Author correction: searching thousands of genomes to classify somatic and novel structural variants using stix

Author correction: searching thousands of genomes to classify somatic and novel structural variants using stix

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Correction to: _Nature Methods_ https://doi.org/10.1038/s41592-022-01423-4, published online 8 April 2022. In the version of this article initially published, the Acknowledgements section for Ryan M. Layer did not include the funding information “NIH/NCI grant no. UO1 CA231978.” The grant has been included in the HTML and PDF versions of the article. AUTHOR INFORMATION AUTHORS AND AFFILIATIONS * BioFrontiers Institute, University of Colorado, Boulder, CO, USA Murad Chowdhury & Ryan M. Layer * University Medical Center, Utrecht University, Utrecht, the Netherlands Brent S. Pedersen * Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA Fritz J. Sedlazeck * Department of Human Genetics, University of Utah, Salt Lake City, UT, USA Aaron R. Quinlan * Department of Biomedical Informatics, University of Utah, Salt Lake City, UT, USA Aaron R. Quinlan * Utah Center for Genetic Discovery, University of Utah, Salt Lake City, UT, USA Aaron R. Quinlan * Department of Computer Science, University of Colorado, Boulder, CO, USA Ryan M. Layer Authors * Murad Chowdhury View author publications You can also search for this author inPubMed Google Scholar * Brent S. Pedersen View author publications You can also search for this author inPubMed Google Scholar * Fritz J. Sedlazeck View author publications You can also search for this author inPubMed Google Scholar * Aaron R. Quinlan View author publications You can also search for this author inPubMed Google Scholar * Ryan M. Layer View author publications You can also search for this author inPubMed Google Scholar CORRESPONDING AUTHOR Correspondence to Ryan M. Layer. RIGHTS AND PERMISSIONS OPEN ACCESS This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. Reprints and permissions ABOUT THIS ARTICLE CITE THIS ARTICLE Chowdhury, M., Pedersen, B.S., Sedlazeck, F.J. _et al._ Author Correction: Searching thousands of genomes to classify somatic and novel structural variants using STIX. _Nat Methods_ 19, 770 (2022). https://doi.org/10.1038/s41592-022-01538-8 Download citation * Published: 26 May 2022 * Issue Date: June 2022 * DOI: https://doi.org/10.1038/s41592-022-01538-8 SHARE THIS ARTICLE Anyone you share the following link with will be able to read this content: Get shareable link Sorry, a shareable link is not currently available for this article. Copy to clipboard Provided by the Springer Nature SharedIt content-sharing initiative

Correction to: _Nature Methods_ https://doi.org/10.1038/s41592-022-01423-4, published online 8 April 2022. In the version of this article initially published, the Acknowledgements section


for Ryan M. Layer did not include the funding information “NIH/NCI grant no. UO1 CA231978.” The grant has been included in the HTML and PDF versions of the article. AUTHOR INFORMATION


AUTHORS AND AFFILIATIONS * BioFrontiers Institute, University of Colorado, Boulder, CO, USA Murad Chowdhury & Ryan M. Layer * University Medical Center, Utrecht University, Utrecht, the


Netherlands Brent S. Pedersen * Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA Fritz J. Sedlazeck * Department of Human Genetics, University of Utah, Salt Lake


City, UT, USA Aaron R. Quinlan * Department of Biomedical Informatics, University of Utah, Salt Lake City, UT, USA Aaron R. Quinlan * Utah Center for Genetic Discovery, University of Utah,


Salt Lake City, UT, USA Aaron R. Quinlan * Department of Computer Science, University of Colorado, Boulder, CO, USA Ryan M. Layer Authors * Murad Chowdhury View author publications You can


also search for this author inPubMed Google Scholar * Brent S. Pedersen View author publications You can also search for this author inPubMed Google Scholar * Fritz J. Sedlazeck View author


publications You can also search for this author inPubMed Google Scholar * Aaron R. Quinlan View author publications You can also search for this author inPubMed Google Scholar * Ryan M.


Layer View author publications You can also search for this author inPubMed Google Scholar CORRESPONDING AUTHOR Correspondence to Ryan M. Layer. RIGHTS AND PERMISSIONS OPEN ACCESS This


article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as


you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party


material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s


Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder.


To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. Reprints and permissions ABOUT THIS ARTICLE CITE THIS ARTICLE Chowdhury, M., Pedersen, B.S., Sedlazeck,


F.J. _et al._ Author Correction: Searching thousands of genomes to classify somatic and novel structural variants using STIX. _Nat Methods_ 19, 770 (2022).


https://doi.org/10.1038/s41592-022-01538-8 Download citation * Published: 26 May 2022 * Issue Date: June 2022 * DOI: https://doi.org/10.1038/s41592-022-01538-8 SHARE THIS ARTICLE Anyone you


share the following link with will be able to read this content: Get shareable link Sorry, a shareable link is not currently available for this article. Copy to clipboard Provided by the


Springer Nature SharedIt content-sharing initiative