cancer uncovers therapeutic vulnerabilities

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Comprehensive genomic characterization of squamous cell lung cancers

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Emergence of KRAS mutations and acquired resistance to anti-EGFR therapy in colorectal cancer

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High-throughput detection of actionable genomic alterations in clinical tumor samples by targeted, massively parallel sequencing

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21 June 2018

Intratumor Heterogeneity and Branched Evolution Revealed by Multiregion Sequencing

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VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing

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T790M and acquired resistance of EGFR TKI: a literature review of clinical reports

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30 October 2018

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10.1038/S41598-017-00520-1

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Europe PubMed Central

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15 March 2020

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15 March 2020

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15 March 2020

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