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Data from: Attack of the PCR clones: rates of clonality have little effect on RAD-seq genotype calls
负责人:
关键词:
conservation genetics;Salvelinus fontinalis;methodology;genotyping;Sander vitreus;Fish;PCR duplicates;Oncorhynchus keta;Coregonus artedi;Population Genetics - Empirical
DOI:
doi:10.5061/dryad.3mq4631
摘要:
, investigate the mechanisms that lead to genotype call changes, and test if clones bias heterozygosity estimates. Our RAD-seq datasets contained 30 – 60% PCR
Data from: Long-range PCR allows sequencing of mitochondrial genomes from environmental DNA
负责人:
关键词:
mitogenome sequencing;Actinopterygii;eDNA
DOI:
doi:10.5061/dryad.q5gg0
摘要:
range of ray-finned fishes (Class: Actinopterygii). We tested the primer pair using long-range PCR and Illumina sequencing in vitro on a mock community
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: 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:
), we found that only in the longest PCR product, a marked decrease in prey detection success occurred. Lowering maximum annealing temperatures by 4 °C resulte
Data from: Diagnostic gene expression biomarkers of coral thermal stress
负责人:
关键词:
qPCR;Porites astreoides;cellular stress response;double-gene assay;cellular homeostasis response
DOI:
doi:10.5061/dryad.1h0n1
摘要:
erested in linking organism physiology with large-scale climatic conditions. Here, we assessed the ability of quantitative PCR (qPCR) based gene expression biomarkers
Data from: High herpesvirus diversity in wild rodent and shrew species in central Africa
负责人:
Christian Lange
关键词:
DOI:
doi:10.5061/dryad.7880kj7
摘要:
e sampled and tested by PCR for the presence of herpesvirus DNA. Methods: A broad range PCRs targeting either the Polymerase or the terminase gene were use
Data from: Advanced characterization of DNA molecules in rAAV vector preparations by single-stranded virus next-generation sequencing
负责人:
关键词:
Contaminants;Illumina;Adeno-associated virus;quality control;quantitative PCR;AAV;DNA;bioinformatics;gene therapy;vector;NGS;virus
DOI:
doi:10.5061/dryad.fs4cp
摘要:
with qPCR results and showed a quasi-random distribution of contaminants originating from the packaging cells genome. Finally, we found single-nucleotide
Data from: High Rates of Asymptomatic, Sub-microscopic Plasmodium vivax Infection and Disappearing Plasmodium falciparum Malaria in an Area of Low
负责人:
关键词:
Plasmodium vivax;transmission;gametocytes;sub-microscopic infections;malaria;elimination;Solomon Islands
DOI:
doi:10.5061/dryad.545tv
摘要:
by quantitative PCR (qPCR) and light microscopy (LM). Presence of gametocytes was determined by reverse transcription quantitative PCR (RT-qPCR). Results: By qPCR, 468
Data from: Deep sequencing of the olfactory epithelium reveals specific chemosensory receptors are expressed at sexual maturity in the European eel Anguilla anguilla
负责人:
关键词:
differential gene expression;Anguilla anguilla;transcriptome;olfactory epithelium;olfactory receptors;reproduction
DOI:
doi:10.5061/dryad.qp578
摘要:
Vertebrate genomes encode a diversity of G protein-coupled receptors (GPCR) that belong to large gene families and are used by olfactory system

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