file:Summary of SAGE.svg
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Sanchhipt me
| Baare me |
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] |
| Taarik | |
| Source | Aapan kaam |
| Likhe waala | Thomas Shafee |
| Other versions |
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- ↑ 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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| Din/Time | Chhota chapa | Lambai aur chaurai | Sadasya | Tiprrin | |
|---|---|---|---|---|---|
| abhi waala | 12:21, 13 Farwari 2017 | | 938 × 756 (180 KB) | Evolution and evolvability | text as paths to avoid artefacts |
| 10:48, 13 Farwari 2017 |  | 938 × 756 (104 KB) | Evolution and evolvability | update sequence text to 'sans-serif' open font for more robust rendering | |
| 05:27, 7 Actobar 2016 |  | 938 × 756 (104 KB) | Evolution and evolvability | ce | |
| 05:23, 7 Actobar 2016 |  | 938 × 756 (102 KB) | Evolution and evolvability | ce | |
| 05:16, 7 Actobar 2016 |  | 938 × 756 (104 KB) | Evolution and evolvability | digitag-->tag | |
| 05:08, 5 Actobar 2016 |  | 1,020 × 821 (106 KB) | Evolution and evolvability | User created page with UploadWizard |
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