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FinnGen Handbook
  • Introduction
  • Where to begin
    • Quick guides
      • New to FinnGen
      • Green data users
      • Red data users
    • I'm new to FinnGen, where is the best place for me to start?
    • What kind of questions can I ask of FinnGen data?
    • How do I make a custom endpoint?
    • How do I run a GWAS of a phenotype I created myself?
    • I'm interested in FinnGen rare variant phenotypes
  • Background Concepts
    • Basics of Genetics
    • Linkage Disequilibrium (LD)
    • Genotype Imputation
    • Genotype Data Processing and Quality Control (QC)
    • GWAS Analysis
    • P Values
    • Heritability and genetic correlations
    • Finemapping
    • Conditional analysis
    • Colocalization
    • Using Polygenic Risk Scores
    • PheWAS analysis
    • Survival analysis
    • Longitudinal Data Analysis
    • GWAS Association to Biological Function
    • Genetic Data Resources outside FinnGen
    • Getting Started with Unix
    • Getting Started with R
    • Structure of the FinnGen project
    • Finnish gene pool and health register data
  • FinnGen Data Specifics
    • FinnGen Data Freezes and Releases
    • Analysis proposals
      • What is a FinnGen analysis proposal and when do I need to submit one?
      • How do I submit an analysis proposal?
      • How are analysis proposals handled?
      • What is a FinnGen bespoke analysis proposal and when do I need to submit one?
      • How do I submit a bespoke analysis proposal?
      • How are bespoke analysis proposals handled?
      • What is the difference between FinnGen analysis proposals and FinnGen bespoke analyses?
      • Existing analysis proposals
    • Finnish Health Registries and Medical Coding
      • Finnish health registries
      • Register data pre-processing
      • Data Masking/Blurring of Visit Dates
      • International and Finnish Health Code Sets
      • More information on health code sets
      • VNR code mapping to RxNorm
      • Register code translation files
    • Endpoints
      • FinnGen clinical endpoints
      • History of creating the FinnGen endpoints
      • Location of FinnGen Endpoint and Control Description Files
        • What's new in DF13 endpoints
        • What’s new in DF12 endpoints
        • What’s new in DF11 endpoints
        • What’s new in the DF10 endpoints
        • What’s new in DF9 endpoints
        • What’s new in DF8 endpoints
      • Interpretation of Endpoint Definition file
      • Location of Endpoint Quality Control Report
      • Creating a User-defined Endpoint(s)
      • Requesting a User-defined Endpoint to be included in Core Analysis
      • Complete follow-up time of the FinnGen registries – primary endpoint data
        • Survival analysis using the truncated endpoint file – secondary endpoint data
    • Biobanks in Finland
    • Publishing FinnGen results
      • Preparing manuscripts or conference abstracts
      • The 1-year “Exclusivity Period” Policy
      • List of Publications using FinnGen Data
      • How to share GWAS summary statistics with FinnGen community
      • How to publish GWAS summary statistics
      • Public Result Releases
    • Red Library Data (individual level data)
      • Genotype data
        • Genotype Arrays Used
          • Legacy cohorts and chips
        • Imputation Panel
          • Sisu v4 reference panel
          • Sisu v3 reference panel
          • Sisu v4.2 reference panel
            • Variant-wise QC metrics file
        • Genome build used in FinnGen
        • Genotype Data Processing Flow
        • Genotype Files in Sandbox
          • Imputed genotypes in VCF format
          • Imputed genotypes in BGEN format
          • Imputed genotypes in PLINK format
          • Chip data
          • Imputed HLA alleles
          • Principal components analysis (PCA) data
          • Kinship data
          • Analysis covariates
          • Polygenic risk scores (PRS)
          • Genetic Ancestry
          • Genetic relationships (GRM)
          • Mosaic chromosomal alterations (mCA)
          • Prune data (R9)
          • Imputed STR genotypes (R8)
      • Phenotype data
        • Register data
        • Detailed longitudinal data
          • Splitting combination codes in detailed longitudinal data
        • Service sector data
          • Service sector data code translations
        • Endpoint and endpoint longitudinal data
        • Kanta lab values
          • Data
          • FAQ
          • How-to guides
        • Kanta prescriptions
        • Minimum extended phenotype data
          • Extracting minimum phenotype data per biobank
          • DNA isolation protocols per biobank
        • Minimum longitudinal data
        • Minimum phenotype data (before R11)
        • Cohort data (before R11)
        • Other register data files in Sandbox
          • Register of Congenital Malformations
          • Finnish Registry for Kidney Diseases
          • Reproductive history data
          • Finnish Cancer Registry: Cervical cancer screening
          • Finnish Cancer Registry: Breast cancer screening
          • Finnish Cancer Registry: Detailed cancer data
          • Finnish Register of Visual Impairment
          • Parental cause of death data
          • Ejection fraction data
          • Finnish National Infectious Disease Register
          • Finnish National Vaccination Register
          • Covid-19 primary care data
          • Blood donor data from the Finnish Red Cross Blood Service (FRCBS)
          • Dental data
          • Socioeconomic data
          • Hilmo and avohilmo extended data
      • Omics data
        • Proteomics
          • Expansion Area 5 proteomics data
          • FinnGen 3 proteomics data
        • Metabolomics
        • Single-cell transcriptomics and immune profiling
        • High-content cell imaging
        • Full blood counts and clinical chemistry
      • Hospital administered medications
      • Whole exome sequencing (WES) data
    • Green Library Data (aggregate data)
      • What is "Green" Data?
      • Accessing Green Data
      • Other analyses available
        • Colocalizations in FinnGen
        • Autoreporting – information on overlaps
          • Index of Autoreporting variables
        • HLA
        • LoF burden test
        • Meta-analyses
      • Core analysis results files
        • Recessive GWAS results format
        • Variant annotation file format
        • Genotype cluster plots format
        • GWAS results format
        • Finemapping results format
        • Colocalization results format
          • Results format in colocalization before DF13
        • Autoreporting results format
        • Sex-specific GWAS results format
        • UKBB-FinnGen meta-analysis file formats
        • Pairwise endpoint genetic correlation format
        • Heritabilities
        • Coding variant associations format
        • HLA association results
        • Proteomics results
        • Coding variant results including CHIP EWAS (Exome-Wide Association Scan)
        • Kanta lab association results v1
    • Disease specific Task Force data
      • Inflammatory bowel disease (IBD) SNOMED codes data
    • Expansion Area 3 (EA3) studies
      • EA3 study: Fatty liver disease study and data in Sandbox
      • EA3 study: Age-related macular degeneration study and data in Sandbox
      • EA3 study: Women's health studies
        • EA3 study: Women’s health – Endometriosis and data in Sandbox
        • EA3 study: Human papilloma virus-related gynecological lesions, and data in Sandbox
        • EA3 study: Women’s health – PCOS and infertility study, and data in Sandbox
      • EA3 study: Diabetic Kidney Disease and Rare Kidney Disease study and data in Sandbox
      • EA3 study: Oncology studies
        • EA3 study: Oncology – Breast cancer study and data in Sandbox
        • EA3 study: Oncology –Prostate cancer study and data in Sandbox
        • EA3 study: Oncology – Ovarian cancer study and data in Sandbox
      • EA3 study: Pulmonary diseases (IPF, asthma and COPD) study and data in Sandbox
      • EA3 study: Immune-mediated diseases
      • EA3 study: Heart Failure study and data in Sandbox
      • FinnGen EA3 leads
  • Disease Specific Task Forces
    • Inflammatory bowel disease (IBD)
    • Kidney Diseases
    • Eye Diseases
    • Rheumatic Diseases
    • Atopic Dermatitis
    • Pulmonary Diseases
    • Neurological Diseases
    • Heart Failure
    • Fibrotic Diseases
    • Metabolic diseases
    • Parkinson's diseases
  • Working in the Sandbox
    • How to get started with Sandbox
    • What is Sandbox and what can you do there
    • What do we mean by "red" and "green" data?
    • General workflows for the most common analyses
    • Quirks and Features
      • Managing your files in Sandbox
      • Navigating the Sandbox
      • How to save Sandbox window configuration
      • Copying and pasting in and out of your IVM
      • How to report issues from within the Sandbox
      • Sharing individual-level data within the Sandbox
      • How to download results from your IVM
        • Sandbox download requests – rules and examples for minimum N
      • Keyboard combinations
      • Running analyses in your IVM vs. Pipelines
      • Timeouts and saving your work (backups, github)
      • How to install a R package into Sandbox?
        • How to install R packages with many dependencies
      • Install R and Python packages from the local Sandbox repository
      • How to install a Python package into Sandbox
      • How to install GNU Debian package
      • How to upload your own files to IVM via /finngen/green
      • How to remove files from /finngen/green
      • Using Sandbox as a Chrome application (full screen mode)
      • How to reset your finngen.fi account password
      • Sandbox IVM tool request handling policy
      • Docker images
        • How to get a new Docker image to Sandbox
        • How to mount data into Docker container image
        • Containers available to Sandbox
        • Containers with user customized tool sets
        • How to write a Docker file
        • Anaconda Python environment in the Sandbox
      • Python Virtual Environment in Sandbox
      • How to shut down your IVM
    • Which tools are available?
      • FinnGen exome query tool
      • Custom GWAS tools
        • Custom GWAS GUI tool
        • Custom GWAS command line (CLI) tool
          • Custom GWAS CLI Binary mode
          • Custom GWAS CLI Quantitative mode
        • How to make your summary stats viewable in a PheWeb-style?
        • Finemapping of Custom GWAS analyses
        • PheWeb Users Input Validator tool
        • Conditional analysis of Custom GWAS analyses
      • Pipelines
      • Pre-installed Linux tools
      • PGS Browser
      • Lmod Linux tools
      • Anaconda Python module with ready set of scientific packages
      • Python packages
      • R packages
      • Atlas
        • Quick guide
          • Introduction to OHDSI, OMOP CDM and Atlas
          • From research question to concepts and cohort building
          • Using Atlas in Sandbox
          • Examples on cohort building with Atlas
        • Detailed guide
          • Atlas data model
          • Standard and non-standard codes
          • How to define a cohort in Atlas
            • Select FinnGen data release in Atlas for Search
            • How to define a simple ICD case-control cohort in Atlas
              • Define a simple ICD Concept Set in Atlas
              • Define a simple ICD case cohort in Atlas
              • Define a simple ICD control cohort in Atlas
            • Concept Sets
              • Create Concept Sets using descendants
              • Exclude and Remove codes from Concept Set
              • Simplify Concept Sets that use standard code descendants
              • Create Concept Sets using equivalent standard and non-standard codes
              • View standard code hierarchy in Atlas
            • Cohort Definitions
              • Using the Death register in Atlas
              • Filtering by clinical registries in Atlas
              • Filtering by demographic criteria in Atlas
              • Defining exit rules for a cohort in Atlas
              • Selecting the correct box in Atlas for events and medical codes
            • How to export FinnGen IDs from Atlas
          • Downstream analyses after the Atlas cohorts are created
          • Data Release Summary Statistics in Atlas
          • Cohort Summary Statistics in Atlas
            • Time-dependent Cohort Summary Statistics in Atlas
            • Event inclusion in Cohort Summary Statistics in Atlas
          • Cohort Pathways
      • BigQuery (relational database)
      • Atlas vs BigQuery cohorts
      • Genotype Browser
      • Cohort Operations tool (CO)
        • Upload cohorts to CO
        • Combine cohorts with CO
        • Operate on Atlas cohorts and data with entries and exit events
        • Explore code and endpoint enrichments with CO (CodeWAS)
        • Explore endpoint overlaps with CO
        • Compare custom endpoint to FinnGen endpoint with CO
        • Launch custom GWAS with CO
        • Export FinnGen IDs using CO
        • Understanding phenotypic overlaps using CO
      • Trajectory Visualization Tool (TVT)
        • Running TVT
          • Filtering timelines with TVT
          • Reordering timelines with TVT
          • Clustering timelines with TVT
          • Viewing TVT results
        • Viewing Atlas, CO, and Genotype cohorts in TVT
        • Exporting cohorts from TVT
        • TVT help page
      • LifeTrack
      • Miscellaneous helper scripts/tools
        • Tool to annotate variants with RSIDs
        • Proper translations of medical, service sector and provider codes
        • BigQuery Connection – R
          • Case study – All register data for a person
          • Case study – UpSet plot
          • Case study – Tornado plot
          • Case study – defining simple cohorts using medical codes for running case-control GWAS
        • BigQuery Connection - Python
          • BigQuery Python - Downstream analysis - Active Ingredient - Bar plot
          • BigQuery Python - Case Study - Sex different - Tornado plot
          • BigQuery Python - Case Study - Comorbidity - Upset plot
          • BigQuery Python - Case Study - Patient Timeline - Scatter plot
      • Sandbox internal API for software developers
    • Working with Phenotype Data
      • Variant PheWas
      • How to select controls for your cases
      • Using the R libraries to look at Phenotype data
      • How to check case counts from the data
      • Creating your own user-defined endpoint
    • Working with Genotype Data
      • Genotype Browser how to
      • Cluster Plots
      • ClusterPlot viewer V3C
      • Rare Variant Calling in V3C
      • Create map of allele
      • Genotypes from VCF files
      • Variant PheWas
      • Interpreting rare-variant analysis results
      • Tools for geno-pheno explorations
        • Example: transferring data from Genotype Browser to LifeTrack
        • Example: Visualizing Genotype Browser output data with TVT
    • Running analyses in Sandbox
      • How to run survival analyses
      • How to create custom endpoint using bigquery: example
      • How to use the Pipelines tool
      • How to submit a pipeline from the command line (finngen-cli)
      • How to run genome-wide association studies (GWAS)
        • How to run GWAS using REGENIE
        • Running quantitative GWAS with REGENIE
        • Conditional analysis
        • Conditional Analysis with custom regions and loci
        • How to run GWAS using SAIGE
        • Adding new covariates in GWAS using REGENIE and SAIGE
        • How to run GWAS using plink2 (for unrelated individuals only)
        • How to run GWAS using GATE (survival models)
        • How to run trajGWAS
        • How to run GWAS using the Regenie unmodifiable pipeline
        • How to run an interaction GWAS using the Regenie unmodifiable pipeline
        • How to run survival analysis using GATE unmodifiable pipeline
        • How to run GWAS on imputed HLA alleles using Regenie
      • How to run finemapping pipeline
        • Finemapping with custom regions in DF12
        • Unmodifiable Finemapping pipeline
      • How to run colocalization pipeline
      • How to run the LDSC pipeline
      • How to run PRS pipeline
      • How to calculate PRS weights for FinnGen data
      • Sandbox path and pipeline mappings
      • If your pipeline job fails
      • Tips on how to find a pipeline job ID
      • Managing memory in Sandbox and data filtering tips
      • Using Google Life Sciences API in Sandbox
      • Pipelines is based on Cromwell and WDL
    • Billing information and where to find more details
      • Monitoring Sandbox costs by Sandbox billing report
      • Monitoring Sandbox costs directly from your Google billing account
  • Working outside the Sandbox
    • Risteys
    • Endpoint Browser
    • PheWeb
      • Volcano plots with LAVAA
    • Meta-analysis PheWeb(s)
    • Coding variant browser
    • Multiple Manhattan Plot (MMP)
      • How to prepare an input file for MMP
      • How to use MMP
    • LD browser
    • Green library data
  • FAQ
    • FinnGen Spin Offs
    • FinnGen access and accounts
      • How do I apply for data access?
      • What is "red" or "green" data?
      • I already have green data access, how do I apply for red data access?
      • I cannot access the /finngen/red?
      • How do I enable two-factor authentication (2FA)?
      • I cannot access my FinnGen account?
      • How to reset account credentials
      • What to do if you suspect your account has been compromised
      • Can't access your smartphone for 2FA?
      • How do I access the FinnGen members' area?
      • How do I access FinnGen All Sharepoint?
      • How can I view existing analysis proposals?
      • How can I join the FinnGen Slack?
      • How do I join the FinnGen Teams group?
      • How to apply SES sandbox access
      • How to request a FinnGen account?
    • FinnGen data
      • What to do if I think I found a mistake in the data?
      • What are the field/column names in FinnGen?
      • What covariates are used in FinnGen's core GWAS analyses?
      • Does FinnGen have lab results available?
      • Does FinnGen have family and relatedness information available?
      • Where can I find a list of unrelated individuals in FinnGen?
      • When moving from BCOR to .txt files, what does the column called "correlation" mean?
      • Is there really no participant birth year data?
      • How do I calculate time between events?
      • Can I select only the columns needed for my analysis to import into RStudio?
      • What is the difference is between LD-clumping and the Saige conditional analysis?
      • Can I download all pairwise LD data across the genome at once?
      • How to find latest data releases?
      • Why are there differences in the GWAS results between Data Freezes/Releases?
    • Where can I find
      • COVID association results?
      • Users' Meeting materials?
      • A list of what coding variants are enriched in Finland?
      • A comprehensive list of key file locations in FinnGen?
      • Medical code translations?
    • PheWeb
      • What are QQ and Manhattan plots?
      • How can I access PheWeb?
      • Are fine-mapping results that available in PheWeb also available as flat files?
      • Do the autoreports report the 95% or 99% credible set?
    • Registries
      • What do KELA reimbursement codes map to?
      • What's the cutoff date for FinnGen data?
    • Sandbox
      • What is the FinnGen Sandbox?
      • Why does my IVM freeze while loading data into R/Rstudio
      • Where can I find tutorials and documentation on Sandbox?
      • How do I get my own analysis code into Sandbox?
      • Where to ask for software you'd like to see in Sandbox
      • Can I share individual level data between different Sandbox users?
      • Is there a sun grid engine for running long scripts?
      • How to clear browser cache after sandbox update
      • How do I increase the window resolution on my IVM?
      • How can I view pdf, jpg and HTML files?
      • My Sandbox job was killed - why?
      • How to unzip files in the command line
      • Why aren't my keyboard/shortcuts working in Sandbox like they do in my local computer?
      • How to know if my pipeline job was failed due preemption of worker VM
    • Risteys
      • Why is the case number dropping after the "Check pre-conditions, main-only, mode, ICD version" step?
    • Endpoints
      • Where do I find the most recent list of FinnGen endpoints?
      • What does it mean when an endpoint has “mode” at the end?
      • What scenario would cause an NA (missing data) entry rather than a zero?
      • Does it mean anything when a value is written as $!$ instead of NA?
      • Why is there an inconsistency between ICD10 code J84.1 (IPF) and J84.112?
      • How are control endpoints calculated?
      • Can I get a list of FinnGen IDs by control group for my endpoint?
      • What does Level C mean in the endpoints data table?
      • What does the SUBSET_COV field show?
      • Why is there a "K." prefix on some endpoints?
      • Why there are fewer endpoints going from R5 (N = 2,925) to R8 (N = 2,202)?
      • Should I include primary care registry (PRIM_OUT) codes in my cohort definitions?
      • I found BL_AGE after FU_END_AGE in the endpoint data, how is it possible?
      • Why do individuals who are not dead have death age in endpoint data?
      • I found EVENT_AGE after FU_END_AGE in endpoint data, how is it possible?
    • Pipelines
      • Are there example SAIGE pipelines?
      • How do I apply finemapping to my SAIGE results?
      • Why Pipelines is claiming that my files or folders are not in /finngen/red?
    • Citing
      • How do I cite analysis using publicly available FinnGen results?
      • How do I cite FinnGen results that use individual level data?
    • For biobanks
      • How to apply for data return
    • Data Security and Protection
      • How do I report a data breach?
  • Release Notes
    • Data Releases 2025
    • Data Releases 2024
    • Data Releases 2023
    • Data Releases 2022
    • Data Releases 2021
  • Tool Catalog
  • Glossary
  • User Support
  • Data Protection & Security
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  • Example core analysis result files from FinnGen Release 12 (R12)
  • Example core analysis result files from FinnGen Release 11 (R11)
  • Example core analysis result files from FinnGen Release 10 (R10)

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  1. FinnGen Data Specifics
  2. Green Library Data (aggregate data)

Core analysis results files

PreviousMeta-analysesNextRecessive GWAS results format

Last updated 8 months ago

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FinnGen core analysis results files are available in the Sandbox.

Each core analysis results file is described in the following sections:

See to view all data releases to the Sandbox.

Data freeze/Release specific analysis reports:

Example core analysis result files from FinnGen Release 12 (R12)

Female-/male-specific summary statistics: gs://finngen-production-library-green/finngen_R12/finngen_R12_analysis_data/sex_difference/summary_stats/

Female-male meta-analysis summary statistics: gs://finngen-production-library-green/finngen_R12/finngen_R12_analysis_data/sex_difference/meta_analysis/meta_summary_stats/

Aggregated meta-analysis results (all endpoints, single-sex assoc P<=5E-8): gs://finngen-production-library-green/finngen_R12/finngen_R12_analysis_data/sex_difference/meta_analysis/sex_specific_meta_gwsig_in_either_sex_all_endpoints.tsv.gz

gs://finngen-production-library-green/finngen_R12/finngen_R12_analysis_data/lof/

data: gs://finngen-production-library-green/finngen_R12/finngen_R12_analysis_data/hla/

documentation: gs://finngen-production-library-green/finngen_R12/finngen_R12_analysis_documentation/finngen_R12_hla_analysis.md gs://finngen-production-library-green/finngen_R12/finngen_R12_analysis_documentation/finngen_R12_hla_analysis.pdfFinnGen

  • finemapping data: /finngen/library-green/finngen_R12/finngen_R12_analysis_data/finemap

  • autoreporting data: /finngen/library-green/finngen_R12/finngen_R12_analysis_data/autoreporting

  • documentation: /finngen/library-green/finngen_R12/finngen_R12_analysis_documentation/

  • /finngen/library-red/finngen_R12/hla_1.0/

FinnGen R12 meta-analysis results

  • The data and documentation location in the Sandbox

    • gs://finngen-production-library-green/finngen_R12/finngen_R12_analysis_data/meta_analysis/ukbb/

  • data: gs://finngen-production-library-green/finngen_R12/finngen_R12_analysis_data/summary_stats

  • documentation: gs://finngen-production-library-green/finngen_R12/finngen_R12_analysis_documentation/

  • pheweb link: https://r12.finngen.fi

FinnGen DF12 Annotation file

  • Variant annotation file with INFO scores and other annotations gs://finngen-production-library-green/finngen_R12/finngen_R12_analysis_data/annotations/R12_annotated_variants_v1.gz

Example core analysis result files from FinnGen Release 11 (R11)

  • gs://finngen-production-library-green/finngen_R11/finngen_R11_analysis_data/meta_analysis/ukbb/

  • The data and documentation location in the Green Library

    • gs://finngen-production-library-green/finngen_R11/finngen_R11_analysis_data/coding/

FinnGen R11 HLA analysis results. The data and documentation location in the green library:

  • gs://finngen-production-library-green/finngen_R11/finngen_R11_analysis_data/hla/

  • gs://finngen-production-library-green/finngen_R11/finngen_R11_analysis_documentation/finngen_R11_hla_analysis.md

  • gs://finngen-production-library-green/finngen_R11/finngen_R11_analysis_documentation/finngen_R11_hla_analysis.pdf

FinnGen Release 11 heritability and genetic correlation analysis outputs

  • The data and documentation location in the green library:

    • gs://finngen-production-library-green/finngen_R11/finngen_R11_analysis_data/ldsc/

FinnGen Release 11 GWAS, finemapping, conditional analysis, colocalization and autoreporting data. The data and documentation location in the green library:

  • GWAS:

    • gs://finngen-production-library-green/finngen_R11/finngen_R11_analysis_data/summary_stats

  • Fine-mapping:

    • gs://finngen-production-library-green/finngen_R11/finngen_R11_analysis_data/finemap

  • Conditional analysis:

    • gs://finngen-production-library-green/finngen_R11/finngen_R11_analysis_data/conditional_analysis

  • Autoreporting:

    • gs://finngen-production-library-green/finngen_R11/finngen_R11_analysis_data/autoreporting

  • Colocalization:

    • gs://finngen-production-library-green/finngen_R11/finngen_R11_analysis_data/colocalization

  • Documentation available at:

    • gs://finngen-production-library-green/finngen_R11/finngen_R11_analysis_documentation/

    • Data and documentation location in Sandbox:

      • /finngen/library-red/finngen_R11/cluster_plot_1.0

    • Detailed paths to library red data from manifest:

      • /finngen/library-red/finngen_R11/cluster_plot_1.0/manifest.txt

  • Colocalization between pQTLs and all genome wide significant hits in R10 .

    • Data location in the green library:

      • gs://finngen-production-library-green/finngen_R10/finngen_R10_analysis_data/colocalization/

pQTL analysis and finemapping results

gs://finngen-production-library-green/omics/proteomics/release_2023_03_02/

Example core analysis result files from FinnGen Release 10 (R10)

Colocalization between pQTLs and all genome wide significant hits in R10

gs://finngen-production-library-green/finngen_R10/finngen_R10_analysis_data/colocalization/

  • pQTL analysis and finemapping results

    • 828 and 619 samples from SomaLogic and Olink respectively samples

    • Data location in the green library:

      • gs://finngen-production-library-green/omics/proteomics/release_2023_03_02/

  • Colocalization between pQTLs and all genome wide significant hits in R10 .

    • Data location in the green library:

      • gs://finngen-production-library-green/finngen_R10/finngen_R10_analysis_data/colocalization/

  • Heritabilities and genetic correlations: /finngen/library-green/finngen_R10/finngen_R10_analysis_data/ldsc/

  • Imputed HLA allele genotypes /finngen/library-red/finngen_R10/hla_1

  • GWAS data location:

    • /finngen/library-green/finngen_R10/finngen_R10_analysis_data/summary_stats

    • Sex-specific association analysis results (under summary_stats)

    • Variant annotation file with INFO scores and other annotations /finngen/library-green/finngen_R10/finngen_R10_analysis_data/annotations/

  • Fine-mapping data location:

    • /finngen/library-green/finngen_R10/finngen_R10_analysis_data/finemap

  • Conditional analysis data location:

    • g/finngen/library-green/finngen_R10/finngen_R10_analysis_data/conditional_analysis

  • Autoreporting data location:

    • /finngen/library-green/finngen_R10/finngen_R10_analysis_data/autoreporting

  • Colocalization data location:

    • /finngen/library-green/finngen_R10/finngen_R10_analysis_data/colocalization

  • Documentation location:

    • /finngen/library-green/finngen_R10/finngen_R10_analysis_documentation/

  • FinnGen 10 HLA allele analysis results: /finngen/library-green/finngen_R10/finngen_R10_analysis_data/hla/

    • Documentation available at:

      • /finngen/library-green/finngen_R10/finngen_R10_analysis_documentation/finngen_R10_hla_analysis.pdf

  • Finngen R10 cluster plot data:/finngen/library-green/finngen_R10/cluster_plots/

    • The cluster plot tsv files, that contain genotype intensities per variant for a subset of samples used in the cluster plots are released to the Sandbox at:

      /finngen/library-red/finngen_R10/cluster_plot_1.0/data/

      • Detailed paths of this data from the manifest file: /finngen/library-red/finngen_R10/cluster_plot_1.0/manifest.txt

  • FinnGen R10 PRS data (version 1.0): /finngen/library-red/finngen_R10/prs_1.0/

Example core analysis result files from FinnGen Release 8 (R8)

  • Genotype cluster plot file: /finngen/library-red/finngen_R8/cluster_plot_1.0/

  • GWAS results: /finngen/library-green/finngen_R8/finngen_R8_analysis_data/summary_stats/

  • Finemapping results: /finngen/library-green/finngen_R8/finngen_R8_analysis_data/finemap/

  • Colocalization results: /finngen/library-green/finngen_R8/finngen_R8_analysis_data/colocalization/

  • Autoreporting results: /finngen/library-green/finngen_R8/finngen_R8_analysis_data/autoreporting/

  • UKBB-FinnGen meta-analysis results: /finngen/library-green/finngen_R8/finngen_R8_analysis_data/ukbb_meta/

  • All heritability estimates and genetic correlations calculated by ldsc software: /finngen/library-green/finngen_R8_analysis_data/ldsc/

  • Pairwise endpoint genetic correlation format: /finngen/library-green/finngen_R8_analysis_data/ldsc/finngen_R8_FIN.ldsc.summary.tsv

  • Heritabilities: /finngen/library-green/finngen_R8_analysis_data/ldsc/finngen_R8_FIN.ldsc.heritability.tsv

  • Coding variant subset format:/finngen/library-green/finngen_R8/finngen_R8_analysis_data/summary_stats/coding_variants/coding_variants.tsv.gz (all binary endpoints)

  • All quantitative traits (coding variant subset): /finngen/library-green/finngen_R8/finngen_R8_analysis_data/summary_stats/coding_variants/coding_variants.quantitative.tsv.gz

  • Chip GWAS (will be released for DF9, previously was released for DF5)

  • Annotation file (file including eg. counts of each variant per batch and most_severe_consequence and gene; used by finemapping pipeline and Regenie): /finngen/library-green/finngen_R8_analysis_data/annotations/

  • Mapping for imputed variants: /finngen/library-green/finngen_R8_analysis_data/variant_mapping/finngen.variants.tsv

  • Full dbsnp: /finngen/library-green/finngen_R8_analysis_data/variant_mapping/rsid_map.tsv

  • Phenotype case/control N: finngen/library-green/finngen_R8/finngen_R8_pheno.tsv

  • Release documentation: /finngen/library-green/finngen_R8/finngen_R8_analysis_documentation/

FinnGen DF12 and heterogeneity results:

FinnGen DF12 results:

FinnGen DF12 results data: gs://finngen-production-library-green/finngen_R12/finngen_R12_analysis_data/colocalization/ documentation: green/finngen_R12/finngen_R12_analysis_documentation/finngen_R12_colocalization.md gs://finngen-production-library-green/finngen_R12/finngen_R12_analysis_documentation/finngen_R12_colocalization.pdf

FinnGen DF12 results: gs://finngen-production-library-red/finngen_R12/prs_1.0

FinnGen DF12 and results: gs://finngen-production-library-green/finngen_R12/finngen_R12_analysis_data/genetic_correlation/ gs://finngen-production-library-green/finngen_R12/finngen_R12_analysis_data/conditional_analysis/

FinnGen DF12 analysis results

R12 & results

FinnGen R12

(856 binary and 10 progression endpoints):

FinnGen DF12

(762 endpoints) R11:

FinnGen Release 11 and documentation

Finngen R11 . These data files contain genotype intensities per variant for a subset of samples that are used in cluster plots (released in the green library).

The results are browsable in FinnGen browser (e.g. , scroll down for colocalization table)

The results are browsable in FinnGen browser (e.g. , scroll down for colocalization table)

All green-library files can also be seen outside of the Sandbox, without red-data access, by using . See instructions from . When using google cloud console finngen/library-green/ within the above paths is replaced byproduction-library-green, otherwise the paths are the same.

Genotype cluster plots
GWAS results
Finemapping
Colocalization
Autoreporting data
Sex-specific GWAS results
Recessive GWAS results
UKBB - FinnGen meta-analysis
Pairwise endpoint genetic correlations
Heritabilities
Coding variant subset
HLA association results
Proteomics results
Chip EWAS (Exome-Wide Association Scan)
Release Notes
Analysis report R12
Analysis report R11
Analysis Report R10
Analysis Report R9
Analysis Report R8
Analysis Report R7
Analysis Report R6
Analysis Report R5
sex-specific GWAS
LOF
colocalization
PRS
conditional analysis
genetic correlation
HLA association
autoreporting
finemapping
hla data
FinnGen + UKBB meta-analysis
GWAS data
FinnGen + UKBB meta-analysis
coding variant association results
cluster plot data
https://results.finngen.fi/region/H7_AMD/1:196510779-196910779
https://results.finngen.fi/region/H7_AMD/1:196510779-196910779
google cloud console
here