BACKGROUND: Publicly accessible EST libraries contain valuable information that can be utilized for studies of tissue-specific gene expression and processing of individual genes. This information is, however, confounded by multiple systematic effects arising from the procedures used to generate these libraries. RESULTS: We used alignment of ESTs against a reference set of transcripts to estimate the size distributions of the cDNA inserts and sampled mRNA transcripts in individual EST libraries and show how these measurements can be used to inform quantitative comparisons of libraries. While significant attention has been paid to the effects of normalization and substraction, we also find significant biases in transcript sampling in...
We compared in detail the characteristics of the sequences of the cDNA clones obtained by the oligo-...
In line with the importance of RNA-seq, the bioinformatics community has produced nu-merous data ana...
High-throughput sequencing technologies, such as the Illumina Genome Analyzer, are powerful new tool...
AbstractThe strikingly wide and bimodal gene distribution exhibited by the human genome has prompted...
Library preparation can be a source of bias in RNA-sequencing studies, leading to false positives in...
Abstract Background: RNA-seq is a powerful technique for identifying and quantifying transcription a...
Motivations. In recent years, RNA sequencing (RNA-seq) has rapidly become the method of choice for m...
EST expression profiling provides an attractive tool for studying differential gene expression, but ...
Although RNA sequencing (RNA-seq) has become the most advanced technology for transcriptome analysis...
Creating a cDNA library for deep mRNA sequencing (mRNAseq) is generally done by random priming, crea...
International audienceBACKGROUND:Gene expression profiling has become a tool of choice to study path...
The biochemistry of RNA-Seq library preparation results in cDNA fragments that are not uniformly dis...
Background: Standard RNAseq methods using bulk RNA and recent single-cell RNAseq methods use DNA bar...
BackgroundTranscriptome sequencing is a powerful tool for measuring gene expression, but as well as ...
Background: The availability of fast alignment-free algorithms has greatly reduced the computational...
We compared in detail the characteristics of the sequences of the cDNA clones obtained by the oligo-...
In line with the importance of RNA-seq, the bioinformatics community has produced nu-merous data ana...
High-throughput sequencing technologies, such as the Illumina Genome Analyzer, are powerful new tool...
AbstractThe strikingly wide and bimodal gene distribution exhibited by the human genome has prompted...
Library preparation can be a source of bias in RNA-sequencing studies, leading to false positives in...
Abstract Background: RNA-seq is a powerful technique for identifying and quantifying transcription a...
Motivations. In recent years, RNA sequencing (RNA-seq) has rapidly become the method of choice for m...
EST expression profiling provides an attractive tool for studying differential gene expression, but ...
Although RNA sequencing (RNA-seq) has become the most advanced technology for transcriptome analysis...
Creating a cDNA library for deep mRNA sequencing (mRNAseq) is generally done by random priming, crea...
International audienceBACKGROUND:Gene expression profiling has become a tool of choice to study path...
The biochemistry of RNA-Seq library preparation results in cDNA fragments that are not uniformly dis...
Background: Standard RNAseq methods using bulk RNA and recent single-cell RNAseq methods use DNA bar...
BackgroundTranscriptome sequencing is a powerful tool for measuring gene expression, but as well as ...
Background: The availability of fast alignment-free algorithms has greatly reduced the computational...
We compared in detail the characteristics of the sequences of the cDNA clones obtained by the oligo-...
In line with the importance of RNA-seq, the bioinformatics community has produced nu-merous data ana...
High-throughput sequencing technologies, such as the Illumina Genome Analyzer, are powerful new tool...