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blast
•
reset
0
votes
0
replies
666
views
Visualize blastx output in R
blast
2.9 years ago
kvigil
• 0
1
vote
2
replies
1.9k
views
blastn for selected database and/or organism
blast
blastsequences
updated 7.7 years ago by
James W. MacDonald
68k • written 7.7 years ago by
aush
▴ 40
0
votes
0
replies
1.3k
views
batch blast matrix of protein sequences from R
R
blast
blastsequences
protein
8.0 years ago
andres.susrud
• 0
1
vote
2
replies
2.8k
views
blastSequences queries failing due to BLAST switch to https?
annotate
blastSequences
BLAST
https
updated 9.3 years ago by
Martin Morgan
25k • written 9.3 years ago by
ariel.hecht
• 0
3
votes
8
replies
10k
views
Which package to run blast
blast
updated 9.4 years ago by
Malcolm Cook
★ 1.6k • written 9.4 years ago by
biomiha
▴ 20
0
votes
0
replies
1.2k
views
After mapping one Sanger sequence read (about 900bp) to hg19 using blastn, How can I get variants presented as reference-based position and base ch…
Biostrings
blast
variantannotation
9.4 years ago
li lilingdu
▴ 450
0
votes
1
reply
2.2k
views
Primer-blast with bioconductor packages
primer
blast
updated 9.7 years ago by
Hervé Pagès
16k • written 9.7 years ago by
Vinicius Henrique da Silva
▴ 40
0
votes
5
replies
7.4k
views
Blastp - through R
blast
R
9.9 years ago
maahpishanu
• 0
4
votes
13
replies
6.1k
views
How to create an output file with sequence ID's from multiple BLAST result using blastSequences in "Biostrings"
annotation
blast
biostrings
updated 10.5 years ago by
Martin Morgan
25k • written 10.5 years ago by
Mathilde
• 0
2
votes
2
replies
2.4k
views
BLAST export library 'annotate'
blast
annotate
biostrings
export
fasta
11.2 years ago
b.stielow
• 0
4
votes
3
replies
5.8k
views
Use R/Bioconductor to match BLAST hits to GO terms?
GO
BLAST
annotation
updated 11.3 years ago by
Marc Carlson
★ 7.2k • written 11.3 years ago by
Jon Bråte
▴ 270
11 results • Page
1 of 1
Recent ...
Replies
Comment: Joining different datasets and analyzing using the group-specific condition effe
by
James W. MacDonald
68k
There is an example of how you can do this in the [DESeq vignette][1]. An alternative would be to fit a linear mixed model using the `vari…
Comment: Joining different datasets and analyzing using the group-specific condition effe
by
jason.chai
• 0
@mikelove Could I please ask if a similar method would work my set of samples? I have 255 samples which have been generated from 76 subject…
Comment: Clarification on counting in Rsubread (featureCounts)
by
Luca
• 0
Thanks to both of you for your helpful suggestions. The counting was already strand-specific at both the exon and gene levels. I resolved …
Comment: Clarification on counting in Rsubread (featureCounts)
by
Gordon Smyth
53k
Have you told featureCounts to do strand-specific counting? As pointed out by Frances Turner, you can lose reads if they overlap the gene …
Answer: Clarification on counting in Rsubread (featureCounts)
by
Frances Turner
▴ 20
You should look at the summary files produced by feature counts. This gives a breakdown of what happened to reads that were not assigned. Y…
Votes
Answer: Clarification on counting in Rsubread (featureCounts)
Comment: Clarification on counting in Rsubread (featureCounts)
C: ControlGenes/ housekeeping genes Deseq2
Answer: Clarification on counting in Rsubread (featureCounts)
C: RNA-Seq analysis with Limma/edgeR, time course experiment, aberrant results
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James W. MacDonald
68k
Great Question
to
fl
▴ 20
Popular Question
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Lluís Revilla Sancho
▴ 760
Popular Question
to
Gordon Smyth
53k
Popular Question
to
Aleena_Ensembl
▴ 30
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