Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
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Amplicon sequence variant (ASV) inference from 16S rRNA or ITS amplicon sequencing using DADA2. Covers quality filtering, error learning, denoising, and chimera removal. Use when processing demultiplexed amplicon FASTQ files to generate an ASV table for downstream analysis.
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See how to installReview the instructions the agent will receive before you install.
Reference examples tested with: DADA2 1.30+, cutadapt 4.4+
Before using code patterns, verify installed versions match. If versions differ:
packageVersion('<pkg>') then ?function_name to verify parametersIf code throws ImportError, AttributeError, or TypeError, introspect the installed package and adapt the example to match the actual API rather than retrying.
"Process my 16S amplicon data to get ASVs" → Denoise amplicon sequencing reads into exact amplicon sequence variants (ASVs) through quality filtering, error model learning, and chimera removal.
dada2::filterAndTrim() → learnErrors() → dada() → removeBimeraDenovo()library(dada2)
path <- 'raw_reads'
fnFs <- sort(list.files(path, pattern = '_R1_001.fastq.gz', full.names = TRUE))
fnRs <- sort(list.files(path, pattern = '_R2_001.fastq.gz', full.names = TRUE))
sample_names <- sapply(strsplit(basename(fnFs), '_'), `[`, 1)
# Quality profiles
plotQualityProfile(fnFs[1:2])
plotQualityProfile(fnRs[1:2])
filtFs <- file.path('filtered', paste0(sample_names, '_F_filt.fastq.gz'))
filtRs <- file.path('filtered', paste0(sample_names, '_R_filt.fastq.gz'))
names(filtFs) <- sample_names
names(filtRs) <- sample_names
# Filter parameters depend on amplicon region and read length
out <- filterAndTrim(fnFs, filtFs, fnRs, filtRs,
truncLen = c(240, 160), # Trim to quality scores
maxN = 0, # No ambiguous bases
maxEE = c(2, 2), # Max expected errors
truncQ = 2, # Truncate at first Q <= 2
rm.phix = TRUE, # Remove PhiX
compress = TRUE,
multithread = TRUE)
errF <- learnErrors(filtFs, multithread = TRUE)
errR <- learnErrors(filtRs, multithread = TRUE)
# Visualize error rates
plotErrors(errF, nominalQ = TRUE)
dadaFs <- dada(filtFs, err = errF, multithread = TRUE)
dadaRs <- dada(filtRs, err = errR, multithread = TRUE)
# Check results
dadaFs[[1]]
mergers <- mergePairs(dadaFs, filtFs, dadaRs, filtRs, verbose = TRUE)
# Check merge success
head(mergers[[1]])
seqtab <- makeSequenceTable(mergers)
dim(seqtab)
# Check length distribution
table(nchar(getSequences(seqtab)))
seqtab_nochim <- removeBimeraDenovo(seqtab, method = 'consensus',
multithread = TRUE, verbose = TRUE)
# Percentage retained
sum(seqtab_nochim) / sum(seqtab)
Goal: Generate a per-sample summary table showing how many reads survived each DADA2 processing step for quality assessment.
Approach: Extract read counts from each pipeline stage (filtering, denoising, merging, chimera removal) and combine into a single tracking matrix.
getN <- function(x) sum(getUniques(x))
track <- cbind(out, sapply(dadaFs, getN), sapply(dadaRs, getN),
sapply(mergers, getN), rowSums(seqtab_nochim))
colnames(track) <- c('input', 'filtered', 'denoisedF', 'denoisedR', 'merged', 'nonchim')
rownames(track) <- sample_names
track
# For ITS, use cutadapt to remove primers first (variable length amplicons)
# Then skip truncLen (don't truncate ITS to fixed length)
out_its <- filterAndTrim(fnFs, filtFs, fnRs, filtRs,
maxN = 0, maxEE = c(2, 2), truncQ = 2,
minLen = 50, # Minimum length
rm.phix = TRUE, compress = TRUE, multithread = TRUE)
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Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
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Validate protein designs using AlphaFold2 structure prediction. Use this skill when: (1) Validating designed sequences fold correctly, (2) Predicting binder-target complex structures, (3) Calculating confidence metrics (pLDDT, pTM, ipTM), (4) Self-consistency validation of designs, (5) Multi-chain complex prediction with AlphaFold-Multimer. For faster single-chain prediction, use esm. For QC thresholds, use protein-qc.
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AlphaFold2 / AlphaFold-Multimer structure prediction for validation and confidence scoring. Use this skill when: (1) Validating designed sequences fold correctly, (2) Predicting binder-target complex structures, (3) Calculating confidence metrics (pLDDT, pTM, ipTM), (4) Self-consistency validation of designs, (5) Multi-chain complex prediction with AlphaFold-Multimer. For faster single-chain prediction, use esm2-sequence-scoring. For QC thresholds, use protein-design-qc.
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Workflow for event-level and isoform-level splicing analysis with sashimi-ready outputs and splice QC.
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ATAC-seq processing with assay QC, MACS3 peak calling, consensus peak matrices, differential accessibility, and motif or footprint follow-up.
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End-to-end binder design using BindCraft hallucination. Use this skill when: (1) Designing protein binders with built-in AF2 validation, (2) Running production-quality binder campaigns, (3) Using different design protocols (fast, default, slow), (4) Need joint backbone and sequence optimization, (5) Want high experimental success rate. For backbone-only generation, use rfdiffusion. For QC thresholds, use protein-qc. For tool selection guidance, use binder-design.
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