Zobrazeno 1 - 10
of 64
pro vyhledávání: '"Gamze, Gürsoy"'
Autor:
Emel Uyar, Gamze Gürsoy, Banu Çelikel Acar, Rana Beyoğlu, Aslınur Özkaya Parlakay, Serhan Özcan, Oktay Perk, Esra Koçkuzu, Serhat Emeksiz
Publikováno v:
Journal of Pediatric Emergency and Intensive Care Medicine, Vol 11, Iss 1, Pp 81-84 (2024)
Severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2) typically leads to mild infectious disease in children, although both acute infection and multisystem inflammatory syndrome in children can cause severe complications. Additionally, SARS-Co
Externí odkaz:
https://doaj.org/article/8f28d1eb59ed4a9d8b63873d203228a1
Publikováno v:
Journal of Pediatric Emergency and Intensive Care Medicine, Vol 10, Iss 2, Pp 150-153 (2023)
An adolescent girl applied to the pediatric emergency outpatient clinic with a complaint of acute abdomen. On abdominal ultrasonography, it was suspected of intussusception. However, when her medical history was expanded, it was discovered that she h
Externí odkaz:
https://doaj.org/article/08ad73c67688427ab72bd1651ef3ae87
Publikováno v:
Genome Biology, Vol 23, Iss 1, Pp 1-22 (2022)
Abstract There are major efforts underway to make genome sequencing a routine part of clinical practice. A critical barrier to these is achieving practical solutions for data ownership and integrity. Blockchain provides solutions to these challenges
Externí odkaz:
https://doaj.org/article/fe4ce4c6c7c44a48b2e50498949aceb3
Publikováno v:
Genome Biology, Vol 22, Iss 1, Pp 1-9 (2021)
Abstract With the recent increase in RNA sequencing efforts using large cohorts of individuals, surveying allele-specific gene expression is becoming increasingly frequent. Here, we report that, despite not containing explicit variant information, a
Externí odkaz:
https://doaj.org/article/81a41c5bba57448eb9f65fcf149e6984
Publikováno v:
BMC Medical Genomics, Vol 13, Iss S7, Pp 1-9 (2020)
Abstract Background Genomic variants are considered sensitive information, revealing potentially private facts about individuals. Therefore, it is important to control access to such data. A key aspect of controlled access is secure storage and effic
Externí odkaz:
https://doaj.org/article/2af95aa6869241849e5d14083569447f
Autor:
Jing Zhang, Donghoon Lee, Vineet Dhiman, Peng Jiang, Jie Xu, Patrick McGillivray, Hongbo Yang, Jason Liu, William Meyerson, Declan Clarke, Mengting Gu, Shantao Li, Shaoke Lou, Jinrui Xu, Lucas Lochovsky, Matthew Ung, Lijia Ma, Shan Yu, Qin Cao, Arif Harmanci, Koon-Kiu Yan, Anurag Sethi, Gamze Gürsoy, Michael Rutenberg Schoenberg, Joel Rozowsky, Jonathan Warrell, Prashant Emani, Yucheng T. Yang, Timur Galeev, Xiangmeng Kong, Shuang Liu, Xiaotong Li, Jayanth Krishnan, Yanlin Feng, Juan Carlos Rivera-Mulia, Jessica Adrian, James R Broach, Michael Bolt, Jennifer Moran, Dominic Fitzgerald, Vishnu Dileep, Tingting Liu, Shenglin Mei, Takayo Sasaki, Claudia Trevilla-Garcia, Su Wang, Yanli Wang, Chongzhi Zang, Daifeng Wang, Robert J. Klein, Michael Snyder, David M. Gilbert, Kevin Yip, Chao Cheng, Feng Yue, X. Shirley Liu, Kevin P. White, Mark Gerstein
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-11 (2020)
ENCODE is a resource comprising thousands of functional genomic datasets. Here, the authors present custom annotation within ENCODE for cancer, highlighting a workflow that can help prioritise key elements in oncogenesis.
Externí odkaz:
https://doaj.org/article/d3ef1766b33842a5aa6bd3194efeba4e
Publikováno v:
BMC Bioinformatics, Vol 21, Iss 1, Pp 1-15 (2020)
Abstract Background During transcription, numerous transcription factors (TFs) bind to targets in a highly coordinated manner to control the gene expression. Alterations in groups of TF-binding profiles (i.e. “co-binding changes”) can affect the
Externí odkaz:
https://doaj.org/article/e96a1fd0895d48698bb3580f3a653e9d
Publikováno v:
BMC Medical Genomics, Vol 13, Iss 1, Pp 1-11 (2020)
Abstract Background As pharmacogenomics data becomes increasingly integral to clinical treatment decisions, appropriate data storage and sharing protocols need to be adopted. One promising option for secure, high-integrity storage and sharing is Ethe
Externí odkaz:
https://doaj.org/article/354e2e799d6c4bcb967d891b081ae656
Autor:
Graham S. Erwin, Gamze Gürsoy, Rashid Al-Abri, Ashwini Suriyaprakash, Egor Dolzhenko, Kevin Zhu, Christian R. Hoerner, Shannon M. White, Lucia Ramirez, Ananya Vadlakonda, Alekhya Vadlakonda, Konor von Kraut, Julia Park, Charlotte M. Brannon, Daniel A. Sumano, Raushun A. Kirtikar, Alicia A. Erwin, Thomas J. Metzner, Ryan K. C. Yuen, Alice C. Fan, John T. Leppert, Michael A. Eberle, Mark Gerstein, Michael P. Snyder
Publikováno v:
Nature. 613:96-102
Expansion of a single repetitive DNA sequence, termed a tandem repeat (TR), is known to cause more than 50 diseases1,2. However, repeat expansions are often not explored beyond neurological and neurodegenerative disorders. In some cancers, mutations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0960ace30a01bc4fd6356079f51ab7f5
https://doi.org/10.1038/s41586-022-05515-1
https://doi.org/10.1038/s41586-022-05515-1
Publikováno v:
Bioinformatics. 39
MotivationLinkage disequilibrium (LD) matrices derived from large populations are widely used in population genetics in fine-mapping, LD score regression, and linear mixed models for Genome-wide Association Studies (GWAS). However, these matrices can
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f4efd07f6854819e4bea65be9da0a40
https://doi.org/10.1093/bioinformatics/btad092
https://doi.org/10.1093/bioinformatics/btad092