In DKMS-LSL/dr2s: Dual redundant reference sequencing
knitr::opts_chunk$set(
collapse = TRUE,
comment = "#>",
fig.path = "README-"
)
DR2S - dual redundant reference sequencing
An R package designed to facilitate generating reliable, full-length
phase-defined reference sequences for novel HLA and KIR alleles.
Installation
This package is only available on GitHub for now. It depends on a local installation
of samtools, bwa (>= 0.7.11) and minimap2.
Some used R packages have additional system dependencies.
Bash:
sudo apt-get update
sudo apt-get install \
build-essentials \ # for samtools, bwa
gcc \ # for samtools, bwa
autoconf \ # for samtools, bwa
libxml2-dev \
libssl2-dev \
libz-dev \
libbz2-dev \
liblzma-dev \
libncurses5-dev
R:
install.packages("devtools") # if not already installed
devtools::install_github("DKMS-LSL/DR2S")
A Docker image is also provided for convenience at docker hub.
This can be loaded and used with the following command:
docker pull dkmslsl/dr2s
docker run --rm -p 8788:8787 -e PASSWORD=<yourpassword> -it dkmslsl/dr2s
An rstudio server session can be accessed in your browser at localhost:8788 (The default port 8787 is mapped to the host port 8788 in case you have, like me, rstudio server already running).
Login to rstudio using the username "rstudio" and your set password.
A detailed introduction to use DR2S with example data can be found at the Vignette "DR2S".
Workflow
Input and output
DR2S is designed to integrate long-read HLA and KIR data (e.g., PacBio or Oxford
Nanopore sequences) and shortread shotgun data (Illumina). It is also possible
to run DR2S in "longread-only mode", but don't expect reference-quality
consensus sequences that way.
As input, we expect longread and, optionally, shortread FASTQ files to be placed in
separate subdirectories within a working directory and to follow the naming
convention SAMPLEID_LOCUS_.*.fastq(.gz)?.
SAMPLEID can be any arbitrary unique identification code and LOCUS should
be one of A, B, C, DQB1, DRB1, or DPB1 for HLA, or one of 2DL1,
2DL2, 2DL3, 2DL4, 2DL5A, 2DL5B, 2DP1, 2DS1, 2DS2, 2DS3,
2DS4, 2DS5, 3DL1, 3DL2, 3DL3, 3DP1, or 3DS1 for KIR.
All output is placed in a directory tree under the configured output directory LOCUS\SAMPLEID\.
An example:
~/dr2s_data
|
+-- pacbio
| |-- ID123_DPB1_lbc23.fastq.gz
|
|
+-- illumina
| |-- ID123_DPB1_S23_L001_R1_001.fastq.gz
| |-- ID123_DPB1_S23_L001_R2_001.fastq.gz
|
+-- output
|
+-- DQB1
|
+-- ID123
| --...
| --...
| --...
Usage
Once all input files are put in place a DR2S analysis is started with a call
to the functions createDR2SConf() or readDR2SConf() and InitDR2S():
## a minimal example:
x <- InitDR2S(
createDR2SConf(
sample = "ID123",
locus = "DPB1",
longreads = list(dir = "Sequel", type = "pacbio"),
shortreads = list(dir = "Illumina", type = "illumina"),
datadir = "~/dr2s_data",
outdir = "~/dr2s_data/output",
reference = "DPB1"
))
Arguments
sample: A unique sample identifier. The FASTQs associated with a sample need
need to be prefixed with this identifier.locus: One of the allowed HLA and KIR loci above. If allele information for
a sample is available it can be specified as, e.g. DPB1*04:02:01:01.
In this case this allele will be used as a reference against which an initial
mapping of the longreads is performed. If this information is not given a
generic locus-specific reference is used. NOTE: generic references are not yet
implemented for KIR.longreads: The location, type, and mapper for longreads as a named list
with the fields dir, type ("pacbio" or "nanopore") and mapper
("bwamem" or "minimap").shortreads: (optional) The location, type, and mapper for shortreads as a
named list with the fields dir, type ("illumina") and mapper ("bwamem"
or "minimap").datadir: The data directory (see above).outdir: The output directory (see above).reference: (optional) Path to a fasta file containing the reference sequence.details: (optional) Named list of sample metadata. These data will be
included in the fasta headers of the final sequences and stored in the
config file.opts: (optional) Named list of arguments to the DR2S pipeline steps. They
will be stored in the config file. See below for a detailed descriptions of
options that control the DR2S pipeline.
This call generates an R6 object of class DR2S that encapsulates all data
and methods for all subsequent analysis steps.
An alternative approach is to use yaml or json config files.
An example config file is provided in the toy example at URL to github project:
configFile <- "~/dr2s_data/dr2s_config.yaml"
x <- InitDR2S(
readDR2SConf(configFile)
)
Pipeline
An analysis proceeds in a number of steps that can be chained together
using the pipe %>%:
x %>%
mapInit() %>%
partitionLongreads() %>%
mapIter() %>%
partitionShortreads() %>%
mapFinal() %>%
report() %>%
cache()
Alternatively, the complete pipeline can be run in one go.
There are two available pipelines, one for the standard run (SR), and another for only long-read data (LR).
Which pipeline to run can be configured in the config file.
x$runPipeline()
The individual steps perform the following analyses:
mapInit():
- Map the shortreads (SR) against an initial reference. Construct a tentative
consensus.
- Perform a second SR mapping to the consensus sequence from the
previous step. This expands the reference and may be necessary if there are
extensive repeat structures like microsatellites in your sequence. Construct a
tentative consensus.
- A final SR mapping to the consensus from the previous step.
- A longread (LR) mapping to the consensus from the previous step.
partitionLongreads():
- Infer polymorphic positions from the SR mapping performed in the previous
step.
- Construct a SNP matrix from the LR mapping at the polymorphic positions
infer from the SR mapping.
- Perform hierarchical clustering the LR SNPs.
- Attempt to detect chimeric reads.
- Assign a haplotype and a haplotype_membership_coefficient to each read.
- Pick longreads that best represent the allele haplotypes based on the
haplotype_membership_coefficient from the previous step.
- Extract the selected longreads from the alignment file and output the data
as FASTQs into subdirectories for each haplotype.
mapIter():
- Construct a consensus sequence for each haplotype from the initial LR mapping
whilst using only reads that have been assigned to that haplotype.
- Iteratively refine the longread consensus sequences by remapping longreads
per haplotype to the latest haplotype consensus.
partitionShortreads():
- Partition the shortreads into haplotypes using the inferred longread
haplotypes and the initial SR mapping.
mapFinal():
- Map the shortreads against the refined longread consensus sequences.
report():
- Report the finalised shortread-based consensus sequences as FASTA files.
Provide a tsv file with suspicious positions that may warrant manual inspection.
Report the alignment of all haplotypes.
Throughout this process a number of diagnostic plots are produced and placed
in the output directory for later inspection.
While this process works remarkably well, there are situations where alignment
artefacts or plain bad luck may introduce errors in the final consensus
sequences. You should never accept the result as ground truth without
some manual and visual consistency checks!
DR2S provides some facilities to aid checking and signing-off of finalised
consensus sequences.
Postprocessing
A typical post-processing workflow may look as follows:
run_igv(x, 3000)
check_alignment_file(x)
refineAlignment(x, "A")
run_igv(x, "refine")
report_checked_consensus(x)
-
run_igv:
Opens an instance of the IGV Genome Browser for each haplotype at a specified position
(one for each allele) displaying both the long read and short read data
for manual inspection.
-
check_alignment_file :
Opens a pairwise or multiple alignment of the final consensus sequences in your text
editor. Use this to perform any manual edits on the consensus sequences.
Editor options are: "subl", "gvim" and "gedit". Defaults to systems standard editor.
-
report_checked_consensus:
Export final consensus sequences from the edited pairwise or multiple alignment
as FASTAs into a separate subdirectory ./checked in the output
directory.
DR2S creates bash scripts for the convenient access to important postprocessing functions:
- run_checkConsensus.sh
Runs the
check_alignment_file command.
- runIGV_mapInit.sh
Opens an IGV instance of the initial mapping.
- runIGV_mapIter.sh
Opens an IGV instance of the results of the mapIter step.
- runIGV_mapFinal.sh
Opens an IGV instance of the final mapping
- run_remap[X].sh
Remap the reads of a haplotype to the manuall curated sequence to look if it
is finally correct. This command is available for all found haplotypes
- run_reportCheckedConsensus.sh
report the manually checked consensus and state that its finished and can
be used.
Pipeline control options
A more fine-grained control of the DR2S pipeline is available via a json-based
config file. This config file can be created externally and read in using the
readDR2Sconf() function. Alternatively the config file is created by the
createDR2Sconf() function. Pipeline control options are set using the opts
argument in createDR2Sconf(), e.g.:
conf <- createDR2SConf(
sample = "ID12912701",
locus = "A*01:01:01:01",
longreads = list(dir = "pacbio", type = "pacbio", mapper = "minimap"),
shortreads = list(dir = "illumina", type = "illumina", mapper = "bwamem"),
datadir = "~/dr2s_data",
outdir = "~/dr2s_data/output",
opts = list(
mapInit = list(topx = "auto",
createIgv = FALSE),
partitionLongreads = list(threshold = 1/5,
noGapPartitioning = TRUE,
selectCorrelatedPositions = TRUE,
selectAllelesBy = "distance"),
mapIter = list(iterations = 2),
mapFinal = list(createIgv = FALSE),
report = list(createIgv = FALSE)
))
The complete set of available options and their defaults are:
##
## mapInit() defaults ####
##
mapInit = list(
## <includeDeletions>: include deletions in pileup.
includeDeletions = TRUE,
## <includeInsertions>: include insertions in pileup.
includeInsertions = TRUE,
## <callInsertionThreshold>: if <includeInsertions == TRUE>, an insertion
## needs to be at frequency <callInsertionThreshold> for it to be included
## in the pileup.
callInsertionThreshold = 1/5,
## <microsatellite>: if <pipeline == "SR">, perform a second mapping of
## shortreads to the inferred reference. Set to TRUE if you suspect
## microsatellites or repetitive regions in your sequence. This extends
## the reference to a maximum length and enables a better mapping.
microsatellite = FALSE,
## <forceMapping>: set to TRUE if you want to force processing of "bad"
## shortreads when the distribution of coverage is heavily unequal.
## Aborts the program if maximum coverage > 75 % quantile * 5.
forceMapping = FALSE,
## <minMapq>: don't filter longreads for mapping quality unless specified.
## NOTE: for shortreads <minMapq = 50> is hardcoded.
minMapq = 0,
## <topx>: pick the x top-scoring reads. Set to an integer value to pick
## a fixed number of reads. Set to "auto" to use a dynamically determined
## number of reads to be selected.
topx = FALSE,
## <pickiness>: if <topx == "auto">: <pickiness < 1>: bias towards higher
## scores/less reads; <pickiness > 1>: bias towards lower scores/more reads
pickiness = 1,
## <increasePickiness>: if <topx == "auto">: increase pickiness for the
## second iteration of LR mapping
increasePickiness = 1,
## <lowerLimit>: if <topx == "auto"> or <topx > 0>: the minimum number
## of reads to pick if available.
lowerLimit = 200,
## <updateBackgroundModel>: estimate the indel noise in a pileup and use
## this information to update the background model for PWM scoring
updateBackgroundModel = FALSE,
## <createIgv>: subsample bam files for visualisation with IgvJs in the
## DR2S shiny app.
createIgv = TRUE,
## <plot>: generate diagnostic plots.
plot = TRUE
)
##
## partitionLongreads() defaults ####
##
partitionLongreads = list(
## Threshold to call a polymorphic position. A minority nucleotide frequency
## below this threshold is considered noise rather than a valid polymorphism.
threshold = 1/5,
## The expected number of distinct alleles in the sample. This should be 2
## for heterozygous samples, 1 for homozygous samples may be >2 for some
## KIR loci.
distAlleles = 2,
## The minumum frequency of the gap character required to call a gap position.
skipGapFreq = 2/3,
## Don't partition based on gaps. Useful for samples with only few SNPs but
## with homopolymers. The falsely called gaps could mask the real variation.
## Set to override global default.
noGapPartitioning = TRUE,
## Correlate polymorphic positions and cluster based on the absolute
## correlation coefficient. Extract positions from the cluster with the
## higher absolute mean correlation coefficient. This gets rid of positions
## that are not well distributed across the two alleles.
selectCorrelatedPositions = FALSE,
## if <selectCorrelatedPositions> == TRUE, use <measureOfAssociation>
## ("cramer.V" or "spearman") to determine linkage between all polymorphic
## positions.
measureOfAssociation = "cramer.V",
## We perform an equivalence test on clusters of polymorhic positions:
## Calculate the lower 1-sigma bound of the high-association cluster i.
## Calculate the upper 1-sigma bound of the low-association cluster j.
## Reject the clusters, if this bounds overlap by more than <proportionOfOverlap>
## of the average distance (dij) between clusters.
proportionOfOverlap = 1/3,
## By how much do we expect 2 clusters to minimally differ in mean Cramér's V.
## BIC-informed model-based clustering tends to split rather than lump
## and this is a heuristical attempt to forestall this.
minimumExpectedDifference = 0.06,
## If more than <distAlleles> clusters are found select clusters based on:
## (1) "distance": The hamming distance of the resulting variant consensus
## sequences or (2) "count": Take the clusters with the most reads as the
## true alleles.
selectAllelesBy = "distance",
## Minimum size of an allele cluster
minClusterSize = 20,
## When selecting reads from allele clusters using a dynamic threshold:
## pickiness < 1: bias towards higher scores/less reads
## pickiness > 1: bias towards lower scores/more reads
pickiness = 1,
## When selecting reads from allele clusters the minimum number of
## reads to pick if available.
lowerLimit = 40,
## Generate diagnostic plots.
plot = TRUE
)
##
## mapIter() defaults ####
##
mapIter = list(
## Number of <mapIter> iterations. How often are the
## clustered reads remapped to updated reference sequences.
iterations = 1,
## Minimum occupancy (1 - fraction of gap) below which
## bases at insertion position are excluded from from consensus calling.
columnOccupancy = 2/5,
## an insertion needs to be at frequency <callInsertionThreshold> for it
## to be included in the pileup.
callInsertionThreshold = 1/5,
## Generate diagnostic plots.
plot = TRUE
)
##
## mapFinal() defaults ####
##
mapFinal = list(
## include deletions in pileup.
includeDeletions = TRUE,
## include insertions in pileup.
includeInsertions = TRUE,
## an insertion needs to be at frequency <callInsertionThreshold> for it
## to be included in the pileup.
callInsertionThreshold = 1/5,
## (for shortreads only) trim softclips and polymorphic ends of reads before
## the final mapping
trimPolymorphicEnds = FALSE,
## Subsample bam files for visualisation with IgvJs in the
## DR2S shiny app.
createIgv = TRUE,
## Generate diagnostic plots.
plot = TRUE
)
##
## report() defaults ####
##
report = list(
## Maximum number of sequence letters per line in pairwise alignment.
blockWidth = 80,
## Suppress remapping of reads against final consensus.
remap = TRUE,
## Subsample bam files for visualisation with IgvJs in the
## DR2S shiny app.
createIgv = TRUE
)
An example config file:
{
"sampleId": "ID123",
"locus": "A",
"datadir": "/home//dr2s_data",
"outdir": "/home/user/dr2s_data/A/ID12912701",
"reference": "HLA-A*01:01:01:01",
"longreads": {
"dir": "pacbio",
"type": "pacbio",
"mapper": "minimap"
},
"shortreads": {
"dir": "illumina",
"type": "illumina",
"mapper": "bwamem"
},
"pipeline": "SR",
"opts": {
"mapInit": {
"includeDeletions": true,
"includeInsertions": true,
"callInsertionThreshold": 0.2,
"microsatellite": true,
"forceMapping": false,
"minMapq": 0,
"topx": false,
"pickiness": 1,
"increasePickiness": 1,
"lowerLimit": 200,
"updateBackgroundModel": false,
"createIgv": false,
"plot": true
},
"partitionLongreads": {
"threshold": 0.2,
"distAlleles": 2,
"skipGapFreq": 0.6667,
"noGapPartitioning": true,
"selectCorrelatedPositions": false,
"measureOfAssociation": "cramer.V",
"proportionOfOverlap": 0.3333,
"minimumExpectedDifference": 0.06,
"selectAllelesBy": "distance",
"minClusterSize": 20,
"pickiness": 1,
"lowerLimit": 40,
"plot": true
},
"mapIter": {
"iterations": 2,
"columnOccupancy": 0.4,
"callInsertionThreshold": 0.2,
"plot": true
},
"mapFinal": {
"includeDeletions": true,
"includeInsertions": true,
"callInsertionThreshold": 0.2,
"trimPolymorphicEnds": false,
"createIgv": false,
"plot": true
},
"report": {
"blockWidth": 80,
"remap": true,
"createIgv": false
}
},
"format": "json"
}
Longread-only workflow DR2S-LR
If you want to find allele sequences only based on longreads you just need to set
shortreads = NULL in createDR2SConf() and skip the the partitionShortreads()
step in the DR2S pipeline.
x <- InitDR2S(createDR2SConf(
sample = "ID12912701",
locus = "DPB1",
longreads = list(dir = "pacbio", type = "pacbio", mapper = "minimap"),
datadir = "~/dr2s_data",
outdir = "~/dr2s_data/output"
)) %>%
mapInit() %>%
partitionLongreads() %>%
mapIter() %>%
mapFinal() %>%
report() %>%
cache()
DKMS-LSL/dr2s documentation built on March 14, 2021, 2:46 p.m.
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knitr::opts_chunk$set( collapse = TRUE, comment = "#>", fig.path = "README-" )
DR2S - dual redundant reference sequencing
An R package designed to facilitate generating reliable, full-length phase-defined reference sequences for novel HLA and KIR alleles.
Installation
This package is only available on GitHub for now. It depends on a local installation
of samtools, bwa (>= 0.7.11) and minimap2.
Some used R packages have additional system dependencies.
Bash:
sudo apt-get update sudo apt-get install \ build-essentials \ # for samtools, bwa gcc \ # for samtools, bwa autoconf \ # for samtools, bwa libxml2-dev \ libssl2-dev \ libz-dev \ libbz2-dev \ liblzma-dev \ libncurses5-dev
R:
install.packages("devtools") # if not already installed devtools::install_github("DKMS-LSL/DR2S")
A Docker image is also provided for convenience at docker hub. This can be loaded and used with the following command:
docker pull dkmslsl/dr2s docker run --rm -p 8788:8787 -e PASSWORD=<yourpassword> -it dkmslsl/dr2s
An rstudio server session can be accessed in your browser at localhost:8788 (The default port 8787 is mapped to the host port 8788 in case you have, like me, rstudio server already running). Login to rstudio using the username "rstudio" and your set password. A detailed introduction to use DR2S with example data can be found at the Vignette "DR2S".
Workflow
Input and output
DR2S is designed to integrate long-read HLA and KIR data (e.g., PacBio or Oxford
Nanopore sequences) and shortread shotgun data (Illumina). It is also possible
to run DR2S in "longread-only mode", but don't expect reference-quality
consensus sequences that way.
As input, we expect longread and, optionally, shortread FASTQ files to be placed in
separate subdirectories within a working directory and to follow the naming
convention SAMPLEID_LOCUS_.*.fastq(.gz)?.
SAMPLEID can be any arbitrary unique identification code and LOCUS should
be one of A, B, C, DQB1, DRB1, or DPB1 for HLA, or one of 2DL1,
2DL2, 2DL3, 2DL4, 2DL5A, 2DL5B, 2DP1, 2DS1, 2DS2, 2DS3,
2DS4, 2DS5, 3DL1, 3DL2, 3DL3, 3DP1, or 3DS1 for KIR.
All output is placed in a directory tree under the configured output directory LOCUS\SAMPLEID\.
An example:
~/dr2s_data
|
+-- pacbio
| |-- ID123_DPB1_lbc23.fastq.gz
|
|
+-- illumina
| |-- ID123_DPB1_S23_L001_R1_001.fastq.gz
| |-- ID123_DPB1_S23_L001_R2_001.fastq.gz
|
+-- output
|
+-- DQB1
|
+-- ID123
| --...
| --...
| --...
Usage
Once all input files are put in place a DR2S analysis is started with a call
to the functions createDR2SConf() or readDR2SConf() and InitDR2S():
## a minimal example: x <- InitDR2S( createDR2SConf( sample = "ID123", locus = "DPB1", longreads = list(dir = "Sequel", type = "pacbio"), shortreads = list(dir = "Illumina", type = "illumina"), datadir = "~/dr2s_data", outdir = "~/dr2s_data/output", reference = "DPB1" ))
Arguments
sample: A unique sample identifier. The FASTQs associated with a sample need need to be prefixed with this identifier.locus: One of the allowed HLA and KIR loci above. If allele information for a sample is available it can be specified as, e.g.DPB1*04:02:01:01. In this case this allele will be used as a reference against which an initial mapping of the longreads is performed. If this information is not given a generic locus-specific reference is used. NOTE: generic references are not yet implemented for KIR.longreads: The location, type, and mapper for longreads as a named list with the fieldsdir,type("pacbio" or "nanopore") andmapper("bwamem" or "minimap").shortreads: (optional) The location, type, and mapper for shortreads as a named list with the fieldsdir,type("illumina") andmapper("bwamem" or "minimap").datadir: The data directory (see above).outdir: The output directory (see above).reference: (optional) Path to a fasta file containing the reference sequence.details: (optional) Named list of sample metadata. These data will be included in the fasta headers of the final sequences and stored in the config file.opts: (optional) Named list of arguments to the DR2S pipeline steps. They will be stored in the config file. See below for a detailed descriptions of options that control the DR2S pipeline.
This call generates an R6 object of class DR2S that encapsulates all data
and methods for all subsequent analysis steps.
An alternative approach is to use yaml or json config files.
An example config file is provided in the toy example at URL to github project:
configFile <- "~/dr2s_data/dr2s_config.yaml" x <- InitDR2S( readDR2SConf(configFile) )
Pipeline
An analysis proceeds in a number of steps that can be chained together
using the pipe %>%:
x %>% mapInit() %>% partitionLongreads() %>% mapIter() %>% partitionShortreads() %>% mapFinal() %>% report() %>% cache()
Alternatively, the complete pipeline can be run in one go. There are two available pipelines, one for the standard run (SR), and another for only long-read data (LR). Which pipeline to run can be configured in the config file.
x$runPipeline()
The individual steps perform the following analyses:
mapInit():- Map the shortreads (SR) against an initial reference. Construct a tentative consensus.
- Perform a second SR mapping to the consensus sequence from the previous step. This expands the reference and may be necessary if there are extensive repeat structures like microsatellites in your sequence. Construct a tentative consensus.
- A final SR mapping to the consensus from the previous step.
- A longread (LR) mapping to the consensus from the previous step.
partitionLongreads():- Infer polymorphic positions from the SR mapping performed in the previous step.
- Construct a SNP matrix from the LR mapping at the polymorphic positions infer from the SR mapping.
- Perform hierarchical clustering the LR SNPs.
- Attempt to detect chimeric reads.
- Assign a haplotype and a haplotype_membership_coefficient to each read.
- Pick longreads that best represent the allele haplotypes based on the haplotype_membership_coefficient from the previous step.
- Extract the selected longreads from the alignment file and output the data as FASTQs into subdirectories for each haplotype.
mapIter():- Construct a consensus sequence for each haplotype from the initial LR mapping whilst using only reads that have been assigned to that haplotype.
- Iteratively refine the longread consensus sequences by remapping longreads per haplotype to the latest haplotype consensus.
partitionShortreads():- Partition the shortreads into haplotypes using the inferred longread haplotypes and the initial SR mapping.
mapFinal():- Map the shortreads against the refined longread consensus sequences.
report():- Report the finalised shortread-based consensus sequences as FASTA files. Provide a tsv file with suspicious positions that may warrant manual inspection. Report the alignment of all haplotypes.
Throughout this process a number of diagnostic plots are produced and placed in the output directory for later inspection.
While this process works remarkably well, there are situations where alignment artefacts or plain bad luck may introduce errors in the final consensus sequences. You should never accept the result as ground truth without some manual and visual consistency checks!
DR2S provides some facilities to aid checking and signing-off of finalised
consensus sequences.
Postprocessing
A typical post-processing workflow may look as follows:
run_igv(x, 3000) check_alignment_file(x) refineAlignment(x, "A") run_igv(x, "refine") report_checked_consensus(x)
-
run_igv: Opens an instance of the IGV Genome Browser for each haplotype at a specified position (one for each allele) displaying both the long read and short read data for manual inspection.
-
check_alignment_file : Opens a pairwise or multiple alignment of the final consensus sequences in your text editor. Use this to perform any manual edits on the consensus sequences. Editor options are: "subl", "gvim" and "gedit". Defaults to systems standard editor.
-
report_checked_consensus: Export final consensus sequences from the edited pairwise or multiple alignment as FASTAs into a separate subdirectory
./checkedin the output directory.
DR2S creates bash scripts for the convenient access to important postprocessing functions:
- run_checkConsensus.sh
Runs the
check_alignment_filecommand. - runIGV_mapInit.sh Opens an IGV instance of the initial mapping.
- runIGV_mapIter.sh Opens an IGV instance of the results of the mapIter step.
- runIGV_mapFinal.sh Opens an IGV instance of the final mapping
- run_remap[X].sh Remap the reads of a haplotype to the manuall curated sequence to look if it is finally correct. This command is available for all found haplotypes
- run_reportCheckedConsensus.sh report the manually checked consensus and state that its finished and can be used.
Pipeline control options
A more fine-grained control of the DR2S pipeline is available via a json-based
config file. This config file can be created externally and read in using the
readDR2Sconf() function. Alternatively the config file is created by the
createDR2Sconf() function. Pipeline control options are set using the opts
argument in createDR2Sconf(), e.g.:
conf <- createDR2SConf( sample = "ID12912701", locus = "A*01:01:01:01", longreads = list(dir = "pacbio", type = "pacbio", mapper = "minimap"), shortreads = list(dir = "illumina", type = "illumina", mapper = "bwamem"), datadir = "~/dr2s_data", outdir = "~/dr2s_data/output", opts = list( mapInit = list(topx = "auto", createIgv = FALSE), partitionLongreads = list(threshold = 1/5, noGapPartitioning = TRUE, selectCorrelatedPositions = TRUE, selectAllelesBy = "distance"), mapIter = list(iterations = 2), mapFinal = list(createIgv = FALSE), report = list(createIgv = FALSE) ))
The complete set of available options and their defaults are:
## ## mapInit() defaults #### ## mapInit = list( ## <includeDeletions>: include deletions in pileup. includeDeletions = TRUE, ## <includeInsertions>: include insertions in pileup. includeInsertions = TRUE, ## <callInsertionThreshold>: if <includeInsertions == TRUE>, an insertion ## needs to be at frequency <callInsertionThreshold> for it to be included ## in the pileup. callInsertionThreshold = 1/5, ## <microsatellite>: if <pipeline == "SR">, perform a second mapping of ## shortreads to the inferred reference. Set to TRUE if you suspect ## microsatellites or repetitive regions in your sequence. This extends ## the reference to a maximum length and enables a better mapping. microsatellite = FALSE, ## <forceMapping>: set to TRUE if you want to force processing of "bad" ## shortreads when the distribution of coverage is heavily unequal. ## Aborts the program if maximum coverage > 75 % quantile * 5. forceMapping = FALSE, ## <minMapq>: don't filter longreads for mapping quality unless specified. ## NOTE: for shortreads <minMapq = 50> is hardcoded. minMapq = 0, ## <topx>: pick the x top-scoring reads. Set to an integer value to pick ## a fixed number of reads. Set to "auto" to use a dynamically determined ## number of reads to be selected. topx = FALSE, ## <pickiness>: if <topx == "auto">: <pickiness < 1>: bias towards higher ## scores/less reads; <pickiness > 1>: bias towards lower scores/more reads pickiness = 1, ## <increasePickiness>: if <topx == "auto">: increase pickiness for the ## second iteration of LR mapping increasePickiness = 1, ## <lowerLimit>: if <topx == "auto"> or <topx > 0>: the minimum number ## of reads to pick if available. lowerLimit = 200, ## <updateBackgroundModel>: estimate the indel noise in a pileup and use ## this information to update the background model for PWM scoring updateBackgroundModel = FALSE, ## <createIgv>: subsample bam files for visualisation with IgvJs in the ## DR2S shiny app. createIgv = TRUE, ## <plot>: generate diagnostic plots. plot = TRUE ) ## ## partitionLongreads() defaults #### ## partitionLongreads = list( ## Threshold to call a polymorphic position. A minority nucleotide frequency ## below this threshold is considered noise rather than a valid polymorphism. threshold = 1/5, ## The expected number of distinct alleles in the sample. This should be 2 ## for heterozygous samples, 1 for homozygous samples may be >2 for some ## KIR loci. distAlleles = 2, ## The minumum frequency of the gap character required to call a gap position. skipGapFreq = 2/3, ## Don't partition based on gaps. Useful for samples with only few SNPs but ## with homopolymers. The falsely called gaps could mask the real variation. ## Set to override global default. noGapPartitioning = TRUE, ## Correlate polymorphic positions and cluster based on the absolute ## correlation coefficient. Extract positions from the cluster with the ## higher absolute mean correlation coefficient. This gets rid of positions ## that are not well distributed across the two alleles. selectCorrelatedPositions = FALSE, ## if <selectCorrelatedPositions> == TRUE, use <measureOfAssociation> ## ("cramer.V" or "spearman") to determine linkage between all polymorphic ## positions. measureOfAssociation = "cramer.V", ## We perform an equivalence test on clusters of polymorhic positions: ## Calculate the lower 1-sigma bound of the high-association cluster i. ## Calculate the upper 1-sigma bound of the low-association cluster j. ## Reject the clusters, if this bounds overlap by more than <proportionOfOverlap> ## of the average distance (dij) between clusters. proportionOfOverlap = 1/3, ## By how much do we expect 2 clusters to minimally differ in mean Cramér's V. ## BIC-informed model-based clustering tends to split rather than lump ## and this is a heuristical attempt to forestall this. minimumExpectedDifference = 0.06, ## If more than <distAlleles> clusters are found select clusters based on: ## (1) "distance": The hamming distance of the resulting variant consensus ## sequences or (2) "count": Take the clusters with the most reads as the ## true alleles. selectAllelesBy = "distance", ## Minimum size of an allele cluster minClusterSize = 20, ## When selecting reads from allele clusters using a dynamic threshold: ## pickiness < 1: bias towards higher scores/less reads ## pickiness > 1: bias towards lower scores/more reads pickiness = 1, ## When selecting reads from allele clusters the minimum number of ## reads to pick if available. lowerLimit = 40, ## Generate diagnostic plots. plot = TRUE ) ## ## mapIter() defaults #### ## mapIter = list( ## Number of <mapIter> iterations. How often are the ## clustered reads remapped to updated reference sequences. iterations = 1, ## Minimum occupancy (1 - fraction of gap) below which ## bases at insertion position are excluded from from consensus calling. columnOccupancy = 2/5, ## an insertion needs to be at frequency <callInsertionThreshold> for it ## to be included in the pileup. callInsertionThreshold = 1/5, ## Generate diagnostic plots. plot = TRUE ) ## ## mapFinal() defaults #### ## mapFinal = list( ## include deletions in pileup. includeDeletions = TRUE, ## include insertions in pileup. includeInsertions = TRUE, ## an insertion needs to be at frequency <callInsertionThreshold> for it ## to be included in the pileup. callInsertionThreshold = 1/5, ## (for shortreads only) trim softclips and polymorphic ends of reads before ## the final mapping trimPolymorphicEnds = FALSE, ## Subsample bam files for visualisation with IgvJs in the ## DR2S shiny app. createIgv = TRUE, ## Generate diagnostic plots. plot = TRUE ) ## ## report() defaults #### ## report = list( ## Maximum number of sequence letters per line in pairwise alignment. blockWidth = 80, ## Suppress remapping of reads against final consensus. remap = TRUE, ## Subsample bam files for visualisation with IgvJs in the ## DR2S shiny app. createIgv = TRUE )
An example config file:
{
"sampleId": "ID123",
"locus": "A",
"datadir": "/home//dr2s_data",
"outdir": "/home/user/dr2s_data/A/ID12912701",
"reference": "HLA-A*01:01:01:01",
"longreads": {
"dir": "pacbio",
"type": "pacbio",
"mapper": "minimap"
},
"shortreads": {
"dir": "illumina",
"type": "illumina",
"mapper": "bwamem"
},
"pipeline": "SR",
"opts": {
"mapInit": {
"includeDeletions": true,
"includeInsertions": true,
"callInsertionThreshold": 0.2,
"microsatellite": true,
"forceMapping": false,
"minMapq": 0,
"topx": false,
"pickiness": 1,
"increasePickiness": 1,
"lowerLimit": 200,
"updateBackgroundModel": false,
"createIgv": false,
"plot": true
},
"partitionLongreads": {
"threshold": 0.2,
"distAlleles": 2,
"skipGapFreq": 0.6667,
"noGapPartitioning": true,
"selectCorrelatedPositions": false,
"measureOfAssociation": "cramer.V",
"proportionOfOverlap": 0.3333,
"minimumExpectedDifference": 0.06,
"selectAllelesBy": "distance",
"minClusterSize": 20,
"pickiness": 1,
"lowerLimit": 40,
"plot": true
},
"mapIter": {
"iterations": 2,
"columnOccupancy": 0.4,
"callInsertionThreshold": 0.2,
"plot": true
},
"mapFinal": {
"includeDeletions": true,
"includeInsertions": true,
"callInsertionThreshold": 0.2,
"trimPolymorphicEnds": false,
"createIgv": false,
"plot": true
},
"report": {
"blockWidth": 80,
"remap": true,
"createIgv": false
}
},
"format": "json"
}
Longread-only workflow DR2S-LR
If you want to find allele sequences only based on longreads you just need to set
shortreads = NULL in createDR2SConf() and skip the the partitionShortreads()
step in the DR2S pipeline.
x <- InitDR2S(createDR2SConf( sample = "ID12912701", locus = "DPB1", longreads = list(dir = "pacbio", type = "pacbio", mapper = "minimap"), datadir = "~/dr2s_data", outdir = "~/dr2s_data/output" )) %>% mapInit() %>% partitionLongreads() %>% mapIter() %>% mapFinal() %>% report() %>% cache()
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