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英文字典中文字典相关资料:


  • The human disease methylation database - hrbmu. edu. cn
    The labels indicate the number of differential methylated genes computed by DiseaseMeth version 2 0
  • Help - bio-bigdata. hrbmu. edu. cn
    The human Disease Methylation Database DiseaseMeth version 2 0 The human disease methylation database, DiseaseMeth version 2 0 is a web based resource focused on the aberrant methylomes of human diseases Until recently, bulks of large-scale data are avaible and are increasingly grown, from which more information can be mined to gain further information towards human diseases Our mission is
  • CellMarker2. 0 - hrbmu. edu. cn
    Welcome to CellMarker 2 0 Type I spiral ganglion neuron (1126) Microglial cell (764) Neuron (741)
  • Analyze - bio-bigdata. hrbmu. edu. cn
    1 Disease option is used to select the interested diseases 2 Gene name Transcript ID Genomic Interval are used to set interested genomic regions Users can input multiple items 3 Technology Experimental Platform option is used to select the datatype of methylome 4 Control Type is used to select methylomes of controls that is normal tissues
  • Visualization - hrbmu. edu. cn
    DiseaseMeth version 2 0 The human disease methylation database Home Search Analyze DisMethBrowser Download Help
  • Data download - hrbmu. edu. cn
    The human Disease Methylation Database TCGA data download All the 450k data are arranged in the format of annotation file
  • Search - hrbmu. edu. cn
    2 Curation Level of Disease-Gene Association is used to search the wanted association between diseases and methylation of genes 3 The result will display a heatmap for each disease that is associated with the gene or genomic region 1 Disease option is used to select interested diseases for methylome displayed by a heatmap
  • CellMarker2. 0
    A convenient tool to visualizedetailed distribution of cells and find differentially expressed genes in different clusters
  • LincSNP 2. 0 - bio-bigdata. hrbmu. edu. cn
    LincSNP 2 0 provides a submission page that allows researchers to submit newly identified SNP-lncRNA-disease associations Once approved by the submission review committee, the submitted record will be included in the LincSNP 2 0 database and made available to the public in the update release





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