ライフサイエンスコーパス: environmental DNA

1 majority of sequencing capacity taken up by environmental DNA.

2 equencing of ribosomal RNA genes cloned from environmental DNA.

3 nt in site sediment, detected before only in environmental DNA.

4 tic life that branches with the Fungi, using environmental DNA analyses combined with fluorescent det

5 ch to identify and quantify diatoms found in environmental DNA and RNA samples.

6 High-throughput sequencing of environmental DNA barcodes (metabarcoding) offers an alt

7 the identification of antibacterially active environmental DNA clones, will take approximately 2 week

8 haracterization of gene clusters captured on environmental DNA clones.

9 A 16S rRNA gene sequence found on the same environmental DNA cosmid as NasP is most closely related

10 Here we use sequencing of environmental DNA, culturing of isolates, and analysis o

11 In conclusion, the opposing effects of environmental DNA damage and DNA repair result in elevat

12 nsate for the genome-destabilizing effect of environmental DNA damage and may be expected to result i

13 The epidermis is exposed to a variety of environmental DNA-damaging chemicals, principal among wh

14 of transcription factors found in sequenced environmental DNA-derived biosynthetic gene clusters, in

15 e recovery and heterologous expression of an environmental DNA-derived gene cluster encoding the bios

16 o the silent, cryptic pseudogene-containing, environmental DNA-derived Lzr gene cluster.

17 N-acylphenylalanine antibiotics by NasP, an environmental DNA-derived N-acyl amino acid synthase, is

18 High-throughput amplicon sequencing of environmental DNA (eDNA metabarcoding) represents a prom

19 ve real time polymerase chain reaction-based environmental DNA (eDNA) approach to detect the presence

20 The use of environmental DNA (eDNA) as a species detection tool is

21 To test the accuracy of environmental DNA (eDNA) as an early indicator of specie

22 Analysis of environmental DNA (eDNA) enables the detection of specie

23 en hampered by the inability to easily clone environmental DNA (eDNA) fragments large enough to captu

24 Degradation of environmental DNA (eDNA) in aquatic habitats can affect

25 The use of environmental DNA (eDNA) in biodiversity assessments off

26 While environmental DNA (eDNA) is now being regularly used to

27 ryptophan dimer (TD) biosynthesis by probing environmental DNA (eDNA) libraries for chromopyrrolic ac

28 ly been limited to the screening of existing environmental DNA (eDNA) libraries.

29 these OxyC sequences, a 10,000,000-membered environmental DNA (eDNA) megalibrary was created from a

30 ere we pilot a novel, rapid and non-invasive environmental DNA (eDNA) metabarcoding approach specific

31 Environmental DNA (eDNA) surveillance holds great promis

32 Analysis of environmental DNA (eDNA) to identify macroorganisms and

33 The use of environmental DNA (eDNA) to monitor mussel distributions

34 rom species in aquatic ecosystems, including environmental DNA (eDNA), have improved species monitori

35 Rapid expansion in the use of environmental DNA (eDNA), paired with the advancement of

36 primary hosts' DNA in environmental samples [environmental DNA (eDNA)], hydrological variables, and w

37 tracted directly from environmental samples (environmental DNA, eDNA) provides a means of exploring t

38 shotgun sequences of multiple organisms from environmental DNA extracts (metagenomic sequences).

39 Sequence-tag-guided screening of soil environmental DNA libraries can be used to guide the dis

40 Environmental DNA libraries contain large reservoirs of

41 Similar homology-based screening of large environmental DNA libraries is likely to permit the dire

42 Using high throughput screening of complex environmental DNA libraries more than 40 novel microbial

43 Environmental DNA megalibraries, like the one constructe

44 Whole genome shotgun (WGS) sequencing of environmental DNA (metagenomics) can be used to study th

45 achieved by a combination of discovery from environmental DNA of DERAs with improved activity and re

46 beneficial effects of the expanded access to environmental DNA offered by mutators on the adaptive po

47 ty of techniques collectively referred to as environmental DNA or 'eDNA'.

48 that organisms release into the environment (environmental DNA, or eDNA) has enormous potential for a

49 e libraries of small subunit rRNA genes from environmental DNA provided phylogenetic diversity estima

50 We tested this protocol on freshwater environmental DNA, revealing a wide diversity of Perkins

51 econd GH11 xylanase, EnXyn11A (encoded by an environmental DNA sample), bound to ferulic acid-1,5-ara

52 genes representing minor constituents of an environmental DNA sample.

53 Indeed, environmental DNA samples have been shown to encode many

54 Sgx9260b ( gi|44479596 ), were derived from environmental DNA samples originating from the Sargasso

55 These include environmental DNA samples that have proven difficult to

56 ation to estimate organismal abundances from environmental DNA sequence data.

57 he second one (Sgx9355e) was derived from an environmental DNA sequence originally isolated from the

58 Environmental DNA sequence samples are complex mixtures

59 The analytical power of environmental DNA sequences for modeling microbial ecosy

60 lt or impossible to detect without examining environmental DNA sequences, indicating that numerous RN

61 Modern metagenomic environmental DNA studies are almost completely reliant

62 s restricted to a single gene amplified from environmental DNA, the 18S rRNA gene (small subunit [SSU

63 Environmental DNA transported in river networks offers a

64 Because the environmental DNA was derived from many closely related