1.4. Access to datasets in the database

When you access https://jmorp.megabank.tohoku.ac.jp, the top page of the jMorp website appears.

../../_images/access_to_datasets-top.en.png

There are roughly three blocks on the top page (keyword search, genome browser, and category index).

1.4.2. Genome browser view

You can browse the genome-related data in the genome browser by clicking the link on the bottom left of the jMorp top page. There are three different types of genome browsers available now: GRCh37/hg19, GRCh38/hg38, and JG2.1.0. The genome-related data stored in jMorp uses different reference genomes for analysis, and the data that can be browsed differs depending on the selection of genome browsers.

  • GRCh37/hg19
    • Genome Variation
      • 3.5KJPNv2: SNV/INDEL frequency panel derived from short-read whole genome analysis of 3,500 samples

      • 4.7KJPN: SNV/INDEL frequency panel derived from short-read whole genome analysis of 4,700 samples

      • 8.3KJPN: SNV/INDEL frequency panel derived from short-read whole genome analysis of 8,300 samples

      • 8.3KJPN-SV: Structual variation (SV) frequency panel derived from short-read whole genome analysis of 8,300 samples

    • Genome (others)
      • Genome Accessibility: Mean depth data calculated from TMM short-read whole genome sequencing data

  • GRCh38/hg38
    • Genome Variation
      • 14KJPN: SNV/INDEL frequency panel derived from short-read whole genome analysis of 14,000 samples

      • 38KJPN: SNV/INDEL frequency panel derived from short-read whole genome analysis of 38,000 samples

      • 54KJPN: SNV/INDEL frequency panel derived from short-read whole genome analysis of 54,000 samples

      • JCNVv1: CNV frequency panel derived from short-read whole genome analysis of 48,000 samples

      • JSV1: Structual variation (SV) frequency panel derived from long-read whole genome analysis of 222 samples

    • Genome (others)
      • Genome Accessibility: Mean depth data calculated from TMM short-read whole genome sequencing data

  • JG2.1.0
    • Genome Sequence
      • JG2.1.0: JG2.1.0 Japanese reference genome sequence

    • Genome Variation
      • 38KJPN: SNV/INDEL frequency panel derived from short-read whole genome analysis of 38,000 samples (liftover from GRCh38 version)

      • 54KJPN: SNV/INDEL frequency panel derived from short-read whole genome analysis of 54,000 samples (liftover from GRCh38 version)

For instructions on using the genome browser, see Genome browser.

1.4.3. Category index

There is a list of the datasets that are part of jMorp on the right side of the top page. To view the list of entries in a dataset, click on the dataset name. For example, clicking on Metabolome 2023 brings up the table below, which contains a list of the metabolites that are included in the metabolome dataset.

../../_images/access_to_datasets-metabolite_list.en.png

Additionally, you can browse the metabolite’s detailed information by clicking the metabolite ID.

The category index is the best option if you want to quickly see what kind of data is contained in jMorp.

Note

For categories with a lot of entries, like Genome Variation (SNV/INDEL), lists of entries are not available. Please make use of the keyword search and genome browser views.