Graham Reference Dataset Repository
Since May 2021 we have been testing a Network File System (NFS) data mount to provide our users with some commonly used datasets in Bioinformatics and AI. This data mount is provided in an effort to better serve our users and to lower the usage on their project accounts with commonly used datasets. These datasets are mounted on /datashare/
. You can explore the top directories by listing the mount:
[jshleap@gra-login1 ~]$ ls -lL /datashare/
total 152
drwxrwxr-x 9 jshleap sn_staff 4096 Jul 6 11:14 1000genomes
drwxrwxr-x 2 jshleap sn_staff 94208 Jun 4 15:30 BLASTDB
drwxrwxr-x 2 jshleap sn_staff 107 Jun 4 15:30 BLAST_FASTA
drwxrwxr-x 5 jshleap sn_staff 229 Jun 4 18:49 CIFAR-10
drwxrwxr-x 5 jshleap sn_staff 221 Jun 4 18:49 CIFAR-100
drwxrwxr-x 6 jshleap sn_staff 115 Apr 27 10:00 COCO
drwxrwxr-x 2 jshleap sn_staff 135 Jun 10 18:23 DIAMONDDB_2.0.9
drwxrwxr-x 6 jshleap sn_staff 321 Feb 4 17:39 EggNog
drwxrwxr-x 2 jshleap sn_staff 6 Mar 16 16:42 github_mirror
drwxrwxr-x 3 jshleap sn_staff 46 Mar 23 14:23 hg38
drwxrws--- 9 jshleap imagenet-optin 244 Jun 16 09:22 ImageNet
drwxrwxr-x 8 jshleap sn_staff 4096 Jun 7 16:58 kraken2_dbs
drwxrwxr-x 2 jshleap sn_staff 191 Jun 4 18:49 MNIST
drwxrwxr-x 2 jshleap sn_staff 50 Jun 4 18:51 MPI_SINTEL
drwxrwxr-x 2 jshleap sn_staff 4096 Jun 9 17:09 NCBI_taxonomy
drwxrwxr-x 6 jshleap sn_staff 145 Feb 4 22:44 PANTHER
drwxrwxr-x 5 jshleap sn_staff 4096 Apr 19 17:24 PFAM
drwxrwxr-x 7 jshleap sn_staff 4096 Mar 29 09:52 SILVA
drwxrwxr-x 6 jshleap sn_staff 257 Feb 4 22:46 SVHN
drwxrwxr-x 4 jshleap sn_staff 189 Apr 19 17:59 UNIPROT
drwxrwx--- 5 jshleap voxceleb-optin 98 Apr 23 15:15 VoxCeleb
Below a detailed description of each dataset and how to access them.
Bioinformatics
Bioinformatics software often uses reference datasets (often referred to as databases) to work properly. In [www.sharcnet.ca SHARCNET] we are providing a set of these datasets for bioinformatics:
1000 Genomes
In human genetics, the 1000 genomes project (1KGP) was an effort to catalogue human genetic variation and has become a reference and a comparison point to many studies. We provide their data from their FTP site, and will be checked for updates twice a year (June and December).
Directory structure
1000 Genomes directory tree (up to level 2):
├── CHANGELOG ├── data_collections │ ├── 1000G_2504_high_coverage │ ├── 1000G_2504_high_coverage_SV │ ├── 1000_genomes_project │ ├── gambian_genome_variation_project │ ├── gambian_genome_variation_project_GRCh37 │ ├── geuvadis │ ├── han_chinese_high_coverage │ ├── HGDP │ ├── HGSVC2 │ ├── hgsv_sv_discovery │ ├── HLA_types │ ├── illumina_platinum_pedigree │ ├── index.html │ ├── README_data_collections.md │ └── simons_diversity_data ├── historical_data │ ├── former_toplevel │ ├── index.html │ └── README_historical_data.md ├── index.html ├── phase1 │ ├── analysis_results │ ├── data │ ├── index.html │ ├── phase1.alignment.index │ ├── phase1.alignment.index.bas.gz │ ├── phase1.exome.alignment.index │ ├── phase1.exome.alignment.index.bas.gz │ ├── phase1.exome.alignment.index.HsMetrics.gz │ ├── phase1.exome.alignment.index.HsMetrics.stats │ ├── phase1.exome.alignment.index_stats.csv │ ├── README.phase1_alignment_data │ └── technical ├── phase3 │ ├── 20130502.phase3.analysis.sequence.index │ ├── 20130502.phase3.exome.alignment.index │ ├── 20130502.phase3.low_coverage.alignment.index │ ├── 20130502.phase3.sequence.index │ ├── 20130725.phase3.cg_sra.index │ ├── 20130820.phase3.cg_data_index │ ├── 20131219.populations.tsv │ ├── 20131219.superpopulations.tsv │ ├── data │ ├── index.html │ ├── integrated_sv_map │ ├── README_20150504_phase3_data │ └── README_20160404_where_are_the_phase3_variants ├── pilot_data │ ├── data │ ├── index.html │ ├── paper_data_sets │ ├── pilot_data.alignment.index │ ├── pilot_data.alignment.index.bas.gz │ ├── pilot_data.sequence.index │ ├── README.alignment.index │ ├── README.bas │ ├── README.sequence.index │ ├── release │ ├── SRP000031.sequence.index │ ├── SRP000032.sequence.index │ ├── SRP000033.sequence.index │ └── technical ├── PRIVACY-NOTICE.txt ├── README_ebi_aspera_info.md ├── README_file_formats_and_descriptions.md ├── README_ftp_site_structure.md ├── README_missing_files.md ├── README_populations.md ├── README_using_1000genomes_cram.md ├── release │ ├── 2008_12 │ ├── 2009_02 │ ├── 2009_04 │ ├── 2009_05 │ ├── 2009_08 │ ├── 20100804 │ ├── 2010_11 │ ├── 20101123 │ ├── 20110521 │ ├── 20130502 │ └── index.html └── technical ├── browser ├── index.html ├── method_development ├── ncbi_varpipe_data ├── other_exome_alignments ├── other_exome_alignments.alignment_indices ├── phase3_EX_or_LC_only_alignment ├── pilot2_high_cov_GRCh37_bams ├── pilot3_exon_targetted_GRCh37_bams ├── qc ├── README.reference ├── reference ├── retired_reference ├── simulations ├── supporting └── working
As per their README, the directory structure is:
changelog_details
This directory contains a series of files detailing the changes made to the FTP site over time.
data_collections
The data_collections directory contains directories for various collections of data, typically generated by different projects. Among the data collections is the 1000 Genomes Project data.
For each collection of data, within the directory for that collection, README and index files provide information on the collection. Under each collection directory, there is a data directory, under which files are organised by population and then sample. Further information can be found in/datashare/1000genomes/data_collections/README_data_collections.md.
historical_data
This directory was created during a rearrangement of the FTP site in September 2015. It houses README and index files that were formerly present at the toplevel of this site, including dedicated index directories. Further information is available in /datashare/1000genomes/historical_data/README_historical_data.md.
phase1
This directory contains data that supports the publications associated with phase 1 of the 1000 Genomes Project.
phase3
This directory contains data that supports the publications associated with phase 3 of the 1000 Genomes Project.
pilot_data
This directory contains data that supports the publications associated with the pilot phase of the 1000 Genomes Project.
release
The release directory contains dated directories which contain analysis results sets plus README files explaining how those data sets were produced.
Originally, the date in release subdirectory names was the date on which the given release was made. Thereafter, the release subdirectory dates were based on the date in the name of the corresponding YYYYMMDD.sequence.index file. In future, the date in the directory name will be chosen in a manner appropriate to the data and the nature of the release.
Examples of release subdirectories are: - /datashare/1000genomes/release/2008_12/
In cases where release directories are named based on the date of the YYYYMMDD.sequence.index, the SNP calls, indel calls, etc. in these directories are based on alignments produced from data listed in the YYYYMMDD.sequence.index file.
For example, the directory /datashare/1000genomes/release/20100804/ contains the release versions of SNP and indel calls based on the /datashare/1000genomes/historical_data/former_toplevel/sequence_indices/20100804.sequence.index file.
technical
The technical directory contains subdirectories for other data sets such as simulations, files for method development, interim data sets, reference genomes, etc..
An example of data stored under technical is /datashare/1000genomes/datashare/1000genomes/technical/simulations/.
WARNING: /datashare/1000genomes/technical/working/ The working directory under technical contains data that has experimental (non-public release) status and is suitable for internal project use only. Please use with caution.
BLASTDB
BLAST uses a standard set of BLAST databases for nucleotide, protein, and translated BLAST searches. These databases contain the sequence information deposited in the NCBI and are made available here as pre-formatted databases with the same structure as the /db directory of the BLAST ftp site.
The pre-formatted databases offer the following advantages:
- Pre-formatting removes the need to run makeblastdb
- Species-level taxonomy ids are included for each database entry
- Sequences in FASTA format can be generated from the pre-formatted databases by using the blastdbcmd utility
IMPORTANT: The BLAST databases found in this folder are version 5 (v5). Information on newly enabled features with the v5 databases can be find here.
All Pre-formatted databases available are located in Graham's /datashare/BLASTDB
and will be updated every 3 months (Jan, Apr, Jul, Oct).
Directory structure
/datashare/BLASTDB
contains all the pre-formatted without any subfolder. We include the Following:
Name | Type | Title |
---|---|---|
16S_ribosomal_RNA | DNA | 16S ribosomal RNA (Bacteria and Archaea type strains) |
18S_fungal_sequences | DNA | 18S ribosomal RNA sequences (SSU) from Fungi type and reference material |
28S_fungal_sequences | DNA | 28S ribosomal RNA sequences (LSU) from Fungi type and reference material |
Betacoronavirus | DNA | Betacoronavirus |
GCF_000001405.38_top_level | DNA | Homo sapiens GRCh38.p12 [GCF_000001405.38] chromosomes plus unplaced and unlocalized scaffolds |
GCF_000001635.26_top_level | DNA | Mus musculus GRCm38.p6 [GCF_000001635.26] chromosomes plus unplaced and unlocalized scaffolds |
ITS_RefSeq_Fungi | DNA | Internal transcribed spacer region (ITS) from Fungi type and reference material |
ITS_eukaryote_sequences | DNA | ITS eukaryote BLAST |
env_nt | DNA | environmental samples |
nt | DNA | Nucleotide collection (nt) |
patnt | DNA | Nucleotide sequences derived from the Patent division of GenBank |
pdbnt | DNA | PDB nucleotide database |
ref_euk_rep_genomes | DNA | RefSeq Eukaryotic Representative Genome Database |
ref_prok_rep_genomes | DNA | Refseq prokaryote representative genomes (contains refseq assembly) |
ref_viroids_rep_genomes | DNA | Refseq viroids representative genomes |
ref_viruses_rep_genomes | DNA | Refseq viruses representative genomes |
refseq_rna | DNA | NCBI Transcript Reference Sequences |
refseq_select_rna | DNA | RefSeq Select RNA sequences |
env_nr | Protein | Proteins from WGS metagenomic projects (env_nr) |
landmark | Protein | Landmark database for SmartBLAST |
nr | Protein | All non-redundant GenBank CDS translations+PDB+SwissProt+PIR+PRF excluding environmental samples from WGS projects |
pdbaa | Protein | PDB protein database |
pataa | Protein | Protein sequences derived from the Patent division of GenBank |
refseq_protein | Protein | NCBI Protein Reference Sequences |
refseq_select_prot | Protein | RefSeq Select proteins |
swissprot | Protein | Non-redundant UniProtKB/SwissProt sequences |
split-cdd | Protein | CDD split into 32 volumes |
tsa_nr | Protein | Transcriptome Shotgun Assembly (TSA) sequences |
Usage
The most efficient way to use these databases is to copy the specific database to $SLURM_TMPDIR
at the begining of your sbatch script. This will add between 5 to 30 minutes (depending on the database you are moving), so use it only when you know that your blast run will take longer than one hour. For example, your sbatch script can look something like this:
#!/bin/bash #SBATCH --time=02:00:00 #SBATCH --mem=32G #SBATCH --cpus-per-task=8 #SBATCH --account=def-someuser module load StdEnv/2020 gcc/9.3.0 blast+/2.11.0 # load blast and dependencies tar cf - /datashare/BLASTDB/nr | (cd ${SLURM_TMPDIR}; tar xvf -) && # copy the required database (in this case nr) to $SLURM_TMPDIR blastp -db ${SLURM_TMPDIR}/nr -num_threads ${SLURM_CPUS_PER_TASK} -query myquery.fasta
Note that the example above assumes that you have launched the job from the same directory where myquery.fasta is located, that myquery.fasta is a set of protein sequences, and that nr is required as database.
You can also use /datashare/BLASTDB/nr
(as per example), but it might be slower than having the databases in the local disk.
Other Compute Canada Sources
Blast databases can also be found in all cluster through a CVMFS repository (see https://docs.computecanada.ca/wiki/Genomics_data) unfortunately, these databases are based on the cloud ftp from NCBI which is out of date.