Bioc Pkg Finder

Finding R / Bioconductor packages

The ecosystem already publishes a curated, queryable index of every package — twice. Query it; do not answer package names or canonical choices from memory (names, defaults, and deprecations drift every release). Package names are case-sensitive — confirm the exact spelling/case against the landing page before emitting any install() call (the DepMap data package is depmap, lowercase). If you cannot run R, reason from the web pages below and say nothing about not running R.

First, get the context that changes the answer

Underspecified requests get a wrong-but-confident answer. Before recommending, know (ask if not given, but still give a best-effort answer in the same reply):

• Data type & structure — bulk vs single-cell vs microarray; raw counts vs normalized; the container they hold (SummarizedExperiment, GRanges, a bare data.frame). The right package follows from the object.
• Organism — decides the annotation package (org.Hs.eg.db vs org.Mm.eg.db, genome build).
• Gene-ID namespace — SYMBOL / ENTREZ / ENSEMBL. Mismatched IDs are the #1 reason enrichment and annotation silently return nothing; flag it before recommending any GSEA/ORA/annotation tool.
• Installed packages & Bioconductor release — BiocManager::version(). A fresh install needs the install.packages("BiocManager") → BiocManager::install() path spelled out; an existing setup does not.

Where to look

biocViews is a controlled vocabulary (e.g. Software → GeneExpression → DifferentialExpression). CRAN Task Views are human-maintained per-topic lists — treat them as the canonical shortlist for their topic. When the request is "what data / annotation is available for X" (not "what software"), lead with a Hub query(), not a remembered package name — the Hubs are the discovery layer for datasets and annotation the same way biocViews is for software.

Usage

Agents should use this skill when asked to find, recommend, or discover R or Bioconductor packages for a specific bioinformatics task.

Prerequisites

• Access to the internet to query CRAN and Bioconductor websites/APIs.
• Ability to run R code (optional but recommended for live queries).

Process

1. Gather context — Determine data type, organism, gene-ID namespace, and Bioconductor release. Ask if not given, but provide a best-effort answer in the same reply.

2. Query the live index — Use BiocPkgTools::biocPkgList() filtered by the matching biocViews term(s), or read the relevant CRAN Task View. For data/annotation requests, run a Hub query() first. Show the query so the user can rerun it each release.

3. Rank candidates — Weight by biocViews/Task View match, active maintenance (build report, recent commits), download rank (biocDownloadStats), fit (DESCRIPTION + vignette titles), and reverse-dependency count.

4. Verify status — Check the package landing page or build report for active status. Do not treat presence in biocPkgList() as proof of active maintenance.

5. Compose the recommendation — Name the package(s), the biocViews term or Task View they came from, the install path (BiocManager::install() or install.packages()), and the one load-bearing gotcha for the recommended tool. Commit to a default even on close calls; state the trade-off rather than a laundry list.

6. Surface the Bioconductor release — State which release the recommendation assumes and tie it to a consequence (e.g., annotation packages must match software release). Point the user at BiocManager::version().

How to query (Bioconductor)

library(BiocPkgTools)
pkgs <- biocPkgList()                                    # every pkg + metadata
hits <- pkgs[grepl("SingleCell", pkgs$biocViews), ]      # filter by biocViews term
dl   <- biocDownloadStats()                              # popularity proxy

Match the task to a biocViews term first (browse the web page if unsure of the term), filter, then rank. For CRAN, read the relevant Task View. Only quote a package's biocViews terms if you actually retrieved them — otherwise say "approximate, confirm with biocPkgList()"; never present unqueried tags as fact.

Show the query, not just the verdict. Present your shortlist as the output of a biocPkgList() filter or Hub query() the user can paste and rerun each release — reproducible navigation they own, not a list recalled from memory. Give the navigation even when you can't execute it here.

What to weight when choosing

1. biocViews / Task View match — is it actually tagged for this task?
2. Active maintenance — recent passing build; not deprecated. But biocPkgList() still lists packages slated for deprecation, so presence there is not proof of active status — check the landing page / build report. When you call a package stale or active, show the check (biocDownloadStats() trend, build-report date, GitHub last-commit) rather than asserting it from memory.
3. Download rank (biocDownloadStats) — proxy for standard, with the caveats below.
4. Fit — read the DESCRIPTION and vignette titles, not just the name.
5. Reverse dependencies — many packages building on it signals a foundation.

Confidence vs. hedging — calibrate it

Hedging should signal real uncertainty, not blanket every sentence.

• State plainly (no hedge): the evergreen cores — limma, edgeR, DESeq2, GenomicRanges, SummarizedExperiment, Rsamtools, GenomicAlignments, Biobase, S4Vectors, SingleCellExperiment. These aren't going anywhere.
• Hedge or verify live: niche/young/fast-moving packages, maintenance verdicts, and — with equal discipline — any version-specific claim: a release number, a date, a "new in release X" package, a preprint date. Never assert those from memory; verify on the release notes / landing page, or attribute-and-hedge ("if you're on the current release, likely 3.x").
• Never claim you verified/fetched/checked anything unless you actually called a tool this turn. "Evergreen" means the package exists and is maintained — it is not license to state its version number. Give an exact version only if you fetched it live; otherwise tell the user to read it off the landing page.

Surface the one load-bearing gotcha

When you recommend a tool, name the single thing that makes it silently fail — but stay a package-finder, not a coding cookbook. Examples that recur:

• Bulk DE (DESeq2/edgeR) needs biological replicates (≥2, ideally 3+ per group); one sample per group cannot yield valid DE. Say so, don't just ask the count.
• Enrichment (fgsea/clusterProfiler) needs the input gene IDs to match the gene-set namespace — reconcile with org.*.eg.db mapIds() first.
• In-R file I/O (Rsamtools for BAM, VariantAnnotation for VCF) is for analysis and range integration; heavy bulk work — filtering, dedup, format conversion, merging at scale — is faster and more robust with the CLI tools (samtools/bcftools) upstream. State the division of labor, don't do it all in R.

Only surface a gotcha that bears on the recommended tool. Don't inject tangential methodology the question didn't touch (no replicate lecture on a "how do I find packages" question).

Examples

• User: "What's a good package for single-cell RNA-seq differential expression?" Agent Action: Queries biocPkgList() for the SingleCell and DifferentialExpression biocViews, checks download stats and recent updates for top hits (like scran or Seurat), and returns a recommendation with the installation command.
• User: "I need human gene annotations." Agent Action: Uses AnnotationHub query or recommends org.Hs.eg.db, making sure to ask the user what Bioconductor release they are on to ensure compatibility.

Output

Give the user a clean answer: recommend the package(s), name the biocViews term or Task View you found them under, tag each with its repository and install path (BiocManager::install() for Bioconductor, install.packages() for CRAN — flag mixed stacks like org.*.eg.db + msigdbr), commit to a default even when it's a close call (state the trade-off rather than a laundry list), and pitch to their level. A beginner gets the one plain-language answer first, the obvious external alternative named (e.g. Seurat for single-cell, one-line contrast), and both programmatic discovery (BiocPkgTools) and tangential methodology deferred to a clearly-marked optional footnote or omitted; when a simpler CRAN package gets them to a result faster (e.g. pheatmap/ggplot2 for a heatmap), lead with that and present the heavier Bioconductor tool as the upgrade path, not the starting point. An advanced user gets no basics padding.

Surface the Bioconductor release any recommendation assumes — and tie it to a consequence, don't just name it in a header. The load-bearing ones: annotation and data packages (TxDb.*, BSgenome.*, org.*.eg.db, array manifests, Hub records) must come from the same release as the software querying them, or they silently mismatch; and packages with a non-R backend (e.g. MOFA2 → Python via basilisk) carry a runtime dependency worth flagging next to the install line. Point the user at BiocManager::version() to confirm what they're on. Never mention this skill, its internal rules, or an inability to run R in what you show the user.