DE-kupl is a pipeline that finds differentially expressed k-mers between RNA-Seq datasets.
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DE-kupl is a pipeline that finds differentially expressed k-mers between RNA-Seq datasets.
Dekupl-run handles the first part of the DE-kupl pipeline from raw FASTQ to the production of contigs from differentially expressed k-mers.
REFERENCES: DE-kupl: exhaustive capture of biological variation in RNA-seq data through k-mer decomposition Jérôme Audoux, Nicolas Philippe, Rayan Chikhi, Mikaël Salson, Mélina Gallopin, Marc Gabriel, Jérémy Le Coz, Emilie Drouineau, Thérèse Commes and Daniel Gautheret https://doi.org/10.1186/s13059-017-1372-2
DOCKER CREATOR and MAINTAINER: Emilie Drouineau: [email protected]
For any question, please contact: eBio: [email protected]
CONFIGURATION (config.json)
fastq_dir: Location of FASTQ files
nb_threads: Default number of thread to use (unless specified in the snakemake command-line
kmer_length: Length of k-mers (default: 31). This value shoud not exceed 32.
lib_type: Paired-end library type (default: rf). You can specify either rf for reverse-forward strand-specific libraries, fr for strand-specific forward-reverse, or unstranded for unstranded libraries.
output_dir: Location of DE-kupl results (default: DEkupl_result).
dekupl_counter:
Ttest:
Samples: An array of samples. Each sample is described by a name and a condition. The FASTQ files for a sample will be located using the following command fastq_dir/sample_name_{1,2}.fastq.gz
FAQ
If new samples are added to the config.json, make sure to remove the sample_conditions.tsv file in order to force SnakeMake to re-make all targets that depends on this file
OPTIONS:
-test
get data to test the pipeline
-getconf
get the default configuration file to run dekulp (config.json)
-nbthread
fix the thread numbers when running, by default value=1
-run
run dekupl with the config file
docker run --rm --privileged -v $(pwd):/data ebio/dekupl -nbthread NB -runContent type
Image
Digest
Size
1018.8 MB
Last updated
over 8 years ago
docker pull ebio/dekupl