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    • A

      10x vdj数据分析
      免疫组学 • • anneng

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      https://www.sc-best-practices.org/air_repertoire/ir_profiling.html
      56a55e24-8f0e-4b43-a73b-0ee7beaf8d4e-image.png

      VDJ过程
      adc29db5-511a-48a1-bd0f-e9269ac0a751-image.png

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      免疫组学基础
      免疫组学 • • anneng

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    • Z

      rook-ceph磁盘删除重新添加
      问题记录及解决 • • zhanglu

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    • Z

      blast_gpu
      软件部署及教程 • • zhanglu

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      测试

      gpu time /cephfs_data/app/blast_gpu/ncbi-blast-2.2.28+-src/c++/GCC480-ReleaseMT64/bin/blastp -query /cephfs_data/app/blast_gpu/database/test2.fa -db /cephfs_data/app/blast_gpu/database/nr -gpu t -num_threads 30 real 13m42.160s user 38m52.082s sys 0m13.170s cpu

      time /cephfs_data/app/blast_gpu/ncbi-blast-2.2.28+-src/c++/GCC480-ReleaseMT64/bin/blastp -query /cephfs_data/app/blast_gpu/database/test2.fa -db /cephfs_data/app/blast_gpu/database/nr -gpu f -num_threads 30

      real 23m23.076s
      user 695m50.953s
      sys 1m35.377s

    • Z

      tmp
      张方琳 • • zhangfanglin

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      Z

      /cephfs_data/genostack_v3/genostack_php/source_v3/reportHtml/2024_09/a9cc132fd641478e84caacd66ab8502e.zip

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      细胞类型注释
      单细胞分析 • • anneng

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      A

      https://www.sciencedirect.com/science/article/pii/S2215016123001966
      Negative markers combined with positive markers can increase the specificity of cell type identification, reducing the likelihood of misclassification and improving the overall accuracy of the analysis
      [3]
      . By default, the signature genes are expected to be highly expressed in one cell type compared to all other cell types. However, depending on the underlying data, these canonical markers may not be enough to segregate cell types with similar expression profiles (e.g., sub-groups of T-cells in the human blood). When this occurs, genes that are expected not to be detected in a specific cell type (e.g., CD8A in CD4 T cells) can be utilized to improve segregation. Therefore, genes that are characteristically lowly expressed in one cell type compared to the other cell types are introduced as the “negative markers”.

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      siRNA和建模
      RNA-Seq数据分析 • • anneng

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    • A

      R 在jupyter中提示killed
      小技巧 • • anneng

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    • A

      merge vs integrate
      单细胞分析 • • anneng

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      https://www.perplexity.ai/search/seurat-merge-vs-integrate-4wIsp710SlSXnWASiWuvjg
      The functions merge() and IntegrateData() in Seurat serve distinct purposes in handling single-cell RNA sequencing (scRNA-seq) data, particularly when working with multiple datasets.
      merge()
      The merge() function is primarily used to concatenate two or more Seurat objects. This method combines the raw count matrices of the specified objects into a single object. Key characteristics include:
      Concatenation of Counts: merge() combines the raw count data from the input objects. If there are unique genes in either dataset, those genes are included in the merged object, resulting in a comprehensive count matrix that reflects all genes present across the datasets.
      Loss of Normalization: By default, merging erases any previously normalized and scaled data matrices, meaning that it does not account for differences in data distributions between the datasets. If normalization is desired, it must be performed after merging.
      Use Cases: This function is suitable for datasets with minimal batch effects or when combining technical replicates, where the primary goal is to create a larger dataset from similar conditions.
      IntegrateData()
      In contrast, IntegrateData() is designed for more complex scenarios where datasets may have inherent differences, such as batch effects or biological variability. Its main features include:
      Anchor-Based Integration: This function utilizes a method based on identifying "anchor" cells that are shared across datasets. This approach allows for the integration of datasets while accounting for differences in gene expression profiles, enabling better comparison of shared cell populations.
      Focus on Shared Variance: The result of IntegrateData() is a single integrated dataset that retains only the genes shared among the datasets, which facilitates comparative analysis of gene expression profiles across different conditions or batches.
      Use Cases: It is recommended for situations where datasets are expected to have substantial biological differences or batch effects, such as datasets generated from different platforms or experimental conditions.
      Summary
      In summary, use merge() when you want to combine datasets with minimal differences and retain all gene information, while IntegrateData() is preferred for integrating datasets with significant variability to ensure that shared cell populations are accurately represented and analyzed. The choice between the two depends on the experimental design and the nature of the datasets being analyzed.

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      新冠单细胞数据分析样例 covid19_sc
      单细胞分析 • • anneng

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      A

      conda install -c conda-forge fftw
      由于jupyter的环境是在conda里面 所以当报一些包找不到时 用conda安装 用apt安装 可能路径不对 还是找不到

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      GenoStack Jupyterlab 插件清单
      大数据 • • anneng

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      https://github.com/jupyterlab-contrib/jupyter-archive 这个插件可以在UI上直接解压文件或者压缩文件夹并下载 对于生信的场景很有用 空了可以安装升级下

      https://github.com/silx-kit/jupyterlab-h5web 还有这个 可以直接打开h5ad文件 对于单细胞来说很有用

    • Z

      ubuntu 22.04 docker 安装
      软件部署及教程 • • zhanglu

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    • A

      k8s 常用命令
      小技巧 • • anneng

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      https://www.digitalocean.com/community/tutorials/how-to-inspect-kubernetes-networking

      k8s网络

    • A

      Linux 网络命令
      小技巧 • • anneng

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    • A

      晶能UI适配需求
      软件架构设计 • • anneng

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    • A

      ceph故障问题记录
      问题记录及解决 • • anneng

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      A

      ceph tools中执行ceph status会卡死 重启tools pod
      这个问题可能和mgr状态不对有关

    • A

      k8s 启动时 很多pod无法挂载volume
      问题记录及解决 • • anneng

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    • Z

      GS集成AI方案与功能
      软件架构设计 • • zhangfanglin

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    • Z

      GS对接Slurm相关功能
      软件架构设计 • • zhangfanglin

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    • Z

      GS报告升级方案
      软件架构设计 • • zhangfanglin

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