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nf-core/kmermaid

k-mer similarity analysis pipeline

Version: 0.1.0-alpha Git revision: 0.1.0-alpha Commit: Content hash:
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Repository: nf-core/kmermaid
Workflow: main.nf

nf-core/kmermaid

Compare DNA/RNA/protein sequences on k-mer content.

Build Status Nextflow

install with bioconda Docker

Introduction

Workflow overview

The pipeline is built using Nextflow, a workflow tool to run tasks across multiple compute infrastructures in a very portable manner. It comes with docker containers making installation trivial and results highly reproducible.

Quick Start

i. Install nextflow

ii. Install either Docker or Singularity for full pipeline reproducibility (please only use Conda as a last resort; see docs)

iii. Download the pipeline and test it on a minimal dataset with a single command

nextflow run nf-core/kmermaid -profile test,<docker/singularity/conda/institute>

Please check nf-core/configs to see if a custom config file to run nf-core pipelines already exists for your Institute. If so, you can simply use -profile <institute> in your command. This will enable either docker or singularity and set the appropriate execution settings for your local compute environment.

iv. Start running your own analysis!

nextflow run nf-core/kmermaid -profile <docker/singularity/conda/institute> --reads '*_R{1,2}.fastq.gz' --genome GRCh37

See usage docs for all of the available options when running the pipeline.

Documentation

The nf-core/kmermaid pipeline comes with documentation about the pipeline, found in the docs/ directory:

  1. Installation
  2. Pipeline configuration
  3. Running the pipeline
  4. Output and how to interpret the results
  5. Troubleshooting

Usage

With a samples.csv file

nextflow run nf-core/kmermaid --outdir s3://olgabot-maca/nf-kmer-similarity/ --samples samples.csv

With R1, R2 read pairs

nextflow run nf-core/kmermaid --outdir s3://olgabot-maca/nf-kmer-similarity/ \
  --read_pairs 's3://olgabot-maca/sra/homo_sapiens/smartseq2_quartzseq/*{R1,R2}*.fastq.gz,s3://olgabot-maca/sra/danio_rerio/smart-seq/whole_kidney_marrow_prjna393431/*{1,2}.fastq.gz'

With SRA ids

nextflow run nf-core/kmermaid --outdir s3://olgabot-maca/nf-kmer-similarity/ --sra SRP016501

With fasta files

nextflow run nf-core/kmermaid --outdir s3://olgabot-maca/nf-kmer-similarity/ \
  --fastas '*.fasta'

With bam file

nextflow run czbiohub/nf-kmer-similarity --outdir s3://olgabot-maca/nf-kmer-similarity/ \
  --bam 'possorted_genome_bam.bam'

With split kmer

nextflow run czbiohub/nf-kmer-similarity --outdir s3://olgabot-maca/nf-kmer-similarity/ --samples samples.csv --split_kmer --subsample 1000

Credits

nf-core/kmermaid was originally written by Olga Botvinnik.

Contributions and Support

If you would like to contribute to this pipeline, please see the contributing guidelines.

For further information or help, don't hesitate to get in touch on Slack (you can join with this invite).

Citation

You can cite the nf-core publication as follows:

The nf-core framework for community-curated bioinformatics pipelines.

Philip Ewels, Alexander Peltzer, Sven Fillinger, Harshil Patel, Johannes Alneberg, Andreas Wilm, Maxime Ulysse Garcia, Paolo Di Tommaso & Sven Nahnsen.

Nat Biotechnol. 2020 Feb 13. doi: 10.1038/s41587-020-0439-x.
ReadCube: Full Access Link

65 parameter(s) in 10 group(s)

bam options#

Options to adjust parameters and filtering criteria for read alignments.

10x sam tags

type string

Number of alignment to contain in each sharded bam file

type integer

Path to single barcode save the fastas inside the output directory where the results will be saved.

type string

For bam files, Optional absolute path to a .tsv barcodes file if the input is unfiltered 10x bam file

type string

For bam files, Optional absolute path to a .tsv Tab-separated file mapping 10x barcode name to new name, e.g. with channel or cell annotation label

type string

A barcode is only considered a valid barcode read and its signature is written if number of umis are greater than tenx_min_umi_per_cell

type integer

For bam files, Csv file name relative to outdir/barcode_metadata to write number of reads and number of umis per barcode. This csv file is empty with just header when the tenx_min_umi_per_cell is zero i.e Reads and umis per barcode are calculated only when the barcodes are filtered based on tenx_min_umi_per_cell

type string

10x Cell pattern

type string

10x UMI pattern

type string

Generic options#

Less common options for the pipeline, typically set in a config file.

Display help text.

type boolean

Workflow name.

More detail

A