Timeline for Complete human rDNA sequence
Current License: CC BY-SA 4.0
6 events
| when toggle format | what | by | license | comment | |
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| Jun 9, 2018 at 1:19 | comment | added | JayCkat | Welcome to the "gaps" in human genome. Parts of the genome of eukaryote that are very difficult to explore must less experiment with. Here is a reference but it does quite cover recombinational instability of repeat arrays that prevent other methods to study them. ncbi.nlm.nih.gov/pmc/articles/PMC5098217 | |
| Jun 8, 2018 at 19:05 | comment | added | David | Reference in support of this assertion please. I thought methodological developments in sequencing meant that this situation could be dealt with. | |
| Jun 8, 2018 at 14:12 | comment | added | JayCkat | Yes, there must be sequence variability in the non-coding region. However as rDNA arrays are rather unstable and recombine within a yeast or ecoli host. Hence isolating rDNA repeat array and making a rough map of rDNA repeat arrays is next to impossible. | |
| Jun 8, 2018 at 14:08 | history | edited | JayCkat | CC BY-SA 4.0 |
added 11 characters in body
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| Jun 8, 2018 at 10:31 | comment | added | matk | Great, that's useful to know. I assume that there must be mutations in at least some of the noncoding regions that would enable positional information for certain sequences. | |
| Jun 8, 2018 at 9:33 | history | answered | JayCkat | CC BY-SA 4.0 |