Web & Frontend

theneoai Bundle

Frontend Developer

theneoai Bundle

Expert-level UX Designer skill covering user research, information architecture, interaction design, usability testing, design systems, accessibility (WCAG 2.1), and design critique

theneoai Bundle

Expert Educational Technologist specializing in learning management systems, instructional technology integration, online learning design, and EdTech implementation. Expert in LMS administration, SCORM/xAPI standards, accessibility compliance, and digital pedagogy transformation. Use when: edtech, learning-management-system, online-learning, instructional-technology, lms-administration,

theneoai Bundle

Elite Full-Stack Developer skill with mastery of modern frontend frameworks (React, Vue, TypeScript), backend systems (Node.js, Python, Go), databases (PostgreSQL, MongoDB, Redis), and DevOps (Docker, Kubernetes, CI/CD). Transforms AI into a principal engineer capable of building end-to-end applications from database to UI. Use when: full-stack, web-development, react, nodejs,

fridrichmethod Bundle

Orchestrates the end-to-end bulk RNA-seq differential-expression pipeline from FASTQ to an annotated DE gene table, chaining fastp QC/trim, Salmon (decoy-aware) or STAR+featureCounts quantification, tximport gene-level collapse, DESeq2/edgeR/limma-voom testing, apeglm shrinkage, and VST-based visualization. Use when committing the reference release and gene-ID namespace once for the whole run, sequencing steps in the defensible order (tximport before DE, raw counts into the model, VST only for viz/clustering), choosing alignment-free vs align-then-count and the DE engine, setting strandedness correctly, keeping batch in the design instead of correcting-then-testing, or handing the signed ranking statistic to downstream enrichment. Hands mechanism to the component skills; not a re-teach of any single step.

fridrichmethod Bundle

Orchestrates the GWAS pipeline from genotypes to association results, chaining PLINK2 QC (variant-then-sample missingness, controls-only HWE, KING relatedness), panel harmonization + joint phasing/imputation to dosages, long-range-LD-excluded PCA, and an engine chosen by sample structure (PLINK2-GLM / regenie / SAIGE / BOLT-LMM), with LDSC-intercept diagnostics. Use when committing the genome build + ancestry-matched imputation panel once (ancestry match > panel size), running the strand/allele harmonization gate (drop intermediate-frequency palindromes), imputing cases+controls TOGETHER on dosages, excluding long-range-LD regions before PCA, choosing an LMM when relatedness/structure is present (PCs cannot remove a covariance), or separating polygenicity from confounding via the LDSC intercept. Hands mechanism to the population-genetics and phasing-imputation component skills; not a re-teach of any single step.

fridrichmethod Bundle

Creates sashimi-style plots showing RNA-seq read coverage and splice junction counts using ggsashimi (general-purpose, condition-grouped overlays), rmats2sashimiplot (rMATS-output-aware), MAJIQ-VOILA (LSV posteriors interactive HTML), leafviz (leafcutter clusters Shiny), Jutils (tool-agnostic heatmaps and sashimi for rMATS/leafcutter/MntJULiP/MAJIQ output), or pyGenomeTracks (multi-track publication figures). Tool choice depends on the upstream differential-splicing tool's output format and the publication vs interactive use case. Use when visualizing specific splicing events, validating differential splicing calls, or producing publication-quality figures.

fridrichmethod Bundle

Runs all-in-one FASTQ preprocessing with fastp in a single pass - adapter trimming via paired-end overlap analysis, quality/length filtering, 2-color poly-G removal, base correction, optional dedup/UMI/merge, and HTML/JSON reports. Use when preprocessing bulk Illumina data and wanting one fast tool instead of separate Cutadapt, Trimmomatic, and FastQC steps. For precise small-RNA/amplicon adapters use adapter-trimming; for molecule-accurate UMI dedup use umi-processing.

fridrichmethod Bundle

Build enhancer-driven gene regulatory networks (eGRNs) by integrating single-cell RNA-seq and ATAC-seq using SCENIC+, CellOracle base GRNs, Pando, FigR, DIRECT-NET, TRIPOD, and scMEGA. Covers the accessibility-defines-enhancers principle, peak-to-gene linking and its cell-composition confound, the paired-vs-unpaired decision, and TF-region-gene eRegulon triplets. Use when analyzing 10x multiome or paired/unpaired scRNA+scATAC to infer cis-regulatory GRNs. For RNA-only regulons see scenic-regulons; for in silico TF perturbation see perturbation-simulation.

fridrichmethod Bundle

Runs parameterized Jupyter notebooks as reproducible batch report generators with papermill, renders them to HTML/PDF with nbconvert, aggregates results across samples, and makes notebook outputs trustworthy. Use when generating per-sample analysis reports, executing a notebook template across many datasets, or fixing notebooks that do not reproduce.

fridrichmethod Bundle

Analyze TF motif accessibility variability across samples or single cells using chromVAR. Use when identifying TF motifs whose accessibility correlates with conditions, computing per-sample motif z-scores after matched background correction, comparing to ArchR / Signac equivalents, or distinguishing motif-accessibility signal from per-site footprinting.

fridrichmethod Bundle

Analyze single-cell ATAC-seq with Signac/ArchR (R) and SnapATAC2 (Python alternative). Use when processing scATAC fragments, choosing a framework, calling consensus peaks, running TF-IDF/LSI while diagnosing the depth component, scoring chromVAR motif deviations against GC-matched backgrounds, detecting homotypic vs heterotypic doublets, or deciding whether to binarize the count matrix.

fridrichmethod Bundle

Orchestrates the end-to-end bulk ATAC-seq pipeline from FASTQ to differential accessibility and TF footprints, chaining Nextera-aware fastp QC, Bowtie2 alignment, chrM removal, dedup, a single Tn5 +4/-5 shift, MACS3 peak calling, Corces fixed-width consensus, DiffBind/csaw differential accessibility, and TOBIAS footprinting. Use when committing the reference build + blacklist once, recognizing ATAC has NO input control (the shift-extend model IS the background), applying the Tn5 shift exactly once (never combining -f BAMPE with --shift/--extsize), removing chrM before calling, building a fixed-width consensus so per-sample counts are comparable, or choosing MACS3 vs Genrich vs HMMRATAC. Hands mechanism to the atac-seq component skills; not a re-teach of any single step.

fridrichmethod Bundle

Orchestrates the end-to-end ChIP-seq pipeline from FASTQ to blacklist-filtered, annotated peaks, chaining fastp QC, Bowtie2 alignment, pre-dedup library-complexity QC (NRF/PBC), duplicate removal, chrM + ENCODE-blacklist filtering, MACS3 peak calling against a matched input, IDR/consensus reproducibility, deepTools signal tracks, and ChIPseeker annotation. Use when committing the reference build + blacklist version + effective genome size once, pairing each IP with its matched control, computing complexity metrics BEFORE dedup, choosing narrow vs broad and MACS3 vs SEACR/Genrich, keeping per-replicate peaks for IDR, or avoiding depth-normalization that erases a spike-in global shift. Hands mechanism to the chip-seq component skills; not a re-teach of any single step.

fridrichmethod Bundle

Infer cis-regulatory connections (peak-to-peak co-accessibility) from scATAC-seq using Cicero, ArchR getCoAccessibility, or SCENIC+. Use when linking enhancer accessibility to promoter accessibility, identifying enhancer-gene pairs from chromatin alone (without paired RNA), running gene-regulatory inference combining ATAC + RNA, or comparing predicted regulatory contacts against Hi-C/Micro-C ground truth.

theneoai Bundle

Expert mobile repair technician specializing in smartphone and tablet diagnostics, screen replacement, component-level repair, micro-soldering, water damage treatment, and data recovery

fridrichmethod Bundle

Orchestrates the untargeted LC-MS metabolomics pipeline end-to-end (xcms 4.x feature extraction, QC/drift/normalization, confidence-stratified annotation, permutation-validated statistics, background-aware pathway mapping), naming what each stage decides and where it silently fails. Use when running a full LC-MS metabolomics study from raw mzML to enriched pathways and needing the honest handoffs between stages. Each stage defers to its component skill for parameters and traps; for stable-isotope flux (a separate branch, not this untargeted flow) see metabolomics/isotope-tracing.

fridrichmethod Skill

Designing scientific schematics, diagrams, and graphical abstracts. Covers tool selection (BioRender, Inkscape, Affinity, PowerPoint), design principles for pathway diagrams, mechanism schematics, experimental workflows, and journal graphical abstracts. Includes composition, icon sourcing, color for biological entities, and accessibility. Use when creating illustrative (not data-driven) scientific figures.

fridrichmethod Bundle

Orchestrates the cell-free DNA / liquid-biopsy pipeline from plasma sequencing to tumor monitoring, forking tumor-naive (screening) vs tumor-informed (MRD), and chaining pre-analytic QC, UMI/duplex error-suppression (fgbio), fragment QC, ichorCNA tumor fraction (sWGS) or VarDict low-VAF calling (panel), CHIP subtraction against matched WBC, optional fragmentomics/methylation, and longitudinal tracking. Use when treating pre-analytics as the irreversible sensitivity ceiling (tube/time-to-plasma/hemolysis), running error-suppression BEFORE calling (single-strand consensus does not remove deamination; only duplex does), reporting a VAF only with input genome-equivalents (TF ~ 2x VAF only for clonal-het-diploid), subtracting CHIP before reporting somatic, or keeping tube/panel/pipeline identical across a longitudinal MRD series. Hands mechanism to the liquid-biopsy component skills; not a re-teach of any single step.

fridrichmethod Bundle

Gene and region-based rare-variant aggregation - burden/collapsing, SKAT, SKAT-O, ACAT-V/ACAT-O, annotation-weighted STAAR - with regenie (--vc-tests), SAIGE-GENE+, and the SKAT R package. Single-variant tests are powerless at low minor allele count, so rare variants are aggregated across a gene or region under an explicit mask (functional class plus a MAF cutoff). A burden test collapses variants into one score assuming a single effect direction (powerful when true, near-zero power when risk and protective variants cancel); SKAT is a variance-component test robust to mixed directions; SKAT-O blends the two; ACAT/STAAR are dependence-robust and annotation-weighted. The mask is the hypothesis, imbalance needs SPA or Firth, and testing burden is per-gene-per-mask. Use when aggregating rare coding or regulatory variants into gene or region tests, choosing burden vs SKAT vs SKAT-O, or building masks. For single-variant GWAS see association-testing; for mask annotations see variant-calling/variant-annotation.

fridrichmethod Skill

Guide for choosing and creating scientific visualizations for publications and talks. Covers chart-type selection by data structure, color theory for accessibility/print, figure composition, journal formatting (Nature, Cell, ACS), and common pitfalls. Consult when visualizing data or preparing submission figures.

fridrichmethod Bundle

Identify differentially accessible chromatin regions across conditions using DiffBind, csaw, DESeq2, or edgeR. Use when comparing ATAC-seq accessibility between treatment groups, choosing between consensus-peak vs sliding-window approaches, picking the correct normalization (full library vs reads-in-peaks), correcting batch with SVA/RUVseq, or interpreting log2FC and FDR thresholds in a chromatin context.

fridrichmethod Bundle

Orchestrates genome annotation from assembled contigs to functional annotation, forking prokaryotic (Bakta one-step, genetic-code table from GTDB-Tk) vs eukaryotic (RepeatMask -> BRAKER3 -> functional -> ncRNA), then eggNOG/InterProScan functional assignment and Infernal/tRNAscan ncRNA. Use when committing the pro-vs-eukaryotic path and the genetic-code table from taxonomy (never guessing), annotating ONLY a decontaminated QC-passed assembly (CheckM2 before prokaryotic annotation is non-negotiable), committing the evidence set (RNA-seq + protein drives BRAKER3 training), soft-masking with a curated repeat library before gene prediction, or pinning the tool + DB version for any pangenome comparison. Hands mechanism to the genome-annotation component skills; not a re-teach of any single step.

fridrichmethod Bundle

Orchestrates genome-scale metabolic modeling from a protein FASTA to flux predictions, chaining CarveMe/gapseq reconstruction, memote QC, gap-filling, media-constrained FBA/FVA, gene essentiality, and context-specific models. Use when committing the reconstruction tool (which locks the identifier NAMESPACE forever - BiGG vs ModelSEED vs KEGG, no automatic translation), setting the medium BEFORE FBA (the exchange bounds ARE the medium; essentiality and gap-fill are computed relative to it), curating iteratively (stoichiometric-consistency first, then mass/charge, then directionality, then GPR) with energy-generating-cycle removal, and reading a MEMOTE score as well-formedness NOT correctness. Hands mechanism to the systems-biology component skills; not a re-teach of any single step.

fridrichmethod Bundle

Analyze transcription factor motif accessibility variability using chromVAR. Use when identifying which TF motifs show variable accessibility across samples or conditions in ATAC-seq data.

fridrichmethod Bundle

Detect allele-specific chromatin accessibility from ATAC-seq using WASP, GATK ASEReadCounter, or RASQUAL. Use when mapping cis-regulatory genetic variants from heterozygous SNPs, separating cis from trans regulation, building chromatin QTL (caQTL) maps, validating GWAS variant function with allelic imbalance, or detecting reference allele mapping bias before downstream analysis.

fridrichmethod Bundle

Process and analyze single-cell ATAC-seq data with Signac, ArchR, SnapATAC2, or Cell Ranger ATAC. Use when handling 10X scATAC or 10X Multiome (paired RNA+ATAC) data, performing per-cell QC, choosing between ArchR/Signac/SnapATAC2 ecosystems, building per-cluster consensus peaksets, integrating with paired scRNA-seq, doublet detection (AMULET vs ArchR vs scDblFinder), or running pseudobulk differential accessibility per cluster.

fridrichmethod Bundle

Orchestrates the end-to-end spatial transcriptomics pipeline from Space Ranger / vendor output to spatial domains and statistics, branching FIRST on platform class (imaging in-situ Xenium/MERFISH/CosMx vs sequencing/capture Visium/Visium HD/Slide-seq). Use when deciding segmentation-vs-deconvolution and the QC floors from the platform class, committing the coordinate/image-registration frame and panel identity, deconvolving multi-cell spots against an annotated scRNA reference (never relabeling spot clusters as cell types), building the spatial neighbor graph on PHYSICAL not expression space, gating spatially-variable genes on FDR, or using a real domain method (BANKSY/BayesSpace/STAGATE) rather than clustering the spatial graph alone. Hands off deconvolution and cell-cell communication to the component skills; not a re-teach of any single step.

fridrichmethod Bundle

Build a differential-ready consensus peakset from per-replicate ATAC-seq peaks using iterative overlap removal, fixed-width re-centering, and majority-rule overlap. Use when generating a stable peak coordinate system for downstream differential accessibility, ML feature engineering, cross-sample comparison, or fixed-width peak counts; covers Corces 2018 iterative overlap (501 bp), DiffBind summit re-centering, and ENCODE consistency rules.

fridrichmethod Bundle

Orchestrates the end-to-end germline short-variant pipeline from FASTQ to a filtered, normalized, benchmarked VCF, chaining QC/trim, BWA-MEM2 alignment, duplicate marking, optional BQSR, calling (bcftools/GATK HaplotypeCaller/DeepVariant/DRAGEN), normalization, site+genotype filtering, annotation, and hap.py/vcfeval benchmarking. Use when deciding the pipeline-wide reference-genome commitment (GRCh38 analysis set vs T2T, ALT/decoy handling), sequencing the steps in the defensible order (normalize BEFORE annotate, filter site- then genotype-level), choosing the calling engine and single-sample vs cohort joint-calling, picking a filtering strategy by cohort size, or benchmarking stratified within GIAB confident regions. Hands off mechanism to the variant-calling and read-alignment component skills; not a re-teach of any single step.

fridrichmethod Bundle

Designs novel molecules using REINVENT 4 (de novo, scaffold decoration, linker design, R-group, molecular optimization), MolMIM, Diffusion-based generators (DiGress, DiffSMol), and JT-VAE with explicit handling of multi-parameter optimization (MPO), goal-directed scoring functions, transfer/reinforcement/curriculum learning, synthetic accessibility scoring, and chemical space exploration vs exploitation. Use when designing new chemical matter against a target, decorating a scaffold, linking fragments, or optimizing a hit for multiple ADMET / activity properties simultaneously.

fridrichmethod Bundle

Calls significant loops from protein-directed and targeted 3C assays (HiChIP, PLAC-seq, Capture Hi-C/PCHi-C, ChIA-PET) where the contact background is peak-anchored and coverage-biased, so generic Hi-C loop callers (cooltools dots, Juicer HiCCUPS) use the wrong null. Covers FitHiChIP (config-driven coverage+distance-decay spline regression, peak-to-peak vs peak-to-all foreground, loose vs stringent background, coverage vs ICE bias), MAPS (positive Poisson regression on bias factors for PLAC-seq/HiChIP), hichipper (restriction-site-distance bias model + library QC), CHiCAGO (Delaporte two-component Brownian+technical background for asymmetric bait x other-end Capture Hi-C), the with/without separate-ChIP anchor decision, and differential loops via diffloop. Use when calling loops from HiChIP/PLAC-seq/Capture Hi-C, choosing FitHiChIP/MAPS/CHiCAGO, picking peak-to-all vs peak-to-peak, setting the loop FDR, supplying ChIP peaks as anchors, QCing a HiChIP library, or comparing loops between conditions.

fridrichmethod Bundle

Orchestrates the end-to-end 10x Multiome (paired scRNA + scATAC) pipeline from Cell Ranger ARC output to a jointly-embedded, annotated object, chaining per-modality QC, AMULET fragment-based ATAC doublet detection, per-modality normalization (RNA SCT/PCA; ATAC TF-IDF/LSI), WNN (or MultiVI) integration, joint clustering, RNA-based annotation, and LinkPeaks peak-to-gene linking. Use when enforcing the shared cell-barcode intersection between modalities (cellranger-ARC not -atac), keeping per-modality QC/doublets before the joint embedding, dropping the depth-correlated LSI component, annotating identity from RNA (ATAC is regulatory state), treating peak-to-gene links as correlational hypotheses, or aggregating to pseudobulk for cross-condition DE. Hands mechanism to the single-cell and atac-seq component skills; not a re-teach of any single step.

fridrichmethod Bundle

Orchestrates genomic-epidemiology outbreak investigation from pathogen isolates to transmission networks, forking bacterial (snippy -> Gubbins recombination-masking -> IQ-TREE -> TreeTime -> TransPhylo) vs viral (Nextstrain/augur), with parallel MLST typing (cgMLST delegated to epidemiological-genomics/pathogen-typing) and AMR surveillance. Use when committing ONE reference genome for SNP calling (every isolate and distance inherits its coordinates), applying MANDATORY Gubbins recombination-masking on core.full.aln before the tree for recombining bacteria (skipping it inflates the clock 2-5x), gating time-scaling on a temporal-signal test (TempEst R2 >= 0.3), using a pathogen- AND population-specific cluster threshold rather than a universal SNP cutoff, or pinning pangolin-data/Nextclade/Freyja versions for the viral route. Hands mechanism to the epidemiological-genomics component skills; not a re-teach of any single step.

fridrichmethod Bundle

Creates reproducible R Markdown analysis reports (HTML, PDF, Word) with knitr, covering the render pipeline, the interactive-vs-knit session trap, cache invalidation, bookdown cross-references, parameterization, and environment pinning. Use when generating an R-based analysis report, debugging a report that knits differently than it runs interactively, or fixing caching or cross-references.

fridrichmethod Bundle

Orchestrates the end-to-end single-cell RNA-seq pipeline from 10x Cell Ranger output to annotated cell types, chaining ambient-RNA removal, doublet detection, MAD-adaptive QC, normalization, integration, clustering, marker annotation, and (separately) pseudobulk DE + differential abundance. Use when honoring the made-once counting commitments (reference build/Ensembl vintage, --include-introns, cell-calling, feature namespace), ordering correct-then-detect-then-normalize (ambient before doublet before normalize), running per-sample QC before merge, integrating-then-clustering (never testing on integrated values), aggregating to pseudobulk for condition DE instead of cells-as-replicates, or pairing DE with differential abundance. Hands mechanism to the single-cell component skills; not a re-teach of any single step.