Results 241 to 250 of about 107,065 (275)
Global Change Biology Communications, EarlyView.Modeling of current and future spatial distribution of Antarctic lecideoid lichens shows that warming will strongly increase the potential habitat. Under three climate‐change scenarios, most fungal and algal partners are projected to expand inland. Overall, climate change drives widespread range shifts and promotes colonization of interior Antarctica ...
Anna Götz +6 more
wiley +1 more source
Most soil and litter arthropods are unidentifiable based on current DNA barcode reference libraries. [PDF]
Curr ZoolRecuero E, Etzler FE, Caterino MS.
europepmc +1 more source
Characterising the north-western European species of Phaenoglyphis Förster, 1869 (Hymenoptera: Figitidae: Charipinae) with novel insights from DNA barcode data. [PDF]
Biodivers Data JVogel J +3 more
europepmc +1 more source
Dataset on intergenic spacer regions of chloroplast genome and potential DNA barcode of Hoya varticillata var varticillata in Vietnam. [PDF]
Data BriefHoang CV, Tu TQ, Lo TTM, Chu MH.
europepmc +1 more source
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DNA barcoding is a technique used to identify plant species by using specific sections of DNA. The conventional approach to species identification is gradually diminishing due to constraints such as potential misinterpretation, overlooking morphologically cryptic.The two key coding regions, rbcL and matK, serve as primary DNA barcode markers for ...
Arun K. Pandey +3 more
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Arun K. Pandey +3 more
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2012
This chapter is an overview of the techniques for DNA barcoding of fishes from field collection to DNA sequence analysis. Recommendations for modifications of field protocols and best tissue sampling practices are made. A variety of DNA extraction protocols is provided, including high-throughput robot-assisted methods. A pair of well-tested forward and
Lee A, Weigt +3 more
openaire +2 more sources
This chapter is an overview of the techniques for DNA barcoding of fishes from field collection to DNA sequence analysis. Recommendations for modifications of field protocols and best tissue sampling practices are made. A variety of DNA extraction protocols is provided, including high-throughput robot-assisted methods. A pair of well-tested forward and
Lee A, Weigt +3 more
openaire +2 more sources
2012
Conventional DNA barcoding uses an approximately 650 bp DNA barcode of the mitochondrial gene COI for species identification in animal groups. Similar size fragments from chloroplast genes have been proposed as barcode markers for plants. While PCR amplification and sequencing of a 650 bp fragment is consistent in freshly collected and well-preserved ...
Mehrdad, Hajibabaei, Charly, McKenna
openaire +2 more sources
Conventional DNA barcoding uses an approximately 650 bp DNA barcode of the mitochondrial gene COI for species identification in animal groups. Similar size fragments from chloroplast genes have been proposed as barcode markers for plants. While PCR amplification and sequencing of a 650 bp fragment is consistent in freshly collected and well-preserved ...
Mehrdad, Hajibabaei, Charly, McKenna
openaire +2 more sources
Genome, 2016
Fungi are ubiquitous in both natural and human-made environments. They play important roles in the health of plants, animals, and humans, and in broad ecosystem functions. Thus, having an efficient species-level identification system could significantly enhance our ability to treat fungal diseases and to monitor the spatial and temporal patterns of ...
openaire +2 more sources
Fungi are ubiquitous in both natural and human-made environments. They play important roles in the health of plants, animals, and humans, and in broad ecosystem functions. Thus, having an efficient species-level identification system could significantly enhance our ability to treat fungal diseases and to monitor the spatial and temporal patterns of ...
openaire +2 more sources
Protist, 2006
We have developed a simple method for subtyping the intestinal protistan parasite Blastocystis using an approach equivalent to DNA barcoding in animals. Amplification of a 600 bp region of the small subunit ribosomal RNA gene followed by single primer sequencing of the PCR product provides enough data to assign isolates to specific subtypes ...
Stephanie M, Scicluna +2 more
openaire +2 more sources
We have developed a simple method for subtyping the intestinal protistan parasite Blastocystis using an approach equivalent to DNA barcoding in animals. Amplification of a 600 bp region of the small subunit ribosomal RNA gene followed by single primer sequencing of the PCR product provides enough data to assign isolates to specific subtypes ...
Stephanie M, Scicluna +2 more
openaire +2 more sources