AI Plugin Indexngs-dna-germline-variants alternatives
The most used alternatives to ngs-dna-germline-variants are alphafold-database-fetch-and-analyze, daily-paper-generator, control-traffic. All are science and health skills with an active GitHub repository, ranked below by GitHub stars and recent activity.
| # | Skill | What it does | Runs | Updated | Stars |
|---|---|---|---|---|---|
| ref | ngs-dna-germline-variants openai | Runs or plans germline DNA variant calling for WGS, WES, and targeted panel data, from FASTQ, BAM, or CRAM. It is for analysts working on singleton, cohort, duo, or trio samples. | Skill | 16 days ago | 7.6k |
| 1 | alphafold-database-fetch-and-analyze google-deepmind | Retrieves and analyzes AlphaFold predicted structures for a protein from a UniProt Accession ID. Built for researchers who need pLDDT confidence, domain boundaries, or disorder assessment. | Skill | yesterday | 3.3k |
| 2 | daily-paper-generator Galaxy-Dawn | Use when the user asks to generate daily paper digests on a general topic. This skill supports both arXiv and bioRxiv (or either one), then produces structured Chinese/English summaries for selected papers. | Skill | 5 days ago | 5.9k |
| 3 | control-traffic carla-simulator | Tunes the CARLA Traffic Manager that drives autopilot vehicles — global and per-vehicle speed, following distance, running lights/signs, lane-change behaviour, lane offset, TM-managed lights, deterministic seed, hybrid physics, and TM sync mode. Use when the user asks to "make the traffic faster/slower", "let cars run red lights", "keep more distance", "stop lane changes", "make traffic deterministic", or otherwise change how autopilot cars behave. For manually driving one car, use control-vehicle. | Skill | yesterday | 15k |
| 4 | submission-packager zhnnky329 | Package a G6-approved mathematical-modeling paper and its exact supporting code, data, results, and figures without changing their behavior or the workspace. | Skill | 1 month ago | 1.1k |
| 5 | citations synthetic-sciences | Resolves, verifies and formats references for academic drafts. It checks each citation against Crossref, OpenAlex, arXiv or PubMed before adding it to a .bib file. | Skill | yesterday | 4.2k |
| 6 | borzoi aipoch | Predict genome-wide functional tracks (RNA-seq, CAGE, DNase, ChIP) from DNA sequence with Borzoi. Use this skill when: (1) Scoring the regulatory effect of a variant on expression/accessibility, (2) Generating predicted coverage tracks for a locus, (3) Prioritising non-coding variants by predicted track delta. | Skill | today | 5.4k |
| 7 | bindingdb-skill openai | Submits compact BindingDB REST API requests for ligand-target binding lookups by PDB ID, UniProt ID, or SMILES similarity. Built for users who want concise BindingDB summaries. | Skill | 16 days ago | 7.6k |
| 8 | oral-health-analyzer sickn33 | 分析口腔健康数据、识别口腔问题模式、评估口腔健康状况、提供个性化口腔健康建议。支持与营养、慢性病、用药等其他健康数据的关联分析。 | Skill | 5 days ago | 48k |
| 9 | Novelty danielmiessler | Evolutionary explanation-discovery engine for hard-to-vary causal theories of unknown phenomena. USE WHEN develop a new theory, explain a mystery, solve an explanatory gap, discover a mechanism, consciousness, origin, or scientific breakthrough. Also use for multi-cycle creative exploration. NOT FOR a single-pass divergent brainstorm (use BeCreative) or delivery validation alone (use Evals). | Skill | 1 month ago | 20k |
| 10 | extract-clinical-entities-to-fhir maziyarpanahi | Extract clinical entities from synthetic or already de-identified text with OpenMed and map them into deterministic FHIR R4 resources and a Bundle. Use when an agent must turn local clinical NER output into Conditions, MedicationStatements, Observations, or other FHIR resources without inventing terminology codes. | Skill | yesterday | 5.7k |
| 11 | data-science-visualization VisActor | 从真实表格或已有统计与模型结果生成简洁的交互数据科学图表 HTML，按问题与数据条件选图，支持按需交互和对话改图。用于看数据和展示结果；完整分析报告或应用开发使用对应工作流。 | Skill | yesterday | 1.9k |
| 12 | tooluniverse-metagenomics-analysis mims-harvard | Microbiome and metagenomics analysis using MGnify, GTDB taxonomy, ENA sequencing data, and EuropePMC literature. Covers taxonomic classification, genome quality assessment, biome-clinical phenotype linkage, and pathway interpretation. Use for amplicon/shotgun metagenomics study analysis. | Skill | today | 1.8k |
Questions
What is the best alternative to ngs-dna-germline-variants?
By usage, alphafold-database-fetch-and-analyze is the most popular alternative, with 3.3k GitHub stars. The right choice depends on which features and hosting you need.
Is ngs-dna-germline-variants still maintained?
Its last commit was 16 days ago. You can see current activity on its listing page.