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We converted the required format using Picard tools ([http://picard.sourceforge.net/command-line-overview.shtml ref]).
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We combined MiSeq_Ecoli_MG1655_110721_PF_R1.fastq and MiSeq_Ecoli_MG1655_110721_PF_R2.fastq to MiSeq_PE.fastq.
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java -jar SamToFastq.jar INPUT=Ecoli_MG1655_s_6_1_bfast.bam FASTQ=Ecoli_MG1655_s1.fastq
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The data in frg format were downloaded from [ftp://ftp.cbcb.umd.edu/pub/data/PBcR/closure_paper/K12/miseq.100X.frg.bz2 Miseq100X]
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java -jar SamToFastq.jar INPUT=Ecoli_MG1655_s_6_2_bfast.bam FASTQ=Ecoli_MG1655_s2.fastq
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== 118X (HQ) ==
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We have trimmed the sequence reads to be of error probability less than 0.05. The paired-end reads were discarded if one read is shorter than 150bp.
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We combined MiSeq_Ecoli_MG1655_110721_PF_R1.fastq and MiSeq_Ecoli_MG1655_110721_PF_R2.fastq to MiSeq_PE.fastq.
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We therefore obtained 1,839,935 paired-end reads (~118X) with high quality for further analysis.
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java convertFastqToFastaAndQual MiSeq_PE.fastq MiSeq_PE.fna MiSeq_PE.qual |
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java convertFastqToFastaAndQual MiSeq_PE.fastq MiSeq_PE.fna MiSeq_PE.qual |