Cargando…

Linnorm: improved statistical analysis for single cell RNA-seq expression data

Mostrar otras versiones (1)

Detalles Bibliográficos
Autores principales:	Yip, Shun H., Wang, Panwen, Kocher, Jean-Pierre A., Sham, Pak Chung, Wang, Junwen
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Oxford University Press 2017
Materias:	Corrigendum
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5728397/ https://www.ncbi.nlm.nih.gov/pubmed/29161425 http://dx.doi.org/10.1093/nar/gkx1189

Ejemplares similares

Linnorm: improved statistical analysis for single cell RNA-seq expression data
por: Yip, Shun H., et al.
Publicado: (2017)

UClncR: Ultrafast and comprehensive long non-coding RNA detection from RNA-seq
por: Sun, Zhifu, et al.
Publicado: (2017)

A fast and powerful W-test for pairwise epistasis testing
por: Wang, Maggie Haitian, et al.
Publicado: (2016)

Wellington: a novel method for the accurate identification of digital genomic footprints from DNase-seq data
por: Piper, Jason, et al.
Publicado: (2014)

SpliceNet: recovering splicing isoform-specific differential gene networks from RNA-Seq data of normal and diseased samples
por: Yalamanchili, Hari Krishna, et al.
Publicado: (2014)

Author Correction: UClncR: Ultrafast and comprehensive long non-coding RNA detection from RNA-seq
por: Sun, Zhifu, et al.
Publicado: (2018)

GWASdb v2: an update database for human genetic variants identified by genome-wide association studies
por: Li, Mulin Jun, et al.
Publicado: (2016)

Exploring genetic associations with ceRNA regulation in the human genome
por: Li, Mulin Jun, et al.
Publicado: (2017)

ChIP-Array: combinatory analysis of ChIP-seq/chip and microarray gene expression data to discover direct/indirect targets of a transcription factor
por: Qin, Jing, et al.
Publicado: (2011)

GWAS4D: multidimensional analysis of context-specific regulatory variant for human complex diseases and traits
por: Huang, Dandan, et al.
Publicado: (2018)

RefSeq microbial genomes database: new representation and annotation strategy
por: Tatusova, T., et al.
Publicado: (2015)

Statistical Issues in the Analysis of ChIP-Seq and RNA-Seq Data
por: Ghosh, Debashis, et al.
Publicado: (2010)

An evaluation of statistical differential analysis methods in single-cell RNA-seq data
por: Li, Dongmei, et al.
Publicado: (2023)

cepip: context-dependent epigenomic weighting for prioritization of regulatory variants and disease-associated genes
por: Li, Mulin Jun, et al.
Publicado: (2017)

Measure transcript integrity using RNA-seq data
por: Wang, Liguo, et al.
Publicado: (2016)

qDNAmod: a statistical model-based tool to reveal intercellular heterogeneity of DNA modification from SMRT sequencing data
por: Feng, Z., et al.
Publicado: (2015)

mTCTScan: a comprehensive platform for annotation and prioritization of mutations affecting drug sensitivity in cancers
por: Li, Mulin Jun, et al.
Publicado: (2017)

PTHGRN: unraveling post-translational hierarchical gene regulatory networks using PPI, ChIP-seq and gene expression data
por: Guan, Daogang, et al.
Publicado: (2014)

A systematic analysis of the silencing effects of an active siRNA at all single-nucleotide mismatched target sites
por: Du, Quan, et al.
Publicado: (2005)

CORRIGENDUM to Image Statistics and the Fine Lines of Material Perception
Publicado: (2016)

RNA-MoIP: prediction of RNA secondary structure and local 3D motifs from sequence data
por: Yao, Jason, et al.
Publicado: (2017)

Indel detection from RNA-seq data: tool evaluation and strategies for accurate detection of actionable mutations
por: Sun, Zhifu, et al.
Publicado: (2017)

FastPval: a fast and memory efficient program to calculate very low P-values from empirical distribution
por: Li, Mulin Jun, et al.
Publicado: (2010)

Identification of metabolically stable 5΄-phosphate analogs that support single-stranded siRNA activity
por: Prakash, Thazha P., et al.
Publicado: (2017)

Corrigendum to: An examination of multivariable Mendelian randomization in the single-sample and two-sample summary data settings
por: Sanderson, Eleanor, et al.
Publicado: (2020)

A survey of statistical software for analysing RNA-seq data
por: Gao, Dexiang, et al.
Publicado: (2010)

The bench scientist's guide to statistical analysis of RNA-Seq data
por: Yendrek, Craig R, et al.
Publicado: (2012)

GWASdb: a database for human genetic variants identified by genome-wide association studies
por: Li, Mulin Jun, et al.
Publicado: (2012)

Determining mutational burden and signature using RNA-seq from tumor-only samples
por: Jessen, Erik, et al.
Publicado: (2021)

A statistical method for the detection of variants from next-generation resequencing of DNA pools
por: Bansal, Vikas
Publicado: (2016)

Corrigendum to “Polychromatic Iterative Statistical Material Image Reconstruction for Photon-Counting Computed Tomography”
por: Weidinger, Thomas, et al.
Publicado: (2018)

Corrigendum to “Biomarker MicroRNAs for Diagnosis of Oral Squamous Cell Carcinoma Identified Based on Gene Expression Data and MicroRNA-mRNA Network Analysis”
por: Zhang, Hui, et al.
Publicado: (2017)

Cdk1 gates cell cycle-dependent tRNA synthesis by regulating RNA polymerase III activity
por: Herrera, Maria C, et al.
Publicado: (2018)

Opportunities for improving data sharing and FAIR data practices to advance global mental health–Corrigendum
por: Sadeh, Yaara, et al.
Publicado: (2023)

Corrigendum to “Data for proteomic analysis of murine cardiomyocytic HL-1 cells treated with siRNA against tissue factor” [Data Brief 3 (2015) 117–119]
por: Brioschi, Maura, et al.
Publicado: (2015)

Assessment of statistical methods from single cell, bulk RNA-seq, and metagenomics applied to microbiome data
por: Calgaro, Matteo, et al.
Publicado: (2020)

LTMG: a novel statistical modeling of transcriptional expression states in single-cell RNA-Seq data
por: Wan, Changlin, et al.
Publicado: (2019)

Differential Expression Analysis of Single-Cell RNA-Seq Data: Current Statistical Approaches and Outstanding Challenges
por: Das, Samarendra, et al.
Publicado: (2022)

Corrigendum: Single-nucleotide polymorphism screening and RNA sequencing of key messenger RNAs associated with neonatal hypoxic-ischemia brain damage
Publicado: (2020)

The nuclear and organellar tRNA-derived RNA fragment population in Arabidopsis thaliana is highly dynamic
por: Cognat, Valérie, et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_ilgabt1qvui1glsqb9oklf6gtd