Primeomicx/laya-nextflow-nfcore
Text Classification β’ 0.4B β’ Updated
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 βtestβ 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 |
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).
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: ~45β65 ms on Apple Silicon |
noul decisions evaluating idiomatic DSL2 patterns (tuple val(meta), path(reads), publishDir, take/main/emit) versus common anti-patterns.| Split | Records | File |
|---|---|---|
| Train | 5,529 | data/train.jsonl |
| Validation | 691 | data/validation.jsonl |
| Test | 691 | data/test.jsonl |
laya_training/
βββ README.md # Hugging Face Dataset Card & Documentation
βββ requirements.txt # Dependencies
βββ inputs/ # Raw source corpora
β βββ nfcore_corpus.json # Complete 2,153 nf-core module corpus
β βββ nfcore_pipeline_catalog.json # Complete 101 nf-core pipeline catalog
βββ data/ # Hugging Face standard dataset format
β βββ train.jsonl # 5,529 training records
β βββ validation.jsonl # 691 validation records
β βββ test.jsonl # 691 test records
β βββ cached_train_h.pt # Pinned ModernBERT hidden state cache
β βββ cached_val_h.pt # Validation hidden state cache
β βββ dataset_dict.json # Dataset metadata
βββ scripts/ # Training, evaluation & upload pipeline
β βββ 01_build_dataset.py # Generates JSONL splits from corpora
β βββ 02_train_laya.py # RAM-cached ModernBERT decision trainer
β βββ 03_evaluate.py # 100-question Nextflow benchmark runner
β βββ 04_push_to_hub.py # Hugging Face Hub upload utility
βββ checkpoints/ # Checkpoints ready for HF Hub & Laya Agent
β βββ laya-nfcore-v1/
β βββ model.safetensors # Tuned weights (1.6 GB)
β βββ rl_agent_config.json # Laya config
β βββ encoder/ # ModernBERT configuration
β βββ tokenizer/ # Tokenizer vocabulary & configs
βββ results/ # Benchmark reports & training logs
βββ baseline_benchmark_100.json
βββ post_training_benchmark_100.json
βββ test_set_evaluation.json
βββ training_history.json
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
}
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)
python scripts/02_train_laya.py --epochs 8 --batch_size 32 --lr 6e-5 --device mps
python scripts/03_evaluate.py --model_path checkpoints/laya-nfcore-v1
python scripts/04_push_to_hub.py --dataset-repo <your-username>/nfcore-laya-decisions --model-repo <your-username>/laya-nextflow-nfcore