oarfish is a program, written in Rust (https://www.rust-lang.org/), for quantifying transcript-level expression from long-read (i.e. Oxford nanopore cDNA and direct RNA and PacBio) sequencing technologies. oarfish requires a sample of sequencing reads aligned to the transcriptome (currntly not to the genome). It handles multi-mapping reads through the use of probabilistic allocation via an expectation-maximization (EM) algorithm.
It optionally employs many filters to help discard alignments that may reduce quantification accuracy. Currently, the set of filters applied in oarfish are directly derived from the NanoCount1 tool; both the filters that exist, and the way their values are set (with the exception of the --three-prime-clip filter, which is not set by default in oarfish but is in NanoCount).
Additionally, oarfish provides options to make use of coverage profiles derived from the aligned reads to improve quantification accuracy. The use of this coverage model is enabled with the --model-coverage flag. You can read more about oarfish2 in the preprint. Please cite the preprint if you use oarfish in your work or analysis.
Also, please note that oarfish is scientific software in active development. Therefore, please check the GitHub Release page to make sure that you are using the latest version
oarfish can be installed in a variety of ways.
Binaries are available via GitHub Releases.
You can quickly install the latest release using the following helper script:
curl --proto '=https' --tlsv1.2 -LsSf https://github.com/COMBINE-lab/oarfish/releases/latest/download/oarfish-installer.sh | shIf you have cargo installed, you can install oarfish directly from the source code:
cargo install oarfishYou can find the crate on crates.io.
oarfish is available via Bioconda:
conda install -c bioconda oarfishThe usage can be provided by passing -h at the command line.
A fast, accurate and versatile tool for long-read transcript quantification.
Usage: oarfish [OPTIONS] --output <OUTPUT> <--alignments <ALIGNMENTS>|--reads <READS>>
Options:
--quiet
be quiet (i.e. don't output log messages that aren't at least warnings)
--verbose
be verbose (i.e. output all non-developer logging messages)
-o, --output <OUTPUT>
location where output quantification file should be written
--single-cell
input is assumed to be a single-cell BAM and to have the `CB:z` tag for all read records
-j, --threads <THREADS>
number of cores that oarfish will use during different phases of quantification. Note: This value will be at least 2 for bulk quantification and at least 3 for single-cell quantification due to the use of d
edicated parsing threads [default: 3]
--num-bootstraps <NUM_BOOTSTRAPS>
number of bootstrap replicates to produce to assess quantification uncertainty [default: 0]
-h, --help
Print help
-V, --version
Print version
alignment mode:
-a, --alignments <ALIGNMENTS> path to the file containing the input alignments
raw read mode:
--reads <READS> path to the file containing the input reads
--reference <REFERENCE> path to the file containing the reference transcriptome (or existing index) against which to map
--index-out <INDEX_OUT> path where minimap2 index will be written (if provided)
--seq-tech <SEQ_TECH> sequencing technology in which to expect reads if using mapping based mode [possible values: ont-cdna, ont-drna, pac-bio, pac-bio-hifi]
--best-n <BEST_N> maximum number of secondary mappings to consider when mapping reads to the transcriptome [default: 100]
filters:
--filter-group <FILTER_GROUP>
[possible values: no-filters, nanocount-filters]
-t, --three-prime-clip <THREE_PRIME_CLIP>
maximum allowable distance of the right-most end of an alignment from the 3' transcript end [default: *4294967295]
-f, --five-prime-clip <FIVE_PRIME_CLIP>
maximum allowable distance of the left-most end of an alignment from the 5' transcript end [default: *4294967295]
-s, --score-threshold <SCORE_THRESHOLD>
fraction of the best possible alignment score that a secondary alignment must have for consideration [default: *0.95]
-m, --min-aligned-fraction <MIN_ALIGNED_FRACTION>
fraction of a query that must be mapped within an alignemnt to consider the alignemnt valid [default: *0.5]
-l, --min-aligned-len <MIN_ALIGNED_LEN>
minimum number of nucleotides in the aligned portion of a read [default: *50]
-d, --strand-filter <STRAND_FILTER>
only alignments to this strand will be allowed; options are (fw /+, rc/-, or both/.) [default: .]
coverage model:
--model-coverage apply the coverage model
-b, --bin-width <BIN_WIDTH> width of the bins used in the coverage model [default: 100]
output read-txps probabilities:
--write-assignment-probs[=<WRITE_ASSIGNMENT_PROBS>]
write output alignment probabilites (optionally compressed) for each mapped read
EM:
--max-em-iter <MAX_EM_ITER>
maximum number of iterations for which to run the EM algorithm [default: 1000]
--convergence-thresh <CONVERGENCE_THRESH>
maximum number of iterations for which to run the EM algorithm [default: 0.001]
-q, --short-quant <SHORT_QUANT>
location of short read quantification (if provided)
Assume that you have ONT cDNA sequencing reads in a file named sample1_reads.tar.gz, and you'd like to quantify the transcripts in a transcriptome reference in the file transcripts.fa.
To accomplish this with oarfish, you can use either alignment-based or read-based mode. Here we give a brief example
of each. To use alignment-based mode, we assume you have minimap2 and samtools installed.
You can quantify the transcript abundances in this sample using the following commands:
$ minimap2 -t 16 -ax map-ont transcripts.fa sample1_reads.tar.gz | samtools view -@4 -b -o alignments.bam
$ oarfish -j 16 -a alignments.bam -o sample1 --filter-group no-filters --model-coverage
This will produce several output files, as described below.
In read-based mode, you can quantify the transcript abundances in this sample using the following commands:
$ oarfish -j 16 --reads sample1_reads.tar.gz --reference transcripts.fa --seq-tech ont-cdna -o sample1 --filter-group no-filters --model-coverage
If you are going to quantify more than one sample against these reference transcripts, it makes sense to save the minimap2 index that the above command creates. This can be done using the following command:
$ oarfish -j 16 --reads sample1_reads.tar.gz --reference transcripts.fa --index-out transcripts.mmi --seq-tech ont-cdna -o sample1 --filter-group no-filters --model-coverage
Then, in subsequent runs (say when quantifying sample2_reads.tar.gz), you can directly provide the minimap2 index in place of the reference to
speed up quantification. That command would look like the following:
$ oarfish -j 16 --reads sample2_reads.tar.gz --reference transcripts.mmi --seq-tech ont-cdna -o sample2 --filter-group no-filters --model-coverage
As with alignment-based mode, these commands will produce several output files, as described below.
Oarfish can accept as input either a bam file containing reads aligned to the transcriptome as specified below, or
raw sequencing reads themselves (along with a reference transcriptome), which are then mapped to the reference using minimap2-rs
and subsequently processed with oarfish. With equivalent alignment options, the results of these input modes should be equivalent, so which to use is therefore
based on the preference of the user.
The read-based input mode takes as input a reference (specified with the --reference argument), which can be either a FASTA file containing a transcriptome reference
or an pre-build minimap2 index, as well as a set of reads (specified with the --reads argument), and a --seq-tech argument specifying the sequencing technology
type of the reads to be mapped.
The mapping between the potential values that can be passed to oarfish's --seq-tech argument and the minimap2 presets is as follows:
oarfishseq-techont-cdnacorresponds tominimap2presetmap-ontoarfishseq-techont-drnacorresponds tominimap2presetmap-ontoarfishseq-techpac-biocorresponds tominimap2presetmap-pboarfishseq-techpac-bio-hificorresponds tominimap2presetmap-hifi
Given these inputs, oarfish will either load the pre-built minimap2 index, or build one according to the parameter specified by --seq-tech, and will then align
the reads to this index using minimap2-rs. Optionally, the maximum multimapping rate (i.e. the number of secondary alignments
corresponding to the minimap2 parameter -N) can be specified with the command line parameter --best-n. The default value of this parameter is 100.
In alignment-based mode, oarfish processes pre-computed alignments of hte read to the transcriptome. The input should be a bam format file, with reads aligned using minimap2 against the transcriptome. That is, oarfish does not currently handle spliced alignment to the genome. Further, the output alignments should be name sorted (the default order produced by minimap2 should be fine). Specifically, oarfish relies on the existence of the AS tag in the bam records that encodes the alignment score in order to obtain the score for each alignment (which is used in probabilistic read assignment), and the score of the best alignment, overall, for each read. ### Choosing minimap2 alignment options Since the purpose of oarfish is to estimate transcript abundance from a collection of alignments to the target transcriptome, it is important that the alignments are generated in a fashion that is compatible with this goal. Primarily, this means that the aligner should be configured to report as many optimal (and near-optimal) alignments as exist, so that oarfish can observe all of this information and determine how to allocate reads to transcripts. We recommend using the following options with minimap2 when aligning data for later processing by oarfish * For ONT data (either dRNA or cDNA): please use the flags --eqx -N 100 -ax map-ont For PacBio data: please use the flags --eqx -N 100 -ax pacbio Note (1): It may be worthwile using an even larger N value (e.g. the TranSigner manuscript recommends -N 181). A larger value should not diminish the accuracy of oarfish, but it may make alignment take longer and produce a larger bam file.
Note (2): For very high quality PacBio data, it may be most appropriate to use the -ax map-hifi flag in place of -ax pacbio. We are currently evaluating the effect of this option, and also welcome feedback if you have experiences to share on the use of data aligned with these different flags with oarfish.
The parameters above should be explained by their relevant help option, but the -d/--strand-filter is worth noting explicitly. By default, alignments to both strands of a transcript will be considered valid. You can use this option to allow only alignments in the specified orientation; for example -d fw will allow only alignments in the forward orientation and -d rc will allow only alignments in the reverse-complement orientation and -d both (the default) will allow both. The -d filter, if explicitly provided, overrides the orientation filter in any provided "filter group" so e.g. passing --filter-group no-filters -d fw will disable other filters, but will still only admit alignments in the forward orientation.
In general, if you apply a filter-group, the group options will be applied first and then any explicitly provided options given will override the corresponding option in the filter-group.
oarfish has the ability to output read-level assignment probabilities. That is, for each input read, what is the probability, conditioned on the final estimate of transcript abundances, that the read was sequenced from each transcript to which it aligned. By default, this information is not recorded (as it's not required, or commonly used, for most standard analyses). To enable this output, you should pass the --write-assignment-probs option to oarfish. Optionally, you may also pass --write-assignment-probs=compressed to write the output to a compressed (lz4) stream --- the default
output is to an uncompressed text file.
The format of the read assignment probabilities is as follows --- where all fields below on a single line are \t delimited:
<m> <n>
<tname_1>
<tname_2>
...
<tname_m>
<rname_1> <k_1> <tid_11> <tid_21> ... <tid_{k_1}1> <p_11> <p_21> ... <p_{k_1}1>
...
<rname_n> <k_1> <tid_1n> <tid_2n> ... <tid_{k_n}n> <p_1n> <p_2n> ... <p_{k_n}n>
Here, <m> is the number of transcripts in the reference, <n> is the number of mapped reads. The following m lines consist of the names of the transcripts in the order they will be referred to in the file. The following n lines after that provide the actual alignment information and assignment probabilities for each read.
The format of each of these lines is as follows; <rname> is the name of the read, <k> is the number of alignments for which probabilities are reported (if it is determined an alignment is invalid under the model, it may not be reported). Subsequently, there is a list of k integers, and k floating point numbers. Each of the k integers is the index of some transcript in the list of m transcripts given at the start of the file, and the subsequent list of k floating point numbers are the assignment probabilities of this read to each of the transcripts.
For example:
5 3
txpA
txpB
txpC
txpD
txpE
readX 2 0 2 0.4 0.6
readY 3 1 3 4 0.1 0.2 0.7
readZ 1 4 1.0
This file provides an example with 5 reference transcripts and 3 mapped reads. The first read (readX) maps to transcripts 0 and 2 (so txpA and txpC) with probabilities 0.4 and 0.6 respectively. The next read (readY) maps to 3 transcripts, txpB, txpD and txpE with probabilities 0.1, 0.2, and 0.7 respectively. Finally, the last read (readZ) maps uniquely to transcript txpE with probability 1.
The compressed output (i.e. what is generated if one passes --write-assignment-probs=compressed) is exactly the same format, except instead of residing in a plain text file, it is written to an lz4 compressed text file. You can either decompress this file first with an lz4 decompressor, or decompress it on-the-fly as you are parsing the file using the lz4 library in your favorite language.
Starting with version 0.6.1 oarfish incorporates the first single-cell quantification capabilities. Given a bam file, collated by cell barcode and with already (UMI) deduplicated reads, this mode, enabled with the --single-cell flag, will allow oarfish to produce a single-cell quantification matrix. Currently, this mode can not be used with read-based mode, and the input bam file should be properly formatted for this purpose.
Formatting requirements of BAM input in single-cell mode: All alignment records for the same cell barcode should be adjacent in the bam file, and a count will be obtained for each read record, so UMI de-duplication should have been performed if those are the counts you want. In the future, counting UMIs directly may be supported, and some of these other restrictions may be lifted.
oarfish has the ability to compute inferential replicates of its quantification estimates. This is performed by bootstrap sampling of the original read mappings, and subsequently performing inference under each resampling. These inferential replicates allow assessing the variance of the point estimate of transcript abundance, and can lead to improved differential analysis at the transcript level, if using a differential testing tool that takes advantage of this information. The generation of inferential replicates is controlled by the --num-bootstraps argument to oarfish. The default value is 0, meaning that no inferential replicates are generated. If you set this to some value greater than 0, the the requested number of inferential replicates will be generated. It is recommended, if generating inferential replicates, to run oarfish with multiple threads, since replicate generation is highly-parallelized. Finally, if replicates are generated, they are written to a Parquet, starting with the specified output stem and ending with infreps.pq.
The --output option passed to oarfish corresponds to a path prefix (this prefix can contain the path separator character and if it refers to a directory that does not yeat exist, that directory will be created). Based on this path prefix, say P, oarfish will create 2 files:
P.meta_info.json- a JSON format file containing information about relevant parameters with whichoarfishwas run, and other relevant inforamtion from the processed sample apart from the actual transcript quantifications.P.quant- a tab separated file listing the quantified targets, as well as information about their length and other metadata. Thenum_readscolumn provides the estimate of the number of reads originating from each target.P.infreps.pq- aParquettable where each row is a transcript and each column is an inferential replicate, containing the estimated counts for each transcript under each computed inferential replicate.P.ambig_info.tsv- a tab separated file listing, for each transcript (in the same order in which they appear inP.quant) the number of uniquely mapped, ambiguously mapped, and total reads. The quantification estimate for each transcript, in general, should reside between the number of uniquely aligned reads and the total number of reads (i.e. these provide, respectively lower and upper bounds for the number of reads assigned to each transcript). Note that the total in this file is the total number of reads that align to this transcript with a sufficiently high alignment score --- it is not, in general, an estimate of the number of reads originating from this transcript as many of those reads can be multimapping and, in fact, potentially better described by other transcripts.
Footnotes
-
Josie Gleeson, Adrien Leger, Yair D J Prawer, Tracy A Lane, Paul J Harrison, Wilfried Haerty, Michael B Clark, Accurate expression quantification from nanopore direct RNA sequencing with NanoCount, Nucleic Acids Research, Volume 50, Issue 4, 28 February 2022, Page e19, https://doi.org/10.1093/nar/gkab1129 ↩
-
Zahra Zare Jousheghani, Rob Patro. Oarfish: Enhanced probabilistic modeling leads to improved accuracy in long read transcriptome quantification, bioRxiv 2024.02.28.582591; doi: https://doi.org/10.1101/2024.02.28.582591 ↩
