What problem does it solve? Genomic interval analysis with tools like bioframe is slow and memory-bound on large datasets. This Skill provides high-performance interval arithmetic (overlap, nearest, merge, coverage, complement, subtract) and file I/O for BED, VCF, BAM, CRAM, GFF/GTF, FASTA, and FASTQ, with streaming execution and cloud-native reads from S3, GCS, and Azure. ## Core Features & Use Cases - Interval Operations: Run overlap, nearest, merge, cluster, coverage, complement, and subtract on Polars DataFrames with chrom/start/end columns, returning LazyFrames for out-of-core processing. - Bioinformatics File I/O: Read, scan, write, and sink BED, VCF, BAM, CRAM, GFF, GTF, FASTA, FASTQ, SAM, and Hi-C pairs files, including BGZF-compressed and cloud-hosted files. - SQL and Pileup: Register genomic files as DataFusion SQL tables and compute CIGAR-aware per-base read depth from BAM/CRAM alignments. - Use Case: Overlap millions of ChIP-seq peaks against gene annotations by scanning BED files lazily, running pb.overlap with parallel partitions, and collecting results with the streaming engine without loading everything into RAM. ## Quick Start Ask the AI to install polars-bio and find overlapping intervals between two BED files using pb.scan_bed and pb.overlap, then collect the result as a Polars DataFrame.