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SNPs
•
reset
1
vote
2
replies
3.1k
views
Any tool to calculate Fst on haploid data?
snps
VCF
updated 2.8 years ago by
Arafat
• 0 • written 8.0 years ago by
rkdonthu
▴ 10
0
votes
1
reply
774
views
Error running hierClust
hierClust
R
SNPs
clustering
updated 2.9 years ago by
James W. MacDonald
68k • written 2.9 years ago by
sekhwal
• 0
0
votes
0
replies
1.2k
views
How to extract genomic positions of SNPs using snp-sites or using any R package?
SNPs
5.9 years ago
pltbiotech_tkarthi
• 0
0
votes
0
replies
1.4k
views
vcf to venn diagram
snps
vcf
venn diagram
ggplot2
6.1 years ago
mictadlo
▴ 10
0
votes
6
replies
1.5k
views
Physical position to gene positions
bioconductor
molecular biology
snps
updated 6.2 years ago by
James W. MacDonald
68k • written 6.2 years ago by
jebreen20
• 0
2
votes
5
replies
2.9k
views
Error with R package motifbreakR while trying to read a vcf file with snps.from.file function
motifbreakR
vcf
snps
motif analysis
updated 6.6 years ago by
Valerie Obenchain
★ 6.8k • written 6.6 years ago by
svlachavas
▴ 840
3
votes
4
replies
1.7k
views
No annotation for single SNPs
variantannotation
SNPs
txdb.hsapiens.ucsc.hg19.knowngene
ucsc
updated 7.6 years ago by
Valerie Obenchain
★ 6.8k • written 7.6 years ago by
Lna
• 0
0
votes
1
reply
1.6k
views
Extract SNPs and INDELs
hsapiens
snps
indels
updated 9.2 years ago by
Hervé Pagès
16k • written 9.2 years ago by
kredens
• 0
0
votes
1
reply
1.8k
views
Counting SNPs where ambiguity codes represent heterozygosity.
Biostrings
SNPs
alignment
updated 9.6 years ago by
Hervé Pagès
16k • written 9.6 years ago by
ben.ward
▴ 30
0
votes
4
replies
2.1k
views
Marking and annotating several SNPs on Ideogram track by Gviz package.
gviz
ideogram
snps
updated 10.0 years ago by
florian.hahne@novartis.com
★ 1.6k • written 10.0 years ago by
vnyirongo
• 0
4
votes
3
replies
2.5k
views
Overlap the snps
overlap
snps
granges
iranges
updated 10.3 years ago by
Michael Lawrence
★ 11k • written 10.4 years ago by
anastasiya-terskih
▴ 10
11 results • Page
1 of 1
Recent ...
Replies
Comment: accounting for vs. removing batch effects with DESeq2 in RNAseq analysis
by
Blair
• 0
@[Sprunki][1] wrote: Please read the vignette and think about adhering to the author's best practice, which discusses batch impacts. [1…
Comment: error in ChAMP loading file
by
81becky
• 0
hi Giulia, it sounds like you're facing a frustating issue with your chAMP import. One common suggestion is to double-check your CSV fomat…
Answer: DESeq2 adujsted p-value cutoff seemingly not working
by
James W. MacDonald
68k
From `?results' ``` On p-values: By default, independent filtering is performed to select a set of genes for multiple tes…
Comment: Issue with assigning transcript IDs to reads when using summarizeOverlaps(mode =
by
SofieK
• 0
Thank you, I will try this and see.
Comment: DiffBind - question on the use of filtered or unfiltered input data
by
deltaexploitss
• 0
Data input is the adding of data into a computer. This can take place through an input device such as a keyboard. A user inputs data, which…
Votes
A: Effect of lfcThreshold on p-value in DESeq2
Answer: What benchmark should I use for setting the EdgeR filterByExpr min.count paramet
What benchmark should I use for setting the EdgeR filterByExpr min.count parameter?
Answer: Issue with assigning transcript IDs to reads when using summarizeOverlaps(mode =
Comment: Unused arguments error without used arguments in GSVA?
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