「clinical」の検索結果

Retrieves ClinGen gene-disease validity assertions for a public gene or disease, and reviews source-linked public evidence and literature for one supported GRCh38 germline nuclear SNV or simple indel through Folklore Clinical Variant Interpretation MCP. Used when a scientific agent must branch deterministically on resolved, ambiguous, not-found, invalid, unsupported, or unavailable variant outcomes; chain a resolved public variant into related literature or publication details; or preserve evidence provenance without accepting patient, phenotype, family, segregation, or private case data.

日本語の概要は準備中です。原文の説明を表示しています。

Looks up precomputed AlphaGenome Atlas effects for any GRCh38 single-nucleotide variant (AVI score with Phred and 18 SHAP feature attributions, plus raw and quantile scores for RNA-seq, DNase, ATAC, ChIP-TF, ChIP-histone, CAGE, PRO-cap, splicing, polyadenylation and contact-map tracks), scores variants or scans windows on demand with the AlphaGenome model for human and mouse (variant scoring, in silico mutagenesis, REF-versus-ALT track prediction), and builds Atlas website deep links. Use when the user mentions AlphaGenome, AlphaGenome Atlas, AVI or AlphaGenome Variant Impact, DeepMind variant effect prediction, or wants to prioritise or mechanistically interpret non-coding, regulatory, splicing, enhancer, promoter, or chromatin-accessibility effects of SNVs from a VCF, credible set, or region. Research use only; not a clinical tool.

日本語の概要は準備中です。原文の説明を表示しています。

Vocational / technical training courses. Plans the course as a hands-on work task with an operation flow, tool and equipment state, safety boundaries and GO/STOP judgements, instead of a concept lecture. Use when the requirement names a real occupational task, a piece of equipment, a clinical or industrial procedure, or a certification skill.

日本語の概要は準備中です。原文の説明を表示しています。

结构化医学学习产物的统一格式校验。四条硬格式与 validate_output.py 单次标准输入流程。指南章节、路径图、诊断、备考、医保、更新和每日单元使用；普通医学问答走 clinical-q-and-a 的轻量自检，通用任务不套用。

日本語の概要は準備中です。原文の説明を表示しています。

Route retrieval of Chinese medical guidelines, consensus statements, regulatory documents, drug information, safety notices, standards, and public-health materials through authoritative originals and verified fallback copies. Use when a canonical medical source is blocked, slow, unavailable, moved, paywalled, or difficult to parse, or when designing and auditing domestic medical-source fallback rules. Do not treat secondary summaries or reposts as independent clinical evidence.

日本語の概要は準備中です。原文の説明を表示しています。

快速回答普通教育性医学问题与常见误区。默认用一份国内现行权威指南/共识完成轻量核验并立即作答；不用于个体诊疗、处方剂量、精确推荐定位、药品高风险事实、医保监管或跨版本比较。

日本語の概要は準備中です。原文の説明を表示しています。

Transform unstructured clinical encounters into comprehensive SOAP notes with ICD codes and care plans

日本語の概要は準備中です。原文の説明を表示しています。

Submit compact PharmGKB API requests for genes, variants, clinical annotations, dosing guidelines, and search. Use when a user wants concise PharmGKB summaries

日本語の概要は準備中です。原文の説明を表示しています。

Submit compact cBioPortal API requests for studies, molecular profiles, mutations, clinical data, and samples. Use when a user wants concise cBioPortal summaries

日本語の概要は準備中です。原文の説明を表示しています。

Submit compact ClinVar Clinical Tables and NCBI Variation requests for search, VCV, RCV, SCV, and RefSNP lookups. Use when a user wants variant-level summaries or identifier mapping

日本語の概要は準備中です。原文の説明を表示しています。

Generate a therapeutic indication dossier. Covers the patient population, epidemiology, disease biology, standard of care, regulatory precedent, and landmark clinical trials.

日本語の概要は準備中です。原文の説明を表示しています。

Complete survival analysis library in Python. Handles right-censored data, Kaplan-Meier curves, and Cox regression. Standard for clinical trial analysis and epidemiology.

日本語の概要は準備中です。原文の説明を表示しています。

Unified biological database evidence owner. Use for gene annotation, variant clinical significance, cancer mutation evidence, GWAS trait associations, pathway mapping, target-disease evidence, protein structures, protein interaction networks, reference single-cell census queries, and cross-database biological ID mapping. Do not use for full single-cell analysis, bulk RNA-seq differential expression, BAM/VCF processing, protein embedding models, metabolic flux modeling, genomic interval ML, or flow-cytometry file parsing.

日本語の概要は準備中です。原文の説明を表示しています。

Used for finetuning the NV-Generate-CTMR MAISI VAE from CT/MRI NIfTI datalists. Not for clinical or production data approval.

日本語の概要は準備中です。原文の説明を表示しています。

Used for finetuning NV-Generate-CTMR MR-Brain v1 for T1, T2, FLAIR, SWI, or MRA data from a NIfTI datalist. Not for clinical or production data approval.

日本語の概要は準備中です。原文の説明を表示しています。

Run NV-Reason-CT inference on user-provided 3D NIfTI chest or abdominal CT volumes for engineering and research workflows. Not for diagnosis, treatment, or clinical reporting.

日本語の概要は準備中です。原文の説明を表示しています。

Used for command-shape or live NV-Reason-CXR chest X-ray reasoning smoke tests. Not for diagnosis or clinical reporting.

日本語の概要は準備中です。原文の説明を表示しています。

Runs standard or fixed-channel softmax finetuning of NV-Segment-CT VISTA3D on CT NIfTI image/label datasets, with optional MONAI-native MLflow tracking and checkpoint evidence. Uses softmax for predefined, mutually exclusive classes; keeps the standard workflow when point prompts or runtime-variable classes are needed. Not for clinical validation.

日本語の概要は準備中です。原文の説明を表示しています。

Used for running NV-Segment-CTMR on CT or MRI NIfTI volumes and recording label-map evidence. Not for clinical interpretation.

日本語の概要は準備中です。原文の説明を表示しています。

Exports sanitized metadata, parameters, reproducibility details, quality metrics, and optional review artifacts from Medical AI inference runs or evidence packs to MLflow. Use after inference, including NV-Generate runs; not for live training tracking, model registration, or clinical use.

日本語の概要は準備中です。原文の説明を表示しています。

Used for converting one CT DICOM series folder to a HU NIfTI volume with affine evidence. Not for multi-frame DICOM or clinical use.

日本語の概要は準備中です。原文の説明を表示しています。

Used for header-only preflight of one DICOM series folder before conversion or inference. Not for de-identification or clinical clearance.

日本語の概要は準備中です。原文の説明を表示しています。

Used for extracting selected metadata from one DICOM file and flagging standard-tag PHI presence. Not for anonymization or clinical use.

日本語の概要は準備中です。原文の説明を表示しています。

Use when you want to look up, map, and search for short genetic variants (SNPs, indels) in NCBI's dbSNP database. Resolves between rsIDs, genomic coordinates in VCF format, and HGVS strings. For an rsID, returns variant type, gene associations, clinical significance, allele frequencies, and genomic coordinates (GRCh38).

日本語の概要は準備中です。原文の説明を表示しています。