Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Jingsi Ming"'
Autor:
Julia Eve Olivieri, Roozbeh Dehghannasiri, Peter L Wang, SoRi Jang, Antoine de Morree, Serena Y Tan, Jingsi Ming, Angela Ruohao Wu, Tabula Sapiens Consortium, Stephen R Quake, Mark A Krasnow, Julia Salzman
Publikováno v:
eLife, Vol 10 (2021)
The extent splicing is regulated at single-cell resolution has remained controversial due to both available data and methods to interpret it. We apply the SpliZ, a new statistical approach, to detect cell-type-specific splicing in >110K cells from 12
Externí odkaz:
https://doaj.org/article/541656ebdf3d4406a1040ea2c1b0a374
Publikováno v:
Statistics in Biosciences.
The rapid emergence of large-scale atlas-level single-cell RNA-sequencing (scRNA-seq) datasets from various sources presents remarkable opportunities for broad and deep biological investigations through integrative analyses. However, harmonizing such
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a2169e3a26cdab5c832e4a09712bebfd
https://doi.org/10.1101/2021.11.16.468892
https://doi.org/10.1101/2021.11.16.468892
Autor:
Peter L. Wang, Serena Y. Tan, Julia Salzman, Angela Ruohao Wu, Mark A. Krasnow, Jingsi Ming, Julia Eve Olivieri, Antoine de Morrée, SoRi Jang, Roozbeh Dehghannasiri, Stephen R. Quake
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5674660e8a4a4009d84dc2ad452268fe
https://doi.org/10.7554/elife.70692.sa2
https://doi.org/10.7554/elife.70692.sa2
Autor:
Angela Ruohao Wu, Julia Eve Olivieri, Peter L. Wang, Stephen R. Quake, Mark A. Krasnow, Roozbeh Dehghannasiri, Julia Salzman, SoRi Jang, Antoine de Morrée, Serena Y. Tan, Jingsi Ming
More than 95% of human genes are alternatively spliced. Yet, the extent splicing is regulated at single-cell resolution has remained controversial due to both available data and methods to interpret it. We apply the SpliZ, a new statistical approach
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4a8207e02b83d25f51a1a66b1b925809
https://doi.org/10.1101/2021.05.01.442281
https://doi.org/10.1101/2021.05.01.442281
Single-cell RNA-sequencing (scRNA-seq) is being used extensively to measure the mRNA expression of individual cells from deconstructed tissues, organs, and even entire organisms to generate cell atlas references, leading to discoveries of novel cell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::60ad760c06dc2084f630aa7089f0aaff
https://doi.org/10.1101/2020.06.02.129031
https://doi.org/10.1101/2020.06.02.129031
Publikováno v:
Bioinformatics. 34:2788-2796
Motivation Thousands of risk variants underlying complex phenotypes (quantitative traits and diseases) have been identified in genome-wide association studies (GWAS). However, there are still two major challenges towards deepening our understanding o
Publikováno v:
Bioinformatics (Oxford, England). 36(5)
Motivation The results from Genome-Wide Association Studies (GWAS) on thousands of phenotypes provide an unprecedented opportunity to infer the causal effect of one phenotype (exposure) on another (outcome). Mendelian randomization (MR), an instrumen
Autor:
Olivieri, Julia Eve, Dehghannasiri, Roozbeh, Wang, Peter L., SoRi Jang, de Morree, Antoine, Tan, Serena Y., Jingsi Ming, Wu, Angela Ruohao, Consortium, Tabula Sapiens, Quake, Stephen R., Krasnow, Mark A., Salzman, Julia
Publikováno v:
eLife; 11/2/2021, p1-32, 32p
In this paper, we consider a Bayesian bi-level variable selection problem in high-dimensional regressions. In many practical situations, it is natural to assign group membership to each predictor. Examples include that genetic variants can be grouped
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13e9523ccdcb960cac70e95f9415eeb4
http://arxiv.org/abs/1803.10439
http://arxiv.org/abs/1803.10439