Thanks for the reply. From your answer I understand that you suggest creating a single assembly, rather than multiple. How should the assembly be created? from which RNA-seq fastq file? I didn't see an option to create an assembly from multiple fastq files.
Hi.
The data I got was obtained from an experiment with the following structure:
3 similar experiments in separate dates, each included a control group and an experiment group.
Should I create an assembly for each date, or should I create one assembly for data from all 3 dates?
1 answer
If the aim is to create a comprehensive transcriptome first then create an assembly from entire dataset.
You can do an assembly from multiple files, taken from the tool's help:
# If paired reads:
# --left <string> :left reads, one or more file names (separated by commas, not spaces)
# --right <string> :right reads, one or more file names (separated by commas, not spaces)
#
# Or, if unpaired reads:
# --single <string> :single reads, one or more file names, comma-delimited (note, if single file contains pairs, can use flag: --run_as_paired )
#
So basically just put the names separated by commas after the parameters and should be fine.
I was directed in the Trinity Google group to use the --samples_file parameter. If I understand correctly, both options get the same result.
That is correct, and my guess that this is helpful in the downstream analyses like the use of align_and_estimate_abundance.pl from the utils in the Trinity package
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