Latest
Open
Jobs
Tutorials
Tags
About
FAQ
Community
Planet
New Post
Log In
New Post
Latest
Open
News
Jobs
Tutorials
Forum
Tags
Planet
Users
Log In
Sign Up
About
Limit : all time
all time
today
this week
this month
this year
121,963 results • Page
205 of 2440
Sort: Rank
Rank
Views
Votes
Replies
0
votes
0
replies
601
views
Any way to predict hormone biosynthesis pathways in understudied organisms?
genomics
orthologs
biosynthesis-pathway
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
Mark
▴ 60
2
votes
4
replies
1.1k
views
Refseq annotation | Populus trichocarpa
R
RNA-seq
plants
Refseq
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
P
• 0
1
vote
1
reply
737
views
Read Counts from BAM file
bam
samtools
qualimap
readcount
updated 2.0 years ago by
ATpoint
89k • written 2.0 years ago by
Smriti
▴ 40
10
votes
8
replies
2.1k
views
Adding a control sample to bulk RNA-seq
RNA-seq
2.0 years ago by
Chris
▴ 360
19
votes
15
replies
8.8k
views
Forum:
What is the amount of sequencing data produced annually?
data
research
sequencing
updated 16 months ago by
Mohamed
• 0 • written 2.0 years ago by
vincenthus
▴ 70
0
votes
2
replies
839
views
Is it okay to just average the log2FC values across different cell types in pseudobulk scRNA-seq data?
scrna-seq
rna-seq
log2fc
2.0 years ago by
JLee
• 0
3
votes
3
replies
1.4k
views
VDJ reconstitution from 3' 10x genomics platforms
VDJ
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
gal.dadi
▴ 10
0
votes
1
reply
948
views
Identify parent of each read in a GAF
gaf
vgteam
vg
updated 2.0 years ago by
Jordan M Eizenga
▴ 760 • written 2.0 years ago by
cfourps
▴ 10
0
votes
3
replies
1.2k
views
Errors while trying to run Scenic
Scenic
updated 2.0 years ago by
GenoMax
154k • written 2.0 years ago by
Stavroula
• 0
0
votes
3
replies
1.1k
views
How to find target genes From RNA seq data?
Cotton
DGE
RNA-seq
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
Fizzah
▴ 30
3
votes
3
replies
2.9k
views
STAR error EXITING because of FATAL ERROR: failed reading from temporary file
STAR
RNA-seq
updated 13 months ago by
FatihSarigol
▴ 260 • written 2.0 years ago by
erik.burchard
▴ 30
2
votes
3
replies
3.2k
views
Is there an easy to modify the subplot titles in DimPlot (Seurat)?
scRNA-seq
patchwork
DimPlot
Seurat
updated 2.0 years ago by
Nicolas Rosewick
11k • written 2.0 years ago by
alwayshope
▴ 40
0
votes
0
replies
549
views
News:
Course: Data Manipulation and Visualisation with Python
Python
Data-Visualization
Data-Manipulation
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
Physalia-courses
★ 2.6k
0
votes
1
reply
1.1k
views
VCF QUAL field for multiple samples
variants
VCF
updated 2.0 years ago by
DBScan
▴ 530 • written 2.1 years ago by
Ron
• 0
0
votes
3
replies
1.3k
views
CNV calling
CNV
NGS
Variant-Calling
updated 2.0 years ago by
Zhenyu Zhang
★ 1.3k • written 2.7 years ago by
adarsh
▴ 60
2
votes
1
reply
1.0k
views
bedGraphToBigWig: Missing Genome Coordinates
bamtobed
bed
2.0 years ago by
RelativeOptics
▴ 40
0
votes
0
replies
619
views
maftools - median survival time doesn't match plot
R
survival
maftools
K-M
2.0 years ago by
BioGuy
• 0
6
votes
8
replies
2.0k
views
Find potential important genes from bulk-RNA seq experiment
RNA-seq
2.0 years ago by
Chris
▴ 360
0
votes
1
reply
1.1k
views
vg rna pantranscriptome
rna
vg
updated 2.0 years ago by
Jordan M Eizenga
▴ 760 • written 2.0 years ago by
z
• 0
0
votes
0
replies
839
views
Genetic distance in cM from VCF of non-reference species to run Beagle
plink
beagle
vcf
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
AndrMod
• 0
1
vote
4
replies
2.9k
views
ConsensusClusterPlus: How to extract most contributing features for each cluster
R
consensusclusterplus
updated 2.0 years ago by
LChart
5.1k • written 4.6 years ago by
komal.rathi
★ 4.1k
1
vote
4
replies
1.1k
views
rRNA filtering from human RNA-seq data
rRNA
RNA-seq
2.0 years ago by
deniz
▴ 10
0
votes
5
replies
2.0k
views
manhattan plot with vcf information
R
manhattan
vcf
updated 2.0 years ago by
dthorbur
★ 3.1k • written 2.0 years ago by
sooni
▴ 20
6
votes
1
reply
832
views
How to retrieve sample informations from given ID from Sequence Read Archives?
eutils
SRA
updated 22 months ago by
Ram
45k • written 2.0 years ago by
DareDevil
★ 4.4k
2
votes
8
replies
4.3k
views
Read block operation failed with BAM file
bgzip
samtools
bam
pysam
htslib
updated 2.0 years ago by
John Marshall
3.1k • written 2.0 years ago by
Alex Reynolds
36k
0
votes
0
replies
846
views
after gatk VariantAnnotator -V *_com_norm.vcf -A AlleleFraction -O *_norm_AB.vcf There "nan,nan" or "nan" in my vcf file
gatk
AlleleFraction
VariantAnnotator
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
zhuo
• 0
2
votes
0
replies
906
views
the dispersion estimation of edgeR and DESeq2
estimation
dipersion
edgeR
DESeq2
2.0 years ago by
tommy
▴ 40
6
votes
3
replies
1.4k
views
Create 10,000bp windows for a SNP file and assign each SNP to its respective window
genome
snp
vcf
updated 2.0 years ago by
Alex Reynolds
36k • written 2.0 years ago by
nitinra
▴ 50
1
vote
3
replies
1.3k
views
Fastqc loop
fastQC
r
RNA-seq
2.0 years ago by
camillab.
▴ 160
0
votes
2
replies
1.5k
views
News:
The Practice of RADseq: Population Genomics Analysis with Stacks (RADS02) Early bird deadline approaching - 20th September
population-genomics
radseq
stacks
updated 2.0 years ago by
Dave Carlson
★ 2.2k • written 2.0 years ago by
oliverhooker
▴ 110
2
votes
3
replies
1.4k
views
Genewise output help
genewise
updated 2.0 years ago by
Jean-Karim Heriche
27k • written 2.0 years ago by
lorenzoedg
• 0
3
votes
1
reply
1.6k
views
Add samples IDs to Seurat object when integrating different samples to do differential expression analysis
scRNA-seq
Seurat
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
Sara
▴ 280
3
votes
1
reply
965
views
Best Tools and Practices for CNV Variant Calling in WES Data
CNV
WES
updated 2.0 years ago by
Pierre Lindenbaum
166k • written 2.0 years ago by
Nadav
▴ 20
0
votes
2
replies
720
views
Identify genes for mapped reads with combined human-7HPV genome index
star
samtools
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
r.j.lock
• 0
0
votes
0
replies
565
views
News:
Course - GLMMs in R
GLMM
Mixed-Models
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
Physalia-courses
★ 2.6k
0
votes
0
replies
623
views
News:
Introduction to Nextflow (2 seats left)
Nextflow
Workflow
Reproducibility
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
Physalia-courses
★ 2.6k
1
vote
2
replies
1.9k
views
Error executing process > consensus_classification in NanoCLUST
Nanoclust
Nanoporesequence
16SrRNA
updated 2.0 years ago by
Ram
45k • written 3.6 years ago by
yeshirata
▴ 20
3
votes
4
replies
1.5k
views
Generate a fraction of immune cell between two condition from single cell RNAseq
single-cell
2.0 years ago by
synat.keam
▴ 120
4
votes
3
replies
1.3k
views
Batch effect consideration (re-seq the same sample twice)
RNA-seq
batch-effect
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
jkim
▴ 220
3
votes
2
replies
987
views
Scanning for ultra-hot topics in science via pubmed, or using other tools
growth
pubmed
2.0 years ago by
LauferVA
4.8k
0
votes
0
replies
659
views
Data for pathview() (KEGG Pathway Map) after EdgeR
EdgeR
LogFC
pathview
KEGG
2.0 years ago by
Ann
▴ 40
75
votes
19
replies
6.0k
views
11 follow
Blog:
A list of technical advantages of Snakemake over Nextflow | Cloud solution for Snakemake
Snakemake
updated 19 months ago by
LauferVA
4.8k • written 2.1 years ago by
Kenny
▴ 30
7
votes
10
replies
2.8k
views
Batch effect normalization
RNA-seq
batch-effect
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
Smriti
▴ 40
1
vote
3
replies
1.4k
views
How to convert between UniRef50 to EC/enzyme number?
Uniref
conversion
uniprot
enzyme
updated 2.0 years ago by
Elisabeth Gasteiger
★ 2.4k • written 2.0 years ago by
O.rka
▴ 750
0
votes
0
replies
699
views
GTF/Reference genome adjustments? Gene-based differential expression analysis of genetically modified mouse line
RNA-seq
DGE
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
alex
• 0
2
votes
2
replies
1.2k
views
Filter VCF File by VCF Format Variants
SnpSift
Plink
Bcftools
updated 2.0 years ago by
chrchang523
11k • written 2.0 years ago by
another_bioinformatician
• 0
0
votes
0
replies
519
views
cosine simialrity of mutation signature analysis
similarity
Mutational
analysis
signature
cosine
2.0 years ago by
probioquestioner
• 0
1
vote
1
reply
796
views
Significance testing of top vs. random SNPs
SNPs
significance
variance
statistical
updated 2.0 years ago by
dthorbur
★ 3.1k • written 2.0 years ago by
am29
▴ 60
5
votes
2
replies
1.8k
views
Recommended way to normalize SmartSeq2 gene expression matrix to better match 10X expression data
rna-seq
smartseq2
r
updated 23 months ago by
yhdist
▴ 70 • written 2.0 years ago by
Cookin
▴ 10
0
votes
0
replies
559
views
Why we are using filtering >0 for up and <0 for down after TopTags() to extract de genes ids?
EdgeR
logfc
DEG
2.0 years ago by
Ann
▴ 40
121,963 results • Page
205 of 2440
Recent Votes
alternate allele frequency and minor allele frequency
Calculating minor allele frequency for GnomAD VCF file
Hiring FT Remote Nextflow engineer to build ML workflows for cancer genomics
Answer: Gene expression equivalent of polygenic risk score ?
A: TRF output to .gff file
A: GATK ASEReadCounter: Downstream analysis for identifying allele specific express
Comment: Differences between published differential gene expression results and own analy
Recent Locations •
All
Finland,
10 minutes ago
Hong Kong,
14 minutes ago
Japan,
35 minutes ago
UCLA,
36 minutes ago
Singapore,
1 hour ago
United States,
1 hour ago
United States,
1 hour ago
Recent Awards •
All
Popular Question
to
a615ebfb
▴ 60
Popular Question
to
predeus
★ 2.1k
Popular Question
to
raquel
• 0
Popular Question
to
Jeremy Leipzig
23k
Teacher
to
GouthamAtla
12k
Popular Question
to
sacha
★ 2.5k
Popular Question
to
Ann
▴ 40
Recent Replies
Comment: Differences between published differential gene expression results and own analy
by
dsull
★ 7.7k
There are many ways to do normalization and one of the correct ways is simply to plug raw counts into deseq2 (the math that deseq2 uses to …
Comment: tximport error (medianLengthOverIsoform)
by
rfran010
★ 1.6k
Is it the version number in your data? e.g. ENST00000415118.1 vs ENST00000415118 could be causing the mismatch?
Comment: Differences between published differential gene expression results and own analy
by
vernonlim98
• 0
So is there any correct way for normalisation? I know limma recommends CPM via limma-voom and DESeq2 just takes in raw counts and does thei…
Comment: Gene expression equivalent of polygenic risk score ?
by
Picasa
▴ 690
Thanks a lot for your answer. I will check the paper.
Comment: Differences between published differential gene expression results and own analy
by
dsull
★ 7.7k
If those logFCs are different, then that's a normalization issue. The logFC is straight forward arithmetic (it's simply dividing mean of […
Comment: Differences between published differential gene expression results and own analy
by
vernonlim98
• 0
Thanks both for your input. It got me to look at the published methodologies more closely, and you guys were right. One paper that I was re…
Comment: Differences between published differential gene expression results and own analy
by
vernonlim98
• 0
Yes it does not match at all, and those genes that are common in both analysis results have very different logFC and p values
Comment: Errors with RSEM/bowtie2
by
Olivia
• 0
I am not sure what you mean by this, but I believe that is what I did. With Trinity, I matched all the paired reads together, so they shoul…
Answer: Gene expression equivalent of polygenic risk score ?
by
GouthamAtla
12k
I don't think something exists out of the box. With variants, we have a 'weight' for each variant on disease risk (obtained through large s…
Comment: ESTIMATE (Estimation of STromal and Immune cells in MAlignant Tumor tissues usin
by
Ben
• 0
write.table(df1, "df1.txt", sep = "\t", row.names = T, col.names = T, quote = FALSE)
Comment: Errors with RSEM/bowtie2
by
GenoMax
154k
That is good confirmation. Bacl to the error message. > I don't know how to fix this, given that I already did the trimming steps. DId yo…
Comment: Differences between published differential gene expression results and own analy
by
dsull
★ 7.7k
Honestly, those things shouldn't result in a considerable discrepancy. The largest difference will come from the post-processing & analysi…
Answer: Differences between published differential gene expression results and own analy
by
Ales
▴ 50
I second the comment about comparing the top 100 genes - if you see vastly different results, I would lean closer to examining protocols th…
Answer: Help interpreting BLASTn results and phylogenetic tree for genetics practical
by
Mensur Dlakic
★ 30k
I think what you are asking involves too much work for anyone to explain it in granular detail. But who knows, maybe there is a good soul o…
Answer: Differences between published differential gene expression results and own analy
by
yura.grabovska
▴ 830
When you say vastly different, what do you mean exactly? Does your top 100 up/down not match theirs at all?
Traffic: 2905 users visited in the last hour
Content
Search
Users
Tags
Badges
Help
About
FAQ
Access
RSS
API
Stats
Use of this site constitutes acceptance of our
User Agreement and Privacy Policy
.
Powered by the
version 2.3.6