Error: a transcript file must be provide. Error: the output prefix must be provide. Error: the wanted
expression levels must be provided. Warning: no read number is specified. Generating one million reads.
Usage:
For scanning a FASTA/gz file:
/usr/lib/subread/genRandomReads--summarizeFasta \
--transcriptFasta <file> --outputPrefix <string> [--simpleTranscriptId]
For generating read/pairs:
/usr/lib/subread/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.