Skip to main content

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

The Original Article was published on 26 June 2015

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.

Reference

  1. 1.

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

    PubMed Central  Article  Google Scholar 

Download references

Author information

Affiliations

Consortia

Additional information

The online version of the original article can be found under doi:10.1186/s13059-015-0693-2.

Rights and permissions

Open Access This 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.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Saudi Mendeliome Group. Erratum to: Comprehensive gene panels provide advantages over clinical exome sequencing for Mendelian diseases. Genome Biol 16, 226 (2015). https://doi.org/10.1186/s13059-015-0798-7

Download citation

  • Received:

  • Accepted:

  • Published:

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