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bioconductor-bsgenome

Infrastructure shared by all the Biostrings-based genome data packages.

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bioconductor-bsgenome

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Use bioconductor-bsgenome to find occurrences of [nucleotide patterns] across [installed BSgenome package], reporting matches by chromosome and strand; verify chromosome names first and process one chromosome at a time.

Required inputs

  • [nucleotide patterns]
  • [installed BSgenome package]

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SKILL.md

name: bioconductor-bsgenomedescription: Infrastructure shared by all the Biostrings-based genome data packages.when_to_use: "Use when: Chromosome Pattern Matching: Finding or counting the occurrences of an arbitrary nucleotide pattern in a specific chromosome using matchPattern() or countPattern().; Genome-Wide Dictionary Searches: Finding all occurrences of a constant-width dictionary of patterns across an entire genome using PDict() and matchPDict().; Sequence Masking: Applying or toggling masks (e.g., assembly gaps, repeats) o. Not for: For querying remote sequence databases on-the-fly without local storage, use biomaRt instead, as BSgenome relies on locally installed data packages.; For extracting transcript or exon sequences, use GenomicFeatures instead, because BSgenome provides"user-invocable: false

BSgenome

Dependencies & Environment

Package-intrinsic requirements from the Bioconductor landing page — reproduce in any R environment.

  • Version: 1.80.0 · Bioconductor: 3.23 · R: ≥ 4.6
  • Depends: BiocGenerics, S4Vectors, IRanges, Seqinfo, GenomicRanges, Biostrings, BiocIO, rtracklayer
  • Imports: matrixStats, XVector, Rsamtools
  • Install: BiocManager::install("BSgenome")

When to Use

  • Chromosome Pattern Matching: Finding or counting the occurrences of an arbitrary nucleotide pattern in a specific chromosome using matchPattern() or countPattern().
  • Genome-Wide Dictionary Searches: Finding all occurrences of a constant-width dictionary of patterns across an entire genome using PDict() and matchPDict().
  • Sequence Masking: Applying or toggling masks (e.g., assembly gaps, repeats) on chromosome sequences using masks() and active() before performing sequence analysis.

When NOT to Use

  • For querying remote sequence databases on-the-fly without local storage, use biomaRt instead, as BSgenome relies on locally installed data packages.
  • For extracting transcript or exon sequences, use GenomicFeatures instead, because BSgenome provides raw chromosome sequences rather than gene models.

Data Requirements

  • Genome Package: An installed BSgenome data package (e.g., BSgenome.Celegans.UCSC.ce2).
  • Query Patterns: A dictionary of patterns stored in a FASTA file and loaded as a DNAStringSet using readDNAStringSet().

Key Parameters

  • max.mismatch (default): Allows inexact matching by specifying the maximum number of mismatching letters per match in matchPattern().
  • fixed (default): Logical or vector controlling whether to allow ambiguities during pattern matching in countPattern().
  • append (default): Logical indicating whether to append results to an existing file in custom output functions.

Best Practices

  • Verify Chromosome Information: Use seqinfo() and seqnames() to verify chromosome naming conventions and lengths before starting an analysis.
  • Manage Memory: Load only one chromosome sequence into memory at a time (e.g., subject <- genome[[seqname]]) to avoid memory allocation problems on large genomes.
  • Reverse Strand Matching: Find matches on the minus strand by taking the reverseComplement() of the short query pattern rather than the entire chromosome subject.

Common Pitfalls

  • Memory Exhaustion: Loading all chromosome sequences into memory at once. Fix: Iterate through chromosomes using a for loop and seqnames().
  • Inefficient Reverse Complementation: Applying reverseComplement() to an entire chromosome sequence. Fix: Apply reverseComplement() to the short query pattern instead.
  • Masking Confusion: Forgetting that masks might be active, leading to skipped matches or unexpected results. Fix: Explicitly toggle masks using active(masks(chrY)) <- FALSE.

Alternatives

  • Biostrings: For basic sequence manipulation on individual FASTA files without the full genome package infrastructure.
  • GenomicFeatures: For extracting transcript/exon sequences rather than raw genomic intervals.
  • biomaRt: For querying remote sequence databases without local storage.

Citations

  • Pagès, H. (2026). Efficient genome searching with Biostrings and the BSgenome data packages.

References


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