def run_kallisto_singlecell(data): samplename = dd.get_sample_name(data) work_dir = dd.get_work_dir(data) kallisto_dir = os.path.join(work_dir, "kallisto", samplename) gtf_file = dd.get_gtf_file(data) files = dd.get_input_sequence_files(data) if len(files) == 2: fq1, fq2 = files else: fq1, fq2 = files[0], None assert file_exists(gtf_file), "%s was not found, exiting." % gtf_file fasta_file = dd.get_ref_file(data) assert file_exists(fasta_file), "%s was not found, exiting." % fasta_file out_file = kallisto_singlecell(fq1, kallisto_dir, gtf_file, fasta_file, data) data = dd.set_kallisto_quant(data, out_file) return [[data]]
def run_kallisto_rnaseq(data): samplename = dd.get_sample_name(data) work_dir = dd.get_work_dir(data) kallisto_dir = os.path.join(work_dir, "kallisto", samplename) gtf_file = dd.get_gtf_file(data) files = dd.get_input_sequence_files(data) if len(files) == 2: fq1, fq2 = files else: fq1, fq2 = files[0], None assert file_exists(gtf_file), "%s was not found, exiting." % gtf_file fasta_file = dd.get_ref_file(data) assert file_exists(fasta_file), "%s was not found, exiting." % fasta_file assert fq2, ("We don't support kallisto for single-end reads and fusion " "calling with pizzly does not accept single end reads.") out_file = kallisto_rnaseq(fq1, fq2, kallisto_dir, gtf_file, fasta_file, data) data = dd.set_kallisto_quant(data, out_file) return [[data]]
def run_kallisto_rnaseq(data): samplename = dd.get_sample_name(data) work_dir = dd.get_work_dir(data) kallisto_dir = os.path.join(work_dir, "kallisto", samplename) gtf_file = dd.get_gtf_file(data) files = dd.get_input_sequence_files(data) if len(files) == 2: fq1, fq2 = files else: fq1, fq2 = files[0], None assert file_exists(gtf_file), "%s was not found, exiting." % gtf_file fasta_file = dd.get_ref_file(data) assert file_exists(fasta_file), "%s was not found, exiting." % fasta_file assert fq2, ("bcbio doesn't support kallisto for single-end reads, we can " "add support for this if you open up an issue about it here: " "https://github.com/bcbio/bcbio-nextgen/issues") out_file = kallisto_rnaseq(fq1, fq2, kallisto_dir, gtf_file, fasta_file, data) data = dd.set_kallisto_quant(data, out_file) return [[data]]
def run_kallisto_rnaseq(data): samplename = dd.get_sample_name(data) work_dir = dd.get_work_dir(data) kallisto_dir = os.path.join(work_dir, "kallisto", samplename) gtf_file = dd.get_transcriptome_gtf(data, default=dd.get_gtf_file(data)) files = dd.get_input_sequence_files(data) if len(files) == 2: fq1, fq2 = files else: fq1, fq2 = files[0], None assert file_exists(gtf_file), "%s was not found, exiting." % gtf_file fasta_file = dd.get_ref_file(data) assert file_exists(fasta_file), "%s was not found, exiting." % fasta_file assert fq2, ("We don't support kallisto for single-end reads and fusion " "calling with pizzly does not accept single end reads.") out_file = kallisto_rnaseq(fq1, fq2, kallisto_dir, gtf_file, fasta_file, data) data = dd.set_kallisto_quant(data, out_file) return [[data]]
def run_kallisto_rnaseq(data): samplename = dd.get_sample_name(data) work_dir = dd.get_work_dir(data) kallisto_dir = os.path.join(work_dir, "kallisto", samplename) gtf_file = dd.get_gtf_file(data) files = dd.get_input_sequence_files(data) if len(files) == 2: fq1, fq2 = files else: fq1, fq2 = files[0], None assert file_exists(gtf_file), "%s was not found, exiting." % gtf_file fasta_file = dd.get_ref_file(data) assert file_exists(fasta_file), "%s was not found, exiting." % fasta_file assert fq2, ("bcbio doesn't support kallisto for single-end reads, we can " "add support for this if you open up an issue about it here: " "https://github.com/chapmanb/bcbio-nextgen/issues") out_file = kallisto_rnaseq(fq1, fq2, kallisto_dir, gtf_file, fasta_file, data) data = dd.set_kallisto_quant(data, out_file) return [[data]]