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Summary

ᏄᏍᏛ ᏗᎧᏃᏗ
English: Within the organisms, genes are transcribed and spliced (in eukaryotes) to produce mature mRNA transcripts (red). The mRNA is extracted from the organism and reverse transcriptase is used to copy the mRNA into stable ds-cDNA (blue). In SAGE, the ds-cDNA is digested by restriction enzymes (at location ‘X’ and ‘X’+11) to produce 11-nucleotide ‘digitag’ fragments. These digitags are concatenated and sequences using long-read sanger sequencing (different shades of blue indicate digitags from different genes). The sequences are deconvoluted to find the occurrence number of each digitag. Digitag can be used to report on transcription of the gene that the digitag came from is known.[1]
ᎢᎦ
ᏅᏓᏳᏓᎴᏅᎯ Own work
ᏧᏬᏪᎳᏅᎯ Thomas Shafee
Other versions

Also in series:

  • RNA Microarray
    RNA Microarray
  • RNA-Seq
    RNA-Seq
  • SAGE
    SAGE

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  1. ↑ Lowe, Rohan (2017-05-18). "Transcriptomics technologies". PLOS Computational Biology 13 (5): e1005457. DOI:10.1371/journal.pcbi.1005457. PMID 28545146. PMC: PMC5436640. ISSN 1553-7358.

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Serial analysis of gene expression ᎩᎵᏏ

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inception ᎩᎵᏏ

5 ᏚᏂᏅᏗ 2016

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ᎢᎦ/ᎠᏟᎢᎵᏒᎤᏍᏗ ᏓᏟᎶᏍᏛᎢDimensionsᎬᏗᏍᎩᏍᏆᎳ ᎪᏪᎵ
current12:21, 13 ᎧᎦᎵ 2017Thumbnail for version as of 12:21, 13 ᎧᎦᎵ 2017938 × 756 (180 KB)Evolution and evolvabilitytext as paths to avoid artefacts
10:48, 13 ᎧᎦᎵ 2017Thumbnail for version as of 10:48, 13 ᎧᎦᎵ 2017938 × 756 (104 KB)Evolution and evolvabilityupdate sequence text to 'sans-serif' open font for more robust rendering
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05:16, 7 ᏚᏂᏅᏗ 2016Thumbnail for version as of 05:16, 7 ᏚᏂᏅᏗ 2016938 × 756 (104 KB)Evolution and evolvabilitydigitag-->tag
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