quality_trim | R Documentation |
Trim poor quality samples using cutadapt based on the results from quality_test().
quality_trim( per_base, per_seq, pair, threads = 4, scRNA = FALSE, cutadapt_add = NULL )
per_base |
samples with poor per base sequence quality. |
per_seq |
samples with poor per sequence quality scores. |
pair |
'single' for single-end (SE) or 'paired' for paired-end (PE) reads. |
threads |
the number of threads to be used. Default is 4. |
scRNA |
logic, whether single-cell RNA-seq is quantified or not. Default is FALSE. |
cutadapt_add |
additional parameters to customize cutadapt to trim poor quality reads. Default is NULL |
None
quality_trim(per_base = 'test_read_2.fastq', per_seq = 'test_read_2.fastq', pair = 'paired', threads = 4, scRNA = TRUE)
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