User: jnoble333

gravatar for jnoble333
jnoble33320
Reputation:
20
Status:
New User
Location:
Last seen:
1 year ago
Joined:
1 year, 10 months ago
Email:
j********@ufl.edu

Posts by jnoble333

<prev • 9 results • page 1 of 1 • next >
0
votes
1
answer
349
views
1
answers
Answer: A: Prediction of TSS from tuxedo pipeline
... I think in the case of a + strand transcript your TSS would be the leftmost position in exon 1 of the transcripts in the gtf file generated by cufflinks. ...
written 13 months ago by jnoble33320
0
votes
1
answer
341
views
1
answers
Answer: A: Best splicing variant
... What do you mean by best? Would it be the most highly expressed variant? It really comes down to what question you are trying to answer with your data set. ...
written 13 months ago by jnoble33320
0
votes
2
answers
916
views
2
answers
Comment: C: Mapping RNA-Seq data on genome from another species
... That is the post I went by. That threshold works for my dataset for the most part because I have a lot of reads. I'd say try different values and see how your results differ. ...
written 13 months ago by jnoble33320
1
vote
2
answers
916
views
2
answers
Answer: A: Mapping RNA-Seq data on genome from another species
... Hi tlorin, I use STAR to do this frequently with the parameter --outFilterMismatchNmax 8. You can check the alignment percentage in the Log.final.out file and adjust your mismatch threshold accordingly. You may face the issue of reads aligning to a lot of different locations and can filer your bam ...
written 13 months ago by jnoble33320
0
votes
3
answers
728
views
3
answers
Answer: A: RNA-seq analysis with quantitative traits
... Hey Javier, There isn't much work that has been done regressing the transcriptome onto quantitative phenotypic traits. I am attempting to do this as a component of my thesis. Here's a little insight I can provide: Differential expression packages like EdgeR, DeSeq, et al. will not be suitable for ...
written 13 months ago by jnoble33320
0
votes
0
answers
736
views
0
answers
Comment: C: Cuffcompare combined.gtf output contains only exons
... It follows the formate of transcript, exon, exon.... transcript (repeat). It definitely isn't the same as a reference annotation. It does not include a gene field. ...
written 22 months ago by jnoble33320
0
votes
0
answers
736
views
0
answers
Comment: C: Cuffcompare combined.gtf output contains only exons
... I was expecting the merge and compare output gtf's to follow the same format as a cufflinks output gtf, similar to the input gtf files. I do see your point about the redundancy though. My transcriptome assembly was genome guided. I'll give gtf2gtf a try to get the transcript lines added. Thanks! ...
written 22 months ago by jnoble33320
0
votes
0
answers
736
views
0
answers
Comment: A: Cuffcompare combined.gtf output contains only exons
... This also occurs when using cuffmerge on all of the gtf files. ...
written 22 months ago by jnoble33320
2
votes
0
answers
736
views
0
answers
Cuffcompare combined.gtf output contains only exons
... Hello, I have gtf files from a pasa run for 96 samples. My intention was to run cuffcompare on all 96 to produce a master gtf file for all samples. Instead when I run it my results contain only transfrags annotated as "exon". My organism is P. trichocarpa. I am calling cuff compare via: cuffcompar ...
rna-seq written 22 months ago by jnoble33320

Latest awards to jnoble333

No awards yet. Soon to come :-)

Help
Access

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.
Powered by Biostar version 2.3.0
Traffic: 1360 users visited in the last hour