Nanopore assembly and variant calling

Author: Carolina Pita Barros
Contact: carolina.pitabarros@wur.nl
ABG

Assemble nanopore reads and do variant calling with short and long reads

Path to pipeline: /lustre/nobackup/WUR/ABGC/shared/PIPELINES/nanopore-assembly

First follow the instructions here:

Step by step guide on how to use my pipelines
Click here for an introduction to Snakemake

ABOUT

This is a pipeline that uses Flye to create a nanopore assembly. It also does variant calling with long and short reads.
The pipeline starts by using porechop to trim the adaptors, then it uses Flye to create the assembly. After that, ntLink-arks from Lonstitch is used to scaffold the assembly using the nanopore reads. The scaffolded assembly is polished with polca. Bwa-mem2 is used to map the short reads to the assembly and Freebayes to do variant calling using these reads. Minimap2 is used to map the long reads to the assembly, and longshot for variant calling using these. In the end, in addition to your assembly and variant calling results, you'll also get assembly statistics and busco scores before and after the polishing.

Tools used:

• Porechop - trim adaptors
• Flye - assembly
• Seqtk - convert fasta to one line fasta
• LongStitch (ntLink-arks) - scaffolding with nanopore reads
• BUSCO - assess assembly completeness
• MaSuRCA (polca) - polish assembly
• Python - get assembly stats
• Minimap2 - map long reads to reference. Genome alignment
• Samtools - sort and index mapped reads and vcf files
• Longshot - variant calling with nanopore reads
• Bwa-mem2 - map short reads to reference
• Freebayes - variant calling using short reads
• bcftools - vcf statistics
• R - pafCoordsDotPlotly - plot genome alignment

Pipeline workflow

Edit config.yaml with the paths to your files

LONGREADS: <nanopore_reads.fq.gz>
SHORTREADS:
  - /path/to/short/reads_1.fq.gz
  - /path/to/short/reads_2.fq.gz
GENOME_SIZE: <approximate genome size>
PREFIX: <prefix>
OUTDIR: /path/to/outdir
BUSCO_LINEAGE:
  - <lineage>

# genome alignment parameters:
COMPARISON_GENOME: 
  <species>: /path/to/genome/fasta

# filter alignments less than cutoff X bp
MIN_ALIGNMENT_LENGTH: 10000
MIN_QUERY_LENGTH: 50000

• LONGREADS - name of file with long reads. This file should be in the working directory (where this config and the Snakefile are)
• SHORTREADS - paths to short reads fq.gz
• GENOME_SIZE - approximate genome size haploid genome size (bp)(e.g. '3e9' for human genome) from longstitch
• PREFIX - prefix for the created files
• OUTDIR - directory where snakemake will run and where the results will be written to
  

If you want the results to be written to this directory (not to a new directory), open config.yaml and comment out OUTDIR: /path/to/outdir

• BUSCO_LINEAGE - lineage used for busco. Can be one or more (one per line). To see available lineages run busco --list-datasets
• COMPARISON_GENOME - genome for whole genome comparison. Add your species name and the path to the fasta file. ex: chicken: /path/to/chicken.fna.gz. You can add several genomes, one on each line.
  • If you don't want to run the genome alignment step, comment out

COMPARISON_GENOME: 
  <species>: /path/to/genome/fasta

• MIN_ALIGNMENT_LENGTH and MIN_QUERY_LENGTH - parameters for plotting. If your plot is coming out blank or if there's an error with the plotting step, try lowering these thresholds. This happens because the alignments are not large enough.

---

If you have your long reads in several fastq files and need to create one file compressed file with all the reads:

1. In your pipeline directory create one file with all the reads

cat /path/to/fastq/directory/*.fastq > <name of file>.fq

2. Compress the file you just created:

gzip <name of file>.fq

After installing the conda environment (first step of this guide) you'll need to edit the polca.sh file.

First go to the directory where miniconda3 is installed (usually your home directory). Go to /<home>/miniconda/envs/<env_name>/bin and open the file polca.sh. In my case the path looks like this: /home/WUR/<username>/miniconda3/envs/<env_name>/bin/. In your editor open polca.sh and replace this line:

$SAMTOOLS sort -m $MEM -@ $NUM_THREADS <(samtools view -uhS $BASM.unSorted.sam) $BASM.alignSorted 2>>samtools.err && \

With this:

$SAMTOOLS sort -m $MEM -@ $NUM_THREADS <(samtools view -uhS $BASM.unSorted.sam) -o $BASM.alignSorted.bam 2>>samtools.err && \

RESULTS

The most important files are and directories are:

• <run_date>_files.txt dated file with an overview of the files used to run the pipeline (for documentation purposes)
• results directory that contains
  • {prefix}_oneline.k32.w100.ntLink-arks.longstitch-scaffolds.fa.PolcaCorrected.fa final assembly
  • assembly_stats_<prefix>.txt file with assembly statistics for the final assembly
  • variant_calling directory with variant calling VCF files with long and short reads, as well as VCF stats
    • {prefix}_shortreads.vcf.gz
    • {prefix}_shortreads.vcf.gz.stats
    • {prefix}_longreads.vcf.gz
    • {prefix}_longreads.vcf.gz.stats
  • genome_alignment directory with results and figure from whole genome alignment
    • {prefix}_{species}.png
• mapped directory that contains the bam file with long reads mapped to the new assembly
  • {prefix}_longreads.mapped.sorted.bam
• busco_{prefix}_before_polish_ and busco_{prefix}_after_polish directories - contain busco results before and after polishing
  • short_summary.specific.{lineage}.{prefix}_before_polish.txt
  • short_summary.specific.{lineage}.{prefix}_after_polish.txt"
• other_files - directory containing other files created during the pipeline
• assembly - directory containing files created during the assembly step