Take input from stdin (-) and print the SAM header and any reads overlapping a specific region to stdout

Tools for handling high-throughput sequencing (genomics) data.
Used for reading/writing/editing/indexing/viewing of data in SAM/BAM/CRAM format.
More information: <https://www.htslib.org>.
Trick copyright: tl;dr; <https://github.com/tldr-pages/tldr>

{{other_command}} | samtools view -h - chromosome:start-end

click the source code to copy install samtools on any operating system with command-not-found.com