Keeps the subjects, samples, and analysis outputs of a study in one validated object. It starts from a sample manifest with one row per sample, which is read, checked, and split into a subject table and a sample map. Species and assay are plain values in those tables rather than fixed types, so the same object serves any organism and any omics assay. From that object the package writes the sample sheet a pipeline expects, pairs tumor and normal samples on demand, and records where each analysis writes its output so the files can be loaded back in by subject or by pair. Manual corrections are kept in an audit trail. Results can also be translated across genome builds or species, with liftover for coordinates and ortholog mapping for genes.

biocohort keeps the subjects, samples, and analysis outputs of a study in one validated object. Species and assays are values in the data, not columns or classes, so the same functions work for any organism and any omics assay.
See the repository root README for the motivation behind this package.
pak::pak("samuelbharti/biocohort/pkg-r")
r-universe works too:
install.packages("biocohort", repos = "https://samuelbharti.r-universe.dev")
A manifest is one long-format table, one row per sample. Four columns carry
the shape of the study: subject_id, assay, sample_id, role. Every
other column is metadata.
subject_id,species,genotype,assay,sample_id,role
R1,rat,WT,wes,T1,tumor
R1,rat,WT,wes,N1,normal
R2,rat,KO,wes,T2,tumor
R2,rat,KO,wes,N2,normal
library(biocohort)
parsed <- read_manifest("manifest.csv")
cohort <- cohort_new(parsed$subject_tbl, parsed$sample_map)
cohort
#> ── Cohort
#> • 2 subjects (2 rat)
#> • 4 samples (4 wes)
subjects(cohort)
samples(cohort, assay = "wes")
completeness(cohort, wide = TRUE)
Some studies keep one row per subject, with one id column per assay.
manifest_from_wide() turns that into the long form first:
id_cols <- data.frame(
column = c("wes_tumor_id", "wes_normal_id"),
assay = c("wes", "wes"),
role = c("tumor", "normal")
)
long <- manifest_from_wide(wide_table, id_cols)
read_manifest() reads CSV, TSV, or Excel, always as
text, so an id like 007 keeps its leading zero. validate_manifest()
checks it and splits subject-level columns from sample-level ones.cohort_new() builds a Cohort: one table of
subjects, one long table of samples, an optional Study, and a registry
of analyses.subjects(), samples(), completeness(), and
sample_pairs() return plain tibbles. cohort_filter() keeps a subset
and stays valid.cohort_qc() flags or drops subjects or samples
with a required reason. qc_log() reads the audit trail, which survives
later cohort_filter() calls.cohort_groups() groups subjects by one or more
columns. cohort_contrasts() enumerates every pairwise contrast between
those groups.cohort_derive() bins an existing
numeric column at named cutoffs, so a cutoff is a value passed in, not
code. derive_log() reads its provenance.sample_sheet() writes the sample list
a pipeline expects. as_coldata() and join_metadata() carry cohort
metadata into a SummarizedExperiment, a Seurat object, or a data frame.analysis_spec_new() and load_analysis()
resolve a path template per subject or pair, read the files, and record
which ones were found.apply_corrections() applies a table
of documented overrides to a manifest and keeps an audit trail, instead
of a value changing quietly inside a script.translate() moves a feature table across
genome builds or species, through a liftover or an ortholog backend.read_study_yaml() builds a cohort from a
YAML file that names the study, the manifest, the paths, and the
registered analyses.The package website includes:
To build the site locally, run from the repository root:
pkgdown::build_site("pkg-r")
See CONTRIBUTING.md for the development workflow.
MIT