Commit 56a3c8ad authored by Peter van 't Hof's avatar Peter van 't Hof

Fix text comments

parent 97d831f3
......@@ -84,7 +84,7 @@ At this moment the following variant callers can be used
##### Germline
When doing variantcalling mostly germline is used. This will detect variants based on the assumption that there is a fixed number of alleles. Mostly the default used is a ploidy of 2. When this assumption does not hold for your data somatic variantcalling can be a better solution.
When doing variant calling most often germline is used. This will detect variants based on the assumption that there is a fixed number of alleles. Mostly the default used is a ploidy of 2. When this assumption does not hold for your data, somatic variant calling can be a better solution.
| ConfigName | Tool | Description |
| ---------- | ---- | ----------- |
......@@ -101,7 +101,7 @@ When doing variantcalling mostly germline is used. This will detect variants bas
##### Somatic
In contrast to germline variantcalling does somatic variantcalling does not have a direct assumption about the number of alleles. Some can also take a control into account, like MuTect2. Having a control is useful when analysing tumor samples.
In contrast to germline variant calling, somatic variant calling does not have a direct assumption about the number of alleles. Some can also take a control into account, like MuTect2. Having a control is useful when analysing tumor samples.
| ConfigName | Tool | Description |
| ---------- | ---- | ----------- |
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