Accessing the impact of functional variants on human phenotypes by transcriptome analysis in individuals carrying different rSNP alleles Научная публикация
Конференция |
Cognitive Sciences, Genomics and Bioinformatics 06-10 июл. 2020 , Новосибирск |
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Сборник | Proceedings - 2020 Cognitive Sciences, Genomics and Bioinformatics, CSGB 2020 Сборник, IEEE. 2020. 300 c. |
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Вых. Данные | Год: 2020, Номер статьи : 9214706, Страниц : 4 DOI: 10.1109/CSGB51356.2020.9214706 | ||||||
Ключевые слова | 1000 Genomes Project; functional annotation; phenotypic outcome; rSNPs; transcriptome analysis | ||||||
Авторы |
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Организации |
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Реферат:
the problem of functional annotation of regulatory single nucleotide polymorphisms is considered. Previously we have identified 1476 human regulatory SNPs through an integrated epigenome and transcriptome analysis. Here we employed the analysis of differentially expressed genes in order to explore the extensive impact of these regulatory variants on the phenotypic landscape. © 2020 IEEE.
Библиографическая ссылка:
Korbolina E.
, Bryzgalov L.
, Postovalov S.
, Nedelko V.
, Berikov V.
, Merkulova T.
Accessing the impact of functional variants on human phenotypes by transcriptome analysis in individuals carrying different rSNP alleles
В сборнике Proceedings - 2020 Cognitive Sciences, Genomics and Bioinformatics, CSGB 2020. – IEEE., 2020. – C.10-13. DOI: 10.1109/CSGB51356.2020.9214706 Scopus OpenAlex
Accessing the impact of functional variants on human phenotypes by transcriptome analysis in individuals carrying different rSNP alleles
В сборнике Proceedings - 2020 Cognitive Sciences, Genomics and Bioinformatics, CSGB 2020. – IEEE., 2020. – C.10-13. DOI: 10.1109/CSGB51356.2020.9214706 Scopus OpenAlex
Идентификаторы БД:
Scopus: | 2-s2.0-85094827289 |
OpenAlex: | W3091769390 |
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Пока нет цитирований