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Data from: “Direct PCR” optimization yields a rapid, cost-effective, non-destructive, and efficient method for obtaining DNA barcodes without DNA extraction
负责人:
关键词:
ecosystem services;Chironomidae;DNA Barcoding;insects;Invertebrates
DOI:
doi:10.5061/dryad.4q4kf
摘要:
PCR method that skips DNA extraction (“direct PCR”) and that can be used for a broad range of invertebrate taxa. We demonstrate how direct PCR can be optimized
Data from: An examination of the accuracy of a sequential PCR and sequencing test used to detect the incursion of an invasive species: the cas
负责人:
关键词:
scats;predator faeces;specificity;sensitivity;sequential testing;trace DNA;Vulpes vulpes
DOI:
doi:10.5061/dryad.7652s
摘要:
1. Polymerase Chain Reaction (PCR) diagnostic tests are increasingly applied to the identification of wildlife. Yet rigorous verification is rare
Data from: Microfluidic PCR-based target enrichment: a case study in two rapid radiations of Commiphora (Burseraceae) from Madagascar
负责人:
关键词:
Illumina MiSeq;microfluidic PCR;genome-tagged amplification;Miocene;Burseraceae;targeted amplicon sequencing;Commiphora;phylogenomics;Bursera
DOI:
doi:10.5061/dryad.591q3
摘要:
. Here we describe the development and validation of a novel set of 91 nuclear markers for PCR-based target enrichment. Using microfluidic PCR
Data from: Estimating and mitigating amplification bias in qualitative and quantitative arthropod metabarcoding
负责人:
关键词:
Arthropoda;Arthropods
DOI:
doi:10.5061/dryad.fs728
摘要:
can be derived from metabarcoding due to taxon specific PCR amplification biases. PCR-free approaches have been suggested to mitigate this problem
Data from: Optimizing methods for PCR-based analysis of predation
负责人:
关键词:
replicability;Pardosa;Oreonebria castanea;molecular gut content analysis;visualisation methods;annealing temperature;Nebria germari
DOI:
doi:10.5061/dryad.8947
摘要:
alpine carabid beetles and lycosid spiders, we investigated how PCR annealing temperature affects prey DNA detection success and how post-PCR visualization
Data from: Improving PCR detection of prey in molecular diet studies: importance of group-specific primer set selection and extraction protocol
负责人:
Zarzoso-Lacoste, Diane
关键词:
Invasive rats Diet Analysis PCR-based method Extraction protocol performances A260/A280 absorbance ratio Group-specific primer pairs
DOI:
doi:10.5061/dryad.8c134
摘要:
itical step, as PCR inhibitors may be co-extracted. Another critical step consist in carefully select suitable group-specific primer sets that should
Data from: Residual eDNA detection sensitivity assessed by quantitative real-time PCR in a river ecosystem
负责人:
关键词:
Environmental DNA;qRT-PCR;river;Residual;DNA persistence
DOI:
doi:10.5061/dryad.5rf92
摘要:
eDNA detection sensitivity using quantitative real-time polymerase chain reaction (qRT-PCR), in a flowing, uncontrolled river after the eDNA source
Data from: Development of a PCR-RFLP assay to identify Drosophila melanogaster among field-collected larvae
负责人:
Raquin Vincent
关键词:
Fruit fly larvae field samples PCR-RFLP taxonomic identification
DOI:
doi:10.5061/dryad.pm71k02
摘要:
ecially field-derived samples. Here, we developed a Polymerase Chain Reaction-Restriction Fragment Length Polymorphism (PCR-RFLP) assay that discr
Data from: Blood-stage parasitaemia and age determine Plasmodium falciparum and P. vivax gametocytaemia in Papua New Guinea
负责人:
关键词:
asymptomatic infection;Plasmodium vivax;Plasmodium falciparum;age trend;malaria transmission;cross-sectional;gametocyte;submicroscopic infection
DOI:
doi:10.5061/dryad.550p3
摘要:
and gametocytes by detection of pfs25 and pvs25 mRNA transcripts by reverse-transcriptase PCR (qRT-PCR). The parasite prevalence by PCR was 18

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