Update docs (#506)

* update docs * prettier * update params * prettier * parameters * changelog
genomic-medicine-sweden · Nov 19, 2024 · a36ad22 · a36ad22
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diff --git a/CHANGELOG.md b/CHANGELOG.md
@@ -94,6 +94,7 @@ and this project adheres to [Semantic Versioning](https://semver.org/spec/v2.0.0
 - [#502](https://github.com/genomic-medicine-sweden/nallo/pull/502) - Changed to annotating and ranking SNVs per family instead of per project
 - [#502](https://github.com/genomic-medicine-sweden/nallo/pull/502) - Changed output documentation and structure to match `sample` and `family` for all variants
 - [#502](https://github.com/genomic-medicine-sweden/nallo/pull/502) - Changed the way of validating the samplesheet to remove outputing false errors with `ifEmpty`
+- [#506](https://github.com/genomic-medicine-sweden/nallo/pull/506) - Updated documentation
 
 ### `Removed`
 

diff --git a/README.md b/README.md
@@ -52,7 +52,7 @@
 
 ##### Filtering
 
-- Filter SNVs, INDELs, SVs and CNVs with [filter_vep](https://www.ensembl.org/vep) and [bcftools view](https://samtools.github.io/bcftools/bcftools.html).
+- Filter SNVs, INDELs, SVs and CNVs with [filter_vep](https://www.ensembl.org/vep) and [bcftools](https://samtools.github.io/bcftools/bcftools.html)
 
 ## Usage
 

diff --git a/docs/index.md b/docs/index.md
@@ -48,7 +48,7 @@ description: A bioinformatics analysis pipeline for long-reads from both PacBio
 
 ### Filtering
 
-- Filter SNVs, INDELs, SVs and CNVs with [filter_vep](https://www.ensembl.org/vep) and [bcftools view](https://samtools.github.io/bcftools/bcftools.html).
+- Filter SNVs, INDELs, SVs and CNVs with [filter_vep](https://www.ensembl.org/vep) and [bcftools](https://samtools.github.io/bcftools/bcftools.html)
 
 ## Usage