IGVFFI0524YUIL

preview
validated
{
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    "accession": "IGVFFI0524YUIL",
    "aliases": [
        "jesse-engreitz:240908-S029-PPIF_5SpliceSite-IndividualVariantExp-AGGT_TCAG-THP1_Variant-EFFECTS_File_Standardized"
    ],
    "assay_titles": [
        "Variant-EFFECTS"
    ],
    "assembly": "GRCh38",
    "audit": {},
    "award": {
        "@id": "/awards/HG011972/",
        "component": "functional characterization"
    },
    "barcode_map_for": [],
    "checkfiles_version": "v20",
    "content_md5sum": "db9fdff00016f581472510112d5542b2",
    "content_type": "variant effects",
    "controlled_access": false,
    "creation_timestamp": "2025-03-29T00:14:06.868302+00:00",
    "derived_from": [
        "/tabular-files/IGVFFI0706LAPB/"
    ],
    "derived_manually": true,
    "description": "Manually standardized output of Variant-EFFECTS pipeline, formatted for GRCh38 with SPDI variant IDs",
    "file_format": "tsv",
    "file_format_specifications": [
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            "description": "This file type describes results from genome editing experiments that measure the effect of a variant on an endogenous gene in the genome."
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                "taxa": "Homo sapiens"
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                        "@id": "/crispr-modifications/fc6bc0b3-a064-47d0-b95d-a9af14bb1624/",
                        "modality": "prime editing",
                        "status": "released",
                        "summary": "CRISPR prime editing Sp-nCas9-M-MLV RT (PE2)"
                    }
                ],
                "sample_terms": [
                    {
                        "@id": "/sample-terms/EFO_0001253/",
                        "status": "released",
                        "term_name": "THP-1"
                    }
                ],
                "status": "preview",
                "summary": "Homo sapiens (male) THP-1 cell line (sorting details: FACS bin for 26-50% expression of PPIF) modified with CRISPR prime editing Sp-nCas9-M-MLV RT (PE2), transduced (lentivirus) with a guide library",
                "taxa": "Homo sapiens"
            }
        ],
        "status": "preview",
        "summary": "CRISPR prime editing Variant-EFFECTS targeting PPIF integrating a guide (sgRNA) library targeting sequence variants in a genomic locus"
    },
    "file_size": 337,
    "gene_list_for": [],
    "href": "/tabular-files/IGVFFI0524YUIL/@@download/IGVFFI0524YUIL.tsv.gz",
    "input_file_for": [],
    "integrated_in": [],
    "lab": {
        "@id": "/labs/jesse-engreitz/",
        "title": "Jesse Engreitz, Stanford"
    },
    "loci_list_for": [],
    "md5sum": "8f429ab0d9c0061a926aa6b72aaa561d",
    "primer_design_for": [],
    "quality_metrics": [],
    "s3_uri": "s3://igvf-files/2025/03/29/67aada35-700e-419b-b0a1-dbb342282dc4/IGVFFI0524YUIL.tsv.gz",
    "schema_version": "15",
    "status": "preview",
    "submitted_by": {
        "@id": "/users/f9e7cd82-a407-4a20-89ee-f4dc668b0cbe/",
        "title": "Michael Montgomery"
    },
    "submitted_file_name": "PPIF_5PrimeSpliceIndividual_AGGT_TCAG_VariantEffectsFile.tsv.gz",
    "submitter_comment": "The original outputs from the Variant-EFFECTS pipeline report VariantIDs in the hg19 format. To obtain the standardized variant information provided in this file, hg19 coordinates were lifted to hg38 using the UCSC LiftOver tool (https://genome.ucsc.edu/cgi-bin/hgLiftOver). Then, canonical, validated SPDIs were generated and validated using the igvf_spdi_demo tool (https://github.com/mikelove/igvf_spdi_demo).",
    "summary": "GRCh38 variant effects",
    "upload_status": "validated",
    "uuid": "67aada35-700e-419b-b0a1-dbb342282dc4"
}