Provides Python/HTSlib workflows for genomic files. Used when reading, querying, filtering, or writing SAM/BAM/CRAM, VCF/BCF, FASTA/FASTQ, or tabix data with pysam, including pileup, coverage, indexing, and CRAM references.
安装方式：打开 GenHub 客户端 → 技能市场 → 搜索「pysam」→ 一键安装。
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