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fix: command in vcf2cytosure rule and update ReadtheDocs #966
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Codecov Report
@@ Coverage Diff @@
## develop #966 +/- ##
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Coverage 99.24% 99.24%
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Files 29 29
Lines 1714 1714
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Hits 1701 1701
Misses 13 13
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The changes regarding docs looks fine, but it still doesnt render the CLI https://balsamic-docs.readthedocs.io/en/latest/cli_package.html (I tested it in my fork). I will further look into this.
Regarding the content, we discussed some names but maybe you @ashwini06 have some better suggestions how the structure of references/tools should look.
@ivadym @khurrammaqbool : I propose that we can change the existing balsamic readthedocs to a more structured one. How about the following structure? Getting Started
Detailed Documentation:
Development Guide
OTHER INFO:
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The suggested names look good! We have some new entries in develop branch that I included below and me and @khurrammaqbool liked this structure: Getting Started
Detailed Documentation:
Development Guide
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References: References doesn't sound like a correct term here, I would suggest keeping this outside of detailed documentation (like Other info), as it is mostly a Knowledge base resource and the text within it includes a huge collection of tools from various resources. |
@ivadym : Don't forget to add new links to the delivery report, as these |
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few suggestions
docs/balsamic_filters.rst
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- Analysis type | ||
- Somatic/Germline | ||
- Variant type | ||
* - DNAScope |
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* - DNAScope | |
* - DNAscope |
docs/balsamic_filters.rst
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- tumor-normal, tumor-only | ||
- somatic | ||
- SNV, InDel | ||
* - TNScope :superscript:`2` |
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* - TNScope :superscript:`2` | |
* - TNscope :superscript:`2` |
- tumor-normal, tumor-only | ||
- somatic | ||
- SNV, InDel | ||
* - TNScope_umi |
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* - TNScope_umi | |
* - TNscope_umi |
docs/balsamic_filters.rst
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:superscript:`1` TNhaplotyper is only executed for tumor-only if a WGS case is being analysed | ||
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:superscript:`2` TNScope output is being merged with TNhaplotyper calls for TO-WGS analysis |
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:superscript:`2` TNScope output is being merged with TNhaplotyper calls for TO-WGS analysis | |
:superscript:`2` TNscope output is being merged with TNhaplotyper calls for TO-WGS analysis |
docs/balsamic_sv_cnv.rst
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@@ -1,5 +1,5 @@ | |||
************************************ | |||
Structural and Copy Number Variants | |||
Structural and copy-number variants |
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Structural and copy-number variants | |
Structural and Copy Number variants |
CHANGELOG.rst
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@@ -37,6 +37,7 @@ Fixed: | |||
* `run_validate.sh` script https://github.com/Clinical-Genomics/BALSAMIC/pull/952 | |||
* Somatic SV tumor normal rules https://github.com/Clinical-Genomics/BALSAMIC/pull/959 | |||
* Missing `genderChr` flag for `ascat_tumor_normal` rule https://github.com/Clinical-Genomics/BALSAMIC/pull/963 | |||
* Command in vcf2cyosure rule and updated ReadtheDocs https://github.com/Clinical-Genomics/BALSAMIC/pull/966 |
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* Command in vcf2cyosure rule and updated ReadtheDocs https://github.com/Clinical-Genomics/BALSAMIC/pull/966 | |
* Command in vcf2cytosure rule and updated ReadtheDocs https://github.com/Clinical-Genomics/BALSAMIC/pull/966 |
Kudos, SonarCloud Quality Gate passed! 0 Bugs No Coverage information |
This PR:
Changed: ReadtheDocs
Fixed: command in vcf2cytosure rule
Review and tests: