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fix input

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LUYAO REN 6 年之前
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ff97cdf527
共有 2 個檔案被更改,包括 4 行新增2 行删除
  1. +2
    -0
      README.md
  2. +2
    -2
      inputs

+ 2
- 0
README.md 查看文件

@@ -100,9 +100,11 @@ Hard filtration is applied, for GATK do not yet have the RNAseq training/truth r
- `QD < 2.0`Qual By Depth values

```bash
# GATK3, if you are using gatk4, please pay attention to the new arguments
java -jar GenomeAnalysisTK.jar -T VariantFiltration -R hg_19.fasta -V input.vcf -window 35 -cluster 3 -filterName FS -filter "FS > 30.0" -filterName QD -filter "QD < 2.0" -o output.vcf
```
**Reference**

1. GATK best practice https://software.broadinstitute.org/gatk/documentation/article.php?id=3891
2. Sentieon manual https://support.sentieon.com/manual/RNA_call/rna/
3. STAR github https://github.com/alexdobin/STAR

+ 2
- 2
inputs 查看文件

@@ -4,7 +4,7 @@
"{{ project_name }}.PIdocker": "registry-vpc.cn-shanghai.aliyuncs.com/pgx-docker-registry/picard:2.20.2",
"{{ project_name }}.platform": "ILLUMINA",
"{{ project_name }}.dbsnp_dir": "oss://pgx-reference-data/GRCh38.d1.vd1/",
"{{ project_name }}.disk_size": "{{ disk_size }}",
"{{ project_name }}.disk_size": "500",
"{{ project_name }}.SAdocker": "registry-vpc.cn-shanghai.aliyuncs.com/pgx-docker-registry/star:2.7.0",
"{{ project_name }}.fastq_1": "{{ read1 }}",
"{{ project_name }}.machine": "{{ machine }}",
@@ -12,7 +12,7 @@
"{{ project_name }}.library": "{{ library }}",
"{{ project_name }}.fastq_2": "{{ read2 }}",
"{{ project_name }}.dbmills_dir": "oss://pgx-reference-data/GRCh38.d1.vd1/",
"{{ project_name }}.cluster_config": "{{ cluster if cluster != '' else 'OnDemand ecs.sn1ne.8xlarge img-ubuntu-vpc' }}",
"{{ project_name }}.cluster_config": "OnDemand ecs.sn1ne.8xlarge img-ubuntu-vpc",
"{{ project_name }}.SAref_dir": "oss://chinese-quartet/quartet-storage-data/reference_data/STAR_GRCh38_2.7.0d/",
"{{ project_name }}.SAMdocker": "registry-vpc.cn-shanghai.aliyuncs.com/pgx-docker-registry/samtools:v1.3.1",
"{{ project_name }}.STref_dir": "oss://chinese-quartet/quartet-storage-data/reference_data/",

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