Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Gilad Mishne"'
Autor:
Julian R. Homburger, Cynthia L. Neben, Gilad Mishne, Alicia Y. Zhou, Sekar Kathiresan, Amit V. Khera
Publikováno v:
Genome Medicine, Vol 11, Iss 1, Pp 1-12 (2019)
Abstract Background Inherited susceptibility to common, complex diseases may be caused by rare, pathogenic variants (“monogenic”) or by the cumulative effect of numerous common variants (“polygenic”). Comprehensive genome interpretation shoul
Externí odkaz:
https://doaj.org/article/47339bfe7b8a4608881ffa2876af6a9b
Publikováno v:
BMC Genomics, Vol 19, Iss 1, Pp 1-9 (2018)
Abstract Background Next generation sequencing (NGS) has become a common technology for clinical genetic tests. The quality of NGS calls varies widely and is influenced by features like reference sequence characteristics, read depth, and mapping accu
Externí odkaz:
https://doaj.org/article/c5c9a3c058104e22b88773e5cd40c2ec
Autor:
Jimmy Lin, Gilad Mishne
Publikováno v:
Proceedings of the International AAAI Conference on Web and Social Media. 6:503-506
The real-time nature of Twitter means that term distributions in tweets and in search queries change rapidly: the most frequent terms in one hour may look very different from those in the next. Informally, we call this phenomenon "churn". Our interes
Autor:
Gilad Mishne, Serra Kim, Scott Topper, Robert O'Connor, Carmen Lai, Jeroen van den Akker, Raymond C. Chan, Anjali D. Zimmer, Alicia Y. Zhou
Publikováno v:
Human Mutation
Advances in genome sequencing have led to a tremendous increase in the discovery of novel missense variants, but evidence for determining clinical significance can be limited or conflicting. Here, we present Learning from Evidence to Assess Pathogeni
Autor:
Alicia Y. Zhou, Julian R. Homburger, Gilad Mishne, Sekar Kathiresan, Amit Khera, Cynthia L. Neben
Publikováno v:
Genome Medicine, Vol 11, Iss 1, Pp 1-12 (2019)
Genome Medicine
Genome Medicine
Background Inherited susceptibility to common, complex diseases may be caused by rare, pathogenic variants (“monogenic”) or by the cumulative effect of numerous common variants (“polygenic”). Comprehensive genome interpretation should enable
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ced9cdb2591932424587c4f05fbe6b0
Autor:
Ryan Barrett, Alicia Y. Zhou, Cynthia L. Neben, Gilad Mishne, Anjali D. Zimmer, Jeremy Ginsberg, Wendy McKennon
Publikováno v:
Database: The Journal of Biological Databases and Curation
Next generation sequencing multi-gene panels have greatly improved the diagnostic yield and cost effectiveness of genetic testing and are rapidly being integrated into the clinic for hereditary cancer risk. With this technology comes a dramatic incre
Publikováno v:
BMC Genomics
BMC Genomics, Vol 19, Iss 1, Pp 1-9 (2018)
BMC Genomics, Vol 19, Iss 1, Pp 1-9 (2018)
Background Next generation sequencing (NGS) has become a common technology for clinical genetic tests. The quality of NGS calls varies widely and is influenced by features like reference sequence characteristics, read depth, and mapping accuracy. Wit
Autor:
Gilad Mishne
Publikováno v:
Proceedings of the 39th International ACM SIGIR conference on Research and Development in Information Retrieval.
Autor:
Gilad Mishne
Publikováno v:
Proceedings of the 39th International ACM SIGIR conference on Research and Development in Information Retrieval.
Autor:
Guangyu Zhu, Gilad Mishne
Publikováno v:
ACM Transactions on the Web. 6:1-22
User browsing information, particularly non-search-related activity, reveals important contextual information on the preferences and intents of Web users. In this article, we demonstrate the importance of mining general Web user behavior data to impr