Publications by authors named "Yingyi Hao"

Article Synopsis
  • Oncopanel genomic testing is becoming more common in medical practice, but there is a lack of reliable reference samples with many known variants for assessing the analytical quality of these tests.
  • The FDA's SEQC2 consortium analyzed diverse cancer cell lines and developed a reference sample, Sample A, which reveals over 40,000 variants, greatly exceeding existing commercial samples.
  • This new sample provides enhanced tools for evaluating oncopanel performance, offering better quality control and validation options for both traditional and liquid biopsy assays.
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In clinical cancer research, it is a hot topic on how to accurately stratify patients based on genomic data. With the development of next-generation sequencing technology, more and more types of genomic features, such as mRNA expression level, can be used to distinguish cancer patients. Previous studies commonly stratified patients by using a single type of genomic features, which can only reflect one aspect of the cancer.

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Prostate cancer remains the second leading cause of male cancer death, and there is an unmet need for biomarkers to identify patients with such aggressive disease. Piwi-inteacting RNAs (piRNAs) have been classified as transcriptional and posttranscriptional regulators in somatic cells. In this study, we discovered three piRNAs as novel prognostic markers and their association with prostate cancer biochemical recurrence was confirmed in validation data set.

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Drug-induced rhabdomyolysis (DIR) is an idiosyncratic and fatal adverse drug reaction (ADR) characterized in severe muscle injuries accompanied by multiple-organ failure. Limited knowledge regarding the pathophysiology of rhabdomyolysis is the main obstacle to developing early biomarkers and prevention strategies. Given the lack of a centralized data resource to curate, organize, and standardize widespread DIR information, here we present a Drug-Induced Rhabdomyolysis Atlas (DIRA) that provides DIR-related information, including: a classification scheme for DIR based on drug labeling information; postmarketing surveillance data of DIR; and DIR drug property information.

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