The incorporation of unique molecular identifiers (UMIs) in single-cell RNA-seq assays makes possible the identification of duplicated molecules, thereby facilitating the counting of distinct molecules from sequenced reads. However, we show that the na\uefve removal of duplicates can lead to a bias due to a “pooled amplification paradox,” and we propose an improved quantification method based on unseen species modeling. Our correction called BUTTERFLY uses a zero truncated negative binomial estimator implemented in the kallisto bustools workflow. We demonstrate its efficacy across cell types and genes and show that in some cases it can invert the relative abundance of genes
Kindred cells can have different genomes because of dynamic changes in DNA. Single cell sequencing i...
Motivation: Single-cell RNA sequencing has been proved to be revolutionary for its potential of zoom...
Abstract We develop a method, VIPER, to impute the zero values in single-cell RNA sequ...
The incorporation of unique molecular identifiers (UMIs) in single-cell RNA-seq assays allows for th...
BACKGROUND: RNA-seq and small RNA-seq are powerful, quantitative tools to study gene regulation and ...
RNA-seq and small RNA-seq are powerful, quantitative tools to study gene regulation and function. Co...
Currently, quantitative RNA-seq methods are pushed to work with increasingly small starting amounts ...
Unique Molecular Identifiers (UMIs) are random oligonucleotide barcodes that are increasingly used i...
Advances in molecular biology have made it easy to identify different DNA or RNA species and to copy...
BackgroundRecently, measurement of RNA at single cell resolution has yielded surprising insights. Me...
The attachment of unique molecular identifiers (UMIs) to RNA molecules prior to PCR amplification an...
Single cell RNA sequencing methods have been increasingly used to understand cellular heterogeneity....
Potential users of single-cell RNA-sequencing (scRNA-seq) often encounter a choice between high-thro...
Background: Single cell RNA sequencing (scRNA-seq) has rapidly gained popularity for profiling trans...
With the advent of RNA sequencing and other high- throughput molecular assays, RNA biology has recen...
Kindred cells can have different genomes because of dynamic changes in DNA. Single cell sequencing i...
Motivation: Single-cell RNA sequencing has been proved to be revolutionary for its potential of zoom...
Abstract We develop a method, VIPER, to impute the zero values in single-cell RNA sequ...
The incorporation of unique molecular identifiers (UMIs) in single-cell RNA-seq assays allows for th...
BACKGROUND: RNA-seq and small RNA-seq are powerful, quantitative tools to study gene regulation and ...
RNA-seq and small RNA-seq are powerful, quantitative tools to study gene regulation and function. Co...
Currently, quantitative RNA-seq methods are pushed to work with increasingly small starting amounts ...
Unique Molecular Identifiers (UMIs) are random oligonucleotide barcodes that are increasingly used i...
Advances in molecular biology have made it easy to identify different DNA or RNA species and to copy...
BackgroundRecently, measurement of RNA at single cell resolution has yielded surprising insights. Me...
The attachment of unique molecular identifiers (UMIs) to RNA molecules prior to PCR amplification an...
Single cell RNA sequencing methods have been increasingly used to understand cellular heterogeneity....
Potential users of single-cell RNA-sequencing (scRNA-seq) often encounter a choice between high-thro...
Background: Single cell RNA sequencing (scRNA-seq) has rapidly gained popularity for profiling trans...
With the advent of RNA sequencing and other high- throughput molecular assays, RNA biology has recen...
Kindred cells can have different genomes because of dynamic changes in DNA. Single cell sequencing i...
Motivation: Single-cell RNA sequencing has been proved to be revolutionary for its potential of zoom...
Abstract We develop a method, VIPER, to impute the zero values in single-cell RNA sequ...