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I have downloaded my Nebula genomics 30X .cram file. I would like to extract the complete list of snps and genotypes resulting in a 23andme style output file. I have successfully installed WGSExtract …
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Hi Randy,
This is Jeremy again. I've been using WGSExtract over the past few weeks and I've come across an issue. The program has been handling some of the low-quality BAMs I've given it pretty well …
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Ancestry reports mitochondrial (MT/Chr26) SNPs as diploid (e.g. "GG", with two identical alleles), even though there is just one mitochondrial genome, with multiple copies. 23andme reports as haploid …
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Dear authors,
When I hanle the 1000 Genomes dataset by the code 'yhaplo -i 1000y.all.vcf.gz', the linux system responds that ‘ERROR. Could not open: 1000Y.all.vcf.gz’. I have check the path and the…
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Hello,
I downloaded your source code (in mac terminal, bash shell) using the simple copy-paste command you offered. I then pointed the environment label to the proper location by copying and pasting …
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Consider schema and data below:
**schema.yaml**
```
maptest: map(bool())
```
**test.yaml**
```
maptest:
key1: false
key2: xpto
key2: true
```
**Expected behavior: (either o…
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When yamale is run on the command line in a file tree of yaml files and schema files, the program wrongly validates against the schema file in the current directory rather than matching the schema fil…
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Add the following to README.md after the section on Recursion:
##### List
You can specify a list using the Include validator.
This schema:
```yaml
person: list(min=1, include='human')
---
h…
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Currently you use the library like this:
```python
import yamale
schema = yamale.make_schema('./schema.yaml')
# Create a Data object
data = yamale.make_data('./data.yaml')
# Validate data ag…
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Release new major version dropping support for < `7.2`
- [x] Release Provider [23andme](https://github.com/SocialiteProviders/23andme/releases)
- [x] Release Provider [37Signals](https://github.co…