def mergeCufflinksGeneFPKM(infiles, outfile):
'''build aggregate table with cufflinks FPKM values.'''
PipelineRnaseq.mergeCufflinksFPKM(
infiles,
outfile,
identifier="gene_id",
tracking="genes_tracking")
def mergeCufflinksIsoformFPKM(infiles, outfile):
'''build aggregate table with cufflinks FPKM values.'''
PipelineRnaseq.mergeCufflinksFPKM(
infiles,
outfile,
identifier="transcript_id",
tracking="fpkm_tracking")
def quantifyWithStringTie(infiles, outfile):
'''Quantify existing samples against genesets'''
bamfile, gtffile = infiles
outdir = P.snip(outfile, ".log")
RnaSeq.quantifyWithStringTie(bamfile=bamfile,
gtffile=gtffile,
outdir=outdir)
def count_chunks(infiles, outfile):
gtffile = infiles[1]
bamfile = infiles[0]
PipelineRnaseq.runFeatureCounts(gtffile,
bamfile,
outfile,
job_threads=2,
strand=0,
options=' -f -O -T 2 --primary -p -B -C')
def count_chunks(infiles, outfile):
gtffile = infiles[1]
bamfile = infiles[0]
PipelineRnaseq.runFeatureCounts(
gtffile,
bamfile,
outfile,
job_threads=PARAMS["featurecounts_threads"],
strand=PARAMS["stranded"],
options="-f " + PARAMS["featurecounts_options"])
def runSailfishAddModels(infiles, outfiles):
'''
Computes read counts across transcripts and genes based on a fastq
file and an indexed transcriptome using Sailfish.
Runs the sailfish "quant" function across transcripts with the specified
options. Read counts across genes are counted as the total in all
transcripts of that gene (based on the getTranscript2GeneMap table)
'''
infiles, transcript2geneMap = infiles
index, fastqfile = infiles
transcript_outfile, gene_outfile = outfiles
Quantifier = PipelineRnaseq.SailfishQuantifier(
infile=fastqfile,
transcript_outfile=transcript_outfile,
gene_outfile=gene_outfile,
annotations=index,
job_threads=PARAMS["alignment_free_threads"],
job_memory=PARAMS["sailfish_memory"],
options=PARAMS["sailfish_options"],
bootstrap=PARAMS["alignment_free_bootstrap"],
libtype=PARAMS['sailfish_libtype'],
transcript2geneMap=transcript2geneMap)
Quantifier.run_all()
def runKallistoAddModels(infiles, outfiles):
'''
Computes read counts across transcripts and genes based on a fastq
file and an indexed transcriptome using Kallisto.
Runs the kallisto "quant" function across transcripts with the specified
options. Read counts across genes are counted as the total in all
transcripts of that gene (based on the getTranscript2GeneMap table)
'''
infiles, transcript2geneMap = infiles
index, fastqfile = infiles
transcript_outfile, gene_outfile = outfiles
Quantifier = PipelineRnaseq.KallistoQuantifier(
infile=fastqfile,
transcript_outfile=transcript_outfile,
gene_outfile=gene_outfile,
annotations=index,
job_threads=PARAMS["alignment_free_threads"],
job_memory=PARAMS["kallisto_memory"],
options=PARAMS["kallisto_options"],
bootstrap=PARAMS["alignment_free_bootstrap"],
fragment_length=PARAMS["kallisto_fragment_length"],
fragment_sd=PARAMS["kallisto_fragment_sd"],
transcript2geneMap=transcript2geneMap)
Quantifier.run_all()
def buildFeatureCounts(infiles, outfile):
'''counts reads falling into "features", which by default are genes.
A read overlaps if at least one bp overlaps.
Pairs and strandedness can be used to resolve reads falling into
more than one feature. Reads that cannot be resolved to a single
feature are ignored.
'''
bamfile, annotations = infiles
PipelineRnaseq.runFeatureCounts(annotations,
bamfile,
outfile,
nthreads=PARAMS['featurecounts_threads'],
strand=PARAMS['featurecounts_strand'],
options=PARAMS['featurecounts_options'])
def buildFeatureCounts(infiles, outfile):
'''counts reads falling into "features", which by default are genes.
A read overlaps if at least one bp overlaps.
Pairs and strandedness can be used to resolve reads falling into
more than one feature. Reads that cannot be resolved to a single
feature are ignored.
'''
bamfile, annotations = infiles
PipelineRnaseq.runFeatureCounts(
annotations,
bamfile,
outfile,
nthreads=PARAMS['featurecounts_threads'],
strand=PARAMS['featurecounts_strand'],
options=PARAMS['featurecounts_options'])
def runKallisto(infiles, outfiles):
'''
Computes read counts across transcripts and genes based on a fastq
file and an indexed transcriptome using Kallisto.
Runs the kallisto "quant" function across transcripts with the specified
options. Read counts across genes are counted as the total in all
transcripts of that gene (based on the getTranscript2GeneMap table)
Parameters
----------
infiles: list
list with three components
0 - string - path to fastq file to quantify using Kallisto
1 - string - path to Kallisto index file
2 - string - path totable mapping transcripts to genes
kallisto_threads: int
:term: `PARAMS` the number of threads for Kallisto
kallisto_memory: str
:term: `PARAMS` the job memory for Kallisto
kallisto_options: str
:term: `PARAMS` string to append to the Kallisto quant command to
provide specific
options, see https://pachterlab.github.io/kallisto/manual
kallisto_bootstrap: int
:term: `PARAMS` number of bootstrap samples to run.
Note, you need to bootstrap for differential expression with sleuth
if there are no technical replicates. If you only need point estimates,
set to 1. Note that bootstrap must be set to at least 1
kallisto_fragment_length: int
:term: `PARAMS` Fragment length for Kallisto, required for single end
reads only
kallisto_fragment_sd: int
:term: `PARAMS` Fragment length standard deviation for Kallisto,
required for single end reads only.
outfiles: list
paths to output files for transcripts and genes
'''
fastqfile, index, transcript2geneMap = infiles
transcript_outfile, gene_outfile = outfiles
Quantifier = PipelineRnaseq.KallistoQuantifier(
infile=fastqfile,
transcript_outfile=transcript_outfile,
gene_outfile=gene_outfile,
annotations=index,
job_threads=PARAMS["alignment_free_threads"],
job_memory=PARAMS["kallisto_memory"],
options=PARAMS["kallisto_options"],
bootstrap=PARAMS["alignment_free_bootstrap"],
fragment_length=PARAMS["kallisto_fragment_length"],
fragment_sd=PARAMS["kallisto_fragment_sd"],
transcript2geneMap=transcript2geneMap)
Quantifier.run_all()
def runSalmon(infiles, outfiles):
'''
Computes read counts across transcripts and genes based on a fastq
file and an indexed transcriptome using Salmon.
Runs the salmon "quant" function across transcripts with the specified
options. Read counts across genes are counted as the total in all
transcripts of that gene (based on the getTranscript2GeneMap table)
Parameters
----------
infiles: list
list with three components
0 - list of strings - paths to fastq files to merge then quantify
across using sailfish
1 - string - path to sailfish index file
2 - string - path to table mapping transcripts to genes
salmon_threads: int
:term: `PARAMS` the number of threads for salmon
salmon_memory: str
:term: `PARAMS` the job memory for salmon
salmon_options: str
:term: `PARAMS` string to append to the salmon quant command to
provide specific
options, see http://sailfish.readthedocs.io/en/master/salmon.html
salmon_bootstrap: int
:term: `PARAMS` number of bootstrap samples to run.
Note, you need to bootstrap for differential expression with sleuth
if there are no technical replicates. If you only need point estimates,
set to 1.
salmon_libtype: str
:term: `PARAMS` salmon library type
as for sailfish - use
http://sailfish.readthedocs.io/en/master/library_type.html#fraglibtype
outfiles: list
paths to output files for transcripts and genes
'''
fastqfile, index, transcript2geneMap = infiles
transcript_outfile, gene_outfile = outfiles
Quantifier = PipelineRnaseq.SalmonQuantifier(
infile=fastqfile,
transcript_outfile=transcript_outfile,
gene_outfile=gene_outfile,
annotations=index,
job_threads=PARAMS["alignment_free_threads"],
job_memory=PARAMS["salmon_memory"],
options=PARAMS["salmon_options"],
bootstrap=PARAMS["alignment_free_bootstrap"],
libtype=PARAMS['salmon_libtype'],
kmer=PARAMS['alignment_free_kmer'],
transcript2geneMap=transcript2geneMap)
Quantifier.run_all()
def runFeatureCountsAddModels(infiles, outfiles):
'''
First align with hisat2 and then quantify with FeatureCounts
'''
junctions, infile, annotations, sequins_genome_index, transcript_map = infiles
### align with hisat ###
job_threads = PARAMS["hisat_threads"]
job_memory = PARAMS["hisat_memory"]
tmp_outfile = P.getTempFilename()
hisat_index_dir = os.path.dirname(sequins_genome_index)
genome = P.snip(os.path.basename(sequins_genome_index), ".1.ht2")
m = PipelineMapping.Hisat(executable='hisat2',
strip_sequence=0,
stranded=PARAMS["hisat_strandedness"])
statement = m.build((infile, ), tmp_outfile)
P.run()
### quantify with featureCounts ###
transcript_outfile, gene_outfile = outfiles
Quantifier = PipelineRnaseq.FeatureCountsQuantifier(
infile=tmp_outfile,
transcript_outfile=transcript_outfile,
gene_outfile=gene_outfile,
job_threads=PARAMS['featurecounts_threads'],
strand=PARAMS['featurecounts_strand'],
options=PARAMS['featurecounts_options'],
annotations=annotations)
Quantifier.run_all()
os.unlink(tmp_outfile)
def loadStringTieQuant(infiles, outfile):
RnaSeq.mergeAndLoadStringTie(infiles, ".+/(.+)_.+/", outfile)
def loadCufflinks(infile, outfile):
'''load expression level measurements.'''
PipelineRnaseq.loadCufflinks(infile, outfile)
def runCufflinks(infiles, outfile):
'''estimate expression levels in each set using cufflinks.'''
PipelineRnaseq.runCufflinks(infiles, outfile)
def loadCufflinks(infile, outfile):
'''load expression level measurements.'''
PipelineRnaseq.loadCufflinks(infile, outfile)
def runCufflinks(infiles, outfile):
'''estimate expression levels in each set using cufflinks.'''
PipelineRnaseq.runCufflinks(infiles, outfile)
