ctSkennerton
commented
2 years ago You can. There is a small risk that some CRISPR will not be detected in the split files but they would be rare in the data.
On Apr 20, 2022, at 01:16, fanlu-f @.***> wrote:
Hi,
I try to run my data using crass, but there were errors in several data sets.
-I installed crass using conda.
20/04/2022_03:43 -- CRisprASSembler (crass) -- Version: 1.0.1 5m 18s ERR WorkHorse.cpp : int WorkHorse::doWork(Vecstr) : 191: FATAL ERROR: parseSeqFiles failed I try to split the original fastq file into several small files and run them separately. That can solve the problem.
Therefore, I would like to ask whether it is possible to use this method to combine the results of all subsets as the results of the original sample.
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Hi,
I try to run my data using crass, but there were errors in several data sets.
-I installed crass using conda.
I try to split the original fastq file into several small files and run them separately. That can solve the problem.
Therefore, I would like to ask whether it is possible to use this method to combine the results of all subsets as the results of the original sample.