# Quick Start

EVd3x helps you move from a biological question to source-attributed evidence quickly.

## 1) Start a search

You can start with any of these:
- Natural-language query: `show EV cargo linked to Parkinson disease`
- Single molecule: `SNCA` or `hsa-miR-7-5p`
- Collection: `SNCA, LRRK2, RAB10, hsa-miR-7-5p`

## 2) What Analyze does

1. Resolves your query into candidate molecules.
2. Builds a graph state and loads the Summary tab first.
3. If one molecule resolves, EVd3x opens single mode and auto-selects the node.
4. If multiple molecules resolve, EVd3x opens collection mode and loads system summary.
5. Enables deeper tabs and assistant follow-up on the same state.

## 3) Recommended first pass

1. Confirm whether you are in single or collection mode.
2. Read Summary before opening heavier tabs.
3. Check EV Evidence source support.
4. Open Pathway and Disease for functional and disease context.
5. Use Cell, LR, and PPI for follow-up hypotheses.

## 4) High-value prompts

- `open pathway tab`
- `focus on EV evidence only`
- `show top 50 molecules`
- `export current view as csv with gene,score,source`

## 5) Reporting minimum

When sharing findings, include:
- query text,
- mode (single or collection),
- filters and top-N settings,
- exported files used in interpretation,
- relevant caps or thresholds.