Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Pia Kirchmeier"'
Autor:
Pacôme Prompsy, Pia Kirchmeier, Justine Marsolier, Marc Deloger, Nicolas Servant, Céline Vallot
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-9 (2020)
Bulk approaches fail to capture the cell-to-cell heterogeneity of chromatin landscapes, while single-cell approaches provide low coverage datasets. Here, the authors present ChromSCape, a user-friendly interactive application that processes single-ce
Externí odkaz:
https://doaj.org/article/0b906fb8cdfb44efb7ca71d60a8115fd
Autor:
Angela Adler, Pia Kirchmeier, Julian Reinhard, Barbara Brauner, Irmtraud Dunger, Gisela Fobo, Goar Frishman, Corinna Montrone, H.-Werner Mewes, Matthias Arnold, Andreas Ruepp
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-8 (2018)
Abstract Background Thoroughly annotated data resources are a key requirement in phenotype dependent analysis and diagnosis of diseases in the area of precision medicine. Recent work has shown that curation and systematic annotation of human phenome
Externí odkaz:
https://doaj.org/article/b8e4382893a74c09b45949f5d840b90a
Autor:
Pia Kirchmeier, Nicolas Servant, Céline Vallot, Justine Marsolier, Pacôme Prompsy, Marc Deloger
Publikováno v:
Nature Communications
Nature Communications, Nature Publishing Group, 2020, 11, ⟨10.1038/s41467-020-19542-x⟩
Nature Communications, Vol 11, Iss 1, Pp 1-9 (2020)
Nature Communications, Nature Publishing Group, 2020, 11, ⟨10.1038/s41467-020-19542-x⟩
Nature Communications, Vol 11, Iss 1, Pp 1-9 (2020)
Chromatin modifications orchestrate the dynamic regulation of gene expression during development and in disease. Bulk approaches have characterized the wide repertoire of histone modifications across cell types, detailing their role in shaping cell i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::71e7135f190cd99055520d8dcc0ceecb
https://hal.archives-ouvertes.fr/hal-03075604
https://hal.archives-ouvertes.fr/hal-03075604
Autor:
Barbara Brauner, Irmtraud Dunger, Julian Reinhard, Matthias Arnold, Andreas Ruepp, Goar Frishman, Corinna Montrone, H. Werner Mewes, Angela Adler, Pia Kirchmeier, Gisela Fobo
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-8 (2018)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Thoroughly annotated data resources are a key requirement in phenotype dependent analysis and diagnosis of diseases in the area of precision medicine. Recent work has shown that curation and systematic annotation of human phenome data can significant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2fccd4d983af757b447cb078679c6326
http://link.springer.com/article/10.1186/s13023-018-0765-y
http://link.springer.com/article/10.1186/s13023-018-0765-y
Assessing chromatin profiles at single-cell resolution is now feasible thanks to recently published experimental methods such as single cell chromatin immunoprecipitation followed by sequencing (scChIP-seq) (Grosselin et al., 2019; Rotem et al., 2015
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87c514e48c67cb05253fd866c18a6d5c
https://doi.org/10.1101/683037
https://doi.org/10.1101/683037