YaqingLiu

Atjaunināts pirms 1 gada

Automated integrated analysis software for genomics data of the cancer patients.

Atjaunināts pirms 2 gadiem

Atjaunināts pirms 3 gadiem

Annotation of genetic variants detected from human genome hg19 and hg38.

Atjaunināts pirms 3 gadiem

VEP (Variant Effect Predictor) predicts the functional effects of genomic variants. The annotated VCF will be converted into MAF based on vcf2maf.

Atjaunināts pirms 3 gadiem

Germline & Somatic short variant discovery (SNVs + Indels) for WGS & WES.

Atjaunināts pirms 3 gadiem

bcftools-merge is used to merge VCF files into a singe VCF.

Atjaunināts pirms 3 gadiem