High-performance content-based music retrieval via automated navigation and semantic features

Autor: Su, Ja-Hwung, Hong, Tzung-Pei, Chen, Yu-Tang, Chin, Chu-Yu

Publikováno v: In Engineering Applications of Artificial Intelligence October 2022 115

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Structural genome analysis in cultivated potato taxa

Autor: José Héctor Gálvez López, Sai Reddy Achakkagari, Martina V. Strömvik, Xinyi Zhu, Helen H. Tai, Maria Kyriakidou, Noelle L. Anglin, David Ellis, Chen Yu Tang

Publikováno v: TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik

Key message Twelve potato accessions were selected to represent two principal views on potato taxonomy. The genomes were sequenced and analyzed for structural variation (copy number variation) against three published potato genomes. Abstract The comm

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a6221bda383f83864e5bed4626ae72b
http://europepmc.org/articles/PMC7021743

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Phenotype Driven Analysis of Whole Genome Sequencing Identifies Deep Intronic Variants that Cause Retinal Dystrophies by Aberrant Exonization

Autor: Jonathan Karas, Isabelle Audo, Fayçal Zine-Eddine, Erika Tavares, Christina Zeitz, Alexander Pearson, Kit Green-Sanderson, Yuliya Zubak, Gail Billingsley, Michael D. Wilson, Chen Yu Tang, Ajoy Vincent, Anupreet Tumber, Anjali Vig, Antonio Mollica, Shriya Deshmukh, Elise Héon, Matteo Di Scipio, Caberry W. Yu

Publikováno v: Investigative Ophthalmology & Visual Science
Investigative Ophthalmology & Visual Science, Association for Research in Vision and Ophthalmology, 2020, 61 (10), pp.36. ⟨10.1167/iovs.61.10.36⟩
Investigative Ophthalmology & Visual Science, 2020, 61 (10), pp.36. ⟨10.1167/iovs.61.10.36⟩

International audience; Purpose: To demonstrate the effectiveness of combining retinal phenotyping and focused variant filtering from genome sequencing (GS) in identifying deep intronic disease causing variants in inherited retinal dystrophies.Method

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5352df9e05ca74190340c8770fac8c5
https://hal.sorbonne-universite.fr/hal-02940524