Matthew E. Ritchie
Molecular Biology · 2007–2020
A researcher in the Science corpus: 6 papers; trusts 12 researchers and is trusted by 3 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 138 citations into it; #10,393 of 17,773 by trust here, #2,484 by citations
- Genetics — 32 citations into it
- Cancer Research — 21 citations into it
- Artificial Intelligence — 16 citations into it
- Biomedical Engineering — 7 citations into it
- Management Science and Operations Research — 5 citations into it
Whom Matthew E. Ritchie trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Gordon K. Smyth
- Mark D. Robinson
- Carl N. Morris
- Y. H. Yang
- Sandrine Dudoit
- Yihui Xie
- Friedrich Leisch
- Terence P. Speed
- Yang Liao
- Bradley Efron
Who trusts Matthew E. Ritchie overall
- Gordon K. Smyth
- Yunshun Chen
- Aaron T. L. Lun
- Belinda Phipson
- Malte D. Luecken
- Brett K. Beaulieu-Jones
- Yang Liao
- G. Korotkevich
- M. van Iterson
- Aurina Arnatkeviciute
Papers from Matthew E. Ritchie's perspective
Ordered by how strongly the researchers Matthew E. Ritchie trusts endorse each paper. Same corpus, a different order for every researcher.
- A scaling normalization method for differential expression analysis of RNA-seq data (Genome Biology)
- On Differential Variability of Expression Ratios: Improving Statistical Inference about Gene Expression Changes from Microarray Data (J. Comput. Biol.)
- Controlling the false discovery rate: a practical and powerful approach to multiple testing
- edgeR: a Bioconductor package for differential expression analysis of digital gene expression data (Bioinform.)
- Normalization for cDNA microarray data: a robust composite method addressing single and multiple slide systematic variation. (Nucleic Acids Research)
- Sweave: Dynamic Generation of Statistical Reports Using Literate Data Analysis (International Conference on Computational Statistics)
- A comparison of normalization methods for high density oligonucleotide array data based on variance and bias (Bioinform.)
- Understanding mechanisms underlying human gene expression variation with RNA sequencing (Nature)
- RSEM: accurate transcript quantification from RNA-Seq data with or without a reference genome (BMC Bioinformatics)
- HTSeq—a Python framework to work with high-throughput sequencing data (bioRxiv)
Their papers
- limma powers differential expression analyses for RNA-sequencing and microarray studies (2015) — 34,728 citations
- A comparison of background correction methods for two-colour microarrays (2007) — 976 citations
- Opportunities and challenges in long-read sequencing data analysis (2020) — 1,305 citations
- RNA-seq analysis is easy as 1-2-3 with limma, Glimma and edgeR (2016) — 738 citations
- Why weight? Modelling sample and observational level variability improves power in RNA-seq analyses (2015) — 502 citations
- Apoptotic Caspases Suppress mtDNA-Induced STING-Mediated Type I IFN Production (2014) — 921 citations