| name | bio-isoform-switching |
| description | Analyzes isoform switching events and functional consequences using IsoformSwitchAnalyzeR. Predicts protein domain changes, NMD sensitivity, ORF alterations, and coding potential shifts between conditions. Use when investigating how splicing changes affect protein function. |
| tool_type | r |
| primary_tool | IsoformSwitchAnalyzeR |
Isoform Switching Analysis
Identify isoform switches and predict their functional consequences on protein structure and function.
IsoformSwitchAnalyzeR Workflow
library(IsoformSwitchAnalyzeR)
salmonQuant <- importIsoformExpression(
parentDir = 'salmon_quant/',
addIsofomIdAsColumn = TRUE
)
switchAnalyzeRlist <- importRdata(
isoformCountMatrix = salmonQuant$counts,
isoformRepExpression = salmonQuant$abundance,
designMatrix = data.frame(
sampleID = colnames(salmonQuant$counts),
condition = c('control', 'control', 'control', 'treatment', 'treatment', 'treatment')
),
isoformExonAnnoation = 'annotation.gtf',
isoformNtFasta = 'transcripts.fa'
)
switchAnalyzeRlist <- preFilter(
switchAnalyzeRlist,
geneExpressionCutoff = 1,
isoformExpressionCutoff = 0,
removeSingleIsoformGenes = TRUE
)
switchAnalyzeRlist <- isoformSwitchTestDEXSeq(
switchAnalyzeRlist,
reduceToSwitchingGenes = TRUE
)
Functional Annotation
switchAnalyzeRlist <- extractSequence(
switchAnalyzeRlist,
pathToOutput = 'sequences/',
writeToFile = TRUE
)
switchAnalyzeRlist <- analyzeCPC2(
switchAnalyzeRlist,
pathToCPC2resultFile = 'cpc2_results.txt',
removeNoncodinORFs = TRUE
)
switchAnalyzeRlist <- analyzePFAM(
switchAnalyzeRlist,
pathToPFAMresultFile = 'pfam_results.txt'
)
switchAnalyzeRlist <- analyzeSignalP(
switchAnalyzeRlist,
pathToSignalPresultFile = 'signalp_results.txt'
)
switchAnalyzeRlist <- analyzeIUPred2A(
switchAnalyzeRlist,
pathToIUPred2AresultFile = 'iupred2_results.txt'
)
Consequence Analysis
switchAnalyzeRlist <- analyzeSwitchConsequences(
switchAnalyzeRlist,
consequencesToAnalyze = c(
'intron_retention',
'coding_potential',
'ORF_seq_similarity',
'NMD_status',
'domains_identified',
'signal_peptide_identified'
),
dIFcutoff = 0.1,
showProgress = TRUE
)
significantSwitches <- extractSwitchSummary(
switchAnalyzeRlist,
filterForConsequences = TRUE
)
print(significantSwitches)
Visualization
switchPlot(
switchAnalyzeRlist,
gene = 'GENE_OF_INTEREST',
condition1 = 'control',
condition2 = 'treatment'
)
extractConsequenceSummary(
switchAnalyzeRlist,
consequencesToAnalyze = 'all',
plotGenes = FALSE
)
extractConsequenceEnrichment(
switchAnalyzeRlist,
consequencesToAnalyze = 'all'
)
Significance Thresholds
| Parameter | Default | Description |
|---|
| Switch q-value | < 0.05 | Significance of isoform switch |
| dIF (delta isoform fraction) | > 0.1 | Minimum usage change |
| Consequence q-value | < 0.05 | Significance of consequence |
Consequence Types
| Consequence | Impact |
|---|
| NMD sensitive | Transcript targeted for degradation |
| Domain loss/gain | Altered protein function |
| ORF disruption | Truncated/altered protein |
| Signal peptide loss | Changed localization |
| Coding potential loss | Switch to non-coding |
Related Skills
- differential-splicing - Identify differential events first
- splicing-quantification - PSI-level analysis
- pathway-analysis/go-enrichment - Pathway enrichment of switching genes