相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。CNValidator: validating somatic copy-number inference
Lucian P. Smith et al.
BIOINFORMATICS (2019)
The Evolving Genomic Landscape of Barrett's Esophagus and Esophageal Adenocarcinoma
Gianmarco Contino et al.
GASTROENTEROLOGY (2017)
The evolution of tumour phylogenetics: principles and practice
Russell Schwartz et al.
NATURE REVIEWS GENETICS (2017)
Proton Pump Inhibitors Do Not Reduce the Risk of Esophageal Adenocarcinoma in Patients with Barrett's Esophagus: A Systematic Review and Meta-Analysis
Qiang Hu et al.
PLOS ONE (2017)
Universal Patterns of Selection in Cancer and Somatic Tissues
Inigo Martincorena et al.
CELL (2017)
ACG Clinical Guideline: Diagnosis and Management of Barrett's Esophagus
Nicholas J. Shaheen et al.
AMERICAN JOURNAL OF GASTROENTEROLOGY (2016)
Limitations of the Driver/Passenger Model in Cancer Prevention
Mary K. Kuhner et al.
CANCER PREVENTION RESEARCH (2016)
Magnitude of Missed Esophageal Adenocarcinoma After Barrett's Esophagus Diagnosis: A Systematic Review and Meta-analysis
Kavel Visrodia et al.
GASTROENTEROLOGY (2016)
Dynamic clonal equilibrium and predetermined cancer risk in Barrett's oesophagus
Pierre Martinez et al.
NATURE COMMUNICATIONS (2016)
A Molecular Clock Infers Heterogeneous Tissue Age Among Patients with Barrett's Esophagus
Kit Curtius et al.
PLOS COMPUTATIONAL BIOLOGY (2016)
Paired exome analysis of Barrett's esophagus and adenocarcinoma
Matthew D. Stachler et al.
NATURE GENETICS (2015)
Whole-genome sequencing provides new insights into the clonal architecture of Barrett's esophagus and esophageal adenocarcinoma
Caryn S. Ross-Innes et al.
NATURE GENETICS (2015)
Temporal and Spatial Evolution of Somatic Chromosomal Alterations: A Case-Cohort Study of Barrett's Esophagus
Xiaohong Li et al.
CANCER PREVENTION RESEARCH (2014)
Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples
Kristian Cibulskis et al.
NATURE BIOTECHNOLOGY (2013)
NSAIDs Modulate Clonal Evolution in Barrett's Esophagus
Rumen L. Kostadinov et al.
PLOS GENETICS (2013)
Strelka: accurate somatic small-variant calling from sequenced tumor-normal sample pairs
Christopher T. Saunders et al.
BIOINFORMATICS (2012)
A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff: SNPs in the genome of Drosophila melanogaster strain w1118; iso-2; iso-3
Pablo Cingolani et al.
FLY (2012)
LoFreq: a sequence-quality aware, ultra-sensitive variant caller for uncovering cell-population heterogeneity from high-throughput sequencing datasets
Andreas Wilm et al.
NUCLEIC ACIDS RESEARCH (2012)
Residual Embryonic Cells as Precursors of a Barrett's-like Metaplasia
Xia Wang et al.
CELL (2011)
PyMix - The Python mixture package - a tool for clustering of heterogeneous biological data
Benjamin Georgi et al.
BMC BIOINFORMATICS (2010)
Allele-specific copy number analysis of tumors
Peter Van Loo et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)