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用于变异分类的证据的教育评估:分子病理学协会的报告。

An Educational Assessment of Evidence Used for Variant Classification: A Report of the Association for Molecular Pathology.

机构信息

The Variant Interpretation Testing Among Laboratories (VITAL) Working Group of the Clinical Practice Committee, Association for Molecular Pathology (AMP), Rockville, Maryland; HudsonAlpha Institute for Biotechnology, Huntsville, Alabama.

Association for Molecular Pathology (AMP), Rockville, Maryland.

出版信息

J Mol Diagn. 2022 Jun;24(6):555-565. doi: 10.1016/j.jmoldx.2021.12.014. Epub 2022 Apr 13.

Abstract

The Association for Molecular Pathology Variant Interpretation Testing Among Laboratories (VITAL) Working Group convened to evaluate the Standards and Guidelines for the Interpretation of Sequence Variants implementation into clinical practice, identify problematic classification rules, and define implementation challenges. Variants and associated clinical information were provided to volunteer respondents. Participant variant classifications were compared with intended consensus-derived classifications of the Working Group. The 24 variant challenges received 1379 responses; 1119 agreed with the intended response (81%; 95% CI, 79% to 83%). Agreement ranged from 44% to 100%, with 16 challenges (67%; 47% to 82%) reaching consensus (≥80% agreement). Participant classifications were also compared to a calculated interpretation of the ACMG Guidelines using the participant-reported criteria as input. The 24 variant challenges had 1368 responses with specific evidence provided and 1121 (82%; 80% to 84%) agreed with the calculated interpretation. Agreement for challenges ranged from 63% to 98%; 15 (63%; 43% to 79%) reaching consensus. Among 81 individual participants, 32 (40%; 30% to 50%) reached agreement with at least 80% of the intended classifications and 42 (52%; 41% to 62%) with the calculated classifications. This study demonstrated that although variant classification remains challenging, published guidelines are being utilized and adapted to improve variant calling consensus. This study identified situations where clarifications are warranted and provides a model for competency assessment.

摘要

分子病理学协会(AMP)实验室间变异解释测试(VITAL)工作组召开会议,评估标准和指南在临床实践中的实施情况,识别有问题的分类规则,并定义实施挑战。向志愿者受访者提供了变异体和相关临床信息。将参与者的变异分类与工作组的预期共识分类进行比较。这 24 个变异体挑战共收到 1379 条回复;1119 条回复与预期回复一致(81%;95%置信区间,79%至 83%)。一致性范围从 44%到 100%不等,其中 16 个挑战(67%;47%至 82%)达成共识(≥80%的一致性)。参与者的分类也与使用参与者报告的标准作为输入的 ACMG 指南的计算解释进行了比较。这 24 个变异体挑战有 1368 条回复,并提供了具体的证据,其中 1121 条回复(82%;80%至 84%)与计算解释一致。挑战的一致性从 63%到 98%不等;15 个挑战(63%;43%至 79%)达成共识。在 81 名个别参与者中,32 名(40%;30%至 50%)至少与 80%的预期分类和 42 名(52%;41%至 62%)的计算分类达成一致。这项研究表明,尽管变异分类仍然具有挑战性,但已在使用发布的指南并对其进行调整,以提高变异体调用共识。这项研究确定了需要澄清的情况,并为能力评估提供了模型。

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