scRNAseq_pipelines

Comparison of High-Throughput Single-Cell RNA Sequencing Data Processing Pipelines

Install Nextflow

https://www.nextflow.io/docs/latest/getstarted.html#requirements

Requirements

1、Nextflow can be used on any POSIX compatible system (Linux, OS X, etc). It requires Bash 3.2 (or later) and Java 8 (or later, up to 11) to be installed.

$ sudo apt-get install openjdk-8-jdk

2、$ mkdir Nextflow && cd Nextflow

3、$ wget -qO- https://get.nextflow.io | bash

It will create the nextflow main executable file in the current directory.

4、move the nextflow file to a directory accessible by your $PATH variable (this is only required to avoid remembering and typing the full path to nextflow each time you need to run it).

5、Test Nextflow

$ nextflow run hello

Output the following to indicate that the installation was successful

N E X T F L O W  ~  version 19.04.1
Pulling nextflow-io/hello ...
downloaded from https://github.com/nextflow-io/hello.git
Launching `nextflow-io/hello` [nice_wozniak] - revision: a9012339ce [master]
[warm up] executor > local
executor >  local (4)
[bc/a32c37] process > sayHello [100%] 4 of 4 ✔
Ciao world!

Hola world!

Hello world!

Bonjour world!

Install Anaconda

Anaconda 2019.10 for Linux Installer Python 3.7 version

https://repo.anaconda.com/archive/Anaconda3-2019.10-Linux-x86_64.sh

Make sure conda is installed and updated:

$ conda --version
$ conda update conda

Tip:

If this is your first time working with Conda, you may need to edit your configuration paths to ensure Anaconda is invoked when calling conda

Quickstart

Clone Repository

$ git clone [email protected]:xmuyulab/scRNAseq_pipelines.git

Install Dependencies

Configuring the software environment. Provides an execution environment for seven pieces of software, which can be installed as needed

$ conda env create -f scRNAseq_pipelines/envs/UMI-tools.yml
$ conda env create -f scRNAseq_pipelines/envs/umis.yml
$ conda env create -f scRNAseq_pipelines/envs/dropEst.yml
$ conda env create -f scRNAseq_pipelines/envs/zUMIs.yml
$ conda env create -f scRNAseq_pipelines/envs/scPipe.yml
$ conda env create -f scRNAseq_pipelines/envs/Dropseq.yml
$ conda env create -f scRNAseq_pipelines/envs/cellranger.yml

Drop-seq_tools

preprocessing

1、Download Drop-seq_tools software

$ wget -c https://github.com/broadinstitute/Drop-seq/releases/download/v2.3.0/Drop-seq_tools-2.3.0.zip

$ gunzip Drop-seq_tools-2.3.0.zip

$ cd Drop-seq_tools-2.3.0

2、Modify the temporary directory of all executables, all the positions are 10 rows from the bottom.

Attention please!

Except file of Drop-seq_alignment.sh. Replace the following /mnt/data/lmy/TMP_Dropseq with a temporary large space directory. My working directory is broad_tmpdir_root=/mnt/data/lmy/TMP_Dropseq.

Please replace /mnt/data/lmy/TMP_Dropseqto /path/to/tmp，you need to create this directory

$ mkdir -p /path/to/tmp

3、Modify `Drop-seq_alignment.sh`, Add temporary directory `-Djava.io.tmpdir=/mnt/data/lmy`, please modify `/mnt/data/lmy` to `/path/to/javatmp`. And modify STAR argument. Position is located in the follow.

# Stage 2: alignment
$echo_prefix java -Xmx4g -Djava.io.tmpdir=/mnt/data/lmy -jar ${picard_jar} SamToFastq INPUT=${tmpdir}/unaligned_mc_tagged_polyA_filtered.bam \
  FASTQ=$tmpdir/unaligned_mc_tagged_polyA_filtered.fastq
files_to_delete="$files_to_delete $tmpdir/unaligned_mc_tagged_polyA_filtered.fastq"

$echo_prefix $star_executable --genomeDir ${genomedir} --outFileNamePrefix ${tmpdir}/star. \
  --readFilesIn $tmpdir/unaligned_mc_tagged_polyA_filtered.fastq --runThreadN 4 --limitIObufferSize 1500000000 --limitOutSJcollapsed 10000000
files_to_delete="$files_to_delete ${aligned_sam}"

# Stage 3: sort aligned reads (STAR does not necessarily emit reads in the same order as the input)
$echo_prefix java -Dsamjdk.buffer_size=131072 -XX:GCTimeLimit=50 -XX:GCHeapFreeLimit=10 -Xmx4g -Djava.io.tmpdir=/mnt/data/lmy -jar ${picard_jar} \
  SortSam INPUT=${aligned_sam} OUTPUT=${aligned_sorted_bam} SORT_ORDER=queryname TMP_DIR=${tmpdir}
files_to_delete="$files_to_delete ${aligned_sorted_bam}"

# Stage 4: merge and tag aligned reads
$echo_prefix java -Xmx4g -Djava.io.tmpdir=/mnt/data/lmy -jar ${picard_jar} MergeBamAlignment REFERENCE_SEQUENCE=${reference} UNMAPPED_BAM=${tagged_unmapped_bam} \
  ALIGNED_BAM=${aligned_sorted_bam} INCLUDE_SECONDARY_ALIGNMENTS=false PAIRED_RUN=false CLIP_ADAPTERS=false \
  TMP_DIR=${tmpdir} OUTPUT=$tmpdir/merged.bam
files_to_delete="$files_to_delete $tmpdir/merged.bam"

Execute the script

4、$ cd scRNAseq_pipelines/Drop-seq_tools

5、--help parameters help the user with this script.

$ nextflow run drop_seqtools.nf --help

6、$ nextflow run drop_seqtools.nf --I [ ] --gtf [ ] --d [ ] --g [ ] --set_cell_number [ ] --fasta [ ] --tmpdir [ ] --O [ ] --javatmp [ ]

umis

1、$ cd scRNAseq_pipelines/umis