High-fidelity target sequencing of individual molecules identified using barcode sequences: de novo detection and absolute quantitation of mutations in plasma cell-free DNA from cancer patients
about
Circulating tumor DNA as a liquid biopsy target for detection of pancreatic cancerGuide to detecting epidermal growth factor receptor (EGFR) mutations in ctDNA of patients with advanced non-small-cell lung cancerLiquid biopsy genotyping in lung cancer: ready for clinical utility?Integrated digital error suppression for improved detection of circulating tumor DNADetecting very low allele fraction variants using targeted DNA sequencing and a novel molecular barcode-aware variant callerSimple multiplexed PCR-based barcoding of DNA for ultrasensitive mutation detection by next-generation sequencing.A computational method for estimating the PCR duplication rate in DNA and RNA-seq experiments.What the blood knows: interrogating circulating tumor DNA to predict progression of minimal residual disease in early breast cancer.Detection of ESR1 mutations in plasma and tumors from metastatic breast cancer patients using next-generation sequencing.Transient appearance of circulating tumor DNA associated with de novo treatment.Characterization of the T-cell receptor beta chain repertoire in tumor-infiltrating lymphocytes.Numerical indices based on circulating tumor DNA for the evaluation of therapeutic response and disease progression in lung cancer patients.Detection of Rare Mutations in CtDNA Using Next Generation Sequencing.Highly sensitive detection of ESR1 mutations in cell-free DNA from patients with metastatic breast cancer using molecular barcode sequencing.Selective identification of somatic mutations in pancreatic cancer cells through a combination of next-generation sequencing of plasma DNA using molecular barcodes and a bioinformatic variant filter.Rapid Multiplex Small DNA Sequencing on the MinION Nanopore Sequencing Platform.Detecting Rare Mutations and DNA Damage with Sequencing-Based Methods.A review of somatic single nucleotide variant calling algorithms for next-generation sequencing data.AmpUMI: design and analysis of unique molecular identifiers for deep amplicon sequencing.
P2860
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P2860
High-fidelity target sequencing of individual molecules identified using barcode sequences: de novo detection and absolute quantitation of mutations in plasma cell-free DNA from cancer patients
description
2015 nî lūn-bûn
@nan
2015年の論文
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2015年学术文章
@wuu
2015年学术文章
@zh-cn
2015年学术文章
@zh-hans
2015年学术文章
@zh-my
2015年学术文章
@zh-sg
2015年學術文章
@yue
2015年學術文章
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2015年學術文章
@zh-hant
name
High-fidelity target sequencin ...... -free DNA from cancer patients
@en
High-fidelity target sequencin ...... -free DNA from cancer patients
@nl
type
label
High-fidelity target sequencin ...... -free DNA from cancer patients
@en
High-fidelity target sequencin ...... -free DNA from cancer patients
@nl
prefLabel
High-fidelity target sequencin ...... -free DNA from cancer patients
@en
High-fidelity target sequencin ...... -free DNA from cancer patients
@nl
P2093
P2860
P356
P1433
P1476
High-fidelity target sequencin ...... -free DNA from cancer patients
@en
P2093
Fumio Imamura
Junji Uchida
Kikuya Kato
Ryo Matoba
Takuya Hamakawa
Yoji Kukita
Yuichiro Doki
P2860
P304
P356
10.1093/DNARES/DSV010
P577
2015-06-29T00:00:00Z