ConVarT: A search engine for matching human genetic variants with variants from non-human species

dc.contributor.author Pir, Mustafa
dc.contributor.author Bilgin, Halil I.
dc.contributor.author Sayıcı, Ahmet
dc.contributor.author Coşkun, Fatih
dc.contributor.author Torun, Furkan M
dc.contributor.author Zhao, Pei
dc.contributor.author Kang, Yahong
dc.contributor.author Çevik, Sebiha
dc.contributor.author Kaplan, Oktay İsmail
dc.contributor.authorID 0000-0002-8733-0920 en_US
dc.contributor.authorID 0000-0002-0935-1929 en_US
dc.contributor.department AGÜ, Mühendislik Fakültesi, Bilgisayar Mühendisliği Bölümü en_US
dc.contributor.institutionauthor Pİr, Mustafa
dc.contributor.institutionauthor Bilgin, Halil İbrahim
dc.contributor.institutionauthor Sayıcı, Ahmet
dc.contributor.institutionauthor Coşkun, Fatih
dc.contributor.institutionauthor Torun, Furkan M.
dc.contributor.institutionauthor Çevik, Sebiha
dc.contributor.institutionauthor Kaplan, Oktay İsmail
dc.date.accessioned 2022-07-21T07:11:04Z
dc.date.available 2022-07-21T07:11:04Z
dc.date.issued 2022 en_US
dc.description.abstract The availability of genetic variants, together with phenotypic annotations from model organisms, facilitates comparing these variants with equivalent variants in humans. However, existing databases and search tools do not make it easy to scan for equivalent variants, namely 'matching variants' (MatchVars) between humans and other organisms. Therefore, we developed an integrated search engine called ConVarT (http://www.convart.org/) for matching variants between humans, mice, and Caenorhabditis elegans. ConVarT incorporates annotations (including phenotypic and pathogenic) into variants, and these previously unexploited phenotypic MatchVars from mice and C. elegans can give clues about the functional consequence of human genetic variants. Our analysis shows that many phenotypic variants in different genes from mice and C. elegans, so far, have no counterparts in humans, and thus, can be useful resources when evaluating a relationship between a new human mutation and a disease. en_US
dc.description.sponsorship Kaplan Laboratory is supported by Abdullah Gul University Scientific Research Project [TOA-2018-110]. en_US
dc.identifier.endpage 1178 en_US
dc.identifier.issn 03051048
dc.identifier.issue 1 en_US
dc.identifier.startpage 1172 en_US
dc.identifier.uri https://doi.org/10.1093/nar/gkab939
dc.identifier.uri https://hdl.handle.net/20.500.12573/1322
dc.identifier.volume 50 en_US
dc.language.iso eng en_US
dc.publisher Oxford University Press en_US
dc.relation.isversionof 10.1093/nar/gkab939 en_US
dc.relation.journal Nucleic Acids Research en_US
dc.relation.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Animals en_US
dc.subject Caenorhabditis elegans en_US
dc.subject Databases en_US
dc.subject Genetic en_US
dc.subject Genetic Variation en_US
dc.subject Humans en_US
dc.subject Mice en_US
dc.subject Software en_US
dc.title ConVarT: A search engine for matching human genetic variants with variants from non-human species en_US
dc.type article en_US

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