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Titlebook: Genomic Applications in Pathology; George Jabboure Netto,Karen L. Kaul Book 2019Latest edition Springer International Publishing AG, part

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發(fā)表于 2025-3-23 10:00:10 | 只看該作者
Patents and Proprietary Assaysuction of novel diagnostic tests. Opponents argue that patents are unnecessary for discovery and that they raise costs, decrease patient access, and harm innovation in the field of molecular pathology. In two recent Supreme Court cases, . and ., the Court ruled that biological correlations and human
12#
發(fā)表于 2025-3-23 14:35:03 | 只看該作者
13#
發(fā)表于 2025-3-23 20:38:13 | 只看該作者
Transitioning Discoveries from Cancer Genomics Research Laboratories into Pathology Practiceindings essential for the use of novel classes of targeting therapies. Although there is considerable enthusiasm for the use of the discoveries of cancer genomics for personalized medicine in clinical practice, the number of new classes of biomarkers incorporated into cancer diagnosis and treatment
14#
發(fā)表于 2025-3-23 22:31:50 | 只看該作者
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發(fā)表于 2025-3-24 03:40:05 | 只看該作者
16#
發(fā)表于 2025-3-24 07:09:49 | 只看該作者
17#
發(fā)表于 2025-3-24 14:38:47 | 只看該作者
Zu Puayen Tan,Brian Thurow,Shengxian Shils and tissues and is allowing us to better understand alternative splicing and the functional elements of the genome and to identify single-nucleotide variants and new fusion transcripts in cancer. We also review current and potential clinical applications of RNA-Seq technology in inherited, chronic, neoplastic, and infectious diseases
18#
發(fā)表于 2025-3-24 17:39:29 | 只看該作者
https://doi.org/10.1007/978-981-10-0033-1ons in human genes and genotype–phenotype relationships and will help facilitate the introduction of large-scale sequencing into clinical practice. The Supreme Court has thereby encouraged the advancement, development, and implementation of personalized medicine.
19#
發(fā)表于 2025-3-24 20:37:54 | 只看該作者
Getting to Grips with Neuronal Diversity,t the computational processing, analysis, and interpretation of NGS results. These efforts have facilitated a broad dissemination of NGS into every facet of biomedical research and into a growing list of clinical diagnostic applications from targeted multigene panels to whole-genome sequencing.
20#
發(fā)表于 2025-3-25 01:03:43 | 只看該作者
-driven informatic analysis of exomes or genomes. Improved efficiency of molecular genetic testing, driven by the development and implementation of comprehensive disease-targeted gene panels, is propelling the advancement of genomic medicine.
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