Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • iltisanni
    Member
    • Mar 2017
    • 21

    #1

    Nanopolish and pilon are calling wrong bases

    Hi,

    we sequenced and assembled a pichia genome with canu and afterwards polished it with nanopolish and with pilon+illumina reads.

    We noticed that the nanopolish Assembly grows against the canu assembly and that it grows again after using pilon and illumina reads for polishing.

    We then viewed our Assembly together with mapped illumina and nanopore reads in IGV and noticed that canu called some bases which nanopolish and pilon removed while polishing but those bases are correct since we can see them in the reads in IGV.

    Why do nanopolish and pilon remove those bases although they are visible in both, illumina and nanopore reads...

    commands we used for nanopolish and pilon:

    Nanopolish:
    nanopolish index -d PATH/TO/FAST5FILES -s PATH/TO/SEQUENCINGSUMMARY.TXT /PATH/TO/COMBINEDFASTQ

    ~/minimap2-2.10_x64-linux/minimap2 -d draft.mmi trimmed_contig.fasta
    ~/minimap2-2.10_x64-linux/minimap2 -ax map-ont -t 16 draft.mmi /PATH/TO/COMBINED.FASTQ | samtools sort -@ 16 -o reads_vs_trimmed_contig.sorted.bam
    samtools index reads_vs_trimmed_contig.sorted.bam

    python3 /usr/lib/nanopolish/nanopolish_makerange.py /PATH/TO/TRIMMED_CONTIG.FASTA | parallel --results nanopolish.results -P 3 nanopolish variants --consensus polished.{1}.fa -w {1} -r /PATH/TO/COMBINED.FASTQ -b /PATH/TO/READS_VS_TRIMMED_CONTIG.SORTED.BAM -g /PATH/TO/TRIMMED_CONTIG.FASTA -t 4 --min-candidate-frequency 0.1 --faster --fix-homopolymers

    python3 /usr/lib/nanopolish/nanopolish_merge.py polished*.fa > polished_GENOME.fa

    pilon:
    java -jar pilon-1.22.jar \
    --genome test.fasta \
    --bam XXX.sorted.bam \
    --fix "bases" \
    --threads 16 \
    --output test \
    --outdir OUT

Latest Articles

Collapse

  • SEQadmin2
    16S/ITS Profiling vs. Shotgun Metagenomics: What Changes in Your Workflow?
    by SEQadmin2




    NGS has revolutionized clinical microbiology by offering new ways to identify and surveil pathogens without prior knowledge of the target. One popular approach is 16S rRNA and ITS amplicon sequencing, which targets specific microbial markers. But studies are increasingly incorporating shotgun metagenomics, a technique that sequences all DNA from a sample without targeting specific microbial markers. This approach allows more detailed taxonomic classification, detection...
    Today, 06:46 AM
  • SEQadmin2
    Multiomic Liquid Biopsy: What DNA/RNA Panels Reveal That DNA Alone Can’t
    by SEQadmin2



    Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?

    Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating
    ...
    10-14-2026, 09:55 AM

ad_right_rmr

Collapse

News

Collapse

Topics Statistics Last Post
Started by SEQadmin2, 10-28-2026, 09:57 AM
0 responses
22 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 10-28-2026, 09:51 AM
0 responses
14 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 10-22-2026, 11:13 AM
0 responses
67 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 10-22-2026, 10:48 AM
0 responses
47 views
0 reactions
Last Post SEQadmin2  
Working...