transcript database
Recently Published Documents


TOTAL DOCUMENTS

9
(FIVE YEARS 2)

H-INDEX

5
(FIVE YEARS 1)

PeerJ ◽  
2019 ◽  
Vol 7 ◽  
pp. e8206 ◽  
Author(s):  
Ashley J. Waardenberg ◽  
Matthew A. Field

Extensive evaluation of RNA-seq methods have demonstrated that no single algorithm consistently outperforms all others. Removal of unwanted variation (RUV) has also been proposed as a method for stabilizing differential expression (DE) results. Despite this, it remains a challenge to run multiple RNA-seq algorithms to identify significant differences common to multiple algorithms, whilst also integrating and assessing the impact of RUV into all algorithms. consensusDE was developed to automate the process of identifying significant DE by combining the results from multiple algorithms with minimal user input and with the option to automatically integrate RUV. consensusDE only requires a table describing the sample groups, a directory containing BAM files or preprocessed count tables and an optional transcript database for annotation. It supports merging of technical replicates, paired analyses and outputs a compendium of plots to guide the user in subsequent analyses. Herein, we assess the ability of RUV to improve DE stability when combined with multiple algorithms and between algorithms, through application to real and simulated data. We find that, although RUV increased fold change stability between algorithms, it demonstrated improved FDR in a setting of low replication for the intersect, the effect was algorithm specific and diminished with increased replication, reinforcing increased replication for recovery of true DE genes. We finish by offering some rules and considerations for the application of RUV in a consensus-based setting. consensusDE is freely available, implemented in R and available as a Bioconductor package, under the GPL-3 license, along with a comprehensive vignette describing functionality: http://bioconductor.org/packages/consensusDE/.


2019 ◽  
Author(s):  
Ashley J. Waardenberg ◽  
Matt A. Field

AbstractExtensive evaluation of RNA-seq methods have demonstrated that no single algorithm consistently outperforms all others. Removal of unwanted variation (RUV) has also been proposed as a method for stabilizing differential expression (DE) results. Despite this, it remains a challenge to run multiple RNA-seq algorithms to identify significant differences common to multiple algorithms, whilst also integrating and assessing the impact of RUV into all algorithms. consensusDE was developed to automate the process of identifying significant DE by combining the results from multiple algorithms with minimal user input and with the option to automatically integrate RUV. consensusDE only requires a table describing the sample groups, a directory containing BAM files or preprocessed count tables and an optional transcript database for annotation. It supports merging of technical replicates, paired analyses and outputs a compendium of plots to guide the user in subsequent analyses. Herein, we also assess the ability of RUV to improve DE stability when combined with multiple algorithms through application to real and simulated data. We find that, although RUV demonstrated improved FDR in a setting of low replication, the effect was algorithm specific and diminished with increased replication, reinforcing increased replication for recovery of true DE genes. We finish by offering some rules and considerations for the application of RUV in a consensus-based setting.consensusDE is freely available, implemented in R and available as a Bioconductor package, under the GPL-3 license, along with a comprehensive vignette describing functionality: http://bioconductor.org/packages/consensusDE/


PLoS ONE ◽  
2014 ◽  
Vol 9 (1) ◽  
pp. e85568 ◽  
Author(s):  
Oliver Rupp ◽  
Jennifer Becker ◽  
Karina Brinkrolf ◽  
Christina Timmermann ◽  
Nicole Borth ◽  
...  

2010 ◽  
Author(s):  
Makoto Shimada ◽  
Makoto Shimada ◽  
Noriko Haraguchi ◽  
Akila Mayeda

2000 ◽  
Vol 16 (2) ◽  
pp. 176-177 ◽  
Author(s):  
J. Bouck ◽  
M. P. McLeod ◽  
K. Worley ◽  
R. A. Gibbs

1999 ◽  
Author(s):  
Bouckk John ◽  
Michael McLeod ◽  
Kim Worley ◽  
Richard Gibbs

1994 ◽  
Vol 21 (1) ◽  
pp. 157-172 ◽  
Author(s):  
Matthew Rispoli

ABSTRACTPronoun case errors, or overextensions, like *me want it are characteristic of English child language. This paper explores a hypothesis that the morphological structure of a pronoun influences the pattern of these errors. The Language Acquisition Device (LAD) attempts to analyse English pronoun case forms into stems and affixes, but cannot because of their irregularity. Nevertheless the LAD extracts a phonetic core for each pronoun (e.g. /m-/ for the ist sg., /h-/ for the 3rd masc. sg.). The phonetic core blocks the overextension of suppletive nominative forms like I and she. This hypothesis predicts strong differences in the frequency and types of errors between pronouns with suppletive nominatives and those without. Evidence for this hypothesis was found in a transcript database of twelve children, with data collected in one hour samples every month from 1;0 to 3;0. 20,908 pronouns were examined, 1347 of which were errors. Statistical analyses of these data provide support for this hypothesis.


Sign in / Sign up

Export Citation Format

Share Document