MediaWiki API result

This is the HTML representation of the JSON format. HTML is good for debugging, but is unsuitable for application use.

Specify the format parameter to change the output format. To see the non-HTML representation of the JSON format, set format=json.

See the complete documentation, or the API help for more information.

{
    "batchcomplete": "",
    "continue": {
        "gapcontinue": "Sequencing",
        "continue": "gapcontinue||"
    },
    "query": {
        "pages": {
            "1700": {
                "pageid": 1700,
                "ns": 0,
                "title": "Rnaextraction",
                "revisions": [
                    {
                        "contentformat": "text/x-wiki",
                        "contentmodel": "wikitext",
                        "*": "=== RNA Extraction ===\nWe are pleased to offer two methods of RNA extraction. Both methods retain total RNA, including small RNAs.  \n\n== Qiagen miRNeasy ==\nFor most low- to medium-throughput experiments, we recommend the column-based Qiagen miRNeasy. \n\nhttps://www.qiagen.com/us/products/discovery-and-translational-research/dna-rna-purification/rna-purification/mirna/mirneasy-kits?catno=217004\n\nThis kit purifies RNA from up to 5 mg tissue, or cells (up to 1 x 106 cells).\n\nSamples should be provided to the Genome Core frozen in exactly 700 ul of Qiazol (please reach out to us, we can supply this), or Trizol. Please do not use >700 ul of Qiazol. \n\n== MagMAX mirVana ==\nFor high throughput projects, we recommend the 96-well, plate-based MagMAX mirVana Total RNA Isolation Kit from Thermo Fisher. \n\nhttps://www.thermofisher.com/order/catalog/product/A27828\n\nThis kit purifies RNA from 10-30 mg of tissue or 1 \u00d7 106 cells.\n\nSamples should be provided to the Genome Core frozen in the MagMax Processing Plate in MagMax Lysis Binding Mix (please reach out to us, we can supply these), according to your project\u2019s unique specifications. We will work with you to make sure that you have all of the information and supplies."
                    }
                ]
            },
            "1693": {
                "pageid": 1693,
                "ns": 0,
                "title": "Scripts",
                "revisions": [
                    {
                        "contentformat": "text/x-wiki",
                        "contentmodel": "wikitext",
                        "*": "= Tool to convert FASTQ format =\n\nFASTQ read id format conversion - https://github.com/sumeetg23/PROFQ\n\nInternally, the script is available at the following location (Unix): /nfs/WIGTC/pub/Public_apps/Format_Conversion/FASTQ_Format_Conversion_v4.pl"
                    }
                ]
            }
        }
    }
}