tcrsift 0.15.0

T-cell receptor selection for TCR-T studies from antigen specific culture and scRNA/VDJ sequencing

TCRsift

Select antigen-specific TCRs from single-cell sequencing data.

pip install tcrsift
tcrsift run --sample-sheet samples.yaml -o results/

Contents

• Architecture
• Installation
• Quick Start
• Sample Sheet Format
• Core Pipeline Steps
• Supplementary Tools
• Workflows
• API Reference
• Output Files

Architecture

CellRanger VDJ + GEX  -->  tcrsift run  -->  clonotypes.csv
                              |
        load -> phenotype -> clonotype -> filter -> annotate -> assemble

Supplementary: load-sct, annotate-gex, match-til, til-clonotype, til-select, unify

Key Data Structures

Stage	Format	Description
Load → Phenotype	AnnData	Per-cell data with expression matrix + VDJ annotations in .obs
Clonotype → Assemble	DataFrame	Per-clonotype data with aggregated statistics

The transition from AnnData to DataFrame happens at the clonotype aggregation step. After that point, all operations work on clonotype-level DataFrames.

CellRanger Requirements

TCRsift expects standard 10x Genomics CellRanger output directories:

VDJ Directory (from cellranger vdj):

vdj_outs/
├── filtered_contig_annotations.csv   # Required: contig info per cell
├── clonotypes.csv                    # Optional: CellRanger clonotype calls
├── consensus_annotations.csv         # Optional: for sequence assembly
└── filtered_contig.fasta             # Optional: for native leader extraction

Required columns in filtered_contig_annotations.csv:

• barcode, chain (TRA/TRB)
• cdr3 (amino acid sequence)
• v_gene, j_gene, c_gene
• umis, reads
• productive, full_length

GEX Directory (from cellranger count):

gex_outs/
├── filtered_feature_bc_matrix.h5     # Preferred: HDF5 format
└── filtered_feature_bc_matrix/       # Alternative: MTX directory
    ├── matrix.mtx.gz
    ├── features.tsv.gz
    └── barcodes.tsv.gz

The GEX matrix must contain T cell marker genes (CD3D, CD3E, CD3G, CD4, CD8A, CD8B) for phenotyping. Gene names or ENSEMBL IDs are both supported.

Barcode Matching: CellRanger VDJ and GEX may use different barcode suffixes (e.g., ACGT-1 vs ACGT-2). TCRsift strips suffixes and matches on the core barcode.

Installation

pip install tcrsift

Or install from source:

git clone https://github.com/pirl-unc/tcrsift.git
cd tcrsift
pip install -e .

Optional Dependencies

# Common add-on bundles
pip install "tcrsift[reports,assembly,excel]"

# For PDF report generation
pip install "tcrsift[reports]"
brew install wkhtmltopdf  # macOS

# For constant region sequences from Ensembl
pip install "tcrsift[assembly]"
pyensembl install --release 93 --species human

# For SCT Excel input files
pip install "tcrsift[excel]"

Quick Start

Run the Complete Pipeline

tcrsift run \
    --sample-sheet samples.yaml \
    --output-dir results/ \
    --vdjdb /path/to/vdjdb

This runs: load → phenotype → clonotype → filter → annotate → assemble

With Configuration File

# Generate example config with all defaults
tcrsift generate-config -o my_config.yaml

# Edit config, then run
tcrsift run --config my_config.yaml --sample-sheet samples.yaml -o results/

Python API

import tcrsift

# Load samples from sample sheet
adata = tcrsift.load_samples("samples.yaml")

# Phenotype cells (CD4/CD8 classification)
adata = tcrsift.phenotype_cells(adata)

# Aggregate to clonotypes
clonotypes = tcrsift.aggregate_clonotypes(adata)

# Filter by expansion
filtered = tcrsift.filter_clonotypes(clonotypes, method="threshold", tcell_type="cd8")

# Annotate with VDJdb
annotated = tcrsift.annotate_clonotypes(filtered, vdjdb_path="/path/to/vdjdb")

# Assemble full sequences
assembled = tcrsift.assemble_full_sequences(annotated, include_constant=True)

Sample Sheet Format

TCRsift accepts sample sheets in CSV or YAML format.

YAML Format

samples:
  # Culture sample with peptide stimulation
  - sample: "Patient1_Culture"
    vdj_dir: "/data/patient1/vdj"
    gex_dir: "/data/patient1/gex"
    antigen_type: "short_peptide"
    antigen_name: "CMV pp65 495-503"
    epitope_sequence: "NLVPMVATV"
    mhc_allele: "HLA-A*02:01"
    source: "culture"

  # TIL sample (no antigen info needed)
  - sample: "Patient1_TIL"
    vdj_dir: "/data/patient1_til/vdj"
    source: "til"
    tissue: "tumor"

CSV Format

sample,vdj_dir,gex_dir,antigen_type,source
Patient1_Culture,/data/patient1/vdj,/data/patient1/gex,short_peptide,culture
Patient1_TIL,/data/patient1_til/vdj,,,til

Required Fields

Field	Required	Description
sample	Yes	Unique sample identifier
vdj_dir	Yes*	Path to CellRanger VDJ output
gex_dir	No	Path to CellRanger GEX output
source	No	Sample type: culture, til, tetramer, sct
patient_id	No	Donor / patient identifier — enables per-donor analysis
enrichment_method	No	Free-form method label (e.g. AIMpos, tetpos) — enables per-method outputs
timepoint	No	Free-form timepoint label (e.g. D7, D14) — enables per-timepoint filtering
apc_type	No	APC identity (e.g. mDC, B-LCL) — enables per-APC filtering

*At least one of vdj_dir or gex_dir is required.

Multi-donor / multi-method designs

When patient_id and enrichment_method are populated, several behaviors light up automatically:

• Per-(donor, method) aggregations on clonotypes (e.g. n_methods_per_donor, max_methods_per_donor)
• Per-(donor, method) ranked CSVs under data/filtered_by_method/
• Per-donor method × method overlap matrices + recovery panel (see Filter Clonotypes)
• Per-donor FDR scope as the default when donors are unrelated (see --fdr-scope below)

For cohorts where donors share antigen + MHC + experimental cohort and a unified FDR ranking is biologically valid, set the YAML root-level flag:

donors_share_antigen: true
samples:
  - sample: ...
    patient_id: ...
    enrichment_method: ...

This locks --fdr-scope auto resolution to global instead of per-donor.

Antigen Types

Antigen Type	Expected T Cell	Description
short_peptide	CD8	8-11aa peptides (direct MHC-I binding)
long_peptide	mixed	15-25+aa (requires processing)
whole_protein	mixed	Full protein antigens
tetramer_mhc1	CD8	MHC-I tetramer selection
tetramer_mhc2	CD4	MHC-II tetramer selection
sct	CD8	Single-chain trimer (pMHC-I fusion)

Core Pipeline Steps

1. Load Data

Loads CellRanger VDJ and GEX outputs, extracts T cell markers (CD3, CD4, CD8), and combines into a unified AnnData object.

tcrsift load --sample-sheet samples.yaml -o loaded.h5ad

What happens:

1. Reads filtered_contig_annotations.csv for VDJ data
2. Reads filtered_feature_bc_matrix.h5 for gene expression
3. Matches barcodes between VDJ and GEX
4. Extracts CD3D/E/G, CD4, CD8A/B expression per cell
5. Pivots VDJ to get one row per cell with TRA/TRB info

2. Phenotype Cells

Classifies each cell as CD4+ or CD8+ based on gene expression ratios.

tcrsift phenotype -i loaded.h5ad -o phenotyped.h5ad --cd4-cd8-ratio 3.0

Classification logic:

• Confident CD8+: (CD8A + CD8B + 1) / (CD4 + 1) > ratio (default: 3.0)
• Confident CD4+: (CD4 + 1) / (CD8A + CD8B + 1) > ratio
• Likely CD8+: CD8 > 0 and CD4 = 0 (any CD8 without CD4)
• Likely CD4+: CD4 > 0 and CD8 = 0 (any CD4 without CD8)
• Unknown: Similar expression or both near zero

3. Aggregate Clonotypes

Groups cells by CDR3 sequences into clonotypes with aggregated statistics.

tcrsift clonotype -i phenotyped.h5ad -o clonotypes.csv --group-by CDR3ab

Grouping options:

• CDR3ab: Match by both alpha and beta CDR3 (strict pairing)
• CDR3b_only: Match by beta chain only (allows alpha variation)

Output columns:

• CDR3ab: Unique identifier (CDR3_alpha_CDR3_beta)
• cell_count: Number of cells with this TCR
• frequency: Proportion of total cells
• Tcell_type_consensus: Most common phenotype
• samples: Which samples contain this clone

4. Filter Clonotypes

Applies tiered filtering to prioritize expanded clones.

tcrsift filter -i clonotypes.csv -o filtered/ --method threshold --tcell-type cd8

Tier thresholds (default):

Tier	Min Cells	Min Frequency	Max Conditions
1	10	1%	2
2	5	0.5%	3
3	3	0.1%	5
4	2	0.05%	10
5	2	0%	unlimited

FDR scope (--fdr-scope)

Controls the null distribution the FDR-tier filter computes against:

Value	Behavior	Output
auto (default)	Resolves to per-donor for multi-donor cohorts unless donors_share_antigen is set, else global	depends on resolution
global	Single FDR ranking pooled across all samples (pre-0.8.2 behavior)	filtered_tier{1..5}.csv
per-donor	Each donor gets its own FDR null from its own pooled-across-methods samples	filtered_tier{1..5}_<donor>.csv
per-sample	Each sample gets its own FDR null	filtered_tier{1..5}_<sample>.csv

Default flip (0.8.2): Multi-donor cohorts now get per-donor scope by default. Without donors_share_antigen: true on the sheet, pooling unrelated donors into one FDR ranking silently biases the result — a clone abundant in one donor and absent from another is ranked against the wrong distribution. Users running v0.7.x → v0.8.x against multi-donor sheets will see different tier files.

# Multi-donor unrelated → per-donor by default
tcrsift run --sample-sheet sheet.yaml -o results/

# Force the old behavior:
tcrsift run --sample-sheet sheet.yaml -o results/ --fdr-scope global
# or on the sheet:
# donors_share_antigen: true

Method × method overlap + recovery (multi-method designs)

When enrichment_method is populated, tcrsift run emits additional outputs that surface per-(donor, method) performance without users reconstructing it from delimited strings:

data/clone_sample_long.csv                  # long-format (clone, sample) table
data/filtered_by_method/<donor>__<m>.csv    # top-N clones per (donor, method)
data/method_overlap_<donor>.csv             # method × method overlap matrix
plots/method_overlap_<donor>.png            # heatmap
data/method_recovery.csv                    # per-(donor, method) recovery of tier1
plots/method_recovery.png                   # paired-by-donor bar chart

Overlap similarity metric is configurable: --method-overlap-similarity {jaccard,dice,count} (default jaccard). All blocks are no-ops when enrichment_method isn't populated — backwards-compatible with single-method designs.

5. Annotate Clonotypes

Matches against public TCR databases to identify known specificities.

tcrsift annotate -i filtered/tier1.csv -o annotated.csv \
    --vdjdb /path/to/vdjdb \
    --iedb /path/to/iedb

Supported databases:

• VDJdb: Curated TCR-epitope pairs
• IEDB: Immune Epitope Database
• CEDAR: Cancer Epitope Database and Analysis Resource

Viral flagging: Clones matching CMV, EBV, HIV, Influenza, etc. are flagged as is_viral=True for review.

Reference-database cache (tcrsift data)

When --vdjdb / --iedb / --cedar are omitted, tcrsift annotate and tcrsift run auto-discover databases from a managed cache directory. Resolution order (first wins):

1. explicit --cache-dir flag
2. TCRSIFT_DATA_DIR env var
3. $XDG_CACHE_HOME/tcrsift
4. ~/.cache/tcrsift

Manage the cache with the tcrsift data subcommand:

tcrsift data list                  # show cached DBs, sizes, paths
tcrsift data download              # auto-fetch supported DBs (VDJdb + IEDB)
tcrsift data download --db iedb    # fetch one DB
tcrsift data download --force      # refresh
tcrsift data clear --db iedb       # remove one DB
tcrsift data clear                 # remove all

VDJdb is fetched via the GitHub releases API for the latest version; IEDB uses the stable receptor-full-v3 download. CEDAR has no automated download — tcrsift data list shows where to drop it manually. Every downloaded DB gets a _meta.json sidecar with source URL, timestamp, size, and sha256.

# Fresh install: cache the DBs once, then forget about paths.
tcrsift data download
tcrsift run --sample-sheet samples.yaml -o results/    # cache picked up automatically

6. Assemble Full Sequences

Builds full-length TCR sequences with leader peptides and constant regions.

tcrsift assemble -i annotated.csv -o full_sequences.csv \
    --alpha-leader CD28 --beta-leader CD8A --include-constant

Sequence structure:

[Leader] + [V(D)J variable region] + [Constant region]

Single-chain construct:
[Beta full] + [T2A linker] + [Alpha full]

Leader options: CD8A, CD28, IgK, TRAC, TRBC, or from_contig (extract native)

Supplementary Tools

These tools handle data outside the standard CellRanger workflow.

Load SCT Data

Loads TCR data from SCT (single-cell TCR) platform Excel files.

tcrsift load-sct -i sct_data.xlsx -o sct_clonotypes.csv --aggregate

When to use: You have SCT platform data (pMHC tetramer with paired TCR sequencing) that wasn't processed through CellRanger.

Quality filters applied:

• high_quality: SNR ≥ 2.0, reads ≥ 10 per chain, mutation match
• chosen: Stricter criteria (SNR ≥ 3.4, reads ≥ 50, comPACT match)

TIL Matching (Automatic)

When you include TIL samples in your sample sheet with source: til, the run command automatically detects them and adds TIL matching columns to culture clonotypes.

# samples.yaml - TIL samples are auto-detected
samples:
  - sample: "Culture_Pool1"
    vdj_dir: "/data/culture/vdj"
    source: "culture"
  - sample: "Patient1_TIL"
    vdj_dir: "/data/til/vdj"
    source: "til"  # This sample will be used for TIL matching

tcrsift run --sample-sheet samples.yaml -o results/
# TIL matching happens automatically - no extra flags needed!

# You can also explicitly specify TIL samples (overrides auto-detection):
tcrsift run --sample-sheet samples.yaml -o results/ --til-samples Patient1_TIL

Use either --til-samples or repeat --til-sample, not both.

Output columns added:

• til_match (bool): Clone found in TIL
• til_cell_count: Number of TIL cells with this TCR
• til_frequency: Frequency in TIL repertoire

TIL samples are excluded from culture clonotype aggregation and are only used for matching.

Why TIL matching matters: Clones that appear in both antigen-stimulated culture AND tumor tissue provide orthogonal evidence of tumor-reactivity.

Match TIL (Cross-Run)

Use match-til only when TIL data was processed in a separate pipeline run.

tcrsift match-til \
    -i culture_clonotypes.csv \
    --til-h5ad til_processed.h5ad \
    -o matched.csv

# Or provide multiple TIL samples directly (no sample sheet):
tcrsift match-til \
    -i culture_clonotypes.csv \
    -o matched.csv \
    --til-sample T1=csv:/path/to/til_t1.csv \
    --til-sample T2=h5ad:/path/to/til_t2.h5ad \
    --til-sample T3=vdj:/path/to/til_t3_vdj_outs

When to use:

• TIL from a different patient or experiment
• Retrospective matching against archived TIL data
• TIL processed with different parameters

TIL-Only Aggregation

For TIL-only studies (for example, multiple TIL timepoints), aggregate one or more TIL sources directly into clonotype-level counts/frequencies:

tcrsift til-clonotype -o til_clonotypes.csv \
    --til-sample T1=csv:/path/to/til_t1.csv \
    --til-sample T2=h5ad:/path/to/til_t2.h5ad \
    --til-sample T3=vdj:/path/to/til_t3_vdj_outs

This creates a harmonized clonotype table with:

• til_cell_count and til_frequency (combined across all TIL samples)
• til_cell_count.{sample} and til_frequency.{sample} (per-sample columns)

TIL-Only Clone Prioritization (til-select)

For 10x VDJ + GEX tumor timepoints, use til-select to prioritize clones with CD8 bias plus enrichment/immunogenic/cytolytic branch signals.

Input layout per timepoint:

• consensus_annotations.<TP>.csv
• clonotypes.<TP>.csv
• filtered_contig_annotations.<TP>.csv
• sample_filtered_feature_bc_matrix.<TP>.h5

Example (compatible with pfo004/full-length-tcrs-in-TILs/data):

tcrsift til-select \
  --data-dir ~/code/pfo-analysis/pfo004/full-length-tcrs-in-TILs/data \
  --vdjdb ~/code/pfo-analysis/pfo004/full-length-tcrs-in-TILs/data/vdjdb.txt \
  --iedb ~/code/pfo-analysis/pfo004/full-length-tcrs-in-TILs/data/iedb_tcr_full_v3.tsv \
  --cedar ~/code/pfo-analysis/pfo004/full-length-tcrs-in-TILs/data/cedar_tcr_full_v3.tsv \
  --rank-by marker_score_z_mean \
  --verbose

Key outputs in figures/:

• abTCR_master_table.csv
• abTCR_annotated.csv
• selection_masks.csv
• subset_*.csv
• selection_funnel.png
• selected_clones_report.pdf
• marker_cells_<TP>.csv, marker_clonotype_scores_<TP>.csv

Legacy v2 CSV compatibility:

• til-select writes v2-compatible CSV schemas and column ordering by default.
• Using the same inputs/options as v2/harmonize_abtcr_timepoints.py, CSV outputs are expected to match exactly.
• Figure files (.png, .pdf) are not expected to be byte-identical across runs/environments.

Annotate with Gene Expression (annotate-gex)

Adds gene expression data from a 10x HDF5 file to TCR DataFrames.

annotate vs annotate-gex:

Command	Data Source	Purpose
annotate	Public databases (VDJdb, IEDB)	Label clonotypes with known epitope specificities
annotate-gex	10x HDF5 expression file	Add per-cell gene expression values

When GEX data is available:

• Standard pipeline: If gex_dir is in your sample sheet, GEX is loaded automatically at the load step and used for CD4/CD8 phenotyping
• VDJ-only workflows: Use annotate-gex to add expression from a separate HDF5 file

When to use annotate-gex:

• You loaded VDJ-only data (no gex_dir in sample sheet)
• You have a separate 10x HDF5 file with expression data
• You want genes beyond the default CD3/CD4/CD8 markers

# Add per-cell expression from HDF5 file
tcrsift annotate-gex \
    -i cells.csv \
    --gex-file filtered_feature_bc_matrix.h5 \
    -o cells_with_gex.csv

# Add GEX and aggregate to clonotype level
tcrsift annotate-gex \
    -i cells.csv \
    --gex-file filtered_feature_bc_matrix.h5 \
    --aggregate \
    --cd4-cd8-counts \
    -o clonotype_gex.csv

# Custom gene list
tcrsift annotate-gex \
    -i cells.csv \
    --gex-file matrix.h5 \
    --genes "GZMA,GZMB,PRF1,IFNG,TNF" \
    -o cytotoxicity_markers.csv

Output columns:

• gex.{GENE}: Expression per cell
• gex.{GENE}.sum, gex.{GENE}.mean: Aggregated per clonotype (with --aggregate)
• gex.n_reads, gex.n_genes, gex.pct_mito: QC metrics per cell
• CD4_only.count, CD8_only.count: Cells with exclusive expression (with --cd4-cd8-counts)

Note: For most workflows, use gex_dir in your sample sheet and the standard pipeline will handle GEX automatically during loading.

Python API:

from tcrsift import augment_with_gex, aggregate_gex_by_clonotype, compute_cd4_cd8_counts

cells_df = augment_with_gex(cells_df, "filtered_feature_bc_matrix.h5")
clonotype_gex = aggregate_gex_by_clonotype(cells_df, group_col="CDR3_pair")
cd4_cd8 = compute_cd4_cd8_counts(cells_df, group_col="CDR3_pair")

Unify Multiple Experiments

Merges clonotype data from multiple independent pipeline runs into a unified table.

tcrsift unify \
    -i til_results/clonotypes.csv culture_results/clonotypes.csv sct_clonotypes.csv \
    -o unified.csv

Note: Inputs can be standard TCRsift clonotype outputs (CDR3ab) or SCT-style tables (CDR3_pair); tcrsift unify will normalize identifiers automatically.

When to use: You have results from multiple independent runs and want to compare or combine them.

run vs unify:

Scenario	Use
One patient, culture + TIL in same sample sheet	run (TIL auto-detected)
One patient, culture + TIL processed separately	match-til
TIL-only, one or more tumor timepoints (10x VDJ+GEX)	til-select
Multiple patients or experiments	unify
Comparing results across different data sources	unify

Output includes:

• Prefixed columns from each source (e.g., TIL.cell_count, Culture.cell_count)
• Occurrence flags (occurs_in_TIL, occurs_in_Culture)
• Combined statistics (combined.total_cells.count)
• Phenotype confidence based on combined evidence

Generate Mnemonic Names

Creates pronounceable names from CDR3 sequences for easier reference. Similar sequences produce similar names, making it easy to spot related clonotypes.

tcrsift mnemonic -i clonotypes.csv -o clonotypes_named.csv

Example output:

CDR3_beta	mnemonic_name
CASSLGQAYEQYF	Laigqaye Qoy
CASSLAGAYEQYF	Lagaye Qoy
CASSIRASYEQYF	Irasye Qoy
CASSIRANYEQYF	Iranye Qoy

Common conserved prefixes (CASS, CAV) and suffixes (F) are stripped to focus on the variable region. Inserted vowels use diphthongs (ai, oo, ei) to distinguish from original amino acid vowels (A, E, I, Y).

Workflows

Standard Single-Experiment Analysis

tcrsift run --sample-sheet samples.yaml -o results/ --vdjdb /path/to/vdjdb

Culture + TIL Together

When TIL and culture samples are in the same sample sheet, TIL matching happens automatically:

# samples.yaml
samples:
  - sample: "Culture_Pool1"
    vdj_dir: "/data/culture/vdj"
    gex_dir: "/data/culture/gex"
    source: "culture"
  - sample: "TIL"
    vdj_dir: "/data/til/vdj"
    source: "til"  # Auto-detected for TIL matching

tcrsift run --sample-sheet samples.yaml -o results/
# No --til-samples flag needed - auto-detected from source: til

This automatically matches culture clones against TIL samples and adds til_match, til_cell_count, til_frequency columns.

Multi-Source Unification

When combining data from different sources processed separately:

# Process each source
tcrsift til-clonotype -o til_results/clonotypes.csv --sample-sheet til_samples.yaml
tcrsift run --sample-sheet culture_samples.yaml -o culture_results/
tcrsift load-sct -i sct_data.xlsx -o sct_clonotypes.csv --aggregate

# Unify
tcrsift unify \
    -i til_results/clonotypes.csv culture_results/clonotypes.csv sct_clonotypes.csv \
    -o unified_clonotypes.csv

API Reference

Data Loading

from tcrsift import load_samples, load_cellranger_vdj, load_cellranger_gex

# Load all samples from sample sheet
adata = load_samples("samples.yaml")

# Load individual CellRanger outputs
vdj_df = load_cellranger_vdj("/path/to/vdj", sample_name="S1")
adata = load_cellranger_gex("/path/to/gex", sample_name="S1")

Phenotyping

from tcrsift import phenotype_cells, filter_by_tcell_type, get_phenotype_summary

# Classify cells
adata = phenotype_cells(adata, cd4_cd8_ratio=3.0)

# Filter to CD8+ only
cd8_cells = filter_by_tcell_type(adata, tcell_type="cd8")

# Get summary by sample
summary = get_phenotype_summary(adata)

Clonotyping

from tcrsift import aggregate_clonotypes, get_clonotype_summary

# Aggregate by CDR3 pair
clonotypes = aggregate_clonotypes(adata, group_by="CDR3ab", min_umi=2)

# Get summary
summary = get_clonotype_summary(clonotypes)

Filtering

from tcrsift import filter_clonotypes, split_by_tier

# Filter with default tiers
filtered = filter_clonotypes(clonotypes, method="threshold", tcell_type="cd8")

# Split into separate DataFrames by tier
tier_dfs = split_by_tier(filtered)

Annotation

from tcrsift import annotate_clonotypes, load_vdjdb

# Load database
vdjdb = load_vdjdb("/path/to/vdjdb")

# Annotate clonotypes
annotated = annotate_clonotypes(
    clonotypes,
    vdjdb_path="/path/to/vdjdb",
    match_by="CDR3ab",
    exclude_viral=True,
)

TIL Matching

from tcrsift import match_til, get_til_summary

# Match culture clones against TIL data
matched = match_til(culture_clonotypes, til_adata, match_by="CDR3ab")

# Get recovery statistics
summary = get_til_summary(matched)

SCT Data

from tcrsift import load_sct, aggregate_sct, get_sct_specificities

# Load and filter SCT data
df = load_sct("sct_data.xlsx", min_snr=2.0, min_reads_per_chain=10)
hq = df[df.high_quality]

# Aggregate to clonotypes
clonotypes = aggregate_sct(df)

# Get specificity mapping
specificities = get_sct_specificities(clonotypes)

Multi-Experiment Unification

from tcrsift import merge_experiments, add_phenotype_confidence

# Prepare experiments
experiments = [
    (til_clonotypes, "TIL"),
    (culture_clonotypes, "Culture"),
]

# Merge with occurrence flags and combined stats
unified = merge_experiments(experiments, add_occurrence_flags=True)

# Add phenotype confidence
unified = add_phenotype_confidence(unified, ratio_threshold=10.0)

Sequence Assembly

from tcrsift import assemble_full_sequences, export_fasta

# Assemble with leaders and constant regions
assembled = assemble_full_sequences(
    clonotypes,
    alpha_leader="CD28",
    beta_leader="CD8A",
    include_constant=True,
    linker="T2A",
)

# Export FASTA
export_fasta(assembled, "sequences.fasta", sequence_col="single_chain_aa")

Output Files

clonotypes.csv

Column	Description
CDR3ab	Unique identifier (CDR3_alpha_CDR3_beta)
CDR3_alpha	Alpha chain CDR3 sequence
CDR3_beta	Beta chain CDR3 sequence
cell_count	Number of cells
frequency	Proportion of total cells
Tcell_type_consensus	Consensus T cell type
tier	Quality tier (1-5)
db_match	Matched in public database
is_viral	Viral specificity flag
n_donors, n_methods_per_donor, max_methods_per_donor	Multi-donor / multi-method aggregations (populated when patient_id + enrichment_method are set)

Multi-donor / multi-method outputs

Emitted by tcrsift run when the corresponding sheet fields are populated:

File	When	Description
data/clone_sample_long.csv	always	One row per (clone, sample) pair — easier to pivot than the semicolon-delimited samples column
data/filtered_by_method/<donor>__<method>.csv	enrichment_method set	Top-N clones ranked within each (donor, method); --per-method-top-n N
data/method_overlap_<donor>.csv	enrichment_method set, ≥2 methods/donor	method × method overlap matrix; metric via --method-overlap-similarity
plots/method_overlap_<donor>.png	as above, with plots enabled	seaborn heatmap
data/method_recovery.csv	enrichment_method set	Long [donor, method, recovered, total, fraction] — "how does each method perform"
plots/method_recovery.png	as above, with plots enabled	Paired-by-donor bar chart, methods sorted by cross-donor mean recovery
data/filtered_tier{N}_<donor>.csv	--fdr-scope per-donor (default for multi-donor)	Tier files split by donor instead of global tiered files

full_sequences.csv

Column	Description
CDR3ab	Clonotype identifier
alpha_full_aa	Full alpha chain (leader + VDJ + constant)
beta_full_aa	Full beta chain
single_chain_aa	Beta-2A-Alpha construct
single_chain_nt	DNA sequence

Documentation

Full documentation: https://pirl-unc.github.io/tcrsift/

Contributing

See CONTRIBUTING.md for guidelines.

License

Apache License 2.0. See LICENSE for details.

Citation

@software{tcrsift,
  author = {Rubinsteyn, Alex},
  title = {TCRsift: T-cell receptor selection from antigen-specific culture},
  url = {https://github.com/pirl-unc/tcrsift},
  year = {2024}
}