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121,793 results • Page
577 of 2436
Sort: Rank
Rank
Views
Votes
Replies
0
votes
0
replies
693
views
How does PLINK work?
PLINK
logisticRegression
GWAS
4.0 years ago by
L_to_the_m
▴ 10
2
votes
1
reply
903
views
How to create a new file containing contigs of a certain length from another contigs file
fasta
minia
updated 2.4 years ago by
Ram
45k • written 4.0 years ago by
Ashi
▴ 20
0
votes
0
replies
591
views
predixcan error
vcf
predixcan
updated 2.4 years ago by
Ram
45k • written 4.0 years ago by
rheab1230
▴ 150
0
votes
0
replies
574
views
News:
Last call for our online training course "Data visualization with Python"
Python
4.0 years ago by
Physalia-courses
★ 2.6k
0
votes
0
replies
792
views
News:
Online training - Genomic Prediction
Genomics
4.0 years ago by
Physalia-courses
★ 2.6k
1
vote
2
replies
1.1k
views
Plotting chromosomes and target capture baits
plotting
target_capture
Hyb-Seq
R
4.0 years ago by
Begonia_pavonina
▴ 210
1
vote
1
reply
750
views
Problem of visualizing results of PPI network
analyst
network
Cytoscape
updated 4.0 years ago by
Scooter
▴ 310 • written 4.0 years ago by
bookorg
▴ 20
0
votes
0
replies
635
views
Cutoffs for Proxy Identification: D' and R^2
plink2
4.0 years ago by
dec986
▴ 380
5
votes
15
replies
4.2k
views
7 follow
DESeq2 normalization - Found Difference in values when calculated manually
DESeq2
normalization
difference
4.0 years ago by
Sandhiya
▴ 20
0
votes
1
reply
953
views
getting different value list from GATK gc content and CANOES
CNV
GATK
CANOES
updated 4.0 years ago by
nicholasopoku24
• 0 • written 6.1 years ago by
a.tavallaie
• 0
0
votes
1
reply
842
views
How is better perform the analyze the somatic mutations? (the mutations of my interest gene)
somatic
VCF
annotation
Oncoplot
updated 4.0 years ago by
German.M.Demidov
★ 3.0k • written 4.0 years ago by
Sonia
• 0
1
vote
1
reply
921
views
How to load user-defined genome in IGV-webapp
IGV-WEBAPP
IGV
igv
updated 4.0 years ago by
GenoMax
153k • written 4.0 years ago by
Frieda
▴ 60
2
votes
6
replies
1.7k
views
Statistics on RNAseq data
on
Statistics
data
RNAseq
updated 4.0 years ago by
hafiz.talhamalik
▴ 350 • written 4.0 years ago by
margot.27.muller
▴ 30
0
votes
0
replies
856
views
Job:
Bioinformatics position at the spatial transcriptomics facility of Lyon (France)
single-cell
spatial-transcriptomics
updated 2.7 years ago by
Ram
45k • written 4.0 years ago by
yad.ghavi-helm
• 0
1
vote
2
replies
1.4k
views
Error when opening CEL files in python
python
updated 4.0 years ago by
Shred
★ 1.6k • written 4.0 years ago by
Paula
• 0
1
vote
2
replies
1.2k
views
Variant Allele Frequency
Cancer
updated 4.0 years ago by
German.M.Demidov
★ 3.0k • written 4.0 years ago by
adarsh
▴ 60
0
votes
4
replies
2.1k
views
Find NLS in list of proteins.
localization
nuclear
signal
updated 4.0 years ago by
Joe
22k • written 4.0 years ago by
qmarulfiz
▴ 60
1
vote
4
replies
1.5k
views
Multiple hypothesis correction with multiple gene sets
gene-set-enrichment
GO
multiple-test-correction
GO-enrichment
updated 4.0 years ago by
Gordon Smyth
★ 8.3k • written 4.0 years ago by
suragnair
• 0
0
votes
2
replies
1.6k
views
HRD score LST?
cnv
updated 4.0 years ago by
e.rempel
★ 1.1k • written 4.9 years ago by
vctrm67
▴ 90
2
votes
2
replies
1.0k
views
Sudden coverage increase in IGV
IGV
sequencing
coverage
updated 4.0 years ago by
GenomeXP
• 0 • written 4.0 years ago by
mrs97
• 0
1
vote
2
replies
1.2k
views
How to get all genes and their annotations within a LD block?
GWAS
haplotype
SNPs
genome
wheat
Ensembl
4.0 years ago by
b.g.tamang
▴ 20
0
votes
2
replies
3.6k
views
From Bismark to methylkit, which file is better to use?
Bisulfite sequencing
Bismark
methylkit
updated 11 months ago by
Lluís R.
★ 1.2k • written 4.7 years ago by
iraia.munoa
▴ 130
0
votes
1
reply
698
views
Regarding functional similarity analysis by GOSemSim package of R
GOSemSim
updated 4.0 years ago by
Jean-Karim Heriche
27k • written 4.0 years ago by
jyotsnap
• 0
0
votes
2
replies
1.8k
views
trinity run_DE_analysis.pl Failed with error: ‘package ‘limma’ could not be loaded’
run_DE_analysis.pl
trinity
4.0 years ago by
Rajesh
▴ 10
2
votes
4
replies
2.2k
views
Any suggestion on metagenomics pipelines for processing shotgun metagenomics whole genome sequencing samples?
metagenomics_pipelines
WGS
shotgun_metagenomics
antimicrobial_resistance
4.0 years ago by
eli_bayat
▴ 100
1
vote
3
replies
2.0k
views
WGCNA
Installation
WGCNA
updated 4.0 years ago by
tothepoint
▴ 940 • written 4.0 years ago by
Nithya
▴ 10
0
votes
0
replies
628
views
Neighboring index between clusters on a map
connectivity
clustering
4.0 years ago by
thejustpark
▴ 80
2
votes
3
replies
2.3k
views
GIAB Benchmark (High Confidence) Bed Filles
SNPS
GIAB
variants
updated 4.0 years ago by
desouzareis.r
▴ 290 • written 4.0 years ago by
bioinformatics2020
▴ 840
8
votes
10
replies
4.9k
views
UCSC knownCanonical hg19 vs. hg38
genome
UCSC
hg19
hg38
canonical
updated 4.0 years ago by
Luis Nassar
▴ 670 • written 4.5 years ago by
Sanjar
▴ 150
1
vote
2
replies
1.3k
views
Tool:
krust: a k-mer counter in Rust using the rust-bio and rayon crates
Rust
kmer-counting
fasta
kmer
updated 4.0 years ago by
Istvan Albert
103k • written 4.0 years ago by
jlivesey
▴ 10
0
votes
2
replies
929
views
Can i estimate the hormone-receptor binding affinity ?
hormone
updated 2.4 years ago by
Ram
45k • written 4.0 years ago by
dmorfologia3
• 0
1
vote
2
replies
980
views
Edit vcf file 0|0 to 0
linux
vcf
genomics
edit
4.0 years ago by
zoubda
• 0
2
votes
4
replies
1.9k
views
Problem with BAM file headers
SAM
GATK
BAM
4.0 years ago by
Lucas
• 0
0
votes
0
replies
816
views
Weird PCA plot using WGCNA results
cancer
PCA
expression
WGCNA
plot
4.0 years ago by
seta
★ 1.9k
0
votes
1
reply
1.1k
views
List of codon numbers in a panel
browser
codon
list
ucsc
genome
updated 4.0 years ago by
Luis Nassar
▴ 670 • written 4.4 years ago by
ines
• 0
2
votes
6
replies
4.2k
views
GenomeInfoDb (in R) and UCSC just stopped co-operating in terms of mm10
seqlevels
seqlevelsStyle
GenomeInfoDnb
R
UCSC
updated 4.0 years ago by
Alex Reynolds
36k • written 4.2 years ago by
sami.kilpinen
▴ 20
1
vote
3
replies
2.4k
views
clusterProfiler: number of GO terms in results
clusterProfiler
4.0 years ago by
thistleq777
▴ 10
2
votes
2
replies
1.8k
views
PRSice-2 without Ref SNP ID
Catalog
PGS
PRSice
PRS
4.0 years ago by
Jenish
▴ 20
0
votes
0
replies
523
views
How to do virtual screening and determining pharmacore
QSAR
Docking
4.0 years ago by
ashwing.kofficial
▴ 10
8
votes
3
replies
4.1k
views
Please help me understand linkage disequilibrium
LD
Linkage
disequilibrium
SNP
updated 4.0 years ago by
i.sudbery
22k • written 4.0 years ago by
?
▴ 60
0
votes
0
replies
1.2k
views
Job:
PhD student for a computational breast cancer research project
Cancer
PhD
Omics
updated 2.5 years ago by
Ram
45k • written 4.0 years ago by
s.vosberg
• 0
1
vote
1
reply
2.1k
views
Ensembl VEP Docker: cannot write to FASTA lockfile
Ensembl
Docker
VEP
updated 4.0 years ago by
Emily
24k • written 4.0 years ago by
PimPolacko
• 0
0
votes
0
replies
716
views
How to show intermolecular forces between two chains within the same protein in Pymol
protein
python
pymol
antibody
antigen
4.0 years ago by
Lucy
• 0
2
votes
2
replies
1.5k
views
network analysis for microbial amplicon sequencing data
plot
Network
igraph
R
4.0 years ago by
Bioinfonext
▴ 470
0
votes
2
replies
1.6k
views
Unicycler and GNU parallel
Unicycler
parallel
4.0 years ago by
emma.a
▴ 130
0
votes
1
reply
3.0k
views
PROVEAN input script
python
provean
variant effect prediction
updated 4.0 years ago by
TongZhou
• 0 • written 8.0 years ago by
s_herrera
▴ 10
0
votes
0
replies
669
views
GREAT genome ontology top hits criteria?
bed
GREAT
gene-ontology
go
updated 2.5 years ago by
Ram
45k • written 4.0 years ago by
a_bis
▴ 40
0
votes
0
replies
662
views
Job:
Postdoctoral Scientist in Statistical Bioinformatics and Software Development, WEHI, Melbourne, Australia
Australia
4.0 years ago by
Gordon Smyth
★ 8.3k
0
votes
0
replies
793
views
GREAT difference between 'mouse phenotype' and 'mouse phenotype single KO'
bed
gene-ontology
GREAT
go
updated 2.5 years ago by
Ram
45k • written 4.0 years ago by
a_bis
▴ 40
0
votes
1
reply
945
views
Running htseq-count to "grab" long non coding gene_id names
lncRNA
htseq
updated 4.0 years ago by
GenoMax
153k • written 4.0 years ago by
dimitrischat
▴ 210
121,793 results • Page
577 of 2436
Recent Votes
Answer: How to account for solvent controls in DESeq2 when comparing follicular vs lutea
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Custom Selection of GO Terms or Pathways in EnrichR Output
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Answer: How to obtain a refFlat file for the Rat
by
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153k
Please don't ask the same question again in a new thread. This was answered a few weeks back: https://www.biostars.org/p/9613666/#9613671 …
Answer: Is a direct comparison of the number of up- and down-regulated genes meaningful?
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4.1k
Usually it is not very useful. The only situation where it makes sense to use is where you do a gradient treatment (e.g. 0M, 5M, 50M, et…
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No, don't rely on numbers. This can and is strongly influences by the sample size and noise, and by this power. Even at same sample size it…
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Hi, Did you figure this out? In my data some gene expressed in very low number of cells (less than 1% of total cells) appear as differentia…
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Comment: Is a direct comparison of the number of up- and down-regulated genes meaningful?
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153k
What do you mean by "directly compare"? Actual number of genes in the two groups don't have a special meaning. They will change based on …
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Samples for condition B were made into two different sets of libraries for batch 1 and 2. The person who did the experiment has left, so I …
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I would ignore the IgGs and only use it during peak calling. For the IP samples I would do https://www.biostars.org/p/413626/#414440
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CUT&Tag shares protocol similarities with ATAC-seq, so I'd recommend using RPGC normalization via DeepTools. You might also consider testin…
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15k
You generally can't correct for replicates in such a tiny experiment like this, so I'd drop that element. But yes, if you want to do an …
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This is the way
Answer: How to detect divergent domains in AlphaFold models (CDD/InterProscan not workin
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There isn't much beyond InterPro and CDD that would automatically detect divergent domains, as those databases already include almost all o…
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That's a good approach. Personally, I copy-paste text and then extract info from that text file - you can see how prohibitive it can be to …
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Good points. More alternatives with more permissive licenses - https://github.com/jmschrei/memesuite-lite - https://github.com/jmschrei/…
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Yes indeed if you just need the start of your DNAse protected fragment, use `--offset 1`
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