Use my own data in Ensembl
NGS reads and more
Ensembl supports a number of different filetypes for upload and visualisation along the genome.
The most popular page in which to view your data is the Location tab, Region in Detail. Use the 'Add your data' button in the left hand menu (N.B. the button will change to 'Manage your data' once you've added at least one file).
A dialogue will ask you what your file type is. You are allowed to upload smaller files. In the case of large data files, only the url attachment option is available.
Here is an example of sequence reads attached as a BAM file, along chromosome 20.
Find out more:
Alleles and mutations
Use the Variant Effect Predictor (VEP) to determine effects of nucleotide substitutions, insertions and deletions within genes or the genome.
Genes and Transcripts
Use BioMart to get information about a list of gene or transcript IDs, names, symbols, or chromosomal locations. Some examples:
- Convert Ensembl IDs to gene names
- Get SNPs for a list of transcripts
- Export protein sequences for genes on a chromosomal region
Learn how to use it in this 5 minute video:
For more about BLAT/BLAST read the help page.
Your data can be displayed on Ensembl karyotypes, by adding your data and going to the 'Whole Genome' view. Note that sparse data can be displayed as points, whereas larger datasets can only be displayed as density tracks.
You can also create a karyotype display showing the location of selected Ensembl features by clicking on 'Add your data', choosing the 'Features on Karyotype' option in the lefthand menu and inputting a list of gene names.
You can display your own genome-wide variation data in Ensembl by attaching your data as VCF files. See our FAQ for more details. Visualise different consequence terms of your variants on the set of Ensembl genes and transcripts. The different consequence terms are displayed by different colours in the Region in Detail view.