noninvasive detection
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mBio ◽  
2022 ◽  
Author(s):  
Courtney R. Armour ◽  
Begüm D. Topçuoğlu ◽  
Andrea Garretto ◽  
Patrick D. Schloss

Despite being highly preventable, colorectal cancer remains a leading cause of cancer-related death in the United States. Low-cost, noninvasive detection methods could greatly improve our ability to identify and treat early stages of disease.


Author(s):  
Jennifer K. Trittmann ◽  
Hanadi Almazroue ◽  
Leif D. Nelin ◽  
Terri A. Shaffer ◽  
Charanda R. Celestine ◽  
...  

2021 ◽  
Vol 13 (620) ◽  
Author(s):  
Matthijs J. M. Cluitmans ◽  
Laura R. Bear ◽  
Uyên C. Nguyên ◽  
Bianca van Rees ◽  
Job Stoks ◽  
...  

2021 ◽  
pp. 339298
Author(s):  
Gang Li ◽  
Dan Wang ◽  
Liu Guozhong ◽  
Wang Xiaofei ◽  
Kang Wang ◽  
...  

PLoS ONE ◽  
2021 ◽  
Vol 16 (10) ◽  
pp. e0259084
Author(s):  
Stephanie S. Coster ◽  
Megan N. Dillon ◽  
William Moore ◽  
George T. Merovich

Environmental DNA (eDNA) is nuclear or mitochondrial DNA shed into the environment, and amplifying this DNA can serve as a reliable, noninvasive way to monitor aquatic systems for the presence of an invasive species. Assays based on the collection of eDNA are becoming increasingly popular, and, when optimized, can aid in effectively and efficiently tracking invasion fronts. We set out to update an eDNA assay to detect the invasive rusty crayfish, Faxonius rusticus. We tested for species specificity compared to other stream crayfish and field tested the assay at sites with known presence (N = 3) and absence (N = 4) in the Juniata River watershed in central Pennsylvania, USA. To maximize sensitivity, we field tested different storage buffers (Longmire’s buffer and ethanol), DNA extraction methods (Qiagen’s DNEasy and PowerWater kits), and quantitative polymerase chain reaction (qPCR) chemistries (TaqMan and SYBR green). Our assay confirmed the presence data and performed optimally when filter samples were stored in Longmire’s buffer, DNA was extracted with DNeasy Blood and Tissue Kit, and TaqMan qPCR chemistry was utilized. With proper sample processing, our assay allows for accurate, noninvasive detection of F. rusticus in streams.


2021 ◽  
Vol 2021 ◽  
pp. 1-10
Author(s):  
Hans E. Skallevold ◽  
Evan M. Vallenari ◽  
Dipak Sapkota

A very low percentage of lung cancer (LC) cases are discovered at an early and treatable stage of the disease, leading to an abysmally low 5-year survival rate. This underscores the immediate necessity for improved diagnostic, prognostic, and predictive biomarkers for LC. Biopsied lung tissue, blood, and plasma are common sources used for LC diagnosis and monitoring of the disease. A growing number of studies have reported saliva to be a useful biological sample for early and noninvasive detection of oral and systemic diseases. Nevertheless, salivary biomarker discovery remains underresearched. Here, we have compiled the available literature to provide an overview of the current understanding of salivary markers for LC detection and provided perspectives for future clinical significance. Valuable markers with diagnostic and prognostic potentials in LC have been discovered in saliva, including metabolic (catalase activity, triene conjugates, and Schiff bases), inflammatory (interleukin 10, C-X-C motif chemokine ligand 10), proteomic (haptoglobin, zinc-α-2-glycoprotein, and calprotectin), genomic (epidermal growth factor receptor), and microbial candidates (Veillonella and Streptococcus). In combination, with each other and with other established screening methods, these salivary markers could be useful for improving early detection of the disease and ultimately improve the survival odds of LC patients. The existing literature suggests that saliva is a promising biological sample for identification and validation of biomarkers in LC, but how saliva can be utilized most effectively in a clinical setting for LC management is still under investigation.


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