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Sensitive, multiplex and direct quantification of RNA sequences using a modified RASL assay
Author(s) -
H. Benjamin Larman,
Erick R. Scott,
Megan Wogan,
Glenn Oliveira,
Ali Torkamani,
Peter G. Schultz
Publication year - 2014
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/gku636
Subject(s) - biology , multiplex , oligonucleotide , computational biology , rna , dna , multiplex ligation dependent probe amplification , dna ligase , microbiology and biotechnology , genetics , gene , exon
A sensitive and highly multiplex method to directly measure RNA sequence abundance without requiring reverse transcription would be of value for a number of biomedical applications, including high throughput small molecule screening, pathogen transcript detection and quantification of short/degraded RNAs.

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