Advertisement
Browse Subject Areas
?

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

  • Loading metrics

Open Access

Correction

Correction: Identifying Human Genome-Wide CNV, LOH and UPD by Targeted Sequencing of Selected Regions

  • The PLOS ONE Staff
  • Article
  • Metrics
  • Comments
  • Media Coverage

Notice of Republication

This article was republished on June 12, 2015 to correct the omission of Corresponding Author Yu Wang and his affiliation from the Author byline. The publisher apologizes for the error. Please download this article again to view the correct version. The originally published, uncorrected article and the republished, corrected article are provided here for reference.

Supporting Information

S1 File. Originally published, uncorrected article.

https://doi.org/10.1371/journal.pone.0132537.s001

(PDF)

S2 File. Republished corrected article.

https://doi.org/10.1371/journal.pone.0132537.s002

(PDF)

Reference

  1. 1. Wang Y, Li W, Xia Y, Wang C, Tang YT, Guo W, et al. (2015) Identifying Human Genome-Wide CNV, LOH and UPD by Targeted Sequencing of Selected Regions. PLoS ONE 10(4): e0123081. pmid:25919136

Citation: The PLOS ONE Staff (2015) Correction: Identifying Human Genome-Wide CNV, LOH and UPD by Targeted Sequencing of Selected Regions. PLoS ONE 10(7): e0132537. https://doi.org/10.1371/journal.pone.0132537

Published: July 2, 2015

Copyright: © 2015 The PLOS ONE Staff. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited