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  1. Runninng demo
  2. Plotting
  3. params.yaml

Runninng demo

The code in this repository is designed to run on a Linux-based machine with up-to-date versions of Nextflow and Singularity-CE. For installation instructions, please refer to the relevant links:

The container with all the neccessary software can be build if the host machine has enought privileges with make build_container command. Alternatively the container can be downloaded with make download_container command.

Running a demo (assuming that singularity and nextflow with java, wget, make, git and other tools are present):

mkdir /tmp/demo && cd /tmp/demo
git clone https://github.com/bioinfcollab/seqdepth
cd seqdepth
make download_container
make test

Plotting

singularity exec -B $PWD containers/seqdepth.sif Rscript scripts/plotting.r --help
Uage: scripts/plotting.r [options]

Options:
        -c CRM, --crm=CRM
                Chromosome

        -p POSITIONLIST, --positionlist=POSITIONLIST
                Comma separated list of chromosome positions

        -m DATADIR, --datadir=DATADIR
                Directory with median files per chromosome

        -o OUTPUTDIR, --outputdir=OUTPUTDIR
                Directory for the result plot

        -t TYPE, --type=TYPE
                DataType - median or hypergeom

        -h, --help
                Show this help message and exit

Example:

mkdir /tmp/plot
singularity exec -B $PWD containers/seqdepth.sif Rscript scripts/plotting.r --crm 19 --positionlist 51417359,51417369 --datadir "results/hypergeometric/" -t hypergeom --outputdir /tmp/plot

params.yaml

# yaml file, use a text editor!
# validate: perl -MYAML -e 'use YAML;YAML::LoadFile("./params.yaml")'

# datadir: path to bam or bed files, in case when data files are distributed
# over directory structure, use symlinks to create a directory pointing to
# specific set of files from a dataset
datadir:                /path_to/bamfiles
# outdir: directory with the  results
outdir:                 /path_to_results
# seqdepth singularity container with scripts and tools
container:              ./containers/seqdepth.sif
# singularity container options, for example bind mounts '-B /lustre'
containerOptions:
# temporary directory, must be big enough for the results, can be also set
# via TMPDIR env variable
temp:                   '/tmp/test'
# Defines on how many parts a single bed file will be split,
# affects pipeline concurency, since every part will be processed
# as a separate task
# the size of the part is determined as 250000000/split
# thus the maxpossiblepostitions must be divisible on the split number
split:                  5
# number of processes for per task
nproc:                  8
# If defined only a specific chromosome will be extracted and processed
# if not set, the range 1..22, X, Y is assumed
chromosome:             6
# some bam files come with chr prefix, other without,
# check with samtools idxstat what is the correct prefix for the
# current dataset
# current pipeline code is aware only of 'chr' prefix
chrom_prefix:
# optinal, needed for a slurm cluster
hpcproject:	<hpcProj>
# by default only median, second option hypergeometric
task:
## hypergeometric calcucation parameters
#minDepth:
#cureentTotalDepth:
#minAcceptedProb:
#tocheck:

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