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121,963 results • Page
203 of 2440
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0
votes
1
reply
991
views
Gene enrichment analysis of prokaryotes gene
prokaryotes
GO
enrichment
DEG
updated 2.0 years ago by
dthorbur
★ 3.1k • written 2.0 years ago by
Genta
• 0
1
vote
1
reply
1.0k
views
GWAS phenotype
R
GWAS
phenotype
updated 2.0 years ago by
dthorbur
★ 3.1k • written 2.0 years ago by
sooni
▴ 20
0
votes
2
replies
1.7k
views
RSEM not giving .genes.results and isoforms.results ; Plase check if you provide correct parameters/options for the pipeline!
genomics
transcriptome
rsem
ngs
2.0 years ago by
kat.bi
• 0
0
votes
2
replies
992
views
how to create a loop in R
R
offtopic
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
mthm
▴ 80
0
votes
6
replies
1.7k
views
BED files
BED
NGS
Chromosomes
updated 24 months ago by
Ram
45k • written 2.0 years ago by
adarsh
▴ 60
5
votes
7
replies
1.9k
views
How the first sequencing template removed in pair end sequencing
NGS
RNA-seq
WGS
sequence
updated 2.0 years ago by
GenoMax
154k • written 2.0 years ago by
octpus616
▴ 120
0
votes
4
replies
1.4k
views
Saving the output of LD pruning from SNPRelate package as a new GDS file
LD-pruning
SNPRelate
updated 2.0 years ago by
DBScan
▴ 530 • written 2.0 years ago by
Patrick
• 0
0
votes
4
replies
1.8k
views
Average Coverage after Assembly (Spades)
coverage
average
assembly
updated 23 months ago by
Brian Bushnell
20k • written 3.1 years ago by
davidmaimoun
▴ 50
1
vote
5
replies
1.5k
views
Can vg take MUMmer output as input?
vg
updated 2.0 years ago by
Ram
45k • written 4.8 years ago by
ac2278
▴ 20
4
votes
6
replies
4.8k
views
7 follow
Samtools Failing to Install through Conda
samtools
conda
updated 23 months ago by
Awosise
• 0 • written 3.4 years ago by
jjp55
▴ 20
4
votes
11
replies
3.3k
views
Should I Learn Docker to Run Command Line Bioinformatics Tool?
Docker
updated 2.0 years ago by
Yogi
▴ 70 • written 2.0 years ago by
Anisur Rahman
▴ 80
0
votes
1
reply
627
views
GO analysis after DESeq2
GO
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
odi
▴ 10
3
votes
2
replies
1.0k
views
Program for Overlapping DMRs (Differentially Methylated Regions) Between Groups
methylation
DMR
updated 2.0 years ago by
Basti
★ 2.1k • written 2.0 years ago by
epianalysis
• 0
0
votes
0
replies
649
views
News:
New NCBI Datasets APIs to Replace Old Ones
NCBI
API
Datasets
2.0 years ago by
PeterC_NCBI
▴ 520
1
vote
3
replies
1.1k
views
miRDeep2 - identifying miRNAs from deep sequencing data
microRNA
miRDeep2
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
Hasan
• 0
3
votes
4
replies
1.1k
views
Unable to build applet in DNAnexus, .jar file not found
dnanexus
applet
updated 2.0 years ago by
LChart
5.1k • written 2.0 years ago by
_quantum_girl_
▴ 60
1
vote
4
replies
3.9k
views
geom_signif() uses t-test to compare between more than 3 groups... Isn't this wrong?
ggplot2
ANOVA
t-test
2.0 years ago by
RM123
▴ 10
0
votes
1
reply
759
views
Download an example of fully-imputed VCF files ?
VCF
impute
updated 2.0 years ago by
barslmn
★ 2.4k • written 2.0 years ago by
Ben
▴ 10
0
votes
1
reply
816
views
How to find the most representative protein data base ID for your protein?
modelling
protein
database
updated 2.0 years ago by
GenoMax
154k • written 2.0 years ago by
amy__
▴ 250
0
votes
2
replies
944
views
Visualize where kmers are on a reference genome
kmer
visualize
updated 2.0 years ago by
Alex Reynolds
36k • written 2.0 years ago by
Carrie
• 0
7
votes
7
replies
2.1k
views
Filter human transcription factors
transcription-factor
RNA-seq
updated 2.0 years ago by
jared.andrews07
★ 19k • written 2.0 years ago by
Chris
▴ 360
2
votes
6
replies
1.8k
views
obtaining circular RNAs' sequences from circBase
circular-RNA
2.0 years ago by
aminijavad4
▴ 10
0
votes
0
replies
442
views
How to annotate BED for tissue expression?
BED
annotation
2.0 years ago by
Fabio_bie88
• 0
2
votes
0
replies
994
views
Job:
Human Genomics Team Leader
ebi
ensembl
embl
genomics
2.0 years ago by
Ben Moore
★ 2.4k
0
votes
1
reply
2.2k
views
error when running local chlorop1.1
chlorop
updated 2.0 years ago by
Ram
45k • written 9.3 years ago by
gerrychang1985
▴ 40
3
votes
14
replies
3.4k
views
10 follow
Help writing code for a question on my homework
biopython
updated 2.0 years ago by
Joe
22k • written 4.4 years ago by
hannahcheyenna
• 0
1
vote
1
reply
1.2k
views
bedGraph for Coverage of Insert from Paired-End Data?
genome
awk
coverage
bed
paired-end
updated 2.0 years ago by
shelkmike
★ 1.8k • written 2.0 years ago by
RelativeOptics
▴ 40
0
votes
6
replies
1.3k
views
gene correlations in between two groups
gene-expression
correlation
2.0 years ago by
biology_inform
▴ 60
0
votes
1
reply
455
views
Running Ibex on both BCR chains?
BCR
ibex
single-cell
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
actinia94
• 0
7
votes
9
replies
2.2k
views
Calculation of TMB on gene level
genomics
updated 2.0 years ago by
svp
▴ 690 • written 2.0 years ago by
smrutimayipanda
▴ 20
0
votes
0
replies
826
views
Spike-in normalization in ATAC-Seq with DiffBind
ATAC-Seq
spike-in
DiffBind
2.0 years ago by
frueher
• 0
1
vote
2
replies
876
views
Is it normal if regress out the cell cycle effects but the DEGs are quite the similar (no big changes)
regress_out
Cell_cycle
Seurat
2.0 years ago by
alwayshope
▴ 40
1
vote
9
replies
2.1k
views
how to identify uniq genes between two gff files.
Genes
Uniq
Annotation
GFF
2.0 years ago by
nikhil
▴ 20
2
votes
3
replies
1.6k
views
I have performed Trimmomatic run for adapter removal. QC report shows drop in the reads and presence of overrepresented sequences. Seeking help!
NGS
illumina
WGS
updated 24 months ago by
Ram
45k • written 2.0 years ago by
Vijith
▴ 100
0
votes
0
replies
1.2k
views
filtering variants in a Strelka2 VCF file based on AD and AF
Filter
VCF
2.0 years ago by
Bogdan
★ 1.4k
2
votes
4
replies
3.0k
views
Integrated Seurat object change name of the two conditions
R
integrated
Seurat
2.0 years ago by
camillab.
▴ 160
0
votes
4
replies
1.9k
views
Hugo_Symbol to Entrez ID
entrez
R
hugo-symbol
org.hs.eg.db
biomart
updated 24 months ago by
Ram
45k • written 2.0 years ago by
shakyaram079
• 0
2
votes
5
replies
1.6k
views
How to change from gene_id to GeneID/EntrezID using R
identifiers
Deseq2
GeneID
updated 2.0 years ago by
Kevin Blighe
89k • written 2.0 years ago by
Nicolas
• 0
0
votes
4
replies
2.1k
views
Is there a way to get a list of all homogygous sites for each sample with plink (regardless if they are in a run)
plink
updated 2.0 years ago by
chrchang523
11k • written 2.1 years ago by
curious
▴ 890
1
vote
4
replies
1.1k
views
How to sort cd-hit-est cluster file
sort
cd-hit-est
2.0 years ago by
Mo
▴ 50
1
vote
5
replies
1.4k
views
Enrichment of mitochondrial and ribosomal pathways - an artifact?
Pathway
Mitochondria
Ribosome
scRNA-seq
Enrichment
2.0 years ago by
omer.shomrat
• 0
18
votes
10
replies
3.5k
views
8 follow
scRNAseq Differential expression analysis
scRNA-seq
Differential-Expression
Seurat
updated 29 days ago by
ATpoint
89k • written 2.0 years ago by
MVJ
▴ 20
3
votes
4
replies
1.6k
views
Dotplot : how to self-define the range of legend
analysis
seq
RNA
updated 2.0 years ago by
GenoMax
154k • written 2.0 years ago by
Xuhao
• 0
0
votes
0
replies
719
views
News:
RADseq data analysis course
RADseq
Phylogenomics
Stacks
Population-Genomics
23 months ago by
Physalia-courses
★ 2.6k
6
votes
2
replies
1.7k
views
How to create structural variants ground truth for alignment of two long-read genome assemblies?
yeast
assembly
structural-variation
SV-callers
2.0 years ago by
Thomas
▴ 40
0
votes
1
reply
713
views
Merging the filename with tsv files for master file
genomics
updated 2.0 years ago by
barslmn
★ 2.4k • written 2.0 years ago by
smrutimayipanda
▴ 20
4
votes
6
replies
1.8k
views
Hisat2 index and alignment question
ubuntu
rna-seq
index
hisat2
updated 2.0 years ago by
Istvan Albert
103k • written 2.0 years ago by
Athena
• 0
2
votes
5
replies
3.0k
views
Ties in reranked list
fgsea
GSEA
updated 17 months ago by
Gordon
• 0 • written 2.0 years ago by
Hamza
▴ 10
1
vote
5
replies
1.5k
views
Error: cannot open file 2 for reading From Cufflinks Version 2.2.1 When Attempting To Use CuffDiff
CuffDiff
Bash
Cufflinks
2.0 years ago by
Y
▴ 10
0
votes
0
replies
734
views
My rMATS output file is not showing gene symbols and only XLOC gene ID are being shown.
rMATS
rMATS-turbo
2.0 years ago by
Nipan
• 0
121,963 results • Page
203 of 2440
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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
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
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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.
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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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