Results for “ipfs”

Perform high-performance genomic interval operations and bioinformatics file I/O on Polars DataFrames, including overlap, nearest, merge, coverage, complement, subtract, and reading/writing BED, VCF, BAM, GFF, FASTA, and FASTQ formats with streaming and cloud-native support.

Parse RFP/RFI/RFQ documents, score fit per requirement with verifiable proof points, generate win-themes, estimate winrate, and produce a bid/no-bid recommendation using the Shipley method.

Firm-fixed-price cost buildup mirroring 1102 IGCE FFP wrap-rate math (BLS OEWS + GSA CALC+ + GSA Per Diem). USE WHEN the user asks to "build an FFP IGCE", "wrap rate buildup", "FFP cost estimate", "layer fringe overhead G&A fee", "how should we price this FFP task order", or "IGCE parity for our bid". Pulls labor categories from pursuit vault or defaults, stacks fringe/overhead/G&A/fee, exports JSON + XLSX to Studio. DO NOT USE FOR T&M/LH pricing (`igce-builder-lh-tm`), cost-reimbursement (`igce-builder-cr`), OT milestones (`ot-prototype-strategist`), or obligation intel (`competitive-intel`).

Expert guidance for Ibis, the Python dataframe library that provides a pandas-like API but generates SQL for execution on any backend — DuckDB, PostgreSQL, BigQuery, Snowflake, Spark, and more. Helps developers write analytics code once and run it anywhere without rewriting SQL for each database.

Enables fast similarity search and clustering of dense vectors using FAISS, covering index types, GPU acceleration, and integrations with LangChain and LlamaIndex.

Build network traffic baselines from NetFlow/IPFIX data using Python pandas for statistical analysis, z-score anomaly detection, and hourly/daily traffic pattern profiling.

Process and analyze mass spectrometry data: import spectra from MGF, mzML, MSP, and JSON formats; apply 40+ filters for metadata harmonization and peak cleaning; compute spectral similarities (cosine, modified cosine) for compound identification; build reproducible processing pipelines.

Takes raw whole-genome sequencing FASTQ files or a pre-existing VCF through variant calling, quality control, and polygenic risk score computation using the PGS Catalog.