Dataset Viewer
Auto-converted to Parquet Duplicate
id
stringlengths
9
59
category
stringclasses
4 values
state
stringlengths
65
5.22k
question
unknown
target
stringlengths
3
53
target_idx
int64
0
9
mod_metamaps_classify_1
tool_selection
In Nextflow DSL2, which module handles: Strain-level metagenomic assignment (tools: metamaps)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "metamaps_mapdirectly": "Maps long reads to a metamaps database", "metamaps_classify": "Strain-level metagenomic assignment", "samtools_ampliconclip": "Clips read alig...
metamaps_classify
1
pipe_all101_bacass_2
pipeline_routing
We have raw sequencing data and want to run standard QC, alignment, and quantification for assembly. Best pipeline:
{ "type": "choice", "instructions": "Select the optimal nf-core pipeline for this bioinformatic analysis task.", "criteria": { "viralintegration": "Analysis pipeline for the identification of viral integration events in genomes using a chimeric read approach. [chimeri", "bacass": "Simple bacterial assembl...
bacass
1
mod_bcftools_pluginimputeinfo_0
tool_selection
In Nextflow DSL2, which module handles: Adds imputation information metrics to the INFO field based on selected FORMAT tags. Only the IMPUTE2 INFO metric from FORMAT/GP tags is currently available. (tools: bcftools)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "bcftools/index": "Index VCF tools", "hmmer/hmmlogo": "extract logo data from a profile HMM file to produce an HMM logo", "foldseek/easysearch": "Search for protein st...
bcftools/pluginimputeinfo
3
noul_named_process_output_emits_10
dsl2_rules
Is this statement accurate according to standard Nextflow DSL2 behavior? "Nextflow DSL2 supports multi-channel emission from processes using named emit blocks: `path '*.bam', emit: bam`."
{ "type": "noul", "instructions": "Determine whether the Nextflow DSL2 statement or idiom is valid and adheres to standards.", "criteria": { "false": "The statement describes an invalid Nextflow DSL2 syntax, anti-pattern, or deprecated behavior.", "true": "The statement describes a valid, standard, and re...
true
1
mod_custom_clustermetrics_1
tool_selection
In Nextflow DSL2, which module handles: Computes clustering quality metrics (silhouette, Calinski-Harabasz, Davies-Bouldin) and performs k-sweep analysis (tools: scikit-learn)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "custom_clustermetrics": "Computes clustering quality metrics (silhouette, Calinski-Harabasz, Davies-Bouldin) and performs k-sweep analy", "foldmason_easymsa": "Aligns pro...
custom_clustermetrics
0
noul_confusing_combine_with_mix_semantics_1
dsl2_rules
Is this statement accurate according to standard Nextflow DSL2 behavior? "The operator `.combine()` performs the same operation as `.mix()` without cartesian product semantics."
{ "type": "noul", "instructions": "Determine whether the Nextflow DSL2 statement or idiom is valid and adheres to standards." }
false
0
core_tool_fastp_bare_0
tool_selection
Which bioinformatics tool or module is best suited for this task? All-in-one FASTQ preprocessor performing automated adapter trimming, polyG tail clipping, quality filtering, and base correction.
{ "type": "choice", "instructions": "Select the appropriate bioinformatics tool or module for the specified task.", "criteria": { "fastp": null, "fastqc": null, "cutadapt": null, "multiqc": null, "trimmomatic": null } }
fastp
0
pipe_all101_smrnaseq_2
pipeline_routing
We have raw sequencing data and want to run standard QC, alignment, and quantification for small-rna. Best pipeline:
{ "type": "choice", "instructions": "Select the optimal nf-core pipeline for this bioinformatic analysis task.", "criteria": { "rnavar": "gatk4 RNA variant calling pipeline [gatk4, rna, rnaseq]", "eager": "A fully reproducible and state-of-the-art ancient DNA analysis pipeline [adna, ancient-dna-analysis,...
smrnaseq
9
mod_gatk4_asereadcounter_1
tool_selection
In Nextflow DSL2, which module handles: Calculates the allele-specific read counts for allele-specific expression analysis of RNAseq data (tools: gatk4)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "bcftools_query": null, "gatk4_annotateintervals": null, "gatk4_baserecalibrator": null, "jupyternotebook": null, "gatk4_asereadcounter": null } }
gatk4_asereadcounter
4
intent_ask_question_24
intent_routing
Classify this user request: "How does the .mix() operator differ from .combine() in Nextflow?"
{ "type": "choice", "instructions": "Classify the user intent into one category.", "criteria": { "debug_error": "User is reporting a runtime error, exit code (137, 127), task failure, or pipeline crash", "prepare_data": "User needs help creating a samplesheet, parsing FASTQ/BAM filenames, or staging refer...
ask_question
3
noul_publishdir_directive_usage_12
dsl2_rules
Is this statement accurate according to standard Nextflow DSL2 behavior? "Process outputs can be conditionally saved to disk using the `publishDir` directive with `mode: 'copy'` or `mode: 'symlink'`."
{ "type": "noul", "instructions": "Determine whether the Nextflow DSL2 statement or idiom is valid and adheres to standards.", "criteria": { "false": "The statement describes an invalid Nextflow DSL2 syntax, anti-pattern, or deprecated behavior.", "true": "The statement describes a valid, standard, and re...
true
1
mod_bbmap_clumpify_1
tool_selection
In Nextflow DSL2, which module handles: Create 30% Smaller, Faster Gzipped Fastq Files. And remove duplicates (tools: bbmap)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "ariba_getref": "Download and prepare database for Ariba analysis", "fasta_bgzip_index_dict_samtools": "Ensure BGZF compression, index, and produce a sequence size summary...
bbmap_clumpify
3
mod_odgi_viz_0
tool_selection
In Nextflow DSL2, which module handles: Visualize a variation graph in 1D. (tools: odgi)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "fgumi/fastq": "Convert a BAM file to interleaved FASTQ format with fgumi", "pbjasmine": "Identify specific base modifications in PacBio HiFi reads by analyzing polymerase...
odgi/viz
3
pipe_all101_rnasplice_0
pipeline_routing
I need to run an end-to-end bioinformatics workflow to analyze rnasplice is a bioinformatics pipeline for RNA-seq alternative splicing analysis. Topics: alternative-splicing, rna, rna-seq, splicing. . Which nf-core pipeline should I execute?
{ "type": "choice", "instructions": "Select the optimal nf-core pipeline for this bioinformatic analysis task.", "criteria": { "smrnaseq": null, "rnastructurome": null, "scrnaseq": null, "rnasplice": null, "metaboigniter": null } }
rnasplice
3
mod_modkit_pileup_1
tool_selection
In Nextflow DSL2, which module handles: A bioinformatics tool for working with modified bases (tools: modkit)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "hmmer_hmmfetch": null, "bismark_report": null, "bismark_align": null, "modkit_pileup": null, "vcf_filter_bcftools_ensemblvep": null } }
modkit_pileup
3
mod_starfusion_build_1
tool_selection
In Nextflow DSL2, which module handles: Download STAR-fusion genome resource required to run STAR-Fusion caller (tools: star-fusion)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "vcflib_vcffixup": null, "starfusion_build": null, "bedtools_bamtobed": null, "caalm_downloadmodels": null, "aria2": null } }
starfusion_build
1
mod_svanalyzer_svbenchmark_0
tool_selection
In Nextflow DSL2, which module handles: SVbenchmark compares a set of β€œtest” structural variants in VCF format to a known truth set (also in VCF format) and outputs estimates of sensitivity and specificity. (tools: svanalyzer)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "hmmcopy/gccounter": "gcCounter function from HMMcopy utilities, used to generate GC content in non-overlapping windows from a fasta", "svanalyzer/svbenchmark": "SVbenchma...
svanalyzer/svbenchmark
1
mod_virusrecom_1
tool_selection
In Nextflow DSL2, which module handles: Information-theory-based method for recombination detection of viral lineages using weighted information content (WIC). (tools: virusrecom)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "lofreq_indelqual": null, "virusrecom": null, "cobrameta": null, "parsnp": null, "checkv_updatedatabase": null } }
virusrecom
1
pipe_all101_phaseimpute_2
pipeline_routing
We have raw sequencing data and want to run standard QC, alignment, and quantification for genomics. Best pipeline:
{ "type": "choice", "instructions": "Select the optimal nf-core pipeline for this bioinformatic analysis task.", "criteria": { "phaseimpute": "A bioinformatics pipeline to phase and impute genetic data [genomics, genotype, imputation]", "marsseq": "MARS-seq v2 pre-processing pipeline with velocity [facs-s...
phaseimpute
0
mod_pairtools_dedup_1
tool_selection
In Nextflow DSL2, which module handles: Find and remove PCR/optical duplicates (tools: pairtools)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "dedup": "DeDup is a tool for read deduplication in paired-end read merging (e.g. for ancient DNA experiments).", "pairtools_dedup": "Find and remove PCR/optical duplicate...
pairtools_dedup
1
mod_parabricks_indexgvcf_0
tool_selection
In Nextflow DSL2, which module handles: NVIDIA Clara Parabricks GPU-accelerated gvcf indexing tool. (tools: parabricks)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "aardvark/merge": "A tool to evaluate and merge multiple variant calls into a consensus VCF.", "atlas/call": "generate VCF file from a BAM file using various calling metho...
parabricks/indexgvcf
3
mod_bowtie_align_0
tool_selection
In Nextflow DSL2, which module handles: Align reads to a reference genome using bowtie (tools: bowtie)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "picard/collectalignmentsummarymetrics": "Collect metrics about the alignment summary of a paired-end library.", "deepmased/predict": "DeepMAsED predict subcommand: runs t...
bowtie/align
3
mod_llamacpppython_run_0
tool_selection
In Nextflow DSL2, which module handles: Python wrapper for running locally-hosted LLM with llama.cpp (tools: llama-cpp-python)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "stringtie/merge": "Merges the annotation gtf file and the stringtie output gtf files", "huggingface/download": "Download a file from a Hugging Face Hub repository using t...
llamacpppython/run
2
mod_sentieon_coveragemetrics_0
tool_selection
In Nextflow DSL2, which module handles: Accelerated implementation of the GATK DepthOfCoverage tool. (tools: sentieon)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "allelecounter": null, "pmdtools/filter": null, "cnvpytor/histogram": null, "sentieon/coveragemetrics": null, "cnvkit/coverage": null } }
sentieon/coveragemetrics
3
mod_cache_download_ensemblvep_snpeff_1
tool_selection
In Nextflow DSL2, which module handles: downlad annotation cache for snpeff and ensemblvep (tools: cache_download_ensemblvep_snpeff)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "snpeff_download": "Genetic variant annotation and functional effect prediction toolbox", "utils_annotation_cache": "Check the path to the annotation cache depending if lo...
cache_download_ensemblvep_snpeff
3
pipe_all101_differentialabundance_3
pipeline_routing
Recommend the most appropriate nf-core workflow for the following project: Differential abundance analysis for feature/ observation matrices from platforms such as RNA-seq. Topics: atac-seq, chip-seq, deseq2, differential-abundance, differential-expression, gsea.
{ "type": "choice", "instructions": "Select the optimal nf-core pipeline for this bioinformatic analysis task.", "criteria": { "slamseq": null, "rangeland": null, "fastquorum": null, "pairgenomealign": null, "proteinfamilies": null, "hgtseq": null, "differentialabundance": null, "d...
differentialabundance
6
mod_picard_collectvariantcallingmetrics_1
tool_selection
In Nextflow DSL2, which module handles: Collects per-sample and aggregate (spanning all samples) metrics from the provided VCF file (tools: picard)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "checkm2_databasedownload": "CheckM2 database download", "aardvark_compare": "A tool to evaluate variant calling performance by comparing a query VCF against a truth VCF."...
picard_collectvariantcallingmetrics
2
mod_viber_1
tool_selection
In Nextflow DSL2, which module handles: Multisample subclonal deconvolution of cancer genome sequencing data. (tools: viber)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "hackgap_count": "Fast, JIT-compiled k-mer counter supporting both contiguous and gapped k-mers using multi-way bucketed Cuckoo ", "pairtools_sort": "Sort a .pairs/.pairsa...
viber
2
pipe_all101_detaxizer_2
pipeline_routing
We have raw sequencing data and want to run standard QC, alignment, and quantification for de-identification. Best pipeline:
{ "type": "choice", "instructions": "Select the optimal nf-core pipeline for this bioinformatic analysis task.", "criteria": { "oncoanalyser": "A comprehensive cancer DNA/RNA analysis and reporting pipeline [cancer, clinical, ctdna]", "detaxizer": "A pipeline to identify (and remove) certain sequences fro...
detaxizer
1
mod_jvarkit_wgscoverageplotter_1
tool_selection
In Nextflow DSL2, which module handles: Plot whole genome coverage from BAM/CRAM file as SVG (tools: jvarkit)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "metabuli_build": null, "jvarkit_wgscoverageplotter": null, "atlas_splitmerge": null, "holodeck_mutate": null, "atlas_pmd": null } }
jvarkit_wgscoverageplotter
1
pipe_all101_mhcquant_3
pipeline_routing
Recommend the most appropriate nf-core workflow for the following project: Identify and quantify MHC eluted peptides from mass spectrometry raw data. Topics: dda, immunopeptidomics, mass-spectrometry, mhc, openms, peptides.
{ "type": "choice", "instructions": "Select the optimal nf-core pipeline for this bioinformatic analysis task.", "criteria": { "isoseq": null, "references": null, "proteinfamilies": null, "dualrnaseq": null, "rnadnavar": null, "drop": null, "mnaseseq": null, "diaproteomics": null, ...
mhcquant
9
noul_subworkflow_structural_blocks_12
dsl2_rules
Is this statement accurate according to standard Nextflow DSL2 behavior? "Workflows in Nextflow DSL2 define inputs with `take:`, core execution with `main:`, and outputs with `emit:`."
{ "type": "noul", "instructions": "Determine whether the Nextflow DSL2 statement or idiom is valid and adheres to standards.", "criteria": { "false": "The statement describes an invalid Nextflow DSL2 syntax, anti-pattern, or deprecated behavior.", "true": "The statement describes a valid, standard, and re...
true
1
mod_regenie_splitl0_0
tool_selection
In Nextflow DSL2, which module handles: Split REGENIE step 1 level-0 ridge-regression blocks into parallel jobs (tools: regenie)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "rrnatranscripts": "Ribosomal RNA extraction from a GTF file.", "regenie/splitl0": "Split REGENIE step 1 level-0 ridge-regression blocks into parallel jobs", "regenie/...
regenie/splitl0
1
mod_midas_run_0
tool_selection
In Nextflow DSL2, which module handles: A tool to estimate bacterial species abundance (tools: midas)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "abricate/summary": null, "bam_dedup_stats_samtools_umitools": null, "gatk4/shiftfasta": null, "midas/run": null, "amrfinderplus/run": null } }
midas/run
3
mod_picard_sortvcf_1
tool_selection
In Nextflow DSL2, which module handles: Sorts vcf files (tools: picard)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "picard_sortvcf": null, "crisprcleanr_normalize": null, "biscuit_vcf2bed": null, "biobambam_bamsormadup": null, "vireo": null } }
picard_sortvcf
0
mod_gatk4_reblockgvcf_1
tool_selection
In Nextflow DSL2, which module handles: Condenses homRef blocks in a single-sample GVCF (tools: gatk4)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "gatk4_annotateintervals": "Annotates intervals with GC content, mappability, and segmental-duplication content", "gatk4_reblockgvcf": "Condenses homRef blocks in a single...
gatk4_reblockgvcf
1
mod_suppa_psiperevent_1
tool_selection
In Nextflow DSL2, which module handles: Calculate PSI values for alternative splicing events using SUPPA (tools: suppa)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "parabricks_minimap2": "NVIDIA Clara Parabricks GPU-accelerated minimap2 for aligning long read sequences against a large reference da", "suppa_psiperevent": "Calculate PS...
suppa_psiperevent
1
mod_motus_downloaddb_1
tool_selection
In Nextflow DSL2, which module handles: Download the mOTUs database (tools: motus)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "ganon_classify": null, "centrifuge_centrifuge": null, "motus_downloaddb": null, "samtools_calmd": null, "fastq_qc_stats": null } }
motus_downloaddb
2
mod_khmer_normalizebymedian_0
tool_selection
In Nextflow DSL2, which module handles: Module that calls normalize-by-median.py from khmer. The module can take a mix of paired end (interleaved) and single end reads. If both types are provided, only a single file with single ends is possible. (tools: khmer)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "seq2hla": "Precision HLA typing and expression from RNA-seq data using seq2HLA", "khmer/trimlowabund": "Removes low abundance k-mers from FASTA/FASTQ files", "khmer/n...
khmer/normalizebymedian
2
mod_syri_0
tool_selection
In Nextflow DSL2, which module handles: Syri compares alignments between two chromosome-level assemblies and identifies synteny and structural rearrangements. (tools: syri)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "irescue": "Quantification of transposable elements expression in scRNA-seq", "syri": "Syri compares alignments between two chromosome-level assemblies and identifies synt...
syri
1
noul_file_pairing_in_channel_tuples_23
dsl2_rules
Is this statement accurate according to standard Nextflow DSL2 behavior? "In Nextflow DSL2, `tuple val(meta), path('*.vcf.gz'), path('*.tbi')` bundles index files with data files."
{ "type": "noul", "instructions": "Determine whether the Nextflow DSL2 statement or idiom is valid and adheres to standards." }
true
1
mod_vcf2zarr_convert_1
tool_selection
In Nextflow DSL2, which module handles: Convert VCF data to the VCF Zarr specification reliably, in parallel or distributed over a cluster (tools: vcf2zarr)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "bcftools_annotate": "Add or remove annotations.", "vcf2zarr_convert": "Convert VCF data to the VCF Zarr specification reliably, in parallel or distributed over a cluster"...
vcf2zarr_convert
1
mod_metaphlan3_mergemetaphlantables_1
tool_selection
In Nextflow DSL2, which module handles: Merges output abundance tables from MetaPhlAn3 (tools: metaphlan3)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "tidk_plot": null, "deacon_indexunion": null, "metaphlan3_mergemetaphlantables": null, "bracken_bracken": null, "biomformat_convert": null } }
metaphlan3_mergemetaphlantables
2
pipe_all101_scnanoseq_0
pipeline_routing
I need to run an end-to-end bioinformatics workflow to analyze Single-cell/nuclei pipeline for data derived from Oxford Nanopore and 10X Genomics. Topics: 10xgenomics, long-read-sequencing, nanopore, rna-seq, rnaseq, scrna-seq. . Which nf-core pipeline should I execute?
{ "type": "choice", "instructions": "Select the optimal nf-core pipeline for this bioinformatic analysis task.", "criteria": { "scnanoseq": null, "reportho": null, "differentialabundance": null, "proteinfamilies": null, "variantprioritization": null } }
scnanoseq
0
mod_aardvark_merge_1
tool_selection
In Nextflow DSL2, which module handles: A tool to evaluate and merge multiple variant calls into a consensus VCF. (tools: aardvark)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "bcftools_call": "This command replaces the former bcftools view caller.\nSome of the original functionality has been temporarily", "hamronization_rgi": "Tool to convert a...
aardvark_merge
2
mod_samclip_0
tool_selection
In Nextflow DSL2, which module handles: Filters SAM/BAM/CRAM files for soft and hard clipped alignments (tools: samclip)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "rtgtools/rocplot": "Plot ROC curves from vcfeval ROC data files, either to an image, or an interactive GUI. The interactive GUI is", "diann/insilicolibrarygeneration": "G...
samclip
4
mod_snakemake_1
tool_selection
In Nextflow DSL2, which module handles: The Snakemake workflow management system is a tool to create reproducible and scalable data analyses. This module runs a simple Snakemake pipeline based on input snakefile. Expect many limitations." (tools: snakemake)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "semibin_singleeasybin": null, "cpc2": null, "abritamr_run": null, "snakemake": null, "bedtools_coverage": null } }
snakemake
3
mod_pairix_1
tool_selection
In Nextflow DSL2, which module handles: a tool for indexing and querying on a block-compressed text file containing pairs of genomic coordinates (tools: pairix)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "autocycler_combine": null, "bbmap_index": null, "cnvkit_reference": null, "biscuit_index": null, "pairix": null } }
pairix
4
mod_nanofilt_0
tool_selection
In Nextflow DSL2, which module handles: Filtering and trimming of Oxford Nanopore Sequencing data (tools: nanofilt)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "nanofilt": "Filtering and trimming of Oxford Nanopore Sequencing data", "gem2/gemmappability": "Define the mappability of a reference", "mcroni": "Analysis of mcr-1 g...
nanofilt
0
mod_bam2fastx_bam2fastq_1
tool_selection
In Nextflow DSL2, which module handles: Conversion of PacBio BAM files into gzipped fastq files, including splitting of barcoded data (tools: bam2fastx)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "hifiasm": "Whole-genome assembly using PacBio HiFi reads", "gcta_calculateldscores": "Calculate LD scores with GCTA and derive GREML-LDMS SNP groups", "mmseqs_createt...
bam2fastx_bam2fastq
4
mod_links_1
tool_selection
In Nextflow DSL2, which module handles: LINKS is a genomics application for scaffolding genome assemblies with long reads, such as those produced by Oxford Nanopore Technologies Ltd. It can be used to scaffold high-quality draft genome assemblies with any long sequences (eg. ONT reads, PacBio reads, other draft genomes...
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "bbmap_index": "Creates an index from a fasta file, ready to be used by bbmap.sh in mapping mode.", "svtk_rdtest2vcf": "Convert an RdTest-formatted bed to the standard VCF...
links
4
mod_coptr_index_0
tool_selection
In Nextflow DSL2, which module handles: Indexes a directory of fasta files for use with CoPTR (tools: coptr)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "coptr/extract": "Computes the coverage map along the reference genome", "coptr/estimate": "Calculates peak-to-through ratio (PTR) from metagenomic sequence data", "co...
coptr/index
2
noul_deprecated_file_output_syntax_23
dsl2_rules
Is this statement accurate according to standard Nextflow DSL2 behavior? "Declaring `output: file('*.bam')` is the modern DSL2 syntax rather than `path('*.bam')`."
{ "type": "noul", "instructions": "Determine whether the Nextflow DSL2 statement or idiom is valid and adheres to standards." }
false
0
mod_shinyngs_staticdifferential_1
tool_selection
In Nextflow DSL2, which module handles: Make plots for interpretation of differential abundance statistics (tools: shinyngs)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "shinyngs_staticdifferential": "Make plots for interpretation of differential abundance statistics", "dotseq_dotseq": "Detect differential ORF usage (DOU) and ORF-level di...
shinyngs_staticdifferential
0
pipe_all101_clipseq_4
pipeline_routing
Which pipeline implements best-practice processing for: CLIP sequencing analysis pipeline for QC, pre-mapping, genome mapping, UMI deduplication, and multiple peak-calling options.. Topics: clip, clip-seq, peak-calling, rna-rbp-interactions. ?
{ "type": "choice", "instructions": "Select the optimal nf-core pipeline for this bioinformatic analysis task.", "criteria": { "nascent": "Nascent Transcription Processing Pipeline [gro-seq, nascent, pro-seq]", "proteinannotator": "Generation of sequence-level annotations for amino acid sequences [annotat...
clipseq
4
mod_mitohifi_mitohifi_0
tool_selection
In Nextflow DSL2, which module handles: A python workflow that assembles mitogenomes from Pacbio HiFi reads (tools: mitohifi.py)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "mitohifi/mitohifi": null, "oatk": null, "hipstr": null, "bam2fastx/bam2fastq": null, "riker/multi": null } }
mitohifi/mitohifi
0
mod_whatshap_phase_1
tool_selection
In Nextflow DSL2, which module handles: Phase variants in a VCF file using long-read sequencing data (tools: whatshap)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "faa_seqfu_seqkit": "Subworkflow that optionally preprocesses amino acid FASTA sequences\n(seqkit seq/replace/rmdup), computes seque", "hiphase": "Small and structural var...
whatshap_phase
2
mod_rrnatranscripts_0
tool_selection
In Nextflow DSL2, which module handles: Ribosomal RNA extraction from a GTF file. (tools: rrnatranscripts)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "abra2": "Assembly Based ReAligner for next-generation sequencing data", "motus/downloaddb": "Download the mOTUs database", "sylph/profile": "Sylph profile command for...
rrnatranscripts
4
noul_retry_errorstrategy_14
dsl2_rules
Is this statement accurate according to standard Nextflow DSL2 behavior? "The `errorStrategy = 'retry'` directive allows Nextflow to re-execute a failed task up to `maxRetries` times."
{ "type": "noul", "instructions": "Determine whether the Nextflow DSL2 statement or idiom is valid and adheres to standards.", "criteria": { "false": "The statement describes an invalid Nextflow DSL2 syntax, anti-pattern, or deprecated behavior.", "true": "The statement describes a valid, standard, and re...
true
1
mod_tidk_explore_0
tool_selection
In Nextflow DSL2, which module handles: `tidk explore` attempts to find the simple telomeric repeat unit in the genome provided. It will report this repeat in its canonical form (e.g. TTAGG -> AACCT). (tools: tidk)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "tcoffee/align": null, "vcf_filter_bcftools_ensemblvep": null, "tidk/explore": null, "agat/spfilterbyorfsize": null, "alignoth": null } }
tidk/explore
2
noul_subworkflow_structural_blocks_22
dsl2_rules
Is this statement accurate according to standard Nextflow DSL2 behavior? "Workflows in Nextflow DSL2 define inputs with `take:`, core execution with `main:`, and outputs with `emit:`."
{ "type": "noul", "instructions": "Determine whether the Nextflow DSL2 statement or idiom is valid and adheres to standards.", "criteria": { "false": "The statement describes an invalid Nextflow DSL2 syntax, anti-pattern, or deprecated behavior.", "true": "The statement describes a valid, standard, and re...
true
1
mod_msisensor2_msi_0
tool_selection
In Nextflow DSL2, which module handles: msisensor2 detection of MSI regions. (tools: msisensor2)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "tmb/pytmb": "This module calculates Tumor Mutational Burden (TMB) scores from VCF files using the pyTMB tool.", "ichorcna/run": "ichorCNA is an R package for calculating ...
msisensor2/msi
4
mod_snapaligner_index_1
tool_selection
In Nextflow DSL2, which module handles: Create a SNAP index for reference genome (tools: snapaligner)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "biscuit_index": "Indexes a reference genome for use with Biscuit", "pangolin_run": "Phylogenetic Assignment of Named Global Outbreak LINeages", "bam_variant_demix_boo...
snapaligner_index
3
mod_cellranger_mkref_1
tool_selection
In Nextflow DSL2, which module handles: Module to build the reference needed by the 10x Genomics Cell Ranger tool. Uses the cellranger mkref command. (tools: cellranger)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "canvas_germline": "Calls germline copy number variants (CNVs) from whole genome sequencing data using\nIllumina Canvas in SmallPed", "myloasm": "Myloasm is a de novo meta...
cellranger_mkref
4
mod_fasta_newick_epang_gappa_1
tool_selection
In Nextflow DSL2, which module handles: Run phylogenetic placement with a number of query sequences plus a reference alignment and phylogeny. Used in nf-core/phyloplace. (tools: fasta_newick_epang_gappa)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "fasta_newick_epang_gappa": "Run phylogenetic placement with a number of query sequences plus a reference alignment and phylogeny. Used in ", "suppa_diffsplice": "Perform ...
fasta_newick_epang_gappa
0
pipe_all101_longraredisease_0
pipeline_routing
I need to run an end-to-end bioinformatics workflow to analyze Long read sequencing pipeline to identify variants in patients with neurodevelopmental disorders. Topics: nanopore, pacbio. . Which nf-core pipeline should I execute?
{ "type": "choice", "instructions": "Select the optimal nf-core pipeline for this bioinformatic analysis task.", "criteria": { "magmap": null, "drop": null, "proteogenomicsdb": null, "genomeqc": null, "variantbenchmarking": null, "diaproteomics": null, "pacvar": null, "longraredise...
longraredisease
7
mod_hifiasm_0
tool_selection
In Nextflow DSL2, which module handles: Whole-genome assembly using PacBio HiFi reads (tools: hifiasm)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "beagle5/beagle": "Beagle v5.5 is a software package for phasing genotypes and for imputing ungenotyped markers.", "purgedups/pbcstat": "Create read depth histogram and ba...
hifiasm
3
mod_arcashla_extract_0
tool_selection
In Nextflow DSL2, which module handles: Extracts reads mapped to chromosome 6 and any HLA decoys or chromosome 6 alternates. (tools: arcashla)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "t1k/build": "A module to create a reference database and coordinate files for T1K.", "t1k/run": "write your description here", "svim/alignment": "Structural variant d...
arcashla/extract
4
mod_crabs_insilicopcr_1
tool_selection
In Nextflow DSL2, which module handles: CRABS extracts the amplicon region of the primer set by conducting an in silico PCR. (tools: crabs)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "parabricks_indexgvcf": "NVIDIA Clara Parabricks GPU-accelerated gvcf indexing tool.", "primerprospector_analyzeprimers": "Score PCR primers for binding to target sequence...
crabs_insilicopcr
3
mod_samtools_bgzip_0
tool_selection
In Nextflow DSL2, which module handles: DEPRECATED. Use HTSLIB/BGZIPTABIX instead. Converts an arbitrary compressed or uncompressed file to BGZIP (tools: samtools)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "samtools/bgzip": "DEPRECATED. Use HTSLIB/BGZIPTABIX instead. Converts an arbitrary compressed or uncompressed file to BGZIP", "grabix/check": "Checks if the input file is...
samtools/bgzip
0
pipe_all101_chipseq_5
pipeline_routing
I need to run an end-to-end bioinformatics workflow to analyze ChIP-seq peak-calling, QC and differential analysis pipeline.. Topics: chip, chip-seq, chromatin-immunoprecipitation, macs2, peak-calling. . Which nf-core pipeline should I execute?
{ "type": "choice", "instructions": "Select the optimal nf-core pipeline for this bioinformatic analysis task.", "criteria": { "chipseq": "ChIP-seq peak-calling, QC and differential analysis pipeline. [chip, chip-seq, chromatin-immunoprecipitation]", "cutandrun": "Analysis pipeline for CUT&RUN and CUT&TAG...
chipseq
0
mod_fargene_0
tool_selection
In Nextflow DSL2, which module handles: tool that takes either fragmented metagenomic data or longer sequences as input and predicts and delivers full-length antiobiotic resistance genes as output. (tools: fargene)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "blast/blastdbcmd": null, "busco/download": null, "fastavalidator": null, "concoct/extractfastabins": null, "fargene": null } }
fargene
4
intent_build_pipeline_6
intent_routing
Classify this user request: "Write a Nextflow DSL2 workflow that takes raw ONT FASTQ files and runs Flye assembly followed by Medaka polishing."
{ "type": "choice", "instructions": "Classify the user intent into one category.", "criteria": { "debug_error": "User is reporting a runtime error, exit code (137, 127), task failure, or pipeline crash", "ask_question": "User is asking for an explanation, conceptual difference, documentation, or Nextflow ...
build_pipeline
3
mod_rpbp_selectfinalpredictionset_1
tool_selection
In Nextflow DSL2, which module handles: Produce the final filtered set of predicted translated ORFs from the per-ORF Bayes factor table. Applies the standard Rp-Bp prediction rules: a minimum Bayes-factor cutoff (favouring translated over untranslated), a minimum ORF length, and overlap resolution so that among overlap...
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "rpbp_estimatemetagenebayesfactors": "Score how strongly each per-read-length metagene profile shows the\n3-nucleotide periodicity expected of active", "rpbp_getperiodicle...
rpbp_selectfinalpredictionset
4
mod_gunc_mergecheckm_1
tool_selection
In Nextflow DSL2, which module handles: Merging of CheckM and GUNC results in one summary table (tools: gunc)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "bwameth_index": null, "checkm_qa": null, "pairtools_dedup": null, "gunc_mergecheckm": null, "checkm2_predict": null } }
gunc_mergecheckm
3
mod_arriba_visualisation_0
tool_selection
In Nextflow DSL2, which module handles: Arriba is a command-line tool for the detection of gene fusions from RNA-Seq data. (tools: arriba)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "bcftools/rohviz": null, "arriba/visualisation": null, "pretextsnapshot": null, "bandage/image": null, "mmseqs/databases": null } }
arriba/visualisation
1
mod_angsd_soapsnpcalibration_1
tool_selection
In Nextflow DSL2, which module handles: Generate ANGSD SOAPsnp genotype likelihood calibration files (counts/quality matrices) from BAM alignments. (tools: angsd)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "angsd_contamination": null, "gatk4_estimatelibrarycomplexity": null, "angsd_realsfs": null, "angsd_soapsnpcalibration": null, "tsebra": null } }
angsd_soapsnpcalibration
3
mod_archive_extract_0
tool_selection
In Nextflow DSL2, which module handles: Extract archive(s) from any format Currently supported format are .gz, .tar.gz, .zip (tools: archive_extract)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "plink2/pmerge": "Merge a second PLINK 2 fileset into the first and write a new combined PLINK 2 fileset", "archive_extract": "Extract archive(s) from any format\nCurrentl...
archive_extract
1
noul_exit_code_137_cause_20
dsl2_rules
Is this statement accurate according to standard Nextflow DSL2 behavior? "An exit code of 137 in a containerized Nextflow task is typically caused by a missing shell command."
{ "type": "noul", "instructions": "Determine whether the Nextflow DSL2 statement or idiom is valid and adheres to standards.", "criteria": { "false": "The statement describes an invalid Nextflow DSL2 syntax, anti-pattern, or deprecated behavior.", "true": "The statement describes a valid, standard, and re...
false
0
mod_instrain_profile_0
tool_selection
In Nextflow DSL2, which module handles: inStrain is python program for analysis of co-occurring genome populations from metagenomes that allows highly accurate genome comparisons, analysis of coverage, microdiversity, and linkage, and sensitive SNP detection with gene localization and synonymous non-synonymous identifi...
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "amps": "Post-processing script of the MaltExtract component of the HOPS package", "instrain/profile": "inStrain is python program for analysis of co-occurring genome popu...
instrain/profile
1
pipe_all101_chipseq_0
pipeline_routing
I need to run an end-to-end bioinformatics workflow to analyze ChIP-seq peak-calling, QC and differential analysis pipeline.. Topics: chip, chip-seq, chromatin-immunoprecipitation, macs2, peak-calling. . Which nf-core pipeline should I execute?
{ "type": "choice", "instructions": "Select the optimal nf-core pipeline for this bioinformatic analysis task.", "criteria": { "chipseq": null, "cutandrun": null, "genomeqc": null, "methylseq": null, "demo": null } }
chipseq
0
mod_pridepy_downloadfile_1
tool_selection
In Nextflow DSL2, which module handles: Download a single file from the PRIDE Archive by name using pridepy. (tools: pridepy)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "bigslice_downloaddb": "Downloads and extracts the BiG-SLiCE HMM database (biosynthetic and sub Pfams)\nusing the bundled `download_big", "pridepy_downloadfile": "Download...
pridepy_downloadfile
1
mod_last_mafswap_1
tool_selection
In Nextflow DSL2, which module handles: Reorder alignments in a MAF file (tools: last)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "last_lastdb": "Prepare sequences for subsequent alignment with lastal.", "last_mafswap": "Reorder alignments in a MAF file", "last_mafconvert": "Converts MAF alignmen...
last_mafswap
1
intent_ask_question_2
intent_routing
Classify this user request: "How does the .mix() operator differ from .combine() in Nextflow?"
{ "type": "choice", "instructions": "Classify the user intent into one category.", "criteria": { "debug_error": "User is reporting a runtime error, exit code (137, 127), task failure, or pipeline crash", "prepare_data": "User needs help creating a samplesheet, parsing FASTQ/BAM filenames, or staging refer...
ask_question
2
mod_paraphase_0
tool_selection
In Nextflow DSL2, which module handles: HiFi-based caller for highly homologous genes (tools: paraphase)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "autocycler/cluster": "Cluster replicons in compressed assemblies with Autocycler.", "bedtools/unionbedg": "Combines multiple BedGraph files into a single file", "auto...
paraphase
3
mod_seqsero2_1
tool_selection
In Nextflow DSL2, which module handles: Salmonella serotype prediction from reads and assemblies (tools: seqsero2)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "entrezdirect_xtract": "Queries an NCBI database using an UID", "agrvate": "Rapid identification of Staphylococcus aureus agr locus type and agr operon variants", "ltr...
seqsero2
4
mod_paragraph_vcf2paragraph_1
tool_selection
In Nextflow DSL2, which module handles: Convert a VCF file to a JSON graph (tools: paragraph)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "trgt_genotype": "Tandem repeat genotyping from PacBio HiFi data", "dssp_mkdssp": "Calculates secondary structure assignments from PDB files using mkdssp (DSSP).\nDSSP is ...
paragraph_vcf2paragraph
2
noul_file_pairing_in_channel_tuples_18
dsl2_rules
Is this statement accurate according to standard Nextflow DSL2 behavior? "In Nextflow DSL2, `tuple val(meta), path('*.vcf.gz'), path('*.tbi')` bundles index files with data files."
{ "type": "noul", "instructions": "Determine whether the Nextflow DSL2 statement or idiom is valid and adheres to standards.", "criteria": { "false": "The statement describes an invalid Nextflow DSL2 syntax, anti-pattern, or deprecated behavior.", "true": "The statement describes a valid, standard, and re...
true
1
mod_bcftools_stats_1
tool_selection
In Nextflow DSL2, which module handles: Generates stats from VCF files (tools: stats)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "viennarna_rnacofold": null, "igv_js": null, "atlas_call": null, "bcftools_consensus": null, "bcftools_stats": null } }
bcftools_stats
4
mod_pureclip_1
tool_selection
In Nextflow DSL2, which module handles: PureCLIP is a tool to detect protein-RNA interaction footprints from single-nucleotide CLIP-seq data, such as iCLIP and eCLIP. (tools: pureclip)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "icountmini_peaks": "Runs iCount peaks on a BED file of crosslinks", "pureclip": "PureCLIP is a tool to detect protein-RNA interaction footprints from single-nucleotide CL...
pureclip
1
core_tool_picard_markduplicates_described_1
tool_selection
Which bioinformatics tool or module is best suited for this task? Identify and flag PCR and optical duplicate reads in coordinate-sorted BAM files based on 5-prime mapping coordinates.
{ "type": "choice", "instructions": "Select the appropriate bioinformatics tool or module for the specified task.", "criteria": { "picard_markduplicates": "Identifies duplicate reads in BAM files", "samtools": "SAM/BAM utilities", "gatk_markduplicates": "GATK duplicate marking", "sambamba": "Fast ...
picard_markduplicates
0
mod_stringtie_merge_0
tool_selection
In Nextflow DSL2, which module handles: Merges the annotation gtf file and the stringtie output gtf files (tools: stringtie2)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "mapdamage2": "Computational framework for tracking and quantifying DNA damage patterns among ancient DNA sequencing reads ge", "bamtools/stats": "BamTools provides both a...
stringtie/merge
4
core_tool_gatk_haplotypecaller_described_0
tool_selection
Which bioinformatics tool or module is best suited for this task? Germline SNP and Indel variant calling via local de novo haplotype assembly across active genomic regions.
{ "type": "choice", "instructions": "Select the appropriate bioinformatics tool or module for the specified task.", "criteria": { "gatk_haplotypecaller": "Call germline SNPs and indels via local de-novo assembly of haplotypes", "freebayes": "Bayesian genetic variant detector", "mutect2": "Somatic vari...
gatk_haplotypecaller
0
mod_rmats_prep_0
tool_selection
In Nextflow DSL2, which module handles: MATS is a computational tool to detect differential alternative splicing events from RNA-Seq data. (tools: rmats)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "regtools/junctionsextract": null, "rmats/prep": null, "nanomonsv/get": null, "ctatsplicing/prepgenomelib": null, "gatk4/printsvevidence": null } }
rmats/prep
1
mod_bam_variant_calling_sort_freebayes_bcftools_0
tool_selection
In Nextflow DSL2, which module handles: Call variants using freebayes, then sort and index (tools: bam_variant_calling_sort_freebayes_bcftools)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "mmseqs/createtsv": "Create a tsv file from a query and a target database as well as the result database", "bam_variant_calling_sort_freebayes_bcftools": "Call variants us...
bam_variant_calling_sort_freebayes_bcftools
1
noul_channel_operator_map_4
dsl2_rules
Is this statement accurate according to standard Nextflow DSL2 behavior? "The `.map { meta, reads -> [ meta, reads ] }` channel operator transforms channel emissions synchronously."
{ "type": "noul", "instructions": "Determine whether the Nextflow DSL2 statement or idiom is valid and adheres to standards.", "criteria": { "false": "The statement describes an invalid Nextflow DSL2 syntax, anti-pattern, or deprecated behavior.", "true": "The statement describes a valid, standard, and re...
true
1
pipe_all101_methylseq_4
pipeline_routing
Which pipeline implements best-practice processing for: Methylation (Bisulfite-Sequencing) analysis pipeline using Bismark/bwa-meth + MethylDackel or bwa-mem + rastair. Topics: bisulfite-sequencing, dna-methylation, em-seq, epigenome, epigenomics, methyl-seq. ?
{ "type": "choice", "instructions": "Select the optimal nf-core pipeline for this bioinformatic analysis task.", "criteria": { "genomeassembler": "Assembly and scaffolding of haploid / unphased genomes from long ONT or PacBio HiFi reads [genome-assembly]", "methylseq": "Methylation (Bisulfite-Sequencing) ...
methylseq
1
mod_agat_convertgff2bed_1
tool_selection
In Nextflow DSL2, which module handles: Takes a GFF3 file and converts to a bed12 file (tools: agat)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "agat_convertbed2gff": "Takes a bed12 file and converts to a GFF3 file", "agat_convertspgxf2gxf": "Fixes and standardizes GFF/GTF files and outputs a cleaned GFF/GTF file"...
agat_convertgff2bed
2
mod_isoseq3_tag_1
tool_selection
In Nextflow DSL2, which module handles: Extract UMI and cell barcodes (tools: isoseq3)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "gstama_merge": "Merge multiple transcriptomes while maintaining source information.", "purecn_normaldb": "Build a normal database for coverage normalization from all the ...
isoseq3_tag
4
mod_deepvariant_1
tool_selection
In Nextflow DSL2, which module handles: (DEPRECATED - see main.nf) DeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data (tools: deepvariant)?
{ "type": "choice", "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.", "criteria": { "atlas_call": "generate VCF file from a BAM file using various calling methods", "bcftools_call": "This command replaces the former bcftools view caller.\nSome of the orig...
deepvariant
4
End of preview. Expand in Data Studio

nf-core & Nextflow Laya Decision Engine (laya-nfcore-v1)

A standardized decision-layer dataset and fine-tuned model for Laya (System-1 Decision Engines) across Nextflow DSL2 and the complete nf-core bioinformatics ecosystem (2,153 modules, 101 pipelines).

πŸ† Test Set Performance (691 Held-Out Records)

Evaluating laya-nfcore-v1 on the independent held-out test split (data/test.jsonl):

Evaluation Category Test Set Score Accuracy Description
DSL2 Syntax & Rules (noul) 165 / 165 100.0% Full resolution of Nextflow idioms, channel emits, and anti-patterns
Tool & Module Selection 421 / 447 94.18% Disambiguating bioinformatics tools across 2,153 modules
User Intent Routing 27 / 29 93.10% Routing queries to code gen, debugging, config, or indexing
nf-core Pipeline Routing 45 / 50 90.00% Matching assay requirements to official nf-core workflows
OVERALL ACCURACY 658 / 691 95.22% Inference Latency: ~45–65 ms on Apple Silicon

πŸ“Š Dataset Summary

  • Total Decision Records: 6,911
  • Domain Coverage:
    • Tool & Module Selection (4,306 records): Spans all 2,153 nf-core modules and subworkflows with mined hard-negative distractors (aligners, variant callers, QC, trimming, single-cell, assembly, etc.).
    • Pipeline Routing (505 records): Covers all 101 official nf-core pipelines across diverse assay queries (RNA-seq, Sarek variant calling, Ampliseq, ATAC-seq, Viralrecon, etc.).
    • DSL2 Syntax & Rules Check (1,800 records): Balanced binary noul decisions evaluating idiomatic DSL2 patterns (tuple val(meta), path(reads), publishDir, take/main/emit) versus common anti-patterns.
    • Task & Intent Routing (300 records): Intent classification across pipeline execution, error debugging, custom module design, and reference genome preparation.

πŸ—‚οΈ Split Information

Split Records File
Train 5,529 data/train.jsonl
Validation 691 data/validation.jsonl
Test 691 data/test.jsonl

πŸ“ Repository Structure

laya_training/
β”œβ”€β”€ README.md                      # Hugging Face Dataset Card & Documentation
β”œβ”€β”€ requirements.txt               # Dependencies
β”œβ”€β”€ inputs/                        # Raw source corpora
β”‚   β”œβ”€β”€ nfcore_corpus.json         # Complete 2,153 nf-core module corpus
β”‚   └── nfcore_pipeline_catalog.json # Complete 101 nf-core pipeline catalog
β”œβ”€β”€ data/                          # Hugging Face standard dataset format
β”‚   β”œβ”€β”€ train.jsonl                # 5,529 training records
β”‚   β”œβ”€β”€ validation.jsonl           # 691 validation records
β”‚   β”œβ”€β”€ test.jsonl                 # 691 test records
β”‚   β”œβ”€β”€ cached_train_h.pt          # Pinned ModernBERT hidden state cache
β”‚   β”œβ”€β”€ cached_val_h.pt            # Validation hidden state cache
β”‚   └── dataset_dict.json          # Dataset metadata
β”œβ”€β”€ scripts/                       # Training, evaluation & upload pipeline
β”‚   β”œβ”€β”€ 01_build_dataset.py        # Generates JSONL splits from corpora
β”‚   β”œβ”€β”€ 02_train_laya.py           # RAM-cached ModernBERT decision trainer
β”‚   β”œβ”€β”€ 03_evaluate.py             # 100-question Nextflow benchmark runner
β”‚   └── 04_push_to_hub.py          # Hugging Face Hub upload utility
β”œβ”€β”€ checkpoints/                   # Checkpoints ready for HF Hub & Laya Agent
β”‚   └── laya-nfcore-v1/
β”‚       β”œβ”€β”€ model.safetensors      # Tuned weights (1.6 GB)
β”‚       β”œβ”€β”€ rl_agent_config.json   # Laya config
β”‚       β”œβ”€β”€ encoder/               # ModernBERT configuration
β”‚       └── tokenizer/             # Tokenizer vocabulary & configs
└── results/                       # Benchmark reports & training logs
    β”œβ”€β”€ baseline_benchmark_100.json
    β”œβ”€β”€ post_training_benchmark_100.json
    β”œβ”€β”€ test_set_evaluation.json
    └── training_history.json

πŸ“‹ Data Schema

Each row in data/*.jsonl is formatted for direct consumption by Laya agents and Hugging Face datasets:

{
  "id": "mod_angsd_realsfs_1",
  "category": "tool_selection",
  "state": "Which module should be imported to execute angsd for Estimate site frequency spectrum from site allele frequencies?",
  "question": {
    "type": "choice",
    "instructions": "Select the appropriate nf-core module for the specified bioinformatics operation.",
    "criteria": {
      "angsd/dosaf": "Estimate site allele frequencies from BAM files.",
      "angsd/realsfs": "Estimate site frequency spectrum from site allele frequencies",
      "cnvkit/access": "Calculate the sequence-accessible coordinates in chromosomes from the given reference genome",
      "mm2plus/index": "Provides fasta index required by mm2plus alignment."
    }
  },
  "target": "angsd/realsfs",
  "target_idx": 1
}

πŸš€ Quickstart

1. Load via Hugging Face datasets

from datasets import load_dataset

dataset = load_dataset("json", data_files={
    "train": "data/train.jsonl",
    "validation": "data/validation.jsonl",
    "test": "data/test.jsonl"
})
print(dataset)

2. Fine-Tune Laya

python scripts/02_train_laya.py --epochs 8 --batch_size 32 --lr 6e-5 --device mps

3. Evaluate Model

python scripts/03_evaluate.py --model_path checkpoints/laya-nfcore-v1

4. Push to Hugging Face Hub

python scripts/04_push_to_hub.py --dataset-repo <your-username>/nfcore-laya-decisions --model-repo <your-username>/laya-nextflow-nfcore
Downloads last month
-

Models trained or fine-tuned on Primeomicx/nfcore-laya-decisions