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I was reading the PBSIM readme page and have a question regarding the following description:
To run model-based simulation:
pbsim --data-type CLR --depth 20 --model_qc data/model_qc_clr sample/sample.fasta
In the example above, simulated read sequences are randomly sampled from a reference sequence ("sample/sample.fasta") and differences (errors) of the sampled reads are introduced.
I was trying to understand what exactly the phrase “simulated read sequences are randomly sampled from a reference sequence” means. If I use a transcriptome.fasta that contains 500 transcripts to generate the simulated reads, would all 500 transcripts in the transcriptome.fasta generate the simulated reads? Or does it mean that only a subset of the 500 transcripts (e.g. 250 transcripts) that are randomly sampled from the transcriptome.fasta generate the simulated reads?
Thank you very much for your help!
The text was updated successfully, but these errors were encountered:
Hello!
I was reading the PBSIM readme page and have a question regarding the following description:
I was trying to understand what exactly the phrase “simulated read sequences are randomly sampled from a reference sequence” means. If I use a
transcriptome.fasta
that contains 500 transcripts to generate the simulated reads, would all 500 transcripts in thetranscriptome.fasta
generate the simulated reads? Or does it mean that only a subset of the 500 transcripts (e.g. 250 transcripts) that are randomly sampled from thetranscriptome.fasta
generate the simulated reads?Thank you very much for your help!
The text was updated successfully, but these errors were encountered: