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Data from: Distance, flow, and PCR inhibition: eDNA dynamics in two headwater steams
负责人:
关键词:
Environmental DNA;Salvelinus fontinalis;stream;Fish;qPCR;eDNA;lotic
DOI:
doi:10.5061/dryad.7j3g5
摘要:
times from mid-summer through autumn, over flows ranging from approximately 1 to 96 L/sec. We used qPCR to relate DNA copy number to distance from source
Data from: Comparison of capture and storage methods for aqueous macrobial eDNA using an optimized extraction protocol: advantage of enclosed filter
负责人:
关键词:
filter capsule;Environmental DNA;qPCR;eDNA
DOI:
doi:10.5061/dryad.p2q4r
摘要:
quantitative PCR (qPCR) and next-generation sequencing (NGS) applications, quality and quantity of the starting material is crucial, calling for optimized capture, storage
Data from: MicroRNA stability in FFPE tissue samples: dependence on GC content
负责人:
关键词:
human;MiRNA
DOI:
doi:10.5061/dryad.fj0f8
摘要:
in FFPE cardiac tissues instead of miR-1, which was predominant before fixation. Subsequent quantitative PCR (qPCR) analyses revealed that miRNAs
Data from: Dysregulation of valvular interstitial cell let-7c, miR-17, miR-20a, and miR-30d in naturally occurring canine myxomatous mitral valve disease
负责人:
关键词:
Canis lupus familiaris
DOI:
doi:10.5061/dryad.3274k
摘要:
disease-relevant changes in miRNA expression. In primary VIC lines from diseased and control valves, miRNA expression was profiled using RT-qPCR
Data from: Methodological considerations for detection of terrestrial small-body salamander eDNA and implications for biodiversity conservation
负责人:
关键词:
Environmental DNA;species declines;Environmental DNA;Plethodon cinereus;terrestrial eDNA;Red-backed Salamander;Amphibians;herpetofauna conservation;Conservation Biology;Wildlife Management
DOI:
doi:10.5061/dryad.tc29r
摘要:
ke management decisions. The objectives of this project were to use quantitative PCR (qPCR) to: (i) detect spiked salamander DNA in soil, (ii) quantify eDNA degradation ove
Data from: Environmental DNA surveillance for invertebrate species: advantages and technical limitations to detect invasive cr
负责人:
关键词:
efficiency of detection;funnel traps;qPCR;Procambarus clarkii;eDNA;limit of detection;limit of quantification;biological invasions
DOI:
doi:10.5061/dryad.0ck3q
摘要:
, the red swamp crayfish Procambarus clarkii. Species-specific primers and probes were designed; their specificity was tested using in silico PCR simulations and ag
Data from: Diet and trophic interactions of a circumglobally significant gelatinous marine zooplankter, Dolioletta gegenbauri (Uljanin, 1884)
负责人:
Frischer, Marc
关键词:
qPCR Doliolid Pelagic Tunicate Selective Feeding South Atlantic Bight Next Generation Sequencing
DOI:
doi:10.5061/dryad.99p2308
摘要:
of the South Atlantic Bight (SAB), USA. Sequencing-based approaches were complimented with targeted quantitative real time PCR (Polymerase Chain Reaction) analyses. Captive
Data from: Taxon abundance, diversity, co-occurrence and network analysis of the ruminal microbiota in response to dietary changes in dairy cows
负责人:
Tapio, Ilma
关键词:
Diet Bacteria Protozoans Fungi Archaean biology Archaeal taxonomy Oils
DOI:
doi:10.5061/dryad.t6t0q
摘要:
period and DNA was extracted from a combined sample. Diet effect on rumen microbial community was explored by qPCR, T-RFLP and metabarcoding sequencing
Data from: Estimating fish abundance and biomass from eDNA concentrations: variability among capture methods and environmental conditions
负责人:
Anais Lacoursière-Roussel
关键词:
qPCR Conservation Genetics Fish Species detection Water sampling Salmonid
DOI:
doi:10.5061/dryad.46sm5
摘要:
ined by quantitative PCR (qPCR) varied significantly with fish abundance and biomass and type of filters (Mixed-design ANOVA, P < 0.001). Results als

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