Germline & Somatic short variant discovery (SNVs + Indels) for WGS & WES.
Updated 3 years ago
用于miRNA-seq二代测序数据分析
Updated 5 years ago
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Infer and visualize copy number from high-throughput DNA sequencing data.
Updated 3 years ago
only test
Updated 4 years ago
Updated 1 year ago
Updated 5 months ago
prepare junction bed and gtf with novel transcripts for PGA input
Updated 4 years ago
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Updated 4 years ago
Updated 4 years ago
Updated 4 years ago