Evaluation of real-time PCR amplification efficiencies to detect PCR inhibitors.
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Real-Time PCR: Revolutionizing Detection and Expression Analysis of GenesValidation of kinetics similarity in qPCRFactors affecting the STR amplification success in poorly preserved bone samplesA new real-time PCR method to overcome significant quantitative inaccuracy due to slight amplification inhibition.Differential susceptibility of PCR reactions to inhibitors: an important and unrecognised phenomenon.Amplification efficiency: linking baseline and bias in the analysis of quantitative PCR data.Selection of reference genes for expression studies with fish myogenic cell culturesShape based kinetic outlier detection in real-time PCR.Enhanced analysis of real-time PCR data by using a variable efficiency model: FPK-PCR.Effect of DNA extraction methods and sampling techniques on the apparent structure of cow and sheep rumen microbial communities.Accelerating plant DNA barcode reference library construction using herbarium specimens: improved experimental techniques.Simple absolute quantification method correcting for quantitative PCR efficiency variations for microbial community samples.Nucleotide Excision Repair and Transcription-coupled DNA Repair Abrogate the Impact of DNA Damage on Transcription.An instrument for automated purification of nucleic acids from contaminated forensic samples.In-house HIV-1 RNA real-time RT-PCR assays: principle, available tests and usefulness in developing countries.Multi-template polymerase chain reaction.A novel approach for evaluating the performance of real time quantitative loop-mediated isothermal amplification-based methods.Advances in forensic DNA quantification: a review.Powerful qPCR assays for the early detection of latent invaders: interdisciplinary approaches in clinical cancer research and plant pathology.Evaluation of different methods for DNA extraction from human burnt bones and the generation of genetic profiles for identification.Design and validation of a RT-qPCR procedure for diagnosis and quantification of most types of infectious pancreatic necrosis virus using a single pair of degenerated primers.Application of Droplet Digital PCR for Estimating Vector Copy Number States in Stem Cell Gene TherapyPCR inhibitor levels in concentrates of biosolid samples predicted by a new method based on excitation-emission matrix spectroscopy.Enhancing PCR amplification of DNA from recalcitrant plant specimens using a trehalose-based additive.Assessment of bias associated with incomplete extraction of microbial DNA from soil.Pressure cycling technology (PCT) reduces effects of inhibitors of the PCR.A guideline to family-wide comparative state-of-the-art quantitative RT-PCR analysis exemplified with a Brassicaceae cross-species seed germination case study.Qiagen's Investigator™ Quantiplex Kit as a predictor of STR amplification success from low-yield DNA samples.Optimizing techniques to capture and extract environmental DNA for detection and quantification of fish.High DNA stability in white blood cells and buffy coat lysates stored at ambient temperature under anoxic and anhydrous atmosphere.Tracking chromatin states using controlled DNase I treatment and real-time PCR.An investigation of PCR inhibition using Plexor(®) -based quantitative PCR and short tandem repeat amplification.A standard additions method reduces inhibitor-induced bias in quantitative real-time PCR.A simple method for normalization of DNA extraction to improve the quantitative detection of soil-borne plant pathogenic oomycetes by real-time PCR.Direct STR amplification from whole blood and blood- or saliva-spotted FTA without DNA purification.Powdered Activated Carbon: An Alternative Approach to Genomic DNA Purification.Development of internal amplification controls for DNA profiling with the AmpFℓSTR(®) SGM Plus(®) kit.A quantitative PCR assay for rapid detection of Shigella species in fresh produce.Considerations for the development of a reference method for sequencing of haploid DNA – an opinion paper on behalf of the IFCC Committee on Molecular Diagnostics. International Federation of Clinical Chemistry and Laboratory MedicineDetection of plant pathogens using real-time PCR: how reliable are lateCtvalues?
P2860
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P2860
Evaluation of real-time PCR amplification efficiencies to detect PCR inhibitors.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年学术文章
@wuu
2006年学术文章
@zh
2006年学术文章
@zh-cn
2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
@yue
2006年學術文章
@zh-hant
name
Evaluation of real-time PCR amplification efficiencies to detect PCR inhibitors.
@en
Evaluation of real-time PCR amplification efficiencies to detect PCR inhibitors.
@nl
type
label
Evaluation of real-time PCR amplification efficiencies to detect PCR inhibitors.
@en
Evaluation of real-time PCR amplification efficiencies to detect PCR inhibitors.
@nl
prefLabel
Evaluation of real-time PCR amplification efficiencies to detect PCR inhibitors.
@en
Evaluation of real-time PCR amplification efficiencies to detect PCR inhibitors.
@nl
P2860
P1476
Evaluation of real-time PCR amplification efficiencies to detect PCR inhibitors.
@en
P2093
Elias J Kontanis
P2860
P304
P356
10.1111/J.1556-4029.2006.00182.X
P50
P577
2006-07-01T00:00:00Z