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http://hdl.handle.net/10261/18...
Part of book or chapter of book
Data sources: UnpayWall
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Recolector de Ciencia Abierta, RECOLECTA
Part of book or chapter of book . 2019 . Peer-reviewed
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https://doi.org/10.1007/978-1-...
Part of book or chapter of book . 2019 . Peer-reviewed
License: Springer TDM
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Quantitative RNA Analysis Using RNA-Seq

Authors: Myler, P. J.; McDonald, Jacqueline A.; Alcolea, Pedro J.; Sur, Aakash;

Quantitative RNA Analysis Using RNA-Seq

Abstract

High-throughput sequencing of cDNA copies of mRNA (RNA-seq) provides a digital readout of mRNA levels over several orders of magnitude, as well as mapping the transcripts to the nucleotide level. Here we describe two different RNA-seq approaches, including one that exploits the 39-nucleotide mini-exon or spliced leader (SL) sequence found at the 5' end of all Leishmania (and other trypanosomatid) mRNAs.

Keywords

Leishmania, Sequence Analysis, RNA, mRNA, High-Throughput Nucleotide Sequencing, Exons, RNA, Messenger, RNA-seq, Differential gene expression, RNA, Protozoan, Transcriptomes

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
views
OpenAIRE UsageCountsViews provided by UsageCounts
downloads
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3
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