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

Updated 2 years ago

用于miRNA-seq二代测序数据分析

Updated 4 years ago

Updated 2 years ago

Updated 2 years ago

Updated 4 years ago

Updated 3 years ago

Infer and visualize copy number from high-throughput DNA sequencing data.

Updated 3 years ago

only test

Updated 3 years ago

Updated 7 months ago

prepare junction bed and gtf with novel transcripts for PGA input

Updated 3 years ago

Updated 3 years ago

Updated 3 years ago

Updated 3 years ago

Updated 3 years ago

Updated 4 years ago