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## Introduction of PCMH
In 2009, the United States spent 17.5% of its gross domestic product on healthcare, almost eight percentage points more than the average for the member countries of the Orga…
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as of 3/8 this should be available
https://github.com/inform-health-informatics/emap_documentation/blob/main/changelogs/2022-08-change_log.md
2022-09-05
this is still not working reliably
we seem …
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Hello. I was wondering if you couple explain how you are determine the genotype for a cnv. Specifically for each allele what criteria are you using to label it as a 1 or a 0.
Thank you very much
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- ~~[BMC Bioinformatics](https://bmcbioinformatics.biomedcentral.com/about)~~ (already submitted and rejected)
> *BMC Bioinformatics* is an open access, peer-reviewed journal that considers articl…
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### Is there an existing issue for this?
- [X] I have searched the existing issues
### Current Behavior
Hi, this has happened twice today that the mapper has stopped responding. At first I th…
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I am able to run vcf2diploid.jar to create paternal, maternal chain. Then I tried to use these chain to create updated annotation for reference GTF/GFF files. But, I am getting the warning message.
…
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Hi,
I'm seeing an issue on shutdown when having multiple headless instances. I haven't had a chance to hunt this down further. Here is the exception:
```
Exception ignored in atexit callback:…
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Hi,
in some samples, I get the variation record is "chrM 1 CNVnator_dup_1 N . PASS END=17000;SVTYPE=DUP;SVLEN=17000;IMPRECISE;natorRD=inf;natorP1=0;natorP2=0;natorP3=0;nat…
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Hello!
When running `goat-cli taxon search` with a file as input I get an error for each query species which does not exist in goat. For species that do return a hit, the output is as expected. The…
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Hi,
Is it possible to use cnvnator for analyzing datasets where the reference genome is not in the list of valid genomes (NCBI36, hg18, GRCh37, hg19, mm9, hg38, GRCh38)?
When I tried it with ba…