Browsing by Author "Love, Michael I."
Now showing items 1-5 of 5
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A benchmark for RNA-seq quantification pipelines
Teng, Mingxiang; Love, Michael I.; Davis, Carrie A.; Djebali, Sarah; Dobin, Alexander; Graveley, Brenton R.; Li, Sheng; Mason, Christopher E.; Olson, Sara; Pervouchine, Dmitri; Sloan, Cricket A.; Wei, Xintao; Zhan, Lijun; Irizarry, Rafael A. (BioMed Central, 2016)Obtaining RNA-seq measurements involves a complex data analytical process with a large number of competing algorithms as options. There is much debate about which of these methods provides the best approach. Unfortunately, ... -
Differential analyses for RNA-seq: transcript-level estimates improve gene-level inferences
Soneson, Charlotte; Love, Michael I.; Robinson, Mark D. (F1000Research, 2015)High-throughput sequencing of cDNA (RNA-seq) is used extensively to characterize the transcriptome of cells. Many transcriptomic studies aim at comparing either abundance levels or the transcriptome composition between ... -
MAGeCK enables robust identification of essential genes from genome-scale CRISPR/Cas9 knockout screens
Li, Wei; Xu, Han; Xiao, Tengfei; Cong, Le; Love, Michael I; Zhang, Feng; Irizarry, Rafael A; Liu, Jun S; Brown, Myles; Liu, X Shirley (BioMed Central, 2014)We propose the Model-based Analysis of Genome-wide CRISPR/Cas9 Knockout (MAGeCK) method for prioritizing single-guide RNAs, genes and pathways in genome-scale CRISPR/Cas9 knockout screens. MAGeCK demonstrates better ... -
Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2
Love, Michael I; Huber, Wolfgang; Anders, Simon (BioMed Central, 2014)In comparative high-throughput sequencing assays, a fundamental task is the analysis of count data, such as read counts per gene in RNA-seq, for evidence of systematic changes across experimental conditions. Small replicate ... -
RNA-Seq workflow: gene-level exploratory analysis and differential expression
Love, Michael I.; Anders, Simon; Kim, Vladislav; Huber, Wolfgang (F1000Research, 2015)Here we walk through an end-to-end gene-level RNA-Seq differential expression workflow using Bioconductor packages. We will start from the FASTQ files, show how these were aligned to the reference genome, and prepare a ...