User profiles for C. Trapnell
Cole TrapnellAssociate Professor, Dept. of Genome Sciences, University of Washington Verified email at uw.edu Cited by 119486 |
Computational methods for transcriptome annotation and quantification using RNA-seq
… (c) For a gene with two expressed isoforms, exons are colored according to the isoform of …
Trapnell, C. et al. Transcript assembly and quantification by RNA-seq reveals unannotated …
Trapnell, C. et al. Transcript assembly and quantification by RNA-seq reveals unannotated …
Defining cell types and states with single-cell genomics
C Trapnell - Genome research, 2015 - genome.cshlp.org
A revolution in cellular measurement technology is under way: For the first time, we have
the ability to monitor global gene regulation in thousands of individual cells in a single …
the ability to monitor global gene regulation in thousands of individual cells in a single …
How to map billions of short reads onto genomes
C Trapnell, SL Salzberg - Nature biotechnology, 2009 - nature.com
… Cole Trapnell … Cole Trapnell and Steven L. Salzberg are at the Center for
Bioinformatics and Computational Biology, University of Maryland, College Park, Maryland …
Bioinformatics and Computational Biology, University of Maryland, College Park, Maryland …
Transcript assembly and quantification by RNA-Seq reveals unannotated transcripts and isoform switching during cell differentiation
… (a) When abundances of isoforms A, B and C of Myc are grouped by TSS, changes in the …
(c) Myc isoforms are downregulated as the time course proceeds. The width of the colored …
(c) Myc isoforms are downregulated as the time course proceeds. The width of the colored …
Differential gene and transcript expression analysis of RNA-seq experiments with TopHat and Cufflinks
… In the version of this article initially published, the computer script in Box 1 sections B and C,
and in Procedure Step 1, contained errors: the last section of the final three lines of the script …
and in Procedure Step 1, contained errors: the last section of the final three lines of the script …
TopHat: discovering splice junctions with RNA-Seq
Motivation: A new protocol for sequencing the messenger RNA in a cell, known as RNA-Seq,
generates millions of short sequence fragments in a single run. These fragments, or ‘reads’…
generates millions of short sequence fragments in a single run. These fragments, or ‘reads’…
[HTML][HTML] Ultrafast and memory-efficient alignment of short DNA sequences to the human genome
Bowtie is an ultrafast, memory-efficient alignment program for aligning short DNA sequence
reads to large genomes. For the human genome, Burrows-Wheeler indexing allows Bowtie …
reads to large genomes. For the human genome, Burrows-Wheeler indexing allows Bowtie …
[HTML][HTML] TopHat2: accurate alignment of transcriptomes in the presence of insertions, deletions and gene fusions
TopHat is a popular spliced aligner for RNA-sequence (RNA-seq) experiments. In this paper,
we describe TopHat2, which incorporates many significant enhancements to TopHat. …
we describe TopHat2, which incorporates many significant enhancements to TopHat. …
The dynamics and regulators of cell fate decisions are revealed by pseudotemporal ordering of single cells
… , dissociated cells were captured and processed with the C 1 Single-Cell Auto Prep System
(… are captured in each C 1 microfluidic device. In this study, we used one C 1 capture chip at 0…
(… are captured in each C 1 microfluidic device. In this study, we used one C 1 capture chip at 0…
Differential analysis of gene regulation at transcript resolution with RNA-seq
… (c) Methods for performing differential gene expression analysis with RNA-seq based on the
exon-union counting method returned nearly all of the genes returned by Cuffdiff 2. (d) Lung …
exon-union counting method returned nearly all of the genes returned by Cuffdiff 2. (d) Lung …