Review your results

Your run finished — let's look at what it found together. Nothing here is final, and you can revisit any variant as many times as you need.

1

Head to Results and open the sample you want to look at. Every completed run waits for you here, so there's no rush.

Head to Results and open the sample you want to look at. Every completed run waits for you here, so there's no rush.
2

Start with the variants Basepair flagged as significant — they're sorted for you, so the ones worth your attention are right at the top.

Start with the variants Basepair flagged as significant — they're sorted for you, so the ones worth your attention are right at the top.
3

Open any variant to read its supporting evidence. If something looks unclear, that's completely normal — the annotations explain why it was called.

Open any variant to read its supporting evidence. If something looks unclear, that's completely normal — the annotations explain why it was called.
4

When you're ready to write things up, click Filter to show only Pathogenic calls. You can clear it any time to see everything again.

When you're ready to write things up, click Filter to show only Pathogenic calls. You can clear it any time to see everything again.