bio-rna-quantification-tximport-workflow

Version Compatibility

Reference examples tested with: tximport 1.30+, tximeta 1.20+, DESeq2 1.42+, edgeR 4.0+, txdbmaker 1.0+, Salmon 1.10+, kallisto 0.50+

Before using code patterns, verify installed versions match. If versions differ:

• R: packageVersion('<pkg>') then ?function_name to verify parameters

If code throws ImportError, AttributeError, or TypeError, introspect the installed package and adapt the example to match the actual API rather than retrying.

tximport Workflow

"Import Salmon/kallisto results into DESeq2" -> Summarize transcript-level abundance estimates to gene-level counts AND compute a per-gene, per-sample length offset that the DE model consumes.

• R: tximport::tximport(files, type='salmon', tx2gene=tx2gene)

Why this is not just a sum

tximport does not merely add transcript counts to a gene total. The fragment count a gene produces depends on the average length of the isoforms expressed in that sample, because longer molecules yield more fragments (more start positions). When isoform usage shifts between conditions (differential transcript usage), the gene's average effective length changes, so a naive summed count is length-biased in a condition-correlated way and masquerades as differential expression. tximport corrects this by returning a per-gene, per-sample average-length matrix (txi$length) and passing it as a normalization offset to DESeq2/edgeR. A single per-gene length cannot capture this because the bias is sample-specific (Soneson, Love, Robinson 2015).

Basic tximport

Goal: Import transcript-level quantifications into R as gene-level counts plus the length offset for DESeq2 or edgeR.

Approach: Build a transcript-to-gene map, then run tximport over the quant files; the returned txi$counts/txi$length carry both the gene counts and the offset.

library(tximport)

files <- c(sample1 = 'sample1_quant/quant.sf',
           sample2 = 'sample2_quant/quant.sf',
           sample3 = 'sample3_quant/quant.sf')

tx2gene <- read.csv('tx2gene.csv')                 # column order: TXNAME, then GENEID
txi <- tximport(files, type = 'salmon', tx2gene = tx2gene)

txi is a list: $abundance (TPM), $counts (estimated counts), $length (the average-length offset source), $countsFromAbundance.

Decision: countsFromAbundance mode

This argument silently determines correctness; nothing errors when it is wrong.

Mode	What it returns	Use when
'no' (default)	Estimated counts + separate length offset	Full-length library -> DESeq2/edgeR (they consume the offset). The cleanest path.
'lengthScaledTPM'	Counts with the length correction baked in, no separate offset	A tool that cannot take an offset (e.g. limma-voom)
'scaledTPM'	TPM scaled to library size, no length scaling	Transcript-level DTU with txOut=TRUE (DRIMSeq/DEXSeq); the established Love et al. workflow input
'dtuScaledTPM'	Scaled by median isoform length	DTU alternative (tximport >= 1.10), needs tx2gene; helps when isoform lengths within a gene differ widely

For DTU, scaledTPM is the established default; dtuScaledTPM is the newer purpose-built mode, preferable when a gene's isoforms span very different lengths.

The 3'-tag exception: for 3'-end protocols (10x, QuantSeq, Lexogen) a read count does not scale with transcript length, so there is no length bias to correct, and length-correcting injects one. Do not use the length-scaled modes (lengthScaledTPM/dtuScaledTPM) for tag-seq. Import with the default, but build the DESeqDataSet from the plain counts so the length offset is NOT auto-applied:

# 3'-tag: bypass the length offset that DESeqDataSetFromTximport would otherwise apply
dds <- DESeqDataSetFromMatrix(round(txi$counts), colData = coldata, design = ~ condition)

# Full-length, DESeq2/edgeR (default): keep the offset path
txi <- tximport(files, type = 'salmon', tx2gene = tx2gene)

# Transcript-level for DTU (hand off to alternative-splicing/isoform-switching)
txi_tx <- tximport(files, type = 'salmon', txOut = TRUE,
                   countsFromAbundance = 'scaledTPM')

Creating tx2gene

The map is a two-column data frame; column ORDER is load-bearing (TXNAME first, GENEID second), names do not matter.

Goal: Map every quantified transcript ID to its gene, with IDs that exactly match the quant files.

Approach: Derive from the annotation that built the index (GTF, ensembldb, biomaRt, or the index t2g); strip version suffixes to match.

# From a GTF: makeTxDbFromGFF moved to txdbmaker in Bioconductor >= 3.19
# (defunct in GenomicFeatures >= 1.61.1; on older Bioconductor use GenomicFeatures::makeTxDbFromGFF)
library(txdbmaker)
txdb <- makeTxDbFromGFF('annotation.gtf')
k <- keys(txdb, keytype = 'TXNAME')
tx2gene <- AnnotationDbi::select(txdb, keys = k, keytype = 'TXNAME',
                                 columns = c('TXNAME', 'GENEID'))

# From biomaRt (useEnsembl; useMart is deprecated)
library(biomaRt)
mart <- useEnsembl(biomart = 'genes', dataset = 'hsapiens_gene_ensembl')
tx2gene <- getBM(attributes = c('ensembl_transcript_id', 'ensembl_gene_id'), mart = mart)

The #1 silent failure: transcript-ID version mismatch

If quant.sf IDs carry version suffixes (ENST00000456328.4) but tx2gene does not (or vice versa), the IDs do not match. Total non-overlap raises an error; partial mismatch silently drops the non-matching transcripts and prints a summary, deflating affected genes toward zero. Fix by stripping versions consistently or with ignoreTxVersion:

txi <- tximport(files, type = 'salmon', tx2gene = tx2gene,
                ignoreTxVersion = TRUE, ignoreAfterBar = TRUE)

Handoff to DESeq2 (offset applied automatically)

Goal: Build a DESeqDataSet that uses the tximport length offset without any manual step.

Approach: DESeqDataSetFromTximport stores txi$length as the avgTxLength assay and converts it to per-gene normalization factors inside DESeq().

library(DESeq2)
coldata <- data.frame(condition = factor(c('control', 'control', 'treated', 'treated')),
                      row.names = names(files))
dds <- DESeqDataSetFromTximport(txi, colData = coldata, design = ~ condition)
dds <- dds[rowSums(counts(dds)) >= 10, ]   # light pre-filter (speed); results() does the inferential filter
dds <- DESeq(dds)
res <- results(dds)

Passing a countsFromAbundance='no' txi prints "using counts and average transcript lengths from tximport"; a length-scaled txi prints "using just counts" and applies no offset. Both are handled correctly by the function.

Handoff to edgeR (manual offset)

Goal: Carry the length offset into an edgeR DGEList.

Approach: Geometric-mean-center the length matrix, fold in composition-corrected library sizes, log it, attach via scaleOffset.

library(edgeR)
cts <- txi$counts
normMat <- txi$length / exp(rowMeans(log(txi$length)))   # center each gene on its geometric mean
normCts <- cts / normMat
eff.lib <- calcNormFactors(normCts) * colSums(normCts)
normMat <- sweep(normMat, 2, eff.lib, '*')
y <- scaleOffset(DGEList(cts), log(normMat))
y <- y[filterByExpr(y, group = coldata$condition), , keep.lib.sizes = FALSE]   # group-aware filter

Do not double-apply the offset: if countsFromAbundance='lengthScaledTPM' already baked the correction into the counts, do not also attach a length offset. Use 'no' for the offset path, the scaled modes for the no-offset path, never both.

Transcript-level uncertainty (DTE/DTU)

Gene-level estimates are robust because per-isoform assignment uncertainty cancels on summation. Transcript-level testing must propagate it: edgeR catchSalmon deflates counts by per-transcript overdispersion (differential-expression/edger-basics), swish/fishpond tests across Salmon Gibbs samples (alternative-splicing/isoform-switching), and sleuth uses kallisto bootstraps (expression-matrix/counts-ingest). Generate the replicates at quantification time (rna-quantification/alignment-free-quant).

tximeta: provenance by checksum

tximeta hashes the index's reference sequences and looks the digest up against known GENCODE/Ensembl/RefSeq releases, attaching transcript ranges and release metadata automatically, so the exact reference becomes a verified property of the object rather than lab lore.

library(tximeta)
makeLinkedTxome(indexDir = 'salmon_index', source = 'Ensembl', organism = 'Homo sapiens',
                release = '110', genome = 'GRCh38', fasta = 'transcripts.fa', gtf = 'annotation.gtf')
coldata <- data.frame(names = names(files), files = files,
                      condition = c('control', 'control', 'treated', 'treated'))
se <- tximeta(coldata)
gse <- summarizeToGene(se)
dds <- DESeqDataSet(gse, design = ~ condition)

Common Errors

Symptom	Cause	Fix
Many genes import as zero or deflated	Transcript-ID version mismatch (partial drop)	ignoreTxVersion = TRUE; or strip \.\d+$ from both sides
Error: none of the transcripts present in tx2gene	Total ID mismatch (versions or wrong annotation)	Rebuild tx2gene from the annotation that built the index
Summarized at the wrong level, no error	tx2gene columns reversed (GENEID first)	Order as TXNAME, then GENEID
Length bias appears in 3'-tag data	DESeqDataSetFromTximport auto-applied the length offset	Build via DESeqDataSetFromMatrix(round(txi$counts), ...) so no offset is applied
Fold changes inflated near isoform switches with manual edgeR	Offset double-applied or omitted	One path only: 'no'+offset, or scaled mode without offset

Related Skills

• rna-quantification/alignment-free-quant - Upstream Salmon/kallisto and inferential replicates
• differential-expression/deseq2-basics - Gene-level DE from a DESeqDataSet
• differential-expression/edger-basics - edgeR DE and catchSalmon transcript DTE
• alternative

---

Content truncated.