Author Correction: A structural variation reference for medical and population genetics
- PMID: 33536627
- PMCID: PMC8064907
- DOI: 10.1038/s41586-020-03176-6
Author Correction: A structural variation reference for medical and population genetics
Erratum for
-
A structural variation reference for medical and population genetics.Nature. 2020 May;581(7809):444-451. doi: 10.1038/s41586-020-2287-8. Epub 2020 May 27. Nature. 2020. PMID: 32461652 Free PMC article.
Similar articles
-
Author Correction: Discovery and population genomics of structural variation in a songbird genus.Nat Commun. 2021 May 20;12(1):3163. doi: 10.1038/s41467-021-23640-9. Nat Commun. 2021. PMID: 34017009 Free PMC article. No abstract available.
-
Author Correction: RSPO2 inhibition of RNF43 and ZNRF3 governs limb development independently of LGR4/5/6.Nature. 2018 Sep;561(7722):E7. doi: 10.1038/s41586-018-0296-7. Nature. 2018. PMID: 29977062
-
A structural variation reference for medical and population genetics.Nature. 2020 May;581(7809):444-451. doi: 10.1038/s41586-020-2287-8. Epub 2020 May 27. Nature. 2020. PMID: 32461652 Free PMC article.
-
The population genetics of structural variation.Nat Genet. 2007 Jul;39(7 Suppl):S30-6. doi: 10.1038/ng2042. Nat Genet. 2007. PMID: 17597779 Free PMC article. Review.
-
Integration of genetics into clinical teaching in medical school education.Genet Med. 2002 Nov-Dec;4(6 Suppl):33S-38S. doi: 10.1097/00125817-200211001-00007. Genet Med. 2002. PMID: 12544485 Review.
Cited by
-
Comprehensive and accurate genome analysis at scale using DRAGEN accelerated algorithms.bioRxiv [Preprint]. 2024 Jan 6:2024.01.02.573821. doi: 10.1101/2024.01.02.573821. bioRxiv. 2024. PMID: 38260545 Free PMC article. Preprint.
-
Closing the gaps, and improving somatic structural variant analysis and benchmarking using CHM13-T2T.Genome Res. 2025 Apr 14;35(4):621-631. doi: 10.1101/gr.279352.124. Genome Res. 2025. PMID: 40097200
-
De novo structural variants in autism spectrum disorder disrupt distal regulatory interactions of neuronal genes.bioRxiv [Preprint]. 2024 Nov 7:2024.11.06.621353. doi: 10.1101/2024.11.06.621353. bioRxiv. 2024. PMID: 39574698 Free PMC article. Preprint.
-
Comprehensive genome analysis and variant detection at scale using DRAGEN.Nat Biotechnol. 2025 Jul;43(7):1177-1191. doi: 10.1038/s41587-024-02382-1. Epub 2024 Oct 25. Nat Biotechnol. 2025. PMID: 39455800 Free PMC article.
-
Biallelic variants of SEMA3F are associated with nonsyndromic hearing loss.Mol Cells. 2025 Mar;48(3):100190. doi: 10.1016/j.mocell.2025.100190. Epub 2025 Feb 3. Mol Cells. 2025. PMID: 39909336 Free PMC article.
Publication types
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources