Results for “ai-files”
9 skillsGeniml
Train unsupervised machine learning models on genomic interval data from BED files, including region embeddings, single-cell ATAC-seq analysis, and consensus peak building.
30.2k · bundle
Pydicom
Read, write, and modify DICOM medical imaging files, including pixel data extraction, metadata manipulation, anonymization, and format conversion.
30.2k · bundle
Biopython
Manipulate biological sequences, parse FASTA/GenBank/PDB files, access NCBI databases, run BLAST searches, and perform phylogenetics using the Biopython library.
30.2k · bundle
Minimax XLSX
Open, create, read, analyze, edit, or validate Excel/spreadsheet files (.xlsx, .xlsm, .csv, .tsv) using XML-level manipulation for zero format loss.
12.9k · bundle
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Liteparse
Parse PDFs, Office files, and images locally with layout-preserved text, bounding boxes, OCR, and page screenshots for RAG and multimodal agents.
30.2k · bundle
Exploratory Data Analysis
Automatically detect and analyze scientific data files across 200+ formats, generating detailed markdown reports with quality metrics and analysis recommendations.
30.2k · bundle
Flowio
Parse FCS (Flow Cytometry Standard) files v2.0-3.1, extract events as NumPy arrays, read metadata and channels, and convert to CSV or DataFrame for flow cytometry data preprocessing.
30.2k · bundle
Markitdown
Convert files and office documents to Markdown using Microsoft's MarkItDown tool. Supports PDF, DOCX, PPTX, XLSX, images (with OCR), audio (with transcription), HTML, CSV, JSON, XML, ZIP, YouTube URLs, EPubs and more.
30.2k · bundle
Gtars
High-performance toolkit for genomic interval analysis in Rust with Python bindings. Use when working with genomic regions, BED files, coverage tracks, overlap detection, tokenization for ML models, or fragment analysis in computational genomics and machine learning applications.
30.2k · bundle