Provided by: subread_2.0.0+dfsg-1_amd64
NAME
genRandomReads - helper tool from subread suite
USAGE
For scanning a FASTA/gz file: genRandomReads --transcriptFasta <file>\ --outputPrefix <string> --expressionLevels <file> [other options] --summarizeFasta Only output the transcript names and lengths. --transcriptFasta <file> The transcript database in FASTA/gz format. --outputPrefix <string> The prefix of the output files. --totalReads <int> Total read/pairs in output. --expressionLevels <file> Two column table delimited by <TAB>, giving the wanted TPM values. Columns: TranscriptID and TPM --readLen <int> The length of the output reads. 100 by default. --totalReads <int> Total read/pairs in the output. --randSeed <int64> Seed to generate random numbers. UNIXTIME is used as the random seed by default. --qualityRefFile <file> A textual file containing Phred+33 quanlity strings for simulating sequencing errors. The quality strings have to have the same length as the output reads. No sequencing errors are simulated when this option is omitted. --floorStrategy How to deal with round-up errors. 'FLOOR': generate less than wanted reads; 'RANDOM': randomly assign margin reads to transcripts; 'ITERATIVE': find the best M value to have ~N reads. --pairedEnd Generate paired-end reads. --insertionLenMean <float>,--insertionLenSigma <float>,--insertionLenMin <int>, --insertionLenMax <int> Parameters of a truncated normal distribution for deciding insertion lengths of paired-end reads. Default values: mean=160, sigma=30, min=110, max=400 --simpleTranscriptId Truncate transcript names to the first '|' or space. --truthInReadNames Encode the true locations of reads in read names. --noActualReads Do not actually generate reads in fastq.gz files.