Leveraging omic features with F3UTER enables identification of unannotated 3'UTRs for synaptic genes.

Sethi, Siddharth; Zhang, David; Guelfi, Sebastian; Chen, Zhongbo; Garcia-Ruiz, Sonia; Olagbaju, Emmanuel O; Ryten, Mina; Saini, Harpreet; Botia, Juan A

Sethi, Siddharth; Zhang, David; Guelfi, Sebastian; Chen, Zhongbo; Garcia-Ruiz, Sonia; Olagbaju, Emmanuel O; Ryten, Mina; Saini, Harpreet; Botia, Juan A.

Afiliación

Sethi S; Astex Pharmaceuticals, 436 Cambridge Science Park, Cambridge, UK.
Zhang D; Department of Neurodegenerative Disease, Institute of Neurology, University College London, London, UK.
Guelfi S; Genetics and Genomic Medicine, Great Ormond Street Institute of Child Health, University College London, London, WC1E 6BT, UK.
Chen Z; Department of Neurodegenerative Disease, Institute of Neurology, University College London, London, UK.
Garcia-Ruiz S; Verge Genomics, South San Francisco, CA, 94080, USA.
Olagbaju EO; Department of Neurodegenerative Disease, Institute of Neurology, University College London, London, UK.
Ryten M; Genetics and Genomic Medicine, Great Ormond Street Institute of Child Health, University College London, London, WC1E 6BT, UK.
Saini H; NIHR Great Ormond Street Hospital Biomedical Research Centre, University College London, London, UK.
Botia JA; Department of Neurodegenerative Disease, Institute of Neurology, University College London, London, UK.

Nat Commun ; 13(1): 2270, 2022 04 27.

Article en En | MEDLINE | ID: mdl-35477703

Asunto(s)

Transcriptoma; Regiones no Traducidas 3'/genética; Humanos; ARN Mensajero/genética

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Transcriptoma Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Nat Commun Asunto de la revista: BIOLOGIA / CIENCIA Año: 2022 Tipo del documento: Article País de afiliación: Reino Unido

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