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PubMed: Detection of somatic copy number alterations in cancer using targeted exome c Newsbot! Literature Watch 0 04-03-2012 03:30 PM

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Old 10-30-2014, 02:48 PM   #1
etal
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Post CNVkit: Copy number detection and visualization for targeted sequencing using off-tar

CNVkit is a software toolkit to infer and visualize copy number from targeted DNA sequencing data. It is designed for use with hybrid capture, including both whole-exome and custom target panels, and short-read sequencing platforms such as Illumina.

This method uses the nonspecifically captured off-target reads to supplement read depth information from on-target regions. With relatively simple normalization steps to make these read depths comparable across the genome, CNVkit can produce copy ratio estimates extremely close to those by array CGH.

Manuscript preprint:
http://dx.doi.org/10.1101/010876

Source code:
https://github.com/etal/cnvkit

Documentation:
http://cnvkit.readthedocs.org/en/latest/

I've attempted to make CNVkit compatible with other software and easy to integrate into sequencing analysis pipelines. (Currently supported or under development: bcbio-nextgen, Galaxy, THetA2, IGV, BioDiscovery Nexus Copy Number, Java TreeView, probably others.) If you would like to see CNVkit play nicely with another existing program, please let me know.

Last edited by etal; 02-04-2015 at 08:41 AM.
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Old 02-04-2015, 03:56 AM   #2
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Hi etal,

As I am not fluent with python (and certainly not my collagues), I wondered what progress you made with running in Galaxy (is there already a toolshed-version?) and/or the combination with Biodiscovery's Nexus. Would the latter be a report in a txt-format readable by Nexus?

With regards, Jasper
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Old 02-04-2015, 08:37 AM   #3
etal
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Hi Jasper,

If you would like to quickly get started without doing any technical work, I recommend the DNAnexus app, which is essentially complete and free to use initially after you've set up a DNAnexus account.

The Galaxy tool is not feature-complete, but I've made it available for testing in the Test Tool Shed (not the production one) in order to learn how people would like to use it. I'll spend more time on this if there's interest, but at the moment it's not the easiest way to use CNVkit.

The BioDiscovery Nexus Copy Number support in CNVkit is simple: CNVkit can export bin-level log2 copy ratio data to a tabular file which can then be loaded in Nexus Copy Number (e.g. "cnvkit.py export nexus-basic MySample.cnr -o MySample.nexus"). The DNAnexus applet also emits these files. Then, within Nexus Copy Number, load the generated file and specify the "basic" format. The copy number data should then appear similarly to array CGH.

Also, please note that CNVkit does not require Python programming to use, only the Unix/Linux command line. Feel free to let me know if you find any of the commands difficult to use or poorly documented.

Last edited by etal; 02-04-2015 at 08:40 AM.
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Old 02-18-2015, 01:39 AM   #4
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Hi Etal,

For the moment it appears that using a Galaxy is the better solution for us. I am running one in a VMware and installed CNVkit this morning. Now I am uploading some .bam files to work with.

With regards, Jasper
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Old 02-18-2015, 07:09 AM   #5
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Hi Etal,

In the current galaxy wrapper all three .bam files appear in both the 'sample' list, as well the 'Normal' list, without a selection or adjustment option.
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Old 02-18-2015, 12:45 PM   #6
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The BAM files available on your server or under your account (however you've set it up) should be visible under either field in the input form, and you should be able to select the files you want for each field through the usual means, e.g. Ctrl+click. Choose the tumor samples for the "sample" list, and any normal or germline files that were sequenced under the same protocol for the "normal" list.

You can also run it without any "normal" BAM inputs and the results should be reasonably good.
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Old 02-23-2015, 09:57 AM   #7
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Hi etal, I have a more basic question for CNV detection- If I have a custom target panel through Ampliseq multiplex PCR, then is there a way to detect CNVs in that data?

Your CNVkit software works only for hybrid capture target panels like TSCA (Illumina) and Haloplex (Agilent)? Am I getting it correct?

Thanks
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Old 02-23-2015, 04:37 PM   #8
etal
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Yes, CNVkit is designed for hybrid capture target panels like those of Illumina, Agilent and Nimblegen. For best results from amplicon-based targeted resequencing, you should probably use another program like OncoCNV.

I've recently added a little bit of support for running the CNVkit pipeline without using any off-target bins. You can try it by downloading release 0.3.4 and following the instructions here. However, this new feature isn't thoroughly tested and I'm told it doesn't work for everyone, and in any case another layer of gene-level normalizations would be needed to make it perform well on targeted amplicon sequencing data. I'll let SeqAnswers know when that mode is ready for broader use.

Last edited by etal; 02-23-2015 at 08:58 PM.
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Old 02-24-2015, 06:42 AM   #9
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Thanks etal for your reply and this information. I will look into OncoCNV.
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Old 02-25-2015, 08:34 AM   #10
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Default fail to open file?

Hi Etal,

I wanted to test CNVkit on a small set of targeted sequencing data, but it is giving me trouble. With both batch and coverage (I haven't tried the other functions yet), I get the error:

"Processing reads in test.bam
[E::hts_open] fail to open file '-Q'
Segmentation fault: 11"

The indexing right before this worked fine. The chromosome names in my bam-files, fasta and target files are all the same (no "chr" prefix). The tests of cnvkit were all ok, no errors or warnings, and my pysam and pyvcf are up to date.
Any idea what I can do to fix this?

Thanks in advance,
Marlous
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Old 02-25-2015, 09:25 AM   #11
etal
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Hi Marlous,

Thanks for reporting this. Can you show me the commands you used to trigger this error, including any special options you used? Are your BAM files definitely in BAM format, and e.g. "samtools idxstats" works on your BAM files?

I think this error indicates that command line options for "samtools bedcov" on your system are different than those in the versions I tested, missing the "-Q" option to set a minimum mapping quality score when counting reads. This would break CNVkit's coverage command internally. The source code of pysam's bundled samtools (in both pysam 0.8.0 and the current trunk) shows that the bedcov command does still accept the -Q option (using getopt), so either you have a version of pysam/samtools/htslib different from what I looked at, or I'm misunderstanding the error. The bedcov command is barely documented in samtools 1.1 and I can't see why this option might be missing in some versions. Maybe a samtools expert here can help?

In the meantime, you can avoid the call to bedcov with "cnvkit.py coverage --count", which returns similar results to the default strategy but filters out unmapped reads directly using the Pysam API, rather than by calling bedcov with the -Q option.

Best,
Eric

Last edited by etal; 02-25-2015 at 10:28 PM. Reason: Inspected the current pysam/samtools source code.
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Old 02-26-2015, 01:12 AM   #12
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Hey Eric,

Thanks for the quick reply! My bam-files are indeed bam-files, the idxstats works fine. I tried samtools bedcov from the command line (version 1.2), without the '-Q' option it works fine but if I add this option I get the same error message, so it seems to be a samtools-related error indeed...
I was mostly interested in the batch option from CNVkit, is it also possible to run this while circumventing the -Q?

Just to be sure, the command I used for the coverage analysis:
Quote:
python cnvkit.py coverage ~/Documents/CNVkit/testT_dedup.realigned.bam ~/Documents/genomes/design_test4.bed -o ~/Documents/CNVkit/test_dedup.realigned.cnn
Output:
Quote:
Processing reads in testT_dedup.realigned.bam
[E::hts_open] fail to open file '-Q'
Segmentation fault: 11
For the batch analysis:
Quote:
python cnvkit.py batch ~/Documents/CNVkit/*T_dedup.realigned.bam --normal ~/Documents/CNVkit/*R*bam --fasta ~/Documents/genomes/GRCh37_gatk.fasta --access ~/bin/cnvkit/data/access-10kb.hg19_noChr.bed --output-reference ~/Documents/CNVkit/test.cnn --output-dir ~/Documents/test/ -t ~/Documents/genomes/design_test4.bed
Output:
Quote:
Detected file format: BED
Detected file format: BED
Detected file format: BED
Wrote /Users/.../Documents/CNVkit/test/design_test4.antitarget.bed with 1678 background intervals
Building a copy number reference from normal samples...
Processing reads in test1R_dedup.realigned.bam
[E::hts_open] fail to open file '-Q'
Segmentation fault: 11
Thanks again, Marlous
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Old 02-26-2015, 12:33 PM   #13
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I've added the "-c/--count" option from the "coverage" command to the "batch" options as well. If you installed CNVkit from the GitHub repo, you can get the latest by either pulling the new commits or downloading the latest source code Zip file from the master branch and installing that.

Please let me know if that works for you.
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Old 02-27-2015, 04:52 AM   #14
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Thumbs up

Works like a charm, thank you so much.

Also, very pleased with the results!

Last edited by Mulos; 02-27-2015 at 06:25 AM.
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Old 03-02-2015, 02:30 AM   #15
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HI Etal,

Very nice work on a promising tool.

I'm giving it a go as well and what strikes me is that I don't always get the PDF files with the diagram and scatter option in a batch run. Is there a way to get verbose (error) logging?

When I do generate them with the individual scatter/diagram option, they are there, but the diagram is very difficult to read as all the labels overlap each other. Is there a way to influence this, or break all chromosomes to sepperate pages?

If i'm on a X11 terminal I can generate the plots, but when we run analyses on the cluster, there is no display available and we would need the pdf files.

Additionally, it would be great if you could use both sample.bam.bai als sample.bai file as indices.

Best, Ies
ps: and Hi to all the other posters!

Last edited by inijman; 03-02-2015 at 02:42 AM.
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Old 03-12-2015, 01:20 PM   #16
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Hi Ies,

Sorry I missed your post earlier. There isn't a verbose logging mode in CNVkit, but the messages on standard error are fairly verbose already and should always report when there is an error. In particular, if something crashes then you'll see a Python traceback message. However, if you parallelized the batch run (-p >1), the messages from each process will be interleaved, which makes them somewhat harder to intepret.

The scatter and diagram PDFs should always be generated in a batch run; there isn't a special code path where they would be skipped. Does the log say something like "Wrote MySample-scatter.pdf" for the missing PDFs, or not?

The --scatter option uses matplotlib to generate a PDF. On a cluster, the default matplotlib backend (e.g. Wx or Gtk) might not be available, and so I guess it's possible the plotting engine of matplotlib gets confused and silently fails to write the file. You could address that by setting a different backend on your cluster -- create a file called "matplotlibrc" in the current working directory or your home folder, with the contents:

backend : pdf

The --diagram option uses a different backend, Reportlab, which always generates a PDF from scratch and does not have an interactive mode. I can't think of a reason why this one would occasionally fail to write a file. Can you suggest anything unusual about your system's configuration? Outdated software versions, maybe?

If the diagram is showing labels for hundreds of genes, that means:
(a) you did exome sequencing, so there's lots to show;
(b) significant copy number alterations cover large regions of chromosomes in your sample; and/or
(c) the purity of your tumor samples is fairly high.

You can:

- Thin out the labeling to some extent by specifying a higher threshold (-t) log2 ratio value in the diagram command; the default is 0.6, so try 0.8 or 0.9 to only show the higher-amplitude CNAs.
- Drop the labels altogether by specifying a high value for -t or just passing the .cns segment file (with -s), without the .cnr.
- Use the "heatmap" command instead to view the unlabeled CNA regions for many samples at once.
- Use the "gainloss" command to list all genes with log2 ratio amplitudes beyond a given threshold, essentially the labels you're currently seeing on the diagram but in a more manageable plain-text, tabular format.

The diagram is based on Biopython's Graphics/BasicChromosome module. If you're handy with Python and have a specific modification in mind, you could edit cnvlib/diagram.py (202 lines) to do it. For example, you can change PAGE_SIZE to much larger dimensions like 22x17" and the chromosomes will scale proportionally, but the gene labels stay the same size and will be more readable if they were overlapping before.

Thanks for the suggestion on sample.bai, I'll look into it.

Cheers,
Eric
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Old 04-06-2015, 09:44 AM   #17
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When I tried to run more tumor samples using the reference .cnn file from a past normal run, there is no .cnr output.

This gives me .cnr files:
cnvkit.py batch T1.bam T2.bam T3.bam T4.bam T5.bam T6.bam T7.bam T8.bam T9.bam T10.bam --normal Na.bam Nb.bam Nc.bam --targets captures.bed --fasta b37_decoy.fasta --split --access b37.decoy.accessibles.bed --scatter --diagram --output-reference N.cnn --output-dir .


This does not output .cnr pr antitargetcoverage.cnn file:
cnvkit.py batch T1.bam T2.bam T3.bam T4.bam T5.bam T6.bam T7.bam T8.bam T9.bam T10.bam -r N.cnn --targets captures.bed --fasta b37_decoy.fasta --split --access b37.decoy.accessibles.bed --scatter --diagram --output-dir .

What is missing? Thanks.
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Old 04-06-2015, 10:05 AM   #18
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What files were generated by the second run, if any? Can you show me the status messages or any errors that were printed?

When you run CNVkit with a reference, you don't need the "--targets", "--fasta", "--split" and "--access" arguments as that information has already been captured in the reference file. The default output directory is the current directory ("."). Try this instead:

cnvkit.py batch T1.bam T2.bam T3.bam T4.bam T5.bam T6.bam T7.bam T8.bam T9.bam T10.bam -r N.cnn --scatter --diagram
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Old 04-06-2015, 10:15 AM   #19
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Quote:
Originally Posted by etal View Post
What files were generated by the second run, if any? Can you show me the status messages or any errors that were printed?

When you run CNVkit with a reference, you don't need the "--targets", "--fasta", "--split" and "--access" arguments as that information has already been captured in the reference file. The default output directory is the current directory ("."). Try this instead:

cnvkit.py batch T1.bam T2.bam T3.bam T4.bam T5.bam T6.bam T7.bam T8.bam T9.bam T10.bam -r N.cnn --scatter --diagram
Thanks. For the second run where I was having question, there is no error message, and a bunch of .targetcoverage.cnn files are generated.

The status messages are:
Code:
Summary: #bins=292, #reads=7633921, mean=26143.5653, min=212.35, max=224646.99
On-target percentage: 37.877 (of 20154547 mapped)
Wrote ./T4.targetcoverage.cnn
Running the CNVkit pipeline on T9.bam ...
Processing reads in T9.bam
Time: 52.775 seconds (154291 reads/sec, 6 bins/sec)
Summary: #bins=292, #reads=8142711, mean=27885.9981, min=268.94, max=279225.27
On-target percentage: 38.472 (of 21165340 mapped)
Wrote ./T3.targetcoverage.cnn
Running the CNVkit pipeline on T10.bam ...
Processing reads in T10.bam
Time: 55.564 seconds (154063 reads/sec, 5 bins/sec)
Summary: #bins=292, #reads=8560291, mean=29316.0670, min=326.38, max=293055.07
On-target percentage: 38.593 (of 22181003 mapped)
Wrote ./T6.targetcoverage.cnn
Time: 57.101 seconds (149544 reads/sec, 5 bins/sec)
Summary: #bins=292, #reads=8539037, mean=29243.2782, min=302.54, max=292123.56
Time: 57.092 seconds (155098 reads/sec, 5 bins/sec)
Summary: #bins=292, #reads=8854878, mean=30324.9281, min=281.23, max=295576.58
Time: 57.155 seconds (147061 reads/sec, 5 bins/sec)
Summary: #bins=292, #reads=8405294, mean=28785.2540, min=254.16, max=285135.1
On-target percentage: 38.485 (of 22188207 mapped)
On-target percentage: 39.087 (of 22654458 mapped)
On-target percentage: 38.633 (of 21757000 mapped)
Wrote ./T2.targetcoverage.cnn
Wrote ./T8.targetcoverage.cnn
Wrote ./T1.targetcoverage.cnn
Time: 58.704 seconds (143289 reads/sec, 5 bins/sec)
Summary: #bins=292, #reads=8411624, mean=28806.9335, min=241.63, max=282191.54
On-target percentage: 38.845 (of 21654563 mapped)
Wrote ./T7.targetcoverage.cnn
Time: 60.050 seconds (150608 reads/sec, 5 bins/sec)
Summary: #bins=292, #reads=9044023, mean=30972.6832, min=298.46, max=306083.6
On-target percentage: 38.815 (of 23300051 mapped)
Wrote ./T5.targetcoverage.cnn
Time: 50.180 seconds (165905 reads/sec, 6 bins/sec)
Summary: #bins=292, #reads=8325083, mean=28510.5614, min=309.7, max=283705.95
On-target percentage: 38.622 (of 21555485 mapped)
Wrote ./T9.targetcoverage.cnn
Time: 51.261 seconds (173281 reads/sec, 6 bins/sec)
Summary: #bins=292, #reads=8882609, mean=30419.8946, min=299.88, max=296973.17
On-target percentage: 38.693 (of 22956916 mapped)
Wrote ./T10.targetcoverage.cnn


I ran again with the command you suggested, and the results are now as expected, i.e., identical to the first run.

Thanks.
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Old 05-11-2015, 01:33 PM   #20
wisekh
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Default calling LOH from a pair of tumor and normal exome bams

Dear Eric,

I wonder if you can provide an instruction/example on how to generate LOH calls from a pair of tumor and normal exom bams.
I assume this tool can generate them, but I couldn't find a tuturoal in the cnvkit website. probably, I missed it?

thank you very much in advance,

wisekh
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