Changes between Version 6 and Version 7 of SOPs/qc_shortReads


Ignore:
Timestamp:
11/19/13 10:16:23 (11 years ago)
Author:
gbell
Comment:

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Unmodified
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  • SOPs/qc_shortReads

    v6 v7  
    9191   # Sample commands:
    9292   # quality_stats: Sample Solexa reads file: s_1_1_sequence.txt or s_1_1_sequence.txt.gz
    93    fastx_quality_stats -i s_1_1_sequence.txt -o s_1_1_sequence.stats
    94    gunzip -c s_1_1_sequence.txt.gz | fastx_quality_stats -o s_1_1_sequence.stats
     93   fastx_quality_stats -i s_1_1_sequence.txt -o s_1_1_sequence.stats  # fastq input
     94   gunzip -c s_1_1_sequence.txt.gz | fastx_quality_stats -o s_1_1_sequence.stats  # fastq.gz input
    9595   # a figure for Nucleotide Distribution:
    9696   fastx_nucleotide_distribution_graph.sh -i s_1_1_sequence.stats  -o s_1_1_sequence.stats.nuc.png -t "s_1_1_sequence.stats Nucleotide Distribution"
     
    109109 
    110110{{{
    111   fastq_quality_filter -v -q 20 -p 75 -i myFile.fastq -o myFile.fastq.fastx_trim   
    112   gunzip -c myFile.fastq | fastq_quality_filter -v -q 20 -p 75 -o myFile.fastq.fastx_trim
     111  fastq_quality_filter -v -q 20 -p 75 -i myFile.fastq -o myFile.fastq.fastx_trim  # fastq input and output
     112  gunzip -c myFile.fastq | fastq_quality_filter -v -q 20 -p 75 -z -o myFile.fastq.fastx_trim.gz  # fastq.gz input and output
    113113
    114114           [-h]         = This helpful help screen.
     
    132132
    133133{{{
    134 bsub "fastq_quality_trimmer -v -t 20 -l 25 -i input.fastq -o output.fastq"
    135 bsub "gunzip -c input.fastq.gz | fastq_quality_trimmer -v -t 20 -l 25 -z -o output.fastq.gz"   
     134bsub "fastq_quality_trimmer -v -t 20 -l 25 -i input.fastq -o output.fastq"  # fastq input and output
     135bsub "gunzip -c input.fastq.gz | fastq_quality_trimmer -v -t 20 -l 25 -z -o output.fastq.gz"  # fastq.gz input and output
    136136
    137137   [-t N]       = Quality threshold - nucleotides with lower
     
    164164
    165165{{{
    166 bsub "fastx_clipper -a CTGTAGGCACCATCAAT -i s2_sequence.txt -v -l 22 -o s2_sequence_noLinker.txt"
    167 bsub "gunzip -c s2_sequence.txt | fastx_clipper -a CTGTAGGCACCATCAAT -v -l 22 -z -o s2_sequence_noLinker.txt.gz"
     166bsub "fastx_clipper -a CTGTAGGCACCATCAAT -i s2_sequence.txt -v -l 22 -o s2_sequence_noLinker.txt"  # fastq input and output
     167bsub "gunzip -c s2_sequence.txt | fastx_clipper -a CTGTAGGCACCATCAAT -v -l 22 -z -o s2_sequence_noLinker.txt.gz"  # fastq.gz input and output
    168168
    169169
     
    191191 
    192192{{{
    193 bsub "fastx_trimmer -f 1 -l 22  -i s7_sequence_clipped.txt -o s7_sequence_clipped_trimmed.txt"
    194 bsub "gunzip -c s7_sequence_clipped.txt | fastx_trimmer -f 1 -l 22 -z -o s7_sequence_clipped_trimmed.txt.gz"
     193bsub "fastx_trimmer -f 1 -l 22  -i s7_sequence_clipped.txt -o s7_sequence_clipped_trimmed.txt"  # fastq input and output
     194bsub "gunzip -c s7_sequence_clipped.txt | fastx_trimmer -f 1 -l 22 -z -o s7_sequence_clipped_trimmed.txt.gz"  # fastq.gz input and output
    195195     
    196196[-i INFILE]  = FASTA/Q input file. default is STDIN.