Mode 1 (Service)
Inputs:
#1 Job data
json file for job {"reference_genome_id": "1310806.3", \
"output_file": "rnaseq_baumanii_1505311", \
"recipe": ["FASTQC","TRIM","ALIGN"], "output_path": "/[email protected]/home/test",\
"paired_end_libs": [{"read1": "/[email protected]/home/rnaseq_test/MHB_R1.fq.gz",\
"read2": "/[email protected]/home/rnaseq_test/MHB_R2.fq.gz"},\
{"read1": "/[email protected]/home/rnaseq_test/MERO_75_R1.fq.gz",\
"read2": "/[email protected]/home/rnaseq_test/MERO_75_R2.fq.gz"}]}
#2 Server string to get genome from using PATRIC ID system
#3 Override parameter string to govern number of processes used
#4 Output directory
Outputs:
#1 Trimmed Fastq files (2 files for paired samples)
#2 BAM/BAI file of aligned reads
#2.5 Samstat report for BAM/BAI file
#3 FastQC report
#4 A recipe specifying which of these steps to execute
This program will:
#1 Use the given SRA accession and/or fastq files to perform the designated operations:
#1.1 fastqc report
#1.2 fastq trimming
#1.3 read mapping
Dependencies:
Bowtie2
https://github.com/BenLangmead/bowtie2
Samstat
http://samstat.sourceforge.net
Fastqc
http://www.bioinformatics.babraham.ac.uk/projects/fastqc/
Cutadapt
https://github.com/marcelm/cutadapt
Trimgalore
https://github.com/FelixKrueger/TrimGalore
Samtools
http://www.htslib.org/
HISAT2
http://daehwankimlab.github.io/hisat2/
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