Targeted next-generation sequencing of a cancer transcriptome enhances detection of sequence variants and novel fusion transcripts
Joshua Z. Levin(Broad Institute), Andreas Gnirke(Broad Institute), Chad Nusbaum(Broad Institute), Timothy R. Fennell(Broad Institute), Alexandre Melnikov(Broad Institute), Xian Adiconis(Broad Institute), Peter Rogov(Broad Institute), Levi A. Garraway(Broad Institute), Michael F. Berger(Memorial Sloan Kettering Cancer Center)
Cited by 198
Related Papers
Initial sequencing and analysis of the human genome
|Nature|2001|24.6k
Full-length transcriptome assembly from RNA-Seq data without a reference genome
|Nature Biotechnology|2011|22.7k
Model-based Analysis of ChIP-Seq (MACS)
|Genome biology|2008|20k
Analysis of protein-coding genetic variation in 60,706 humans
|Nature|2016|10.3k