Generated August 18, 2020

Welcome to KBase's Narrative Interface!

What's a Narrative? Narratives are shareable, reproducible workflows that can include data, analysis steps, results, visualizations and commentary. Learn more...

Take the Tour: Choose "Narrative Tour" from the "Help" menu above. The tour walks you through the user interface, pointing out various useful aspects of it.

Get Some Data: Click the Add Data button in the Data Panel to search KBase data or upload your own. Mouse over a data object to add it to your Narrative. Learn more...

Analyze It: Use the Apps panel or the App Catalog to browse available analysis apps. Select an app to add it to your Narrative, fill in the fields, and click the "play" button to launch the app. Learn more...

Save and Share Your Narrative: Be sure to save your Narrative frequently. To let collaborators view your analysis steps and results, click the Share button. Or make your Narrative public and help expand the social web that KBase is building to make systems biology research more open, reproducible and collaborative. Learn more...

Find Documentation: For more information, please see the Narrative Interface User Guide or the tutorials.

Questions? Bug reports? Contact us!

Ready to begin adding to your Narrative? You can keep this Welcome cell or delete it by selecting "Delete cell" from the "..." menu in the top right corner of this cell.

from biokbase.narrative.jobs.jobmanager import JobManager
JobManager().get_job('5936c44be4b0b89082da637f')
Out[ ]:
A quality control application for high throughput sequence data.
This app completed without errors in 8m 56s.
Links
Files
These are only available in the live Narrative: https://narrative.kbase.us/narrative/21814
  • ffd705fc-85ce-4dd9-a44f-99b8bee62cbc.fwd_fastqc.zip - Zip file generated by fastqc that contains original images seen in the report
  • bcd70199-be58-4b44-8308-1bf478f3b8f4.rev_fastqc.zip - Zip file generated by fastqc that contains original images seen in the report
Trim paired- or single-end Illumina reads with Trimmomatic.
This app completed without errors in 22m 3s.
Objects
Created Object Name Type Description
JC28-genome-reads-trimmed_paired PairedEndLibrary Trimmed Reads
JC28-genome-reads-trimmed_unpaired_fwd SingleEndLibrary Trimmed Unpaired Forward Reads
JC28-genome-reads-trimmed_unpaired_rev SingleEndLibrary Trimmed Unpaired Reverse Reads
Report
A quality control application for high throughput sequence data.
This app produced errors.
No output found.
Assemble paired-end microbial reads using the A5 assembly pipeline.
This app completed without errors in 2h 58m 45s.
Objects
Created Object Name Type Description
JC28-genome-a5.contigs Assembly Assembled contigs
Summary
============= Raw Contigs ============ QUAST: All statistics are based on contigs of size >= 500 bp, unless otherwise noted (e.g., "# contigs (>= 0 bp)" and "Total length (>= 0 bp)" include all contigs). Assembly a5_contigs # contigs (>= 0 bp) 40 # contigs (>= 1000 bp) 31 Total length (>= 0 bp) 5533243 Total length (>= 1000 bp) 5527245 # contigs 39 Largest contig 1226393 Total length 5532803 GC (%) 43.19 N50 509001 N75 314808 L50 4 L75 8 # N's per 100 kbp 3.16 ========== Filtered Contigs ========== ContigSet saved to: asuria25:narrative_1496760868085/JC28-genome-a5.contigs Assembled into 40 contigs. Average Length: 138331.075 bp. Contig Length Distribution (# of contigs -- min to max basepairs): 29 -- 440.0 to 123035.3 bp 2 -- 123035.3 to 245630.6 bp 2 -- 245630.6 to 368225.9 bp 3 -- 368225.9 to 490821.2 bp 3 -- 490821.2 to 613416.5 bp 0 -- 613416.5 to 736011.8 bp 0 -- 736011.8 to 858607.1 bp 0 -- 858607.1 to 981202.4 bp 0 -- 981202.4 to 1103797.7 bp 1 -- 1103797.7 to 1226393.0 bp
Output from Assemble with A5
The viewer for the output created by this App is available at the original Narrative here: https://narrative.kbase.us/narrative/21814
Assemble short microbial reads using the Velvet assembler.
This app completed without errors in 5m 50s.
Objects
Created Object Name Type Description
JC28-genome-velvet.contigs Assembly Assembled contigs
Summary
============= Raw Contigs ============ QUAST: All statistics are based on contigs of size >= 500 bp, unless otherwise noted (e.g., "# contigs (>= 0 bp)" and "Total length (>= 0 bp)" include all contigs). Assembly velvet_contigs # contigs (>= 0 bp) 592 # contigs (>= 1000 bp) 120 Total length (>= 0 bp) 5461918 Total length (>= 1000 bp) 5395649 # contigs 143 Largest contig 230148 Total length 5410830 GC (%) 43.21 N50 98222 N75 59709 L50 18 L75 37 # N's per 100 kbp 126.15 ========== Filtered Contigs ========== ContigSet saved to: asuria25:narrative_1496760868085/JC28-genome-velvet.contigs Assembled into 169 contigs. Average Length: 32076.1597633 bp. Contig Length Distribution (# of contigs -- min to max basepairs): 110 -- 307.0 to 23291.1 bp 13 -- 23291.1 to 46275.2 bp 20 -- 46275.2 to 69259.3 bp 5 -- 69259.3 to 92243.4 bp 6 -- 92243.4 to 115227.5 bp 5 -- 115227.5 to 138211.6 bp 4 -- 138211.6 to 161195.7 bp 2 -- 161195.7 to 184179.8 bp 1 -- 184179.8 to 207163.9 bp 3 -- 207163.9 to 230148.0 bp
Output from Assemble with Velvet
The viewer for the output created by this App is available at the original Narrative here: https://narrative.kbase.us/narrative/21814
Run QUAST (QUality ASsessment Tool) on a set of Assemblies to assess their quality.
This app is still in progress.
No output found.
Align sequencing reads to long reference prokaryotic genome sequences using Bowtie2
This app completed without errors in 32m 49s.
No output found.
Runs the CheckM lineage workflow to assess the genome quality of isolates, single cells, or genome bins from metagenome assemblies
This app completed without errors in 8m 36s.
Links
Files
These are only available in the live Narrative: https://narrative.kbase.us/narrative/21814
  • full_output.zip - Full output of CheckM
  • plots.zip - Output plots from CheckM

Apps

  1. Align Reads using Bowtie2 - v2.3.2
    • Langmead B, Salzberg SL. Fast gapped-read alignment with Bowtie 2. Nat Methods. 2012;9: 357 359. doi:10.1038/nmeth.1923
    • Langmead B, Trapnell C, Pop M, Salzberg SL. Ultrafast and memory-efficient alignment of short DNA sequences to the human genome. Genome Biol. 2009;10: R25. doi:10.1186/gb-2009-10-3-r25
  2. Assemble with A5
    • Coil, D., Jospin, G. and Darling, A.E., (2014). A5-miseq: an updated pipeline to assemble microbial genomes from Illumina MiSeq data. Bioinformatics, p.btu661.
  3. Assemble with Velvet
    • Zerbino, D. R., Birney, E. (2008) Velvet: Algorithms for de novo short read assembly using de Bruijn graphs. Genome Research, 18(5), 821-829, doi: 10.1101/gr.074492.107
  4. Assess Genome Quality with CheckM - v1.0.18
    • Parks DH, Imelfort M, Skennerton CT, Hugenholtz P, Tyson GW. CheckM: assessing the quality of microbial genomes recovered from isolates, single cells, and metagenomes. Genome Res. 2015;25: 1043 1055. doi:10.1101/gr.186072.114
    • CheckM source:
    • Additional info:
  5. Assess Quality of Assemblies with QUAST - v4.4
    • [1] Gurevich A, Saveliev V, Vyahhi N, Tesler G. QUAST: quality assessment tool for genome assemblies. Bioinformatics. 2013;29: 1072 1075. doi:10.1093/bioinformatics/btt086
    • [2] Mikheenko A, Valin G, Prjibelski A, Saveliev V, Gurevich A. Icarus: visualizer for de novo assembly evaluation. Bioinformatics. 2016;32: 3321 3323. doi:10.1093/bioinformatics/btw379
  6. Assess Read Quality with FastQC - v0.11.5
    • FastQC source: Bioinformatics Group at the Babraham Institute, UK.
  7. Trim Reads with Trimmomatic - v0.36
    • Bolger AM, Lohse M, Usadel B. Trimmomatic: a flexible trimmer for Illumina sequence data. Bioinformatics. 2014;30: 2114 2120. doi:10.1093/bioinformatics/btu170