Plugins
1 pluginResults for “i-mr”
10 skillsSaas Metrics Coach
Calculates SaaS health metrics like ARR, MRR, churn, LTV, and CAC from raw business numbers, benchmarks them against industry standards, and provides prioritized actionable advice.
20.4k · bundle
Saas Metrics Ia
Expert en métriques SaaS (MRR, ARR, churn, LTV, CAC, cohort analysis, unit economics)
6
Bids
Organize, query, validate, and convert neuroscience and biomedical data using the Brain Imaging Data Structure (BIDS) standard.
30.2k · bundle
Bids
Organize, query, validate, and convert neuroscience datasets following the Brain Imaging Data Structure (BIDS) standard, including metadata sidecars and derivatives.
253 · bundle
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Pydicom
Read, write, and manipulate DICOM medical imaging files, including pixel data extraction, metadata editing, anonymization, format conversion, and compression handling.
3 · bundle
Spc
Provides statistical process control guidance including control chart selection, capability indices, and out-of-control rules for quality management.
567 · bundle
Scvelo
Estimate cell state transitions from unspliced/spliced mRNA dynamics using scVelo, infer trajectory directions, compute latent time, and identify driver genes in single-cell RNA-seq data.
30.2k · bundle
Scvelo
Analyze RNA velocity in single-cell RNA-seq data with scVelo, estimating cell state transitions from unspliced/spliced mRNA dynamics, inferring trajectory directions, computing latent time, and identifying driver genes.
253 · bundle
Imaging Data Commons
Query and download public cancer imaging data from NCI Imaging Data Commons using idc-index. Access large-scale radiology (CT, MR, PET) and pathology datasets for AI training or research. No authentication required. Query by metadata, visualize in browser, check licenses.
30.2k · bundle
Alterlab Cbioportal
Query cBioPortal via its keyless REST API for cancer genomics across TCGA, GENIE, MSK-IMPACT and hundreds of studies — somatic mutations, copy-number alterations (GISTIC), mRNA/protein expression, structural variants, and patient-level clinical/survival data. Use when asked how often a gene is mutated/amplified/deleted in a tumor type, to profile oncogenes or tumor suppressors across cancers (pan-cancer alteration frequency), to pull patient-level mutations joined to OS/clinical outcomes, or to validate a cancer target from cohort genomics. For germline variant pathogenicity use alterlab-clinvar; for mutational-signature (SBS) decomposition use alterlab-cosmic; for CRISPR/RNAi gene-dependency use alterlab-depmap; for aggregated target-disease evidence use alterlab-opentargets. Part of the AlterLab Academic Skills suite.
60 · bundle