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You searched on: Topic Area: Bioscience Health Sorted by: title

Displaying records 281 to 284.
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281. Use of a spectrally-tunable source to explore improvement in chromatic contrast for illumination of tissues
Topic: Bioscience & Health
Published: 2/11/2010
Authors: Maritoni Abatayo Litorja, Ben Ecker
Abstract: Human vision by a clinical practitioner is often the first disease detection tool. Illumination for such procedures as endoscopy use broadband white light, with luminance level being the only control available. The use of staining dyes for contrast i ...
http://www.nist.gov/manuscript-publication-search.cfm?pub_id=904910

282. Validated Open Source Nanofiber Diameter Measurement Tool
Topic: Bioscience & Health
Published: 4/30/2015
Authors: Nathan A Hotaling, Kapil Bharti, Haydn Kriel, Carl George Simon Jr.
Abstract: Despite the growing use of nanofiber scaffolds for tissue engineering applications, there is not a validated, readily available (commercial or open source) solution for rapid, automated analysis of nanofiber diameter from scanning electron microscope ...
http://www.nist.gov/manuscript-publication-search.cfm?pub_id=917542

283. Viscosity Measurements of DNA Solutions with and without Condensing Agents
Topic: Bioscience & Health
Published: 7/7/2014
Authors: Arno R Laesecke, Jessica Lynne Burger
Abstract: Aqueous DNA solutions at three concentrations were studied as model sputum by viscosity measurements at ambient pressure. Initial measurements at 25 {degree}C, 37.78 {degree}C, and 50 {degree}C indicated a viscosity increase toward 50 {degree}C. Th ...
http://www.nist.gov/manuscript-publication-search.cfm?pub_id=914036

284. Why human genome sequencing platforms differ: Integrating sequencing datasets to understand biases and form consensus variant calls
Topic: Bioscience & Health
Published: 2/16/2014
Authors: Justin M Zook, Brad Chapman, Winston Hide, Marc L Salit
Abstract: Hundreds of thousands of differences exist between human whole genome variant calls from different sequencing platforms and variant calling pipelines, but the reasons for these differences are poorly understood. Well-characterized whole genome Refer ...
http://www.nist.gov/manuscript-publication-search.cfm?pub_id=912658



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