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Topic Area: Standard Reference Materials
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Displaying records 21 to 24.
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21. Standard Practice for Determining the Relative Spectral Correction Factors for the Emission Signal of Fluorescence Spectrometers
Series: NIST Interagency/Internal Report (NISTIR)
Report Number: 7915
Topic: Standard Reference Materials
Published: 8/15/2013
Author: Paul C DeRose
Abstract: This standard practice is intended to aid in the calibration and qualification of fluorescence spectrometers as part of complying with regulatory and other QA/QC requirements. It specifies the materials and procedures used in three different meth ...
http://www.nist.gov/manuscript-publication-search.cfm?pub_id=913001

22. Standard Reference Material for Her2 Testing: Report of a National Institute of Standards and Technology-Sponsored Consensus Workshop
Topic: Standard Reference Materials
Published: 6/1/2003
Authors: M E Hammond, Peter E. Dr. Barker, S Taube, S Gutman
Abstract: A workshop was sponsored by National Institute of Standards and Technology (NIST) Cancer Diagnosis Program of National Cancer Institute (CDP NCI), Food and Drug Administration (FDA), and College of American Pathologists (CAP) to address the need for ...
http://www.nist.gov/manuscript-publication-search.cfm?pub_id=830374

23. Synthetic spike-in standards improve run-specific systematic error analysis for DNA and RNA sequencing
Topic: Standard Reference Materials
Published: 7/31/2012
Authors: Justin M Zook, Daniel Victor Samarov, Jennifer H McDaniel, Shurjo Sen, Marc L Salit
Abstract: While the importance of random sequencing errors decreases at higher DNA or RNA sequencing depths, systematic sequencing errors (SSEs) dominate at high sequencing depths and can be difficult to distinguish from biological variants. These SSEs can ...
http://www.nist.gov/manuscript-publication-search.cfm?pub_id=910640

24. Why human genome sequencing platforms differ: Integrating sequencing datasets to understand biases and form consensus variant calls
Topic: Standard Reference Materials
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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