A1 |
Load the Registry object with details of genomes available |
A2 |
Check which analyses are available for a species |
A3 |
Get soft-masked sequences from Arabidopsis thaliana |
A4 |
Get BED file with repeats in chr4 |
A5 |
Find the DEAR3 gene |
A6 |
Get the transcript used in Compara analyses |
A7 |
Find all orthologues of a gene |
A8 |
Get markers mapped on chr1D of bread wheat |
A9 |
Find all syntelogues among rices |
A10 |
Print all translations for other features genes |
B1 |
Check plant marts and select dataset |
B2 |
Check available filters and attributes |
B3 |
Download GO terms associated with genes |
B4 |
Get Pfam domains annotated in genes |
B5 |
Get SNP consequences from a selected variation source |
C1 |
Find RNA-seq CRAM files for a genome assembly |
F1 |
Download peptide sequences in FASTA format |
F2 |
Download CDS nucleotide sequences in FASTA format |
F3 |
Download transcripts (cDNA) |
F4 |
Download soft-masked genomic sequences |
F5 |
Upstream/downstream sequences |
F6 |
Get mappings to UniProt proteins |
F7 |
Get indexed, bgzipped VCF file with variants mapped |
F8 |
Get precomputed VEP cache files |
F9 |
Download all homologies in a single TSV file, several GBs |
F10 |
Download UniProt report of Ensembl Plants |
F11 |
Retrieve list of new species in current release |
F12 |
Get current plant species tree cladogram |
S1 |
Check currently supported Ensembl Genomes (EG) core schemas |
S2 |
Count protein-coding genes of a particular species |
S3 |
Get stable_ids of transcripts used in Compara analyses |
S4 |
Get variants significantly associated to phenotypes |
S5 |
Get Triticumaestivumhomeologous genes across A, B, and D subgenomes |
S6 |
Count the number of whole-genome alignments of all genomes |
S7 |
Extract all the mutations and consequence for a known line on triticum_aestivum |
R1 |
Create an HTTP client and helper functions |
R2 |
Get metadata for all plant species |
R3 |
Find features overlapping genomic region |
R4 |
Fetch phenotypes overlapping genomic region |
R5 |
Find homologues of selected gene |
R6 |
Get annotation of orthologous genes/proteins |
R7 |
Fetch variant consequences for multiple variant ids |
R8 |
Check consequences of single SNP within CDS sequence |
R9 |
Retrieve variation sources of a species |
V1 |
Download, install, and update VEP |
V2 |
Unpack downloaded cache file and check SIFT support |
V3 |
Predict effect of variants |
V4 |
Predict effect of variants for species not in Ensembl |