2/ If you need the sequence of a single #gene, you can search for the gene symbol or ID from Ensembl homepage and click on ‘Sequence’ in the menu on the left
3/ From this page, you can download the sequence of the gene by clicking on the blue ‘Download Sequence’ button just above the sequence display.
4/ From the pop-up window, you can select the sequence format and type. Either #FASTA or RTF. FASTA option will allow you to download cDNA, CDS, protein, UTR, Exon, Intron and/or genomic sequences in FASTA format -> really useful to use as input in other tools or platforms!
5/ From the gene tab, you can also search for the exon, cDNA or protein sequences of individual transcripts by clicking on the ‘Show Transcript table’ button and clicking on a transcript stable ID to navigate to the transcript tab.
6/ Click on Exon, cDNA or Protein from the menu on the left hand side to view the sequences. Then you can click on the blue ‘Download Sequence’ button to download in either FASTA or RTF format, just like before!
7/ You can also export the sequence of any genomic region by navigating to the location tab for the region and clicking on the ‘Export Data’ button on the left of the page. Just select ‘FASTA sequence’ from the output menu in the pop-up window and click ‘Next’ to download.
8/ If you have a list of gene, transcript or protein symbols or IDs, you can retrieve their sequences from the #BioMart tool with a single query.
🖥️▶️ Watch our BioMart tutorial on YouTube:
9/ Or if you can code🧑💻 and want to automate downloading the sequences you need, you can write a script in any language to use the GET sequence endpoints in the Ensembl REST API: rest.ensembl.org/documentation/…
10/ or if you want to get whole #genome sequences, the Ensembl FTP site has FASTA files of whole #genome sequences, cDNA, CDS and protein sequences of all protein-coding genes, or ncRNA sequences for every species: ftp.ensembl.org
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2/ The #BioMart tool is what you’re going to need for this task. You can find it in the blue header from the @ensembl homepage: ensembl.org/biomart/martvi…
3/ First, you’ll need to select your database type and species of interest using the drop-down menus. In this case, we want to select ‘Ensembl Genes 111’ and the ‘Human genes’ dataset.
2/ Gene-level tissue-specific expression patterns from @ExpressionAtlas are displayed in the Gene tab. Just search for your gene of interest, click through to the gene tab and then click on ‘Gene Expression’ in the left-hand menu. Let’s use SERPINA3 as an example:
@ExpressionAtlas 3/ On this page, you can view baseline expression results as a heatmap with all tissues studied (columns) in different experiments (rows) in which the gene is expressed above the default minimum expression level.
2/ If you are working with human 🧑🤝🧑 variation data, genome-wide variant deleteriousness rankings from the CADD algorithm are available as well as pathogenicity predictions from SIFT, Polyphen-2, REVEL, MutationAssessor and MetaLR for missense variants.
3/ You can see all this data in the ‘Variant Table’ page in the gene tab
👉 https://t.co/vZAsntjEXYensembl.org/Homo_sapiens/G…
2/ To start, look for the #canonical tag in the flags column of the transcript table. The canonical transcript is based on conservation, expression, concordance with @appris_cnio and @uniprot, length, clinically important variants and completeness.
3/ Many Ensembl #canonical transcripts will also be the #MANESelect, which is our collaboration with @NCBI. These transcripts match perfectly with RefSeq transcripts, so are the best to report variant location.
1/ It’s another Thursday, and that means it’s time for another #tweetorial! Today, we want to show you how you can view RefSeq #annotations on Ensembl 🥳
2/ While Ensembl gene models are annotated directly on the reference genome, #RefSeq are annotated on mRNA sequences. In other words: genome browsers will have different annotation methods, so you might be interested in comparing these annotations side-by-side 📖🤔
3/ 👂🏽You say you want to make direct comparisons of annotations between @NCBI’s RefSeq and Ensembl? Now is your time to try it out on Ensembl! 🏃🏽
2/ The Variant Effect Predictor (VEP) is what you’re going to need for this task. You can find it in the blue header from the @ensembl homepage: ensembl.org/info/docs/tool…
3/ Click the ‘Launch VEP’ button to open the VEP web tool and enter your input data using instructions in the documentation:
👉ensembl.org/info/docs/tool…