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  • Erratum
  • Open Access

Erratum to: Comprehensive gene panels provide advantages over clinical exome sequencing for Mendelian diseases

Genome Biology201516:226

https://doi.org/10.1186/s13059-015-0798-7

Received: 7 October 2015

Accepted: 7 October 2015

Published: 13 October 2015

The original article was published in Genome Biology 2015 16:134

Erratum

Unfortunately, the original version of this article [1] contained a mistake. In the Acknowledgement section of the article the author Saeed Bohlega was incorrectly spelt as Saeed Boholega. We apologise for this error. The author’s name has been included correctly in the list below:

Acknowledgement

This study was supported by a research grant from King Salman Center for Disability Research (FSA) as well as the Saudi Human Genome Project initiative, KACST.Saudi Mendeliome Group (alphabetical order): Abdulwahab, Firdous; Abouelhoda, Mohamed; Abouthuraya, Rula; Abumansour, Iman; Ahmed, Syed O.; Al Rubeaan, Khalid; Al Tassan, Nada; AlAbdulaziz, Basma; AlAbdulrahman, Khalid; Alamer, FH; Alazami, Anas; Al-Baik, Lina A.; Aldahmesh, Mohammed; Al-Dhekri, Hasan; AlDusery, Haya; Algazlan, Sulaiman; Al-Ghonaium, Abdulaziz; Alhamed, Mohammed; Alhashem, Amal; Alhissi, Safa Ahmed; AlIssa, Abdulelah; Aljurf, Mahmoud D.; Alkuraya, Fowzan S; Alkuraya, Hisham; Allam, Rabab; Almasharawi, Iman J; Almoisheer, Agaadir; AlMostafa, Abeer; Al-Mousa, Hamoud; Al-Muhsen, Saleh; Almutairy, Eid A; Alnader, Noukha; AlNaqeb, Dhekra; ALOtaibi, AB; Alotibi, Afaf; Al-Qattan, Sarah; Al-Saud, Bandar; Al-Saud, Haya; Alshammari, M; Alsharif, Hadeel; Alsheikh, Abdulmoneem H; Al-Sulaiman, Ayman; Altamimi, AS; Al-Tayeb, Hamsa; Alwadaee, SM; Al-Younes, B; Alzahrani, Fatima; Anazi, Shamsa; Arnaout, Rand; Bashiri, Fahad; Binamer, Yousef; Binhumaid, FS; Bohlega, Saeed; Broering, Dieter; Burdelski, Martin; Dasouki, Majed Jamil; Dzimiri, Nduna Francis; Elamin, Tanziel; El-Kalioby, Mohamed; Elsiesy, Hussien; Faqeih, Eissa; Faquih, Tariq; Hagos, Samya; Hagr, Abdulrahman A; Hashem, Mais; Hawwari, Abbas; Hazzaa, Selwa; Ibrahim, Niema; Imtiaz, Faiqa; Jabr, Amal; Kattan, Rana; Kaya, Namik; Kentab, Amal; Khalil, Dania; Khan, Arif O; Khier, Omnia; Meyer, Brian; Mohamed, Jawahir; Monies, Dorota; Muiya, Paul N.; Murad, Hatem; Naim, EA; Owaidah, Tarek; Patel, Nisha; Ramzan, Khushnooda; Salih, Mustafa A; Shagrani, Mohammad; Shaheen, Ranad; Shamseldin, Hanan; Sogaty, Sameera; Subhani, Shazia; Taibah, Khalid; Wakil, Salma M.

Notes

Declarations

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Authors’ Affiliations

(1)
Saudi Human Genome Project, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia

Reference

  1. Saudi Mendeliome Group. Comprehensive gene panels provide advantages over clinical exome sequencing for Mendelian diseases. Genome Biol. 2015;16:134.PubMed CentralView ArticleGoogle Scholar

Copyright

© Saudi Mendeliome Group. 2015

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