Plots of the first two PCs with the proportion of total variation for the CESC data to cluster primary factor of interest (keratin-low and keratin-high groups): (A, C) raw counts data, and (B, D) after adjusting the library size (UQ) and removing the effect of batch ID and estimated SVs by use of PCA through normalization. Each point is colored based on either the two keratin groups (biological factor) (A, B) or the14 levels of known batch ID (C, D).</p
Normalization procedures are widely used in high-throughput genomic data analyses to remove various ...
In recent years, RNA-Seq technologies became a powerful tool for transcriptome studies. However, com...
Background: Various normalisation techniques have been developed in the context of microarray analy...
Normalization of RNA-Seq data has proven essential to ensure accurate inferences and replication of ...
Normalization of RNA-Seq data has proven essential to ensure accurate inferences and replication of ...
Normalization before clustering is often needed for proximity indices, such as Euclidian distance, w...
While Illumina microarrays can be used successfully for detecting small gene expression changes due ...
This paper investigates subset normalization to adjust for location biases (e.g., splotches) combine...
Mass spectrometry (MS)-based proteomics has seen significant technical advances during the past two ...
[[abstract]]This paper investigates subset normalization to adjust for location biases (e.g., splotc...
Design matrix contains: (A) workflow 2: known technical artifact (batch ID) along with the primary f...
Evaluation of different normalization and analysis procedures for illumina gene expression microarra...
<p>Shown are standard boxplots of normalized gene expressions. On the x-axis are the different sampl...
In the middle of the 1990’s the microarray technology was introduced. The technology allowed for gen...
Copyright © 2015 J. Zyprych-Walczak et al. This is an open access article distributed under the Crea...
Normalization procedures are widely used in high-throughput genomic data analyses to remove various ...
In recent years, RNA-Seq technologies became a powerful tool for transcriptome studies. However, com...
Background: Various normalisation techniques have been developed in the context of microarray analy...
Normalization of RNA-Seq data has proven essential to ensure accurate inferences and replication of ...
Normalization of RNA-Seq data has proven essential to ensure accurate inferences and replication of ...
Normalization before clustering is often needed for proximity indices, such as Euclidian distance, w...
While Illumina microarrays can be used successfully for detecting small gene expression changes due ...
This paper investigates subset normalization to adjust for location biases (e.g., splotches) combine...
Mass spectrometry (MS)-based proteomics has seen significant technical advances during the past two ...
[[abstract]]This paper investigates subset normalization to adjust for location biases (e.g., splotc...
Design matrix contains: (A) workflow 2: known technical artifact (batch ID) along with the primary f...
Evaluation of different normalization and analysis procedures for illumina gene expression microarra...
<p>Shown are standard boxplots of normalized gene expressions. On the x-axis are the different sampl...
In the middle of the 1990’s the microarray technology was introduced. The technology allowed for gen...
Copyright © 2015 J. Zyprych-Walczak et al. This is an open access article distributed under the Crea...
Normalization procedures are widely used in high-throughput genomic data analyses to remove various ...
In recent years, RNA-Seq technologies became a powerful tool for transcriptome studies. However, com...
Background: Various normalisation techniques have been developed in the context of microarray analy...