This program was primarily designed for the taxonomic assignment of amplicon sequence variants (ASVs), but it works with any sequence data in FASTA format. Many output files are generated, several of which can be directly imported into qiime or other common workflows.
Python3 v3.4.3+
modules: Biopython, argsparse
If your starting data is fastq data from an amplicon based experiment you will need to compute ASVs/OTUs prior to running this program. Here are some great options.
dada2 - https://benjjneb.github.io/dada2/tutorial.html
qiime2 -
mothur -
ncbi's nt database - ftp://ftp.ncbi.nlm.nih.gov/blast/db/
#####To download this database copy and paste the line below (it will take a bit)
mkdir ncbi_nt_database && cd ncbi_nt_database
wget 'ftp://ftp.ncbi.nlm.nih.gov/blast/db/nt*.gz'
tar -xvf nt*SILVA ssuRNA sequence and taxonomy database: https://www.arb-silva.de/download/archive/qiime/
Locate and download the latest NCBI taxonomy database.
You will need the names and nodes file to construct the expanded taxonomy lookup.
Link updated December, 2020
mkdir ncbi_taxonomy/ && cd ncbi_taxonomy/
wget ftp://ftp.ncbi.nih.gov/pub/taxonomy/new_taxdump/new_taxdump.tar.gz
tar xvzf *.tar.gz
Expand the taxonomic lineages into a simplified tsv lookup.
python3 genbank_nodes_and_names_to_taxonomy.py names.dmp nodes.dmp
Rather than relying on a single blast hit the program takes the top X (user defined with --hits_to_consider) blast hits for each sequence.
It then computes the classification for each of these blast hits and determines taxonomy for the query sequence based on the best consensus taxonomy. i.e. If all ten blast hits agree on the same taxonomy than it will give the value to the species level, however if they only agree to the family level then it will stop there.
This aspect has many options, including setting the maximum number of blast hits to consider and the percent sway from the best blast hit. Blast hits are not all treated the same.
If your blast provided 10 blast hits but only 5 of them are within '--percent_sway' the others will not be considered.
For example, if one blast hit has a percent identity of 99% while the others are only 95%, only the top hit will be considered (unless of course you set the --percent_sway option to 4.0 or above). The default --percent_sway value is 0.5, this will gather very similiar hits and ignore those that are less similiar.
If you want to only consider the best blast hit, just set --hits_to_consider to '1'.
The program provides another level of taxonomic certainty based on the blast percentage. For example, if the best blast hit is 90% you can be fairly confident that you cannot provide the species of the organisms but maybe you can provide the phylum. Right now there are three levels that you can set with the program, --cutoff_species, --cutoff_family, and --cutoff_phylum. The phylum level cutoff is also used as an ultimate filter for the blast hits percent identity.
If you want to only keep sequences that are identified to the species level, just set all cutoffs to '97' or '99'.
If you want to leave it to the consensus taxonomy to decide 'best estimated taxonomy', set all three cutoffs low, maybe '80'.
These threshold values were arbitrarily chosen in line with diverse literature sources and investigations that were mostly based on mock communities of selected taxa (Brown et al., 2015; Holovachov 2016; Leasi et al., 2018).
Note: The consensus taxonomy usually does a pretty good job of weeding out incorrect taxonomy, setting all these cutoff values to 80 actually provides pretty great taxonomy in a lot of cases. Especially if you set a high --hits_to_consider and --percent_sway.
By default the program will mask blast hits that have a taxonomic assignment of uncultured, or unclassified. These hits will only be considered as a last resort.
You have the option to set the minimum length coverage for the blast hit (defined by 'length of query'/'length of hit'). The default is 0.8. I like to be stringent here to avoid tiny insignificant blast hits.
You already did YOUR OWN BLAST?? We will import that and save you the step. Just make sure the format is right.
use this format --> -outfmt '6 qseqid qlen sseqid pident length qstart qend sstart send evalue bitscore staxids'
If running your own blast command make sure you run it with the out_seqs.fasta file. I have not added an option to input seqs.fna blast directly into qiime yet… but will if requested.
usage: taxonomy_assignment_BLAST_V2.py [-h] [-v]
[--cutoff_species CUTOFF_SPECIES]
[--cutoff_family CUTOFF_FAMILY]
[--cutoff_phylum CUTOFF_PHYLUM]
[--length_percentage LENGTH_PERCENTAGE]
[--length_cutoff LENGTH_CUTOFF]
[--hits_to_consider HITS_TO_CONSIDER]
[--percent_sway PERCENT_SWAY]
[--blast_evalue BLAST_EVALUE]
[--blast_threads BLAST_THREADS]
[--blast_flavor BLAST_FLAVOR]
[--blast_database BLAST_DATABASE]
[--blast_file BLAST_FILE] [--ncbi_nt]
[--output_dir OUTPUT_DIR]
[--config_file CONFIG_FILE]
sequence_file tax_file
positional arguments:
sequence_file seqs.fna file from qiime or any multifasta, just make
sure header has unique id with a space
tax_file path to silva or customized blast database taxonomy
file
optional arguments:
-h, --help show this help message and exit
-v, --verbose increase output verbosity (default: False)
--cutoff_species CUTOFF_SPECIES
cutoff for finest taxonomic level (default: 97)
--cutoff_family CUTOFF_FAMILY
cutoff for family taxonomic level (default: 90)
--cutoff_phylum CUTOFF_PHYLUM
cutoff for phylum taxonomic level, also acts as
ultimate cutoff value for blast (default: 80)
--length_percentage LENGTH_PERCENTAGE
cutoff for query_hit/length_of_query i.e. query
coverage (default: 0.0)
--length_cutoff LENGTH_CUTOFF
primary cutoff for length of hit (default: 0)
--hits_to_consider HITS_TO_CONSIDER
number of hits to consider when gathering consensus
taxonomy (default: 3)
--percent_sway PERCENT_SWAY
when comparing greater than 1 blast hit, value is the
percent from best hit considered. i.e. if best blast
hit is 99.5 ID, a value of 0.5 will consider
everything 99 and greater when creating the consensus
(default: 0.5)
--blast_evalue BLAST_EVALUE
setting for e-value cutoff for blast, must be in form
1e-X (default: 1e-10)
--blast_threads BLAST_THREADS
set the number of threads for blast (default: 24)
--blast_flavor BLAST_FLAVOR
select blastp, tblastn etc, must have correct database
and query sequence formats (default: blastn)
--blast_database BLAST_DATABASE
path tp blast database, be sure to run makeblastdb on
the database first, type 'IGNORE' if precomputed blast
is given (default: None)
--blast_file BLAST_FILE
precomputed blast results, MUST BE MY CUSTOMIZED
FORMAT, '6 qseqid qlen sseqid pident length qstart
qend sstart send evalue bitscore' (default: None)
--ncbi_nt REQUIRED flag for use of ncbi nt database (default:False)
--output_dir OUTPUT_DIR
output directory name (default: Assigned_Taxonomy)
--config_file CONFIG_FILE
NOT YET IMPLEMENTED, an optional parameters file, any
arguments in this file will override other options
(default: None) ```
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