YaqingLiu
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quartet_wes_vcf
0 0

Updated 1 year ago

rnaseq-expr
0 0

Updated 1 year ago

rnaseq-qc
0 0

Updated 1 year ago

SeqKit-sample
0 0

Updated 1 year ago

WesPipe
0 0

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

Updated 2 years ago

WesPipe-hg19-bam
0 0

Updated 2 years ago

WesPipe-hg19
0 0

Updated 2 years ago

CNVkit-test
0 0

Updated 2 years ago

AnnotSV
0 0

Updated 2 years ago

rmsk
0 0

Updated 3 years ago

ANNOVAR
0 0

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

Updated 3 years ago

VEP
0 0

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

Updated 3 years ago

variant-calling
0 1

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

Updated 3 years ago

bcftools-merge
0 0

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

Updated 3 years ago

arriba3
0 0

Updated 3 years ago