Tagged bioinformatics

Grow a TikTok account with positioning, content DNA, briefs and post reviews

Grow an X account with positioning, content DNA, briefs and post reviews

Build qualitative Kuaishou content DNA reports and reusable production templates

Build qualitative TikTok content DNA reports and reusable production templates

Build qualitative X content DNA reports and reusable production templates

Extract 17-dimension style DNA reports from WeChat articles and build templates

Extract content DNA reports from WeChat Channels videos and reusable briefs

Extract Xiaohongshu content DNA into reports, briefs and image-set templates

Map growth options on the Ansoff Matrix with risk-rated sequencing

Plan a strategic roadmap through prioritization, epics, alignment and sequencing

Look up AlphaFold structure predictions and protein annotations as short summaries

Query Bgee for healthy wild-type gene expression metadata in compact summaries

Design new protein, peptide and antibody binder candidates for a target with Boltz

Screen and rank existing protein or antibody binders against a target with Boltz

Predict structures and binding for one protein, RNA, DNA or ligand complex

Find CELLxGENE single-cell collections and dataset metadata in short summaries

Search ENCODE objects and metadata for regulatory genomics datasets

Look up Ensembl genes, overlaps, cross-references and variants in short summaries

Query EpiGraphDB for ontology, Mendelian randomization and gene-drug evidence

Fetch Genebass gene burden PheWAS results for one Ensembl gene

Query gnomAD for variant frequencies, gene constraint and variant context

Search HMDB for metabolites, proteins, diseases and pathways in short summaries

Look up Human Protein Atlas gene expression by tissue and cell line

Map GWAS loci to ranked candidate genes with reproducible tables and figures

Search NCBI Gene for human genes with autocomplete-style results

Look up NCBI genome assemblies and taxonomy metadata in concise summaries

Search PubMed, Gene and GEO through NCBI Entrez for concise results

Route sequencing data requests to the right NGS analysis skill

Plan or run ATAC-seq QC, peak calling and differential accessibility analysis

Route bulk RNA-seq requests to FASTQ processing or differential expression

Process bulk RNA-seq FASTQ into count matrices with alignment and MultiQC checks

Run bulk RNA-seq differential expression from count matrices with contrast checks

Plan ChIP-seq and CUT&RUN peak calling with QC, controls and spike-ins

Plan germline WGS, WES and panel variant calling with joint calling and QC

Run tumor-normal and cancer panel somatic variant calling with purity and QC checks

Plan UMI-based targeted DNA panel variant calling with duplex consensus and panel QC

Route WGS, WES and panel variant requests to the right germline or somatic workflow

Plan ATAC-seq, ChIP-seq and CUT&RUN peak calling with QC and differential peaks

Check which sequencing tools and packages are installed before running a pipeline

Generate count matrices from single-cell and single-nucleus RNA-seq FASTQ files

Look up PharmGKB gene-drug annotations, variants and dosing guidelines

Query ProteomeXchange PROXI for datasets, peptides, proteins and spectra

Search QuickGO for Gene Ontology terms, annotations and their hierarchy

Browse RNAcentral RNA entries and cross-references in concise summaries

Quality-control, annotate and cluster single-cell RNA-seq data with UMAP views

Pull STRING protein interaction partners, networks and enrichment results

Look up UniProt protein entries, UniRef clusters and FASTA sequences

Send protein designs to a cloud lab for binding, expression and stability assays

Fetch AlphaFold protein structures and pLDDT and PAE confidence by UniProt ID