「census」の検索結果

Access COSMIC cancer mutation database. Query somatic mutations, Cancer Gene Census, mutational signatures, gene fusions, for cancer research and precision oncology. Requires authentication.

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。

Query COSMIC for cancer somatic mutations, gene census, mutational signatures, drug resistance variants. REST API v3.1 supports gene/sample/variant queries; free registration. For germline use clinvar-database; for drug-target data use opentargets-database or chembl-database-bioactivity.

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。

NCBI GEO access via GEOparse and E-utilities. Search by keyword/organism/platform, download GSE series matrices, parse GPL annotations, extract GSM metadata, load expression matrices into pandas. For single-cell use cellxgene-census; for multi-DB access use gget-genomic-databases.

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。

Research population, income, age, housing, and employment around a site. Use for census, demographic, or local-market questions tied to a location.

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。

Annotate copy number variant segments with overlapping genes, dosage-sensitivity scores, cancer driver databases, population frequencies, and clinical-variant content. Covers bedtools/pybedtools interval intersection, AnnotSV comprehensive annotation and ranking, ClinGen haploinsufficiency/triplosensitivity scoring, gnomAD-SV/DGV frequency filtering, COSMIC Cancer Gene Census, and ClinVar overlap. Use when interpreting which genes a CNV affects, distinguishing the driver gene of a focal event from passengers, filtering against population CNVs, separating whole-gene from partial-gene overlap, or preparing CNVs for clinical classification.

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。

GPS-aligned genealogical research assistant for family history, ancestor research, record analysis, source-information-evidence classification, conflict resolution, citations, FAN research, privacy-sensitive document analysis, and proof statements, summaries, or arguments. Use for census, vital, probate, land, military, church, newspaper, DNA-plus-documentary, and other genealogy evidence tasks. Not for GEDCOM creation (use gedcom-creator), general history questions, DNA-kit shopping, or generic writing tasks.

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。

Access COSMIC cancer mutation database. Query somatic mutations, Cancer Gene Census, mutational signatures, gene fusions, for cancer research and precision oncology. Requires authentication.

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。

Compare one or several recorded source states to see whether changes improved Anabasis's climb. Build a state-by-condition census first; compare adjacent states only when prompt, model, command, project lineage, budget and runtime identities support it; read equal windows, earned failures and the mechanisms that fired. Use for 'did the fixes work', 'is this wave better', or before relaunching on a new source.

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Use when a task needs the judgment of a demographer — building a cohort-component population projection, reconciling fertility/mortality rate estimates against ACS or vital-statistics counts, judging whether a population trend is real or sampling/measurement noise, sizing a census undercount adjustment, or advising a public agency on age-structure-driven facility or service demand.

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 a task needs the judgment of an Animal Caretaker — triaging daily husbandry when kennel census exceeds staffing capacity, reading a Fear-Anxiety-Stress (FAS) score change or appetite/output drop against an escalation threshold, deciding brush-out vs. shave-down on a matted coat, or setting isolation and vaccination-lead-time protocol for a new intake or boarding admission.

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。

Annotate copy number variant segments with overlapping genes, dosage-sensitivity scores, cancer driver databases, population frequencies, and clinical-variant content. Covers bedtools/pybedtools interval intersection, AnnotSV comprehensive annotation and ranking, ClinGen haploinsufficiency/triplosensitivity scoring, gnomAD-SV/DGV frequency filtering, COSMIC Cancer Gene Census, and ClinVar overlap. Use when interpreting which genes a CNV affects, distinguishing the driver gene of a focal event from passengers, filtering against population CNVs, separating whole-gene from partial-gene overlap, or preparing CNVs for clinical classification.

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。

Data structure for annotated matrices in single-cell analysis. Use when working with .h5ad files or integrating with the scverse ecosystem. This is the data format skill—for analysis workflows use scanpy; for probabilistic models use scvi-tools; for population-scale queries use cellxgene-census.

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。

Data structure for annotated matrices in single-cell analysis. Use when working with .h5ad files or integrating with the scverse ecosystem. This is the data format skill—for analysis workflows use scanpy; for probabilistic models use scvi-tools; for population-scale queries use cellxgene-census.

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: investigating a legacy, inherited, third-party-built, or otherwise newly-unfamiliar codebase before scoping a migration or major refactor. Formalizes a repeatable five-step investigation pass — entry-point census, business-rule classification, side-effect/idempotency cataloging, implicit-contract discovery, semantic-duplication detection — plus a canonical per-project Open Questions document. Requires checkable signals: ticket keywords or prior documentation gaps. Not a mandatory gate;

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: investigating a legacy, inherited, third-party-built, or otherwise newly-unfamiliar codebase before scoping a migration or major refactor. Formalizes a repeatable five-step investigation pass — entry-point census, business-rule classification, side-effect/idempotency cataloging, implicit-contract discovery, semantic-duplication detection — plus a canonical per-project Open Questions document. Requires checkable signals: ticket keywords or prior documentation gaps. Not a mandatory gate; reserved for entry-point-heavy work in code areas with no prior investigation record.

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。

Annotate copy number variant segments with overlapping genes, dosage-sensitivity scores, cancer driver databases, population frequencies, and clinical-variant content. Covers bedtools/pybedtools interval intersection, AnnotSV comprehensive annotation and ranking, ClinGen haploinsufficiency/triplosensitivity scoring, gnomAD-SV/DGV frequency filtering, COSMIC Cancer Gene Census, and ClinVar overlap. Use when interpreting which genes a CNV affects, distinguishing the driver gene of a focal event from passengers, filtering against population CNVs, separating whole-gene from partial-gene overlap, or preparing CNVs for clinical classification.

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。

Annotate copy number variant segments with overlapping genes, dosage-sensitivity scores, cancer driver databases, population frequencies, and clinical-variant content. Covers bedtools/pybedtools interval intersection, AnnotSV comprehensive annotation and ranking, ClinGen haploinsufficiency/triplosensitivity scoring, gnomAD-SV/DGV frequency filtering, COSMIC Cancer Gene Census, and ClinVar overlap. Use when interpreting which genes a CNV affects, distinguishing the driver gene of a focal event from passengers, filtering against population CNVs, separating whole-gene from partial-gene overlap, or preparing CNVs for clinical classification.

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。

Audit-and-fix method for one user setting area across every repo. Use when a setting seems ignored, duplicated or confusing, on 'audit the X settings' or 'why doesn't my X setting apply', or as a lane of the settings sweep. NOT for adding a new setting (use build-sub-feature).

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。

Working playbook preloaded into the researcher helper; the coach updates its Lessons after each round. Use only when acting as researcher or coaching it. NOT for general research tasks.

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。

Collapsing every copy of one kind of thing (tables, UIs, utilities, hooks, APIs, renderers) into a single canonical one. Use when asked to unify, merge, converge, or 'make one X used everywhere', or before migrating callers onto a new canonical piece. NOT for docs (use docs).

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。