Combining real-time PCR and next-generation DNA sequencing to provide quantitative comparisons of fungal aerosol populations

By K. Dannemiller, N. Lang-Yona, N. Yamamoto, Yinon Rudich, Jordan Peccia. 2014

123 citations recorded by the source corpus.

Subfields: Cell Biology, Ecology, Evolution, Behavior and Systematics, Health, Toxicology and Mutagenesis

View Paper: https://www.semanticscholar.org/paper/9619fc223092e3e7cfe910d20afc0b207b2549d8

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Cell Biology

1. Noah Fierer

In Ecology, Evolution, Behavior and Systematics

1. Jack A. Gilbert
2. Jessica L. Green
3. Noah Fierer

In Health, Toxicology and Mutagenesis

1. Linsey C. Marr

Citations in the corpus

• Ten questions concerning the microbiomes of buildings (2016, background): “16 done in conjunction with DNA sequencing to improve understanding of microbial exposure [111] 356 and to yield quantitative estimates of the concentrations of individual species [112].”
• Quantitative PCR provides a simple and accessible method for quantitative microbiota profiling (2020, methodology): “Moreover, the qPCR-based method can be employed to study also non-bacterial communities where a universal marker gene is available, such as in fungi [12].”