# \--run-trim-repetitive and --sequencer-source not part of Docker, Conda, or Pip

**URL:** <https://forum.biobakery.org/t/run-trim-repetitive-and-sequencer-source-not-part-of-docker-conda-or-pip/1321>\
**Category:** KneadData\
**Created:** [November 22, 2020, 8:47pm UTC](https://forum.biobakery.org/t/run-trim-repetitive-and-sequencer-source-not-part-of-docker-conda-or-pip/1321 "2020-11-22T20:47:53Z")\
**Posts on this page:** 2\
**Page:** 1

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**Author:** ![djbradshaw2](https://yyz1.discourse-cdn.com/flex027/user_avatar/forum.biobakery.org/djbradshaw2/32/1050_2.png) [@djbradshaw2](https://forum.biobakery.org/u/djbradshaw2)\
**Post date:** [November 22, 2020, 8:47pm UTC](https://forum.biobakery.org/t/run-trim-repetitive-and-sequencer-source-not-part-of-docker-conda-or-pip/1321/1 "2020-11-22T20:47:53Z")

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Dear Kneaddata Developers,

Thank you for such a great product. I have been following the tutorial from [https://github.com/biobakery/kneaddata](https://github.com/biobakery/kneaddata). I have tried using Docker, Conda, and Pip to download kneaddata, all had versions 0.7.10, but none of them have the --run-trim-repetitive or  
–sequencer-source options mentioned in the tutorial, as seen below with the Conda version. Is this going to be added a an upcoming version of kneaddata, or am I missing something in my downloading process? Thank you for your time and help.

Sincerely,

David

(base) microbiology@Willow:~ kneaddata --version kneaddata v0.7.10 (base) microbiology@Willow:~ kneaddata --help  
usage: kneaddata [-h] [–version] [-v] -i INPUT -o OUTPUT\_DIR  
[-db REFERENCE\_DB] [–bypass-trim]  
[–output-prefix OUTPUT\_PREFIX] [-t \<1\>] [-p \<1\>]  
[-q {phred33,phred64}] [–run-bmtagger] [–bypass-trf]  
[–run-fastqc-start] [–run-fastqc-end] [–store-temp-output]  
[–remove-intermediate-output] [–cat-final-output]  
[–log-level {DEBUG,INFO,WARNING,ERROR,CRITICAL}] [–log LOG]  
[–trimmomatic TRIMMOMATIC\_PATH] [–max-memory MAX\_MEMORY]  
[–trimmomatic-options TRIMMOMATIC\_OPTIONS]  
[–sequencer-source {NexteraPE,TruSeq2,TruSeq3}]  
[–bowtie2 BOWTIE2\_PATH] [–bowtie2-options BOWTIE2\_OPTIONS]  
[–no-discordant] [–reorder] [–serial]  
[–bmtagger BMTAGGER\_PATH] [–trf TRF\_PATH] [–match MATCH]  
[–mismatch MISMATCH] [–delta DELTA] [–pm PM] [–pi PI]  
[–minscore MINSCORE] [–maxperiod MAXPERIOD]  
[–fastqc FASTQC\_PATH]

KneadData

optional arguments:  
-h, --help show this help message and exit  
-v, --verbose additional output is printed

global options:  
–version show program’s version number and exit  
-i INPUT, --input INPUT  
input FASTQ file (add a second argument instance to run with paired input files)  
-o OUTPUT\_DIR, --output OUTPUT\_DIR  
directory to write output files  
-db REFERENCE\_DB, --reference-db REFERENCE\_DB  
location of reference database (additional arguments add databases)  
–bypass-trim bypass the trim step  
–output-prefix OUTPUT\_PREFIX  
prefix for all output files  
[DEFAULT : $SAMPLE\_kneaddata]  
-t \<1\>, --threads \<1\>  
number of threads  
[Default : 1]  
-p \<1\>, --processes \<1\>  
number of processes  
[Default : 1]  
-q {phred33,phred64}, --quality-scores {phred33,phred64}  
quality scores  
[DEFAULT : phred33]  
–run-bmtagger run BMTagger instead of Bowtie2 to identify contaminant reads  
–bypass-trf option to bypass the removal of tandem repeats  
–run-fastqc-start run fastqc at the beginning of the workflow  
–run-fastqc-end run fastqc at the end of the workflow  
–store-temp-output store temp output files  
[DEFAULT : temp output files are removed]  
–remove-intermediate-output  
remove intermediate output files  
[DEFAULT : intermediate output files are stored]  
–cat-final-output concatenate all final output files  
[DEFAULT : final output is not concatenated]  
–log-level {DEBUG,INFO,WARNING,ERROR,CRITICAL}  
level of log messages  
[DEFAULT : DEBUG]  
–log LOG log file  
[DEFAULT : $OUTPUT\_DIR/$SAMPLE\_kneaddata.log]

trimmomatic arguments:  
–trimmomatic TRIMMOMATIC\_PATH  
path to trimmomatic  
[DEFAULT : $PATH]  
–max-memory MAX\_MEMORY  
max amount of memory  
[DEFAULT : 500m]  
–trimmomatic-options TRIMMOMATIC\_OPTIONS  
options for trimmomatic  
[DEFAULT : ILLUMINACLIP:/-SE.fa:2:30:10 SLIDINGWINDOW:4:20 MINLEN:50]  
MINLEN is set to 50 percent of total input read length  
–sequencer-source {NexteraPE,TruSeq2,TruSeq3}  
options for sequencer-source  
[DEFAULT : NexteraPE]

bowtie2 arguments:  
–bowtie2 BOWTIE2\_PATH  
path to bowtie2  
[DEFAULT : $PATH]  
–bowtie2-options BOWTIE2\_OPTIONS  
options for bowtie2  
[DEFAULT : --very-sensitive]  
–no-discordant do not include discordant alignments for pairs (ie one of the two pairs aligns)  
[DEFAULT : Discordant alignments are included]  
–reorder order the sequences in the same order as the input  
[DEFAULT : With discordant paired alignments sequences are not ordered]  
–serial filter the input in serial for multiple databases so a subset of reads are processed in each database search

bmtagger arguments:  
–bmtagger BMTAGGER\_PATH  
path to BMTagger  
[DEFAULT : $PATH]

trf arguments:  
–trf TRF\_PATH path to TRF  
[DEFAULT : $PATH]  
–match MATCH matching weight  
[DEFAULT : 2]  
–mismatch MISMATCH mismatching penalty  
[DEFAULT : 7]  
–delta DELTA indel penalty  
[DEFAULT : 7]  
–pm PM match probability  
[DEFAULT : 80]  
–pi PI indel probability  
[DEFAULT : 10]  
–minscore MINSCORE minimum alignment score to report  
[DEFAULT : 50]  
–maxperiod MAXPERIOD  
maximum period size to report  
[DEFAULT : 500]

fastqc arguments:  
–fastqc FASTQC\_PATH path to fastqc  
[DEFAULT : $PATH]

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**Author:** ![djbradshaw2](https://yyz1.discourse-cdn.com/flex027/user_avatar/forum.biobakery.org/djbradshaw2/32/1050_2.png) [@djbradshaw2](https://forum.biobakery.org/u/djbradshaw2)\
**Post date:** [November 24, 2020, 8:18pm UTC](https://forum.biobakery.org/t/run-trim-repetitive-and-sequencer-source-not-part-of-docker-conda-or-pip/1321/2 "2020-11-24T20:18:42Z")

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Oops, sorry missed that -sequencer-source was there.
