Using next-generation sequencing for high resolution multiplex analysis of copy number variation from nanogram quantities of DNA from formalin-fixed paraffin-embedded specimens
出版年份 2010 全文链接
标题
Using next-generation sequencing for high resolution multiplex analysis of copy number variation from nanogram quantities of DNA from formalin-fixed paraffin-embedded specimens
作者
关键词
-
出版物
NUCLEIC ACIDS RESEARCH
Volume 38, Issue 14, Pages e151-e151
出版商
Oxford University Press (OUP)
发表日期
2010-06-05
DOI
10.1093/nar/gkq510
参考文献
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。- CNV-seq, a new method to detect copy number variation using high-throughput sequencing
- (2009) Chao Xie et al. BMC BIOINFORMATICS
- High-Throughput Multiplex Sequencing to Discover Copy Number Variants in Drosophila
- (2009) Bryce Daines et al. GENETICS
- DNA Sudoku--harnessing high-throughput sequencing for multiplexed specimen analysis
- (2009) Y. Erlich et al. GENOME RESEARCH
- Sensitive and accurate detection of copy number variants using read depth of coverage
- (2009) S. Yoon et al. GENOME RESEARCH
- Molecular Predictors of Outcome With Gefitinib and Docetaxel in Previously Treated Non–Small-Cell Lung Cancer: Data From the Randomized Phase III INTEREST Trial
- (2009) Jean-Yves Douillard et al. JOURNAL OF CLINICAL ONCOLOGY
- Random DNA fragmentation allows detection of single-copy, single-exon alterations of copy number by oligonucleotide array CGH in clinical FFPE samples
- (2009) Galen Hostetter et al. NUCLEIC ACIDS RESEARCH
- The UCSC Genome Browser database: update 2010
- (2009) B. Rhead et al. NUCLEIC ACIDS RESEARCH
- Genome-Wide Massively Parallel Sequencing of Formaldehyde Fixed-Paraffin Embedded (FFPE) Tumor Tissues for Copy-Number- and Mutation-Analysis
- (2009) Michal R. Schweiger et al. PLoS One
- Systems medicine: the future of medical genomics and healthcare
- (2009) Charles Auffray et al. Genome Medicine
- Microdissection molecular copy-number counting (µMCC)-unlocking cancer archives with digital PCR
- (2008) F McCaughan et al. JOURNAL OF PATHOLOGY
- Accurate whole human genome sequencing using reversible terminator chemistry
- (2008) David R. Bentley et al. NATURE
- Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing
- (2008) Peter J Campbell et al. NATURE GENETICS
- High-resolution mapping of copy-number alterations with massively parallel sequencing
- (2008) Derek Y Chiang et al. NATURE METHODS
- Identification of genetic variants using bar-coded multiplexed sequencing
- (2008) David W Craig et al. NATURE METHODS
- Chromosomal imbalances in oral squamous cell carcinoma: Examination of 31 cell lines and review of the literature
- (2007) Christa Lese Martin et al. ORAL ONCOLOGY
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