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Peer Review reports

From: Sequential filtering for clinically relevant variants as a method for clinical interpretation of whole exome sequencing findings in glioma

Original Submission
18 Nov 2020 Submitted Original manuscript
6 Dec 2020 Reviewed Reviewer Report
6 Dec 2020 Reviewed Reviewer Report
30 Dec 2020 Author responded Author comments - Koray Özduman
Resubmission - Version 2
30 Dec 2020 Submitted Manuscript version 2
6 Jan 2021 Author responded Author comments - Koray Özduman
Resubmission - Version 3
6 Jan 2021 Submitted Manuscript version 3
13 Jan 2021 Reviewed Reviewer Report
Resubmission - Version 4
Submitted Manuscript version 4
Publishing
2 Feb 2021 Editorially accepted
23 Feb 2021 Article published 10.1186/s12920-021-00904-3

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