SCOMP is superior to degenerated oligonucleotide primed-polymerase chain reaction for global amplification of minute amounts of DNA from microdissected archival tissue samples.
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Amplification of multiple genomic loci from single cells isolated by laser micro-dissection of tissuesGenome amplification of single sperm using multiple displacement amplificationLarge fragment Bst DNA polymerase for whole genome amplification of DNA from formalin-fixed paraffin-embedded tissuesProfiling genomic copy number changes in retinoblastoma beyond loss of RB1Microdissection molecular copy-number counting (microMCC)--unlocking cancer archives with digital PCRNon-invasive prenatal detection of trisomy 21 using tandem single nucleotide polymorphismsWhole genome amplification of DNA from laser capture-microdissected tissue for high-throughput single nucleotide polymorphism and short tandem repeat genotypingGenomic alterations in sporadic synchronous primary breast cancer using array and metaphase comparative genomic hybridization.Detection of chromosomal structural alterations in single cells by SNP arrays: a systematic survey of amplification bias and optimized workflow.From latent disseminated cells to overt metastasis: genetic analysis of systemic breast cancer progression.Tumor microenvironmental genomic alterations in juvenile nasopharyngeal angiofibroma.Balanced-PCR amplification allows unbiased identification of genomic copy changes in minute cell and tissue samples.Common chromosomal imbalances and stemness-related protein expression markers in endometriotic lesions from different anatomical sites: the potential role of stem cells.Chromosomal imbalances exclusively detected in invasive front area are associated with poor outcome in laryngeal carcinomas from different anatomical sites.A robust method to analyze copy number alterations of less than 100 kb in single cells using oligonucleotide array CGH.Limited tissue fixation times and whole genomic amplification do not impact array CGH profilesArray-based comparative genomic hybridization from formalin-fixed, paraffin-embedded breast tumorsComparison of whole genome amplification methods for analysis of DNA extracted from microdissected early breast lesions in formalin-fixed paraffin-embedded tissueMolecular evolution of breast cancer.Detecting single DNA copy number variations in complex genomes using one nanogram of starting DNA and BAC-array CGH.Challenges for CTC-based liquid biopsies: low CTC frequency and diagnostic leukapheresis as a potential solution.Disseminated tumour cells with highly aberrant genomes are linked to poor prognosis in operable oesophageal adenocarcinoma.Optimized amplification and fluorescent labeling of small cell samples for genomic array-CGH.Identification of the human/mouse syntenic common fragile site FRA7K/Fra12C1--relation of FRA7K and other human common fragile sites on chromosome 7 to evolutionary breakpoints.Whole genome amplification for CGH analysis: Linker-adapter PCR as the method of choice for difficult and limited samples.Genomic alterations in primary breast cancers compared with their sentinel and more distal lymph node metastases: an aCGH study.Mapping genomic and transcriptomic alterations spatially in epithelial cells adjacent to human breast carcinoma.Diagnostic pathology of early systemic cancer: ERBB2 gene amplification in single disseminated cancer cells determines patient survival in operable esophageal cancer.Evaluation of Phi29-based whole-genome amplification for microarray-based comparative genomic hybridisation.A streamlined workflow for single-cells genome-wide copy-number profiling by low-pass sequencing of LM-PCR whole-genome amplification products.A new workflow for whole-genome sequencing of single human cells.Prognostic impact of CK-20-positive cells in peripheral venous blood of patients with gastrointestinal carcinoma.Genomic alterations detected by comparative genomic hybridization in ovarian endometriomas.Molecular copy-number counting: potential of single-molecule diagnostics.Comparative genomic hybridizationCutaneous T-cell lymphoma-associated lung cancers show chromosomal aberrations differing from primary lung cancer
P2860
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P2860
SCOMP is superior to degenerated oligonucleotide primed-polymerase chain reaction for global amplification of minute amounts of DNA from microdissected archival tissue samples.
description
2002 nî lūn-bûn
@nan
2002 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
SCOMP is superior to degenerat ...... ected archival tissue samples.
@ast
SCOMP is superior to degenerat ...... ected archival tissue samples.
@en
type
label
SCOMP is superior to degenerat ...... ected archival tissue samples.
@ast
SCOMP is superior to degenerat ...... ected archival tissue samples.
@en
prefLabel
SCOMP is superior to degenerat ...... ected archival tissue samples.
@ast
SCOMP is superior to degenerat ...... ected archival tissue samples.
@en
P2093
P2860
P1476
SCOMP is superior to degenerat ...... ected archival tissue samples.
@en
P2093
Andreas Erbersdobler
Christoph A Klein
Jakob R Izbicki
Joachim Diebold
Julian A Schardt
Nikolas H Stoecklein
Oleg Schmidt-Kittler
P2860
P356
10.1016/S0002-9440(10)64155-7
P407
P577
2002-07-01T00:00:00Z