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1 protection from potentially harmful types of environmental DNA.
2 y characterised through the metabarcoding of environmental DNA.
3 ciated with increased translocation rates of environmental DNA.
4 from a background of predominantly host and environmental DNA.
5 majority of sequencing capacity taken up by environmental DNA.
6 equencing of ribosomal RNA genes cloned from environmental DNA.
7 nt in site sediment, detected before only in environmental DNA.
13 tic life that branches with the Fungi, using environmental DNA analyses combined with fluorescent det
15 hat void by using a powerful new technology, environmental DNA analysis, that enabled us to character
18 lly heavily fragmented and contaminated with environmental DNA, and where the retrieval of genetic da
19 of the 'pharmabiome' shows the potential of environmental DNA as a powerful forensic tool to assist
24 the identification of antibacterially active environmental DNA clones, will take approximately 2 week
26 y using a metabarcoding approach on airborne environmental DNA collected by a national ambient air qu
27 omic sequencing assay that is robust against environmental DNA contamination introduced during sample
29 ze microbial communities but is sensitive to environmental DNA contamination, in particular when appl
30 A 16S rRNA gene sequence found on the same environmental DNA cosmid as NasP is most closely related
33 nsate for the genome-destabilizing effect of environmental DNA damage and may be expected to result i
34 The epidermis is exposed to a variety of environmental DNA-damaging chemicals, principal among wh
35 of transcription factors found in sequenced environmental DNA-derived biosynthetic gene clusters, in
36 e recovery and heterologous expression of an environmental DNA-derived gene cluster encoding the bios
38 N-acylphenylalanine antibiotics by NasP, an environmental DNA-derived N-acyl amino acid synthase, is
44 t the rapid application of shotgun long-read environmental DNA (eDNA) analysis for non-invasive biodi
52 ve real time polymerase chain reaction-based environmental DNA (eDNA) approach to detect the presence
57 Here, we challenge this notion by analysing environmental DNA (eDNA) captured along with particulate
59 d a blinded pilot study to determine if such environmental DNA (eDNA) could be detected in eleven sam
60 generally treated as separate reservoirs of environmental DNA (eDNA) derived from the species reside
63 nsi and Ae. aegypti, we validated the use of environmental DNA (eDNA) for simultaneous vector detecti
64 en hampered by the inability to easily clone environmental DNA (eDNA) fragments large enough to captu
65 technology, non-invasive method of detecting environmental DNA (eDNA) from both triatomine bugs and T
67 seasonal variation in mammal diversity using environmental DNA (eDNA) from soil samples collected dur
75 a pipeline that utilizes the airborne plant environmental DNA (eDNA) in settled dust to estimate geo
76 tion and efficacy of sampling and sequencing environmental DNA (eDNA) in terrestrial environments usi
85 sus marine life, including identification of environmental DNA (eDNA) left behind by organisms in the
87 ryptophan dimer (TD) biosynthesis by probing environmental DNA (eDNA) libraries for chromopyrrolic ac
89 these OxyC sequences, a 10,000,000-membered environmental DNA (eDNA) megalibrary was created from a
90 ere we pilot a novel, rapid and non-invasive environmental DNA (eDNA) metabarcoding approach specific
91 ake Bay (USA), we evaluated the potential of environmental DNA (eDNA) metabarcoding for BW monitoring
98 nform management and conservation decisions, environmental DNA (eDNA) methods are used to detect gene
100 developed and validated two species-specific environmental DNA (eDNA) protocols and applied them in t
102 microscopy.(11) Instead, here we used novel environmental DNA (eDNA) sampling and qPCR(12-15) to mea
110 te and invertebrate), and pathogens using 10 environmental DNA (eDNA) water sampling events every two
114 rom species in aquatic ecosystems, including environmental DNA (eDNA), have improved species monitori
116 alysis (SIA), fatty acid analysis (FAA), and environmental DNA (eDNA), to investigate the trophic eco
118 cessing pools of individual samples or using environmental DNA (eDNA)-the genetic material shed into
122 primary hosts' DNA in environmental samples [environmental DNA (eDNA)], hydrological variables, and w
124 Because these DNA-based methods (termed environmental DNA, eDNA) confirm species presence by pro
125 tracted directly from environmental samples (environmental DNA, eDNA) provides a means of exploring t
126 etabarcoding (High-Throughput Sequencing) on environmental DNA extracted from both soil samples and b
127 aft metagenome-assembled genomes (MAGs) from environmental DNA extracted from two hot springs within
128 shotgun sequences of multiple organisms from environmental DNA extracts (metagenomic sequences).
129 omes that will further facilitate the use of environmental DNA for studying host specificity in epizo
133 ectious agents in farmed and wild salmon and environmental DNA highlights a further 4 agents that are
134 ce of known Group 2i Isochrysidales based on environmental DNA in both marine and lacustrine environm
137 Similar homology-based screening of large environmental DNA libraries is likely to permit the dire
138 Using high throughput screening of complex environmental DNA libraries more than 40 novel microbial
145 croclimate, productivity and biodiversity by environmental DNA metabarcoding(6)) across 46 proglacial
148 Whole genome shotgun (WGS) sequencing of environmental DNA (metagenomics) can be used to study th
150 achieved by a combination of discovery from environmental DNA of DERAs with improved activity and re
151 beneficial effects of the expanded access to environmental DNA offered by mutators on the adaptive po
154 that organisms release into the environment (environmental DNA, or eDNA) has enormous potential for a
155 urally leave behind in water or soil (called environmental DNA, or eDNA) to identify the species pres
158 e libraries of small subunit rRNA genes from environmental DNA provided phylogenetic diversity estima
159 ially expanding the application of real-time environmental DNA research from monitoring species distr
161 ka; and (6) phylogenetic analysis of mammoth environmental DNA reveals a previously unsampled mitocho
162 econd GH11 xylanase, EnXyn11A (encoded by an environmental DNA sample), bound to ferulic acid-1,5-ara
166 ility of small sets of noisy genotypes, from environmental DNA samples or functional genomics data, m
167 Sgx9260b ( gi|44479596 ), were derived from environmental DNA samples originating from the Sargasso
171 he second one (Sgx9355e) was derived from an environmental DNA sequence originally isolated from the
174 lt or impossible to detect without examining environmental DNA sequences, indicating that numerous RN
175 maging is also being complemented by in situ environmental-DNA sequencing technologies, allowing the
180 DNA based biodiversity assessments (such as environmental DNA) that can help with the complex task o
181 s restricted to a single gene amplified from environmental DNA, the 18S rRNA gene (small subunit [SSU
186 owever, as the study was based on the use of environmental DNA, which does not unequivocally confirm
187 n is feasible through nanopore sequencing of environmental DNA, with important implications for futur