# download gnomad vcf.bgz.tbi dataset into galaxy

**URL:** <https://help.galaxyproject.org/t/download-gnomad-vcf-bgz-tbi-dataset-into-galaxy/2828>\
**Category:** Uncategorized\
**Tags:** variant-analysis, snpeff\
**Created:** [January 21, 2020, 10:04pm UTC](https://help.galaxyproject.org/t/download-gnomad-vcf-bgz-tbi-dataset-into-galaxy/2828 "2020-01-21T22:04:59Z")\
**Posts on this page:** 1\
**Showing post:** 4

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**Author:** ![jennaj](https://sea2.discourse-cdn.com/flex020/user_avatar/help.galaxyproject.org/jennaj/32/27_2.png) [@jennaj](https://help.galaxyproject.org/u/jennaj)\
**Post date:** [January 23, 2020, 8:53pm UTC](https://help.galaxyproject.org/t/download-gnomad-vcf-bgz-tbi-dataset-into-galaxy/2828/4 "2020-01-23T20:53:17Z")

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Also asked about in this post:

> [@merge multiple VCF files - variant analysis and sample organization](https://help.galaxyproject.org/t/merge-multiple-vcf-files-variant-analysis-and-sample-organization/2796/3):
>
> Thank you for your answer! I followed the tutorial you suggested and also the “Identification of somatic and germline variants from tumor and normal sample pairs” tutorial ([https://galaxyproject.github.io/training-material/topics/variant-analysis/tutorials/somatic-variants/tutorial.html#variant-annotation-and-reporting](https://galaxyproject.github.io/training-material/topics/variant-analysis/tutorials/somatic-variants/tutorial.html#variant-annotation-and-reporting)), successfully. 1)I am interested in learning more about the GEMINI annotate and query and Join files to customize my analysis. I am trying to download the gnomad database but I…

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