Invoke with StarScope

Input

The input sample list file is a simple csv with three columns. The first column sample indicates sample IDs, and multiple fastq files with the same sample ID will be concatenated before further processing (e.g. two pairs of human_pbmc_s1 fastq files will be cat to a single pair). Multiple samples in one single sample list will be submitted parallelly and processed asynchronously. The workflow supports both ThunderBio and 10X ATAC data, please use the suggested configuration below. User could check 10X ATAC library structure from https://teichlab.github.io/scg_lib_structs/.

​
sample,fastq_1,fastq_2
human_pbmc_s1,human_pbmc_s1_R1_001.fastq.gz,human_pbmc_s1_R2_001.fastq.gz
human_pbmc_s1,human_pbmc_s1_R1_002.fastq.gz,human_pbmc_s1_R2_002.fastq.gz
human_pbmc_s2,human_pbmc_s2_R1_001.fastq.gz,human_pbmc_s2_R2_001.fastq.gz
human_tissue_s1,human_tissue_s1_R1_001.fastq.gz,human_tissue_s1_R2_001.fastq.gz
sample,fastq_1,fastq_2,fastq_3
10X_pbmc_10k_v1,10X_pbmc_10k_v1_R1_001.fastq.gz,10X_pbmc_10k_v1_R2_001.fastq.gz,10X_pbmc_10k_v1_R3_001.fastq.gz
10X_pbmc_10k_v1,10X_pbmc_10k_v1_R1_002.fastq.gz,10X_pbmc_10k_v1_R2_002.fastq.gz,10X_pbmc_10k_v1_R3_002.fastq.gz
10X_pbmc_10k_v2,10X_pbmc_10k_v2_R1_001.fastq.gz,10X_pbmc_10k_v2_R2_001.fastq.gz,10X_pbmc_10k_v2_R3_001.fastq.gz
10X_pbmc_10k_v2,10X_pbmc_10k_v2_R1_002.fastq.gz,10X_pbmc_10k_v2_R2_002.fastq.gz,10X_pbmc_10k_v2_R3_002.fastq.gz
Note

All samples in the sampleList will use the same options. Therefore, a combination of samples from different species is not supported.

Warning

We found that seq library doesn’t support fastq file with quality score larger than 40 (denoted as J in the fourth line). Please check the quality encoding on FASTQ wiki page. The error message is like:

KeyError: J

Raised from: std.internal.types.collections.dict.Dict.__getitem__:0
/pipeline/starscope/scATAC-seq/codon/lib/codon/stdlib/internal/types/collections/dict.codon:74:9
/scATAC_test/work/09/284782e6058425c6966542b7a70944/.command.sh: line 9: 684639 Aborted                 (core dumped) /pipeline/starscope/scATAC-seq/codon/bin/codon run -release -plugin seq /pipeline/starscope/scATAC-seq/bin/extract_and_correct_thunderbio_barcode_from_fastq.codon TB_v3_20240429.BC1.tsv,TB_v3_20240429.BC2.tsv,TB_v3_20240429.BC3.tsv test_sample_1.merged.fq.gz test_sample_2.merged.fq.gz test_sample_1.barcode.fq test_sample_2.barcode.fq test_sample_barcode_stats.tsv 8

User could use the command below to convert “J” (Q=41) to “I” (Q=40):

for i in *.fq.gz; do zcat $i | awk 'NR%4==1{print; getline; print; getline; print; getline; gsub("J", "I"); print}' | gzip -c > ${i%%.fq.gz}".modified.fq.gz"; done

Command

Invoke with config file

Since there are too many processes and options, we recommend to invoke pipeline with custom configuration file, which gives users more control on resources management.

starscope atac --input sampleList.csv --config example_docker.config
​
params {
  bwaIndex = "/refdata/human/bwa2_index/GRCh38-2020-A"
  genomeGTF = "/refdata/human/refdata-gex-GRCh38-2020-A/genes/genes.gtf"
  whitelist = "/barcodes/BC1.tsv /barcodes/BC2.tsv /barcodes/BC3.tsv" // TB whitelist
  // trimming options used by cutadapt
  trimOpt = '-a AGATGTGTATAAGAGACAG...CTGTCTCTTATACACATCTCCGAGCCCACGAGAC -A GTCTCGTGGGCTCGGAGATGTGTATAAGAGACAG...CTGTCTCTTATACACATCT'
  // cell filtration
  minCell = 10 // feature obeseved in at least "minCell" cells
  minFeature = 200 // cells with at least "minFeature" features
  publishSaturation = true
  platform = "TB" // TB or 10X
}

// uncomment line below if using slurm, see https://www.nextflow.io/docs/latest/executor.html
// process.executor = 'slurm'

// uncomment below chunk if using conda
// process.conda = "/home/xzx/Tools/mambaforge/envs/starscope_scATAC_env"
// conda.enabled = true

// docker setting, comment chunk below if using conda
process.container = "registry-intl.cn-hangzhou.aliyuncs.com/thunderbio/starscope_scatac_env:0.0.6"
docker.enabled = true
docker.userEmulation = true
docker.runOptions = '--init -u $(id -u):$(id -g) $(for group in $(id -G); do echo "--group-add $group"; done)'

// Resouces for each process
process {
  withLabel: process_high {
    cpus = 16
    memory = 32.GB
  }
  withLabel: process_medium {
    cpus = 16
    memory = 20.GB
  }
  withLabel: process_low {
    cpus = 16
    memory = 20.GB
  }
  withName: CAT_FASTQ {
    cpus = 2
    memory = 10.GB
  }
  withName: CAT_FASTQ_10X {
    cpus = 2
    memory = 10.GB
  }
  withName: REPORT {
    cpus = 8
    memory = 40.GB
  }
  withName: CHECK_BARCODE {
    cpus = 16
    memory = 20.GB
  }
  CHECK_BARCODE_10X {
    cpus = 16
    memory = 20.GB
  }
  withName: TRIM_FASTQ {
    cpus = 16
    memory = 20.GB
  }
  withName: BWA_MAPPING {
    cpus = 16
    memory = 32.GB
  }
  withName: STATS {
    cpus = 4
    memory = 20.GB
  }
  withName: DEDUP {
    cpus = 2
    memory = 20.GB
  }
  withName: CHECK_SATURATION {
    cpus = 4
    memory = 20.GB
  }
  withName: MULTIQC {
    cpus = 4
    memory = 20.GB
  }
  withName: GENERATE_FRAGMENTS {
    cpus = 16
    memory = 40.GB
  }
  withName: SIGNAC {
    cpus = 4
    memory = 40.GB
  }
}

Invoke with command line options

To invoke scATAC pipeline with conda environment:

starscope atac --conda \
               --conda_env /path/to/conda/env \
               --input sampleList.csv \
               --bwaIndex /path/to/STAR/reference/dir \
               --genomeGTF /path/to/genomeGTF \
               --whitelist "/path/to/BC1.tsv /path/to/BC2.tsv /path/to/BC3.tsv" \
               --refGenome hg38 \
               --platform TB

user will have to add --conda and indicate conda env path with --conda_env. To check your env path, please use mamba env list:

# conda environments:
#
base                     /home/xzx/Tools/mambaforge
starscope_scATAC_env     /home/xzx/Tools/mambaforge/envs/starscope_scATAC_env

and provide the second column (e.g. /home/xzx/Tools/mambaforge/envs/starscope_scATAC_env).

Required Options

--bwaIndex: bwa-mem2 reference index path and file prefix.

For instance, a typical file structure of the index folder will be like:

## human hg38
/thunderData/refdata/human/bwa2_index/
├── GRCh38-2020-A.0123
├── GRCh38-2020-A.amb
├── GRCh38-2020-A.ann
├── GRCh38-2020-A.bwt.2bit.64
└── GRCh38-2020-A.pac

To create the index above, use the command below:

bwa-mem2 index -p GRCh38-2020-A genome.fa

user will have to provide --bwaIndex /thunderData/refdata/human/bwa2_index/GRCh38-2020-A to starscope command.

--genomeGTF: reference genome GTF file path.

--refGenome: reference genome assembly ID.

This parameter is used to extract genome size when calling peaks with macs2. Here we support hg38, hg19, mm9 and mm10 for human and mosue genome. User could use --genomeSize to indicate genome size directly.

--platform: StarScope scATAC pipeline supports ATAC data from both the ThunderBio and 10X genomics. Use either TB or 10X here.

--whitelist: The white list file(s) path. For ThunerBio scATAC data, whitelist files were distributed with StarScope:

starscope/whitelist/
├── TB_v3_20240429.BC1.tsv
├── TB_v3_20240429.BC2.tsv
├── TB_v3_20240429.BC3.tsv
└── V2_barcode_seq_210407_concat.txt.gz

Please use the whilelist option below, and don’t forget to add double quote.

--whitelsit "/path/to/starscope/whitelist/TB_v3_20240429.BC1.tsv /path/to/starscope/whitelist/TB_v3_20240429.BC2.tsv /path/to/starscope/whitelist/TB_v3_20240429.BC3.tsv"

Outputs

Each sample will have a separated result folder named with sample ID. The subdirectory final contains all the result files, including html report, fragments file (with all the barcodes) and a list of cell associated barcodes identified (e.g. TB_PBMC_s1_raw_cells.tsv).

The pipeline_info directory contains statistics of the pipeline running resources.

results/
├── TB_PBMC_s1
│   ├── final
│   │   ├── TB_PBMC_s1_combined_stats.tsv
│   │   ├── TB_PBMC_s1_filtered_obj.rds
│   │   ├── TB_PBMC_s1.fragments.sorted.bed.gz
│   │   ├── TB_PBMC_s1.fragments.sorted.bed.gz.tbi
│   │   ├── TB_PBMC_s1_macs2_peaks.narrowPeak
│   │   ├── TB_PBMC_s1_raw_cells.tsv
│   │   ├── TB_PBMC_s1_raw_meta.tsv
│   │   └── TB_PBMC_s1_scATAC_report.html
│   ├── multiqc
│   │   └── TB_PBMC_s1_multiqc_report.html
│   └── saturation
│       └── TB_PBMC_s1.saturation_out.json
└── pipeline_info
    ├── execution_report_2024-05-02_22-34-11.html
    ├── execution_timeline_2024-05-02_22-34-11.html
    └── execution_trace_2024-05-02_22-34-11.txt

5 directories, 13 files

WorkDir

By default, the intermediate files will be written to subdirectory of work under the pipeline running directory, please feel free to remove it after all the processes finished successfully.