Peer Review reports
From: A multiplex PCR amplicon sequencing assay to screen genetic hearing loss variants in newborns
| Original Submission | ||
|---|---|---|
| 25 Nov 2020 | Submitted | Original manuscript |
| Resubmission - Version 2 | ||
| Submitted | Manuscript version 2 | |
| 10 Dec 2020 | Reviewed | Reviewer Report |
| 20 Dec 2020 | Reviewed | Reviewer Report |
| 18 Jan 2021 | Author responded | Author comments - Jiale Xiang |
| Resubmission - Version 3 | ||
| 18 Jan 2021 | Submitted | Manuscript version 3 |
| 20 Jan 2021 | Author responded | Author comments - Jiale Xiang |
| Resubmission - Version 4 | ||
| 20 Jan 2021 | Submitted | Manuscript version 4 |
| 20 Jan 2021 | Author responded | Author comments - Jiale Xiang |
| Resubmission - Version 5 | ||
| 20 Jan 2021 | Submitted | Manuscript version 5 |
| 5 Feb 2021 | Reviewed | Reviewer Report |
| 16 Feb 2021 | Reviewed | Reviewer Report |
| Resubmission - Version 6 | ||
| Submitted | Manuscript version 6 | |
| Publishing | ||
| 16 Feb 2021 | Editorially accepted | |
| 27 Feb 2021 | Article published | 10.1186/s12920-021-00906-1 |
You can find further information about peer review here.