Abstract
Targeted RNA-Seq combines next-generation sequencing with capture of sequences from a relevant subset of a transcriptome. When testing by capturing sequences from a tumor cDNA library by hybridization to oligonucleotide probes specific for 467 cancer-related genes, this method showed high selectivity, improved mutation detection enabling discovery of novel chimeric transcripts, and provided RNA expression data. Thus, targeted RNA-Seq produces an enhanced view of the molecular state of a set of "high interest" genes.
MeSH Terms
Amino Acid Sequence
Base Sequence
DNA, Complementary/genetics
Gene Expression Profiling/methods
Gene Expression Regulation, Neoplastic/genetics
Humans
K562 Cells
Molecular Sequence Data
Mutation/genetics
Neoplasms/genetics
Oncogene Proteins, Fusion/chemistry,genetics,metabolism
RNA, Messenger/genetics,metabolism
Sequence Analysis, DNA/methods
Chemicals
DNA, Complementary
Oncogene Proteins, Fusion
RNA, Messenger
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Levin Joshua Z
Genome Sequencing and Analysis Program, Broad Institute of MIT and Harvard, 320 Charles Street, Cambridge, MA 02141, USA. jlevin@broadinstitute.org
Berger Michael F
Adiconis Xian
Rogov Peter
Melnikov Alexandre
Fennell Timothy
Nusbaum Chad
Garraway Levi A
Gnirke Andreas
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