Using next-generation sequencing for high resolution multiplex analysis of copy number variation from nanogram quantities of DNA from formalin-fixed paraffin-embedded specimens
about
Identification of high-confidence somatic mutations in whole genome sequence of formalin-fixed breast cancer specimensClinical implementation of comprehensive strategies to characterize cancer genomes: opportunities and challengesBovine polledness--an autosomal dominant trait with allelic heterogeneityHigh-throughput RNA sequencing of a formalin-fixed, paraffin-embedded autopsy lung tissue sample from the 1918 influenza pandemicNonculture molecular techniques for diagnosis of bacterial disease in animals: a diagnostic laboratory perspectiveIsolating Viral and Host RNA Sequences from Archival Material and Production of cDNA Libraries for High-Throughput DNA Sequencing.Stratifying tumour subtypes based on copy number alteration profiles using next-generation sequence data.CopywriteR: DNA copy number detection from off-target sequence dataIncreased CNV-region deletions in mild cognitive impairment (MCI) and Alzheimer's disease (AD) subjects in the ADNI sampleNon-invasive analysis of intestinal development in preterm and term infants using RNA-Sequencing.Effect of immunohistochemistry on molecular analysis of tissue samples: implications for microdissection technologiesTargeted high throughput sequencing in clinical cancer settings: formaldehyde fixed-paraffin embedded (FFPE) tumor tissues, input amount and tumor heterogeneityCorrecting for cancer genome size and tumour cell content enables better estimation of copy number alterations from next-generation sequence data.Formalin fixation in the '-omics' era: a primer for the surgeon-scientist.Whole genome sequencing for lung cancer.Selective depletion of rRNA enables whole transcriptome profiling of archival fixed tissue.Characteristics of highly polymorphic segmental copy-number variations observed in Japanese by BAC-array-CGHEvaluating the repair of DNA derived from formalin-fixed paraffin-embedded tissues prior to genomic profiling by SNP-CGH analysis.Experimental design, preprocessing, normalization and differential expression analysis of small RNA sequencing experiments.In vivo ligands of MDA5 and RIG-I in measles virus-infected cells.Next-generation sequencing of RNA and DNA isolated from paired fresh-frozen and formalin-fixed paraffin-embedded samples of human cancer and normal tissue.Future medical applications of single-cell sequencing in cancer.The clonal relationships between pre-cancer and cancer revealed by ultra-deep sequencing.Copy-number variations observed in a Japanese population by BAC array CGH: summary of relatively rare CNVsComparison of Accuracy of Whole-Exome Sequencing with Formalin-Fixed Paraffin-Embedded and Fresh Frozen Tissue SamplesGenomic evidence of pre-invasive clonal expansion, dispersal and progression in bronchial dysplasia.Single-strand DNA library preparation improves sequencing of formalin-fixed and paraffin-embedded (FFPE) cancer DNAClinical and genomic analysis of a randomised phase II study evaluating anastrozole and fulvestrant in postmenopausal patients treated for large operable or locally advanced hormone-receptor-positive breast cancerThe transcriptional consequences of somatic amplifications, deletions, and rearrangements in a human lung squamous cell carcinomaIdentification of hallmarks of lung adenocarcinoma prognosis using whole genome sequencing.Next generation sequencing and a new era of medicine.Evaluating the Feasibility of DNA Methylation Analyses Using Long-Term Archived Brain Formalin-Fixed Paraffin-Embedded Samples.Targeted or whole genome sequencing of formalin fixed tissue samples: potential applications in cancer genomics.Comparison of methods for the extraction of DNA from formalin-fixed, paraffin-embedded archival tissues.CGH and SNP array using DNA extracted from fixed cytogenetic preparations and long-term refrigerated bone marrow specimens.CGH arrays compared for DNA isolated from formalin-fixed, paraffin-embedded material.Past and future impact of next-generation sequencing in head and neck cancer.Nonreciprocal chromosomal translocations in renal cancer involve multiple DSBs and NHEJ associated with breakpoint inversion but not necessarily with transcription.Positional information resolves structural variations and uncovers an evolutionarily divergent genetic locus in accessions of Arabidopsis thaliana.Diagnosis of fetal submicroscopic chromosomal abnormalities in failed array CGH samples: copy number by sequencing as an alternative to microarrays for invasive fetal testing.
P2860
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P2860
Using next-generation sequencing for high resolution multiplex analysis of copy number variation from nanogram quantities of DNA from formalin-fixed paraffin-embedded specimens
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
2010年论文
@zh
2010年论文
@zh-cn
name
Using next-generation sequenci ...... ed paraffin-embedded specimens
@en
Using next-generation sequenci ...... ed paraffin-embedded specimens
@en-gb
type
label
Using next-generation sequenci ...... ed paraffin-embedded specimens
@en
Using next-generation sequenci ...... ed paraffin-embedded specimens
@en-gb
prefLabel
Using next-generation sequenci ...... ed paraffin-embedded specimens
@en
Using next-generation sequenci ...... ed paraffin-embedded specimens
@en-gb
P2093
P2860
P356
P1154
2-s2.0-77955778246
P1476
Using next-generation sequenci ...... ed paraffin-embedded specimens
@en
P2093
Bruce Hayward
Caroline Conway
Catherine Daly
Claire McKinley
David J Adams
Graham R Taylor
Joanne Morgan
Ken MacLennan
Kostas Papagiannopoulos
P2860
P356
10.1093/NAR/GKQ510
P407
P5530
P577
2010-06-04T00:00:00Z
P5875
P6179
1020822593