File tree 4 files changed +7
-7
lines changed
4 files changed +7
-7
lines changed Original file line number Diff line number Diff line change @@ -27,7 +27,7 @@ Clone the most recent release of ngs-bits (the source code package of GitHub doe
27
27
28
28
git clone --recursive https://github.com/imgag/ngs-bits.git
29
29
cd ngs-bits
30
- git checkout 2021_06
30
+ git checkout 2021_09
31
31
git submodule update --recursive --init
32
32
33
33
## Build
Original file line number Diff line number Diff line change @@ -20,7 +20,7 @@ Use git to clone the most recent release (the source code package of GitHub does
20
20
21
21
> git clone --recursive https://github.com/imgag/ngs-bits.git
22
22
> cd ngs-bits
23
- > git checkout 2021_06
23
+ > git checkout 2021_09
24
24
> git submodule update --recursive --init
25
25
26
26
### Resolving proxy issues with git
Original file line number Diff line number Diff line change @@ -25,7 +25,7 @@ Open a *Git CMD* and clone the most recent release (the source code package of G
25
25
26
26
git clone --recursive https://github.com/imgag/ngs-bits.git
27
27
cd ngs-bits
28
- git checkout 2021_06
28
+ git checkout 2021_09
29
29
git submodule update --recursive --init
30
30
31
31
## Build
Original file line number Diff line number Diff line change 1
1
### VariantFilterAnnotations tool help
2
- VariantFilterAnnotations (2021_06-48-gfc326851 )
2
+ VariantFilterAnnotations (2021_06-105-g6f3de776 )
3
3
4
4
Filter a variant list in GSvar format based on variant annotations.
5
5
112
112
build - Genome build used for pseudoautosomal region coordinates [default=hg19] [valid=hg19,hg38]
113
113
Tumor zygosity Filter based on the zygosity of tumor-only samples. Filters out germline het/hom calls.
114
114
Parameters:
115
- het_af_range - Consider allele frequencies of 50% ± het_af_range as heterozygous and thus as germline. [default=0] [min=0] [max=49.9]
116
- hom_af_range - Consider allele frequencies of 100% ± hom_af_range as homozygous and thus as germline. [default=0] [min=0] [max=99.9]
115
+ het_af_range - Consider allele frequencies of 50% ± het_af_range as heterozygous and thus as germline. [default=0] [min=0] [max=49.9]
116
+ hom_af_range - Consider allele frequencies of 100% ± hom_af_range as homozygous and thus as germline. [default=0] [min=0] [max=99.9]
117
117
Variant quality Filter for variant quality
118
118
Parameters:
119
119
qual - Minimum variant quality score (Phred) [default=250] [min=0]
141
141
--tdx Writes a Tool Definition Xml file. The file name is the application name with the suffix '.tdx'.
142
142
143
143
### VariantFilterAnnotations changelog
144
- VariantFilterAnnotations 2021_06-48-gfc326851
144
+ VariantFilterAnnotations 2021_06-105-g6f3de776
145
145
146
146
2018-07-30 Replaced command-line parameters by INI file and added many new filters.
147
147
2017-06-14 Refactoring of genotype-based filters: now also supports multi-sample filtering of affected and control samples.
You can’t perform that action at this time.
0 commit comments