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Systematic bias in genomic classification due to contaminating non-neoplastic tissue in breast tumor samples.由于乳腺肿瘤样本中存在污染的非肿瘤组织,基因组分类存在系统性偏差。
BMC Med Genomics. 2011 Jun 30;4:54. doi: 10.1186/1755-8794-4-54.
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College of American Pathologists/American College of Medical Genetics proficiency testing for constitutional cytogenomic microarray analysis.美国病理学家学院/美国医学遗传学学院的染色体基因组微阵列分析能力验证。
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Preanalytical quality improvement: from dream to reality.分析前质量改进:从梦想变为现实。
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The effect of formaldehyde fixation on RNA: optimization of formaldehyde adduct removal.甲醛固定对 RNA 的影响:甲醛加合物去除的优化。
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Analysis of circulating microRNA: preanalytical and analytical challenges.循环 microRNA 分析:分析前和分析中的挑战。
Clin Chem. 2011 Jun;57(6):833-40. doi: 10.1373/clinchem.2010.157198. Epub 2011 Apr 12.
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Does routine repeat testing of critical values offer any advantage over single testing?常规重复检测危急值是否优于单次检测?
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7
Nucleic acids extraction from laser microdissected FFPE tissue sections.从激光显微切割的福尔马林固定石蜡包埋(FFPE)组织切片中提取核酸。
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8
Gene expression profiles from formalin fixed paraffin embedded breast cancer tissue are largely comparable to fresh frozen matched tissue.福尔马林固定石蜡包埋的乳腺癌组织的基因表达谱与新鲜冷冻匹配组织基本可比。
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9
Genome-wide gene expression profiling of formalin-fixed paraffin-embedded breast cancer core biopsies using microarrays.使用微阵列对福尔马林固定石蜡包埋的乳腺癌核心活检进行全基因组基因表达谱分析。
J Histochem Cytochem. 2011 Feb;59(2):146-57. doi: 10.1369/jhc.2010.956607.
10
Transcriptional profiling and genotyping of degraded nucleic acids from autopsy tissue samples after prolonged formalin fixation times.长时间福尔马林固定后尸检组织样本中降解核酸的转录谱分析和基因分型。
Int J Clin Exp Pathol. 2011 Jan 6;4(2):156-61.

临床实验室中 RNA 表达谱分析的质量保证。

Quality assurance of RNA expression profiling in clinical laboratories.

机构信息

Department of Pathology and Laboratory Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, 27599-7525, USA.

出版信息

J Mol Diagn. 2012 Jan;14(1):1-11. doi: 10.1016/j.jmoldx.2011.09.003. Epub 2011 Oct 20.

DOI:10.1016/j.jmoldx.2011.09.003
PMID:22020152
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3338342/
Abstract

RNA expression profiles are increasingly used to diagnose and classify disease, based on expression patterns of as many as several thousand RNAs. To ensure quality of expression profiling services in clinical settings, a standard operating procedure incorporates multiple quality indicators and controls, beginning with preanalytic specimen preparation and proceeding thorough analysis, interpretation, and reporting. Before testing, histopathological examination of each cellular specimen, along with optional cell enrichment procedures, ensures adequacy of the input tissue. Other tactics include endogenous controls to evaluate adequacy of RNA and exogenous or spiked controls to evaluate run- and patient-specific performance of the test system, respectively. Unique aspects of quality assurance for array-based tests include controls for the pertinent outcome signatures that often supersede controls for each individual analyte, built-in redundancy for critical analytes or biochemical pathways, and software-supported scrutiny of abundant data by a laboratory physician who interprets the findings in a manner facilitating appropriate medical intervention. Access to high-quality reagents, instruments, and software from commercial sources promotes standardization and adoption in clinical settings, once an assay is vetted in validation studies as being analytically sound and clinically useful. Careful attention to the well-honed principles of laboratory medicine, along with guidance from government and professional groups on strategies to preserve RNA and manage large data sets, promotes clinical-grade assay performance.

摘要

RNA 表达谱越来越多地被用于诊断和分类疾病,其依据是多达数千种 RNA 的表达模式。为了确保临床环境中表达谱服务的质量,标准操作规程包括多个质量指标和控制措施,从分析前标本准备开始,贯穿分析、解释和报告的全过程。在检测之前,对每个细胞标本进行组织病理学检查,并进行可选的细胞富集程序,以确保输入组织的充分性。其他策略包括内源性对照,以评估 RNA 的充分性,以及外源性或加标对照,以分别评估测试系统的运行和患者特异性性能。基于阵列的测试的质量保证的独特方面包括针对相关结果特征的对照,这些特征通常取代针对每个单独分析物的对照,对关键分析物或生化途径进行内置冗余,以及软件支持的实验室医生对大量数据的审查,以促进以促进适当医疗干预的方式解释发现。从商业来源获得高质量的试剂、仪器和软件可以促进临床环境中的标准化和采用,一旦在验证研究中证明该测定具有良好的分析性能和临床实用性。仔细关注实验室医学的精细化原则,以及政府和专业团体关于保存 RNA 和管理大数据集的策略指导,可促进临床级别的测定性能。