39 research outputs found

    A practical guide to single-cell RNA-sequencing for biomedical research and clinical applications.

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    RNA sequencing (RNA-seq) is a genomic approach for the detection and quantitative analysis of messenger RNA molecules in a biological sample and is useful for studying cellular responses. RNA-seq has fueled much discovery and innovation in medicine over recent years. For practical reasons, the technique is usually conducted on samples comprising thousands to millions of cells. However, this has hindered direct assessment of the fundamental unit of biology-the cell. Since the first single-cell RNA-sequencing (scRNA-seq) study was published in 2009, many more have been conducted, mostly by specialist laboratories with unique skills in wet-lab single-cell genomics, bioinformatics, and computation. However, with the increasing commercial availability of scRNA-seq platforms, and the rapid ongoing maturation of bioinformatics approaches, a point has been reached where any biomedical researcher or clinician can use scRNA-seq to make exciting discoveries. In this review, we present a practical guide to help researchers design their first scRNA-seq studies, including introductory information on experimental hardware, protocol choice, quality control, data analysis and biological interpretation

    The effectiveness of green advertising: An Australian empirical study

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    Use of hyperspectral reflectance for discrimination between grape varieties

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    Visible-near infrared reflectance characteristics were examined for four varieties (Cabernet Sauvignon, Merlot, Semillon and Shiraz) of grape vine grape (Vitis vinifera) in a southern Australian vineyard. Reflectance measurements over the range 400-900 nm were acquired in the field under solar illumination using a Lastek VNIR spectroradiometer. Both reflectance and first derivative spectra were tested at 2 nm intervals for differences between the four varieties and pairs of varieties showing greatest significance were established using a Tukey post hoc test. The field reflectance spectra showed greatest difference at the red edge (~720 nm), followed by the green reflectance peak and its wings in the visible. Cabernet Sauvignon and Semillon were the most significantly different pair throughout the visible region, while the differences at the red edge were mainly attributed to Semillon. In the derivative spectra regions of significant difference were narrower and potentially attributable to chlorophyll content, leaf structure or water content. Cabernet Sauvignon differed most from the other varieties at approximately 512 nm and 580 nm. The wavelengths that showed the greatest potential for discrimination between all four varieties were 512 nm, 580 nm, 611 nm, 649 nm, 690 nm and 763 nm.F.M. Lacar, M.M. Lewis and I.T. Grierso

    Use of hyperspectral imagery for mapping grape varieties in the Barossa Valley, South Australia

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    The wine industry is important to Australia's economy. With the advances in remote sensing there has been increasing interest in its potential application for vineyard varietal, condition and health mapping. CASI (Compact Airborne Spectrographic Imager) data was obtained over a vineyard in the Barossa Valley, South Australia in an attempt to discriminate between the grape cultivars (Vitis vinifera) , Cabernet Sauvignon and Shiraz. Statistical analysis of sample spectra from the two varieties in the CASI imagery showed that the significant differences in the visible region. Maximum likelihood classification was employed to map the two grape varieties present on the site. Classification was performed using 12 visible and near infrared CASI bands and repeated using a spectral subset of seven bands shown to be most significant in separating the varieties. Discrimination between Cabernet Sauvignon and Shiraz was successful with 91.5% of vine rows correctly classified. Spectral subsetting did not improve classification and led to under classification of vine pixels.F.M. Lacar, M.M. Lewis and I.T. Grierso

    Are cells from a snowman realistic? Cryopreserved tissues as a source for single-cell RNA-sequencing experiments

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    A recently published study in Genome Biology shows that cells isolated from cryopreserved tissues are a reliable source of genetic material for single-cell RNA-sequencing experiments.Please see related Method article: http://genomebiology.biomedcentral.com/articles/10.1186/s13059-017-1171-9
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