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121,962 results • Page
200 of 2440
Sort: Rank
Rank
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Votes
Replies
0
votes
2
replies
3.6k
views
Using infercnv R package
infercnv
r
Seurat
updated 24 months ago by
Ram
45k • written 3.0 years ago by
j.jacob1
• 0
0
votes
0
replies
448
views
CNVkit analysis with different average depths of control normals
CNV
CNVkit
24 months ago by
luna
• 0
1
vote
2
replies
710
views
The meaning of the analysis results when using a new metric in analysis
rna-seq
linear-regression
deseq2
24 months ago by
SH
• 0
9
votes
4
replies
17k
views
Running python script in slurm using conda environment
slurm
python
conda
updated 24 months ago by
filip.buric
▴ 10 • written 2.1 years ago by
sidrah.maryam
▴ 70
0
votes
4
replies
1.3k
views
Cloud Computing w.r.t. AWS, Google Cloud, Microsoft Azure
Google-Cloud
AWS
Azure
24 months ago by
Saurabh
• 0
3
votes
3
replies
4.0k
views
How to choose LiftOver chain file
hg38tohg19
picard
LiftOver
updated 24 months ago by
Giulio Genovese
▴ 630 • written 24 months ago by
ttom
▴ 230
0
votes
0
replies
814
views
Job:
Post-doctoral positions in computational biomedicine
data-science
biomedicine
machine-learning
updated 24 months ago by
Ram
45k • written 24 months ago by
pandey.gaurav
▴ 200
0
votes
1
reply
585
views
Syntenic Analysis
synteny
updated 24 months ago by
Ram
45k • written 24 months ago by
Farzana
• 0
0
votes
0
replies
510
views
scRNA seq vs scRNA seq for microbiome?
microbiome
scRNA
R
data
python
24 months ago by
Athena
• 0
0
votes
0
replies
400
views
Mapping C.Elegans protein onto Aminopeptidase P1 from Arabidopsis thaliana
AlphaFold
24 months ago by
Ethan
• 0
0
votes
1
reply
691
views
DESeq2 : standardising variation between treatments
rna-seq
deseq2
updated 2.0 years ago by
bk11
★ 3.1k • written 2.0 years ago by
ar14g12
▴ 10
1
vote
5
replies
1.9k
views
counting from a single BAM file with multiple samples
cell-barcode
RNA-seq
2.0 years ago by
dr-device
▴ 10
1
vote
1
reply
1.1k
views
Help with error velocyto
velocyto
24 months ago by
Chris
▴ 360
3
votes
26
replies
4.2k
views
6 follow
STAR Genome index Error
STAR
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
Prasanna
• 0
1
vote
3
replies
1.6k
views
pheatmap
pheatmap
heatmap
differential-expression
RNA-seq
updated 2.0 years ago by
bk11
★ 3.1k • written 2.0 years ago by
Sara
▴ 40
1
vote
2
replies
1.5k
views
Commands to do the following in BCFtools or recommendations for another tool
bcftools
vcf
updated 2.0 years ago by
barslmn
★ 2.4k • written 2.0 years ago by
ex_nihilo
• 0
0
votes
0
replies
593
views
InferCNV Step 8 Issues
InferCNV
2.0 years ago by
ccbb7aab4
▴ 20
0
votes
1
reply
645
views
Extract Loci based on the snps number
SNP
NGS
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
safiq713
▴ 10
2
votes
3
replies
1.4k
views
tximport error: vroom
tximport
2.0 years ago by
Maxine
▴ 50
6
votes
4
replies
2.6k
views
Kraken2 is falsely assigning Klebsiella
taxonomy
Kraken2
24 months ago by
SushiRoll
▴ 140
0
votes
0
replies
557
views
News:
Course: Seascape Genomics in R course
R
GEA
Seascape-Genomics
Adaptation-Genomics
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
Physalia-courses
★ 2.6k
1
vote
8
replies
2.7k
views
18S taxonomy assignment SILVA database formatting
assignTaxonomy
18S
dada2
SILVA
2.0 years ago by
mbuenner
• 0
2
votes
4
replies
1.3k
views
Finding sequences in unannotated genomes using reference coordinates
consensus
VCF
2.0 years ago by
Prangan
▴ 20
0
votes
0
replies
511
views
multi-population vcf filtering for population genomics analysis
Filtering
WGS
Genomics
Population
VCF
2.0 years ago by
qstefano
▴ 20
0
votes
2
replies
869
views
Error in checkFullRank(modelMatrix) :
DESeq2
updated 2.0 years ago by
Basti
★ 2.1k • written 2.0 years ago by
jabbari.parnian
▴ 30
2
votes
0
replies
948
views
Job:
Need help to setup a PGS pipeline
bim
plink
fam
bed
PGS
2.0 years ago by
Ben
▴ 10
28
votes
16
replies
34k
views
11 follow
How Do I Convert From Bed Format To Gff Format?
gff
galaxy
bed
updated 23 months ago by
Ram
45k • written 16.0 years ago by
Istvan Albert
103k
2
votes
1
reply
1.7k
views
tensorQTL interaction issue
genomics
eqtl
genetics
qtl
2.0 years ago by
Solal
▴ 10
0
votes
1
reply
855
views
Kimura% of calcDivergenceFromAlign output
repeatlandscape
repeatmasker
2.0 years ago by
睿紘
• 0
0
votes
5
replies
1.4k
views
Understanding mother and father alleles in VCF file
snp
vcf
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
c.
• 0
7
votes
13
replies
2.6k
views
Forum:
How do you validate and verify your pipeline's software updates?
Validation
Verification
Quality-Assurance
updated 23 months ago by
Ram
45k • written 2.0 years ago by
kieran
▴ 10
3
votes
3
replies
1.7k
views
Differentially Expressed Genes between two conditions (scRNA, single GEO dataset with multiple samples and no cell annotations)
scRNA-seq
RNA-Seq
Seurat
updated 2.0 years ago by
bk11
★ 3.1k • written 2.0 years ago by
prietto
▴ 10
0
votes
0
replies
427
views
Help on dendrimer building
dendrimer
gromacs
molecular-dynamics
2.0 years ago by
v.berriosfarias
▴ 140
0
votes
0
replies
645
views
Adding custom annotation to VEP output VCF
bcftools
VEP
vcf
2.0 years ago by
avelarbio46
▴ 30
0
votes
9
replies
1.5k
views
Deseq2 error
R
deseq2
2.0 years ago by
sgadila
• 0
0
votes
3
replies
1.0k
views
WGCNA plotEigengeneNetworks error (coercion to logical)
WGCNA
plotEigengeneNetworks
RNA-seq
RStudio
updated 24 months ago by
Ram
45k • written 2.0 years ago by
Victor
• 0
0
votes
0
replies
592
views
News:
Course :MACHINE LEARNING - A HANDS-ON INTRODUCTION IN R
R
Statistical-Learning
Omics
Machine-Learning
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
Physalia-courses
★ 2.6k
3
votes
2
replies
1.1k
views
Feature plot not applicable for RunTSNE object in seurat?
harmony
Seurat
single-cell
2.0 years ago by
synat.keam
▴ 120
2
votes
2
replies
1.5k
views
Get discordant read pairs from bam
samtools
NGS
updated 2.0 years ago by
benformatics
4.2k • written 2.0 years ago by
paulaotero.sanchez
• 0
0
votes
2
replies
1.5k
views
Low percentage of 'Fraction Antibody Reads Usable' in Feature Barcode Cell Ranger output
scCITE-seq
feature-barcode
10x
scRNA-seq
updated 5 weeks ago by
octopuslegs11
▴ 10 • written 2.5 years ago by
rocio.castellanos
• 0
3
votes
6
replies
2.0k
views
Exporting DEGs obtained from DESeq2
R
Deseq2
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
camillab.
▴ 160
2
votes
2
replies
957
views
I need help with univariate logistic regression in a set of microarray data
R
microarray
odds-ratio
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
Pooria
• 0
0
votes
20
replies
3.1k
views
Rockhoppper - Suspiciously low percentage of perfectly aligned reads
Rockhopper
RNA-seq
23 months ago by
langziv
▴ 70
0
votes
0
replies
461
views
Adding means cluster from fviz_cluster on the PCA
fviz_cluster
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
ayaosama2111
▴ 10
0
votes
0
replies
624
views
DMRcate design
R
Epigenetics
EPIC
DMRcate
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
Bioinfonext
▴ 480
4
votes
5
replies
1.9k
views
Snakemake alignment script
snakemake
alignment
24 months ago by
Begonia_pavonina
▴ 210
21
votes
7
replies
14k
views
Forum:
Bioinformatics short paper journal resource [software/webapps/database]
journal
software
webapp
updated 2.0 years ago by
Gennady Khvorykh
▴ 100 • written 9.5 years ago by
Sukhi Singh
11k
0
votes
1
reply
841
views
Determine kit used for library preparation for whole exome sequencing from fastq files
Agilent
NGS
library-preparation
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
Harinder
• 0
1
vote
1
reply
784
views
Bam sort merge error?
bam
linux
sam
updated 2.0 years ago by
Pierre Lindenbaum
166k • written 2.0 years ago by
Athena
• 0
0
votes
0
replies
479
views
Algorithmic Solutions for Resolving Overlapping Sequences in Sanger Sequencing of PCR Segments
Sanger
pcr
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
Amior
• 0
121,962 results • Page
200 of 2440
Recent Votes
Comment: Differences between published differential gene expression results and own analy
A: Which is the proper RNA-seq count table transformation to perform hierarchial cl
Answer: Differences between published differential gene expression results and own analy
Answer: If TPM is not comparable across cohorts, can it be used as the input for ML mode
Answer: If TPM is not comparable across cohorts, can it be used as the input for ML mode
Answer: Tools to simulate Illumina short read sequences and ONT long reads with a refere
sra-explorer : find SRA and FastQ download URLs in a couple of clicks
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Recent Replies
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?
Comment: Functional prediction for proteins of bacteria.
by
colindaven
8.0k
Have a look at tools like SnpEff or Ensembl VEP. Perhaps your bacterial sp is included.
Comment: Errors with RSEM/bowtie2
by
Olivia
• 0
Yes, I already made the transcriptome with these tools, and the CD-HIT-EST fasta file is the transcript file that I am using for RSEM. Then…
Comment: sra-explorer : find SRA and FastQ download URLs in a couple of clicks
by
Guilherme
• 0
Oh, ok. It seems like NCBI stores the files in SRA format (thus needing conversion and database lookups by sra toolkit tools) and EBI store…
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