Results for “pkcs11”

Import object detection models from HuggingFace or NVIDIA NGC into a DeepStream pipeline with automated ONNX download, TensorRT engine build, custom parser, multi-stream benchmark, and PDF report generation.

Diagnoses and operates Kubernetes clusters: pods, deployments, ingress, HPA, PVC, StorageClass, NetworkPolicy, Secrets, Helm, ArgoCD, cert-manager. Reads before changing; mutations require confirmation and diff review.

Generates kernel device-tree overlay fragments to enable or disable individual PCIe controllers and configure lane count and link speed on Jetson Thor/Orin custom carriers.

Validates inputs, generates samplesheets and launch scripts, and optionally executes nf-core/pacsomatic matched tumor-normal workflows from BAM files, supporting local runs and scheduler submission (LSF/Slurm/PBS/SGE).

Deploy and query Arkime for full packet capture network traffic analysis, including session search, PCAP download, beaconing detection, DNS tunneling analysis, and TLS anomaly identification.

>- Analyze KiCad projects and PDF schematics: schematics, PCB layouts, Gerbers, footprints, symbols, netlists, and design rules. Reviews designs for bugs, traces nets, cross-references schematic to PCB, extracts BOM data, checks DRC/ERC, DFM, power trees, and regulator circuits. Every finding carries a confidence label and evidence source with trust_summary rollup. Analyzes PDF schematics from dev boards, reference designs, eval kits, and datasheets. Supports KiCad 5–10. Use whenever the user mentions .kicad_sch, .kicad_pcb, .kicad_pro, PCB design review, schematic analysis, PDF schematics, reference designs, Gerber files, DRC/ERC, netlist issues, BOM extraction, signal tracing, power budget, DFM, or wants to understand, debug, compare, or review any hardware design. Also for "check my board", "review before fab", "what's wrong with my schematic", "is this ready to order", "check my...

Processes STIX 2.1 threat intelligence bundles from TAXII 2.1 servers, normalizing objects into platform-native schemas and routing them to consuming systems.

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.