![]() |
|
![]() |
||||
Thread | Thread Starter | Forum | Replies | Last Post |
lncRNA study pipeline using STAR | rajeev.vikram | RNA Sequencing | 2 | 04-11-2016 08:33 PM |
Differences between NONCODE and RFAM? | A_Morozov | Bioinformatics | 0 | 12-24-2013 12:25 AM |
RNAseq for lncRNA | wtrypste | RNA Sequencing | 1 | 10-11-2012 09:04 PM |
Noncode Download Page | Francisc | Bioinformatics | 0 | 03-29-2012 01:33 AM |
![]() |
|
Thread Tools |
![]() |
#1 |
Senior Member
Location: Paris Join Date: Aug 2011
Posts: 239
|
![]()
Hello everybody,
Did some of you use lncRNA databases in addition to Gencode annotation to count reads in genes? I heard about MiTranscriptome, which contains ~58,000 lncRNA, and is based only on polyA RNA sequencing. I have ribodepleted samples from which I count the number of reads in each gene based on Gencode annotation. I am interested in coding and non coding elements, in lncRNA in particular. I would like to know if some of the lncRNA databases could help and can be used in combination with Gencode to characterize my RNA repertoire. (I used hg19). I would appreciate any feedback. Thank you |
![]() |
![]() |
![]() |
Thread Tools | |
|
|