User: ooluwayiose
ooluwayiose • 0
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Posts by ooluwayiose
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... Hey. I am working on smallRNA-seq data with the final goal of investigating differential expression analysis.
I used bowtie1 for mapping with the following specification: `bowtie -p 10 -n 2 -m 1 -k 1 --strata --best -x index -q *fq`
The summary statistics I got are as follows:
#reads proces ...
written 9 days ago by
ooluwayiose • 0
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8 days ago by
GenoMax ♦ 96k
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... @GenoMax, thank you so much for your help. I did not know it was possible to count small RNA sorted bam files directly and easily with **samtools idxstats** without either HTseq or featurecounts. That was really helpful.
Also, this may sound naive but I wonder what may be the pros and cons of usin ...
written 21 days ago by
ooluwayiose • 0
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... @GenoMax, thanks for a prompt response. Still confused, please are you referring to a mismatch in my gtf file (columns 3 & 9) or my .bam file. Please how do I make them match in all locations? The URS* in column 3 of the bam file seems to be the RNAcentral ID and I wonder if that needs to change ...
written 21 days ago by
ooluwayiose • 0
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... For some reason, the image icon above appeared not to work. Here are the links again:
gtf: ![https://ibb.co/19sv9WV][1]
mapped.sorted.bam: ![https://ibb.co/0cxmB8w][2]
featureCounts output: ![https://ibb.co/hWmxq8s][3]
[1]: https://i.ibb.co/sF5mFYS/gtf-file.png
[2]: https://i.ibb.co/Bt9c4 ...
written 22 days ago by
ooluwayiose • 0
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22 days ago by
GenoMax ♦ 96k
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... Thanks GenoMax, I used imgbb as recommended in the link.
Please see the links below:
![.gtf][1]
![mapped.sorted.bam][2]
![featureCounts output][3]
[1]: https://ibb.co/19sv9WV
[2]: https://ibb.co/0cxmB8w
[3]: https://ibb.co/hWmxq8s ...
written 22 days ago by
ooluwayiose • 0
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... The is smallRNA-seq data.
My apologies about the images. here are the links to the three images now using googledrive image hoster.
[.gtf][1] [mapped.sorted.bam][2] [featureCounts snapshot][3]
[1]: https://drive.google.com/file/d/1N01yy2w0eBJV9Wc9MXa89aISXA7sm_yp/view?usp=sharing
[2]: https ...
written 22 days ago by
ooluwayiose • 0
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... Hey folks, I'm new with RNAseq analysis and would appreciate your assistance in figuring this out.
I have single end reads from RNAseq data with the goal of profiling all available sncRNAs in the tissue (n = 96 samples). Post-trimming Fastqc distribution ranged between 16 - 50nt. Here are my steps: ...
written 22 days ago by
ooluwayiose • 0
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