Becton Dickinson OMICS-One XT WTA Assay Kit

Becton Dickinson OMICS One XT WTA检测试剂盒

Becton Dickinson has launched the BD Omics-One XT WTA Assay whole-transcriptome amplification kit for automated library preparation in single-cell discovery studies.

Becton Dickinson推出了BD Omics One XT WTA Assay全转录组扩增试剂盒，用于单细胞发现研究中的自动文库制备。

The robotics-ready kit runs on the Hamilton Microlab NGS STAR automated liquid handling platform. The kit and platform can potentially deliver more consistent single-cell results compared to manual methods while also increasing sample throughput, BD said.

机器人就绪套件在汉密尔顿Microlab NGS STAR自动液体处理平台上运行。BD表示，与手动方法相比，该试剂盒和平台可能会提供更一致的单细胞结果，同时还可以提高样品通量。

Proteintech Genomics MultiPro Human Discovery Panel

Proteintech Genomics MultiPro人类发现小组

Proteintech Genomics has launched the MultiPro Human Discovery Panel for single-cell multiomics research. The new panel enables scientists to profile 325 proteins alongside whole-transcriptome analysis in single cells. The panel is built on 10x Genomics' Chromium Single Cell Gene Expression Flex chemistry with Feature Barcode technology, allowing researchers to explore proteins located both within the intracellular compartments and on the surface of cells.

Proteintech Genomics推出了用于单细胞多组学研究的MultiPro人类发现小组。新的小组使科学家能够在单细胞中分析325种蛋白质以及整个转录组分析。该小组基于10x Genomics的铬单细胞基因表达柔性化学和特征条形码技术，使研究人员能够探索位于细胞内区室和细胞表面的蛋白质。

With 346 antibodies against 325 distinct proteins, the panel offers significant coverage of key cellular components, including transcription factors, cytokines, signaling proteins, and phospho-epitopes. Approximately two-thirds of these protein targets are intracellular, while the remaining third are located on the cell surface, Proteintech said..

该小组拥有针对325种不同蛋白质的346种抗体，可显着覆盖关键细胞成分，包括转录因子，细胞因子，信号蛋白和磷酸表位。Proteintech说，这些蛋白质靶标中约有三分之二位于细胞内，而其余三分之一位于细胞表面。。

Breakthrough Genomics Virtual Geneticist

突破基因组学虚拟遗传学家

Breakthrough Genomics has launched a new version of its fully automated genome reader Virtual Geneticist. The newly designed platform is free to use and features a streamlined interface that allows users to enter basic clinical information and accompanying genomic data to receive a genomic interpretation report and rare disease diagnosis in minutes.

突破基因组学推出了其全自动基因组读取器虚拟遗传学家的新版本。新设计的平台可以免费使用，并具有简化的界面，允许用户输入基本的临床信息和伴随的基因组数据，以在几分钟内收到基因组解释报告和罕见疾病诊断。

VG's stripped-down landing page functions more like a Google search rather than requiring a cumbersome and complicated onboarding procedure, meaning it can be easily used as a tool to analyze new genomic testing data or double-check results from prior tests, especially for cases when no diagnostic variant was identified, Breakthrough said..

突破说，VG精简的登录页功能更像是谷歌搜索，而不需要繁琐而复杂的登录程序，这意味着它可以很容易地用作分析新基因组测试数据或重复检查先前测试结果的工具，尤其是对于未发现诊断变异的情况。。

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