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196 results • Page
4 of 4
Sort: Views
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Views
Votes
Replies
0
votes
2
replies
179
views
GOSt Plot
GOSt
ggplot2
updated 1 day ago by
bk11
★ 1.4k • written 1 day ago by
Sarah
• 0
0
votes
2
replies
178
views
chromosome location
visualization
updated 6 days ago by
Ram
40k • written 6 days ago by
Farzana
• 0
3
votes
6
replies
173
views
Exporting DEGs obtained from DESeq2
R
Deseq2
updated 5 hours ago by
Ram
40k • written 7 hours ago by
camillab.
▴ 140
1
vote
1
reply
167
views
Is it possible to convert 3 prime sequencing read counts into TPMs?
RNAseq
TPM
expression
updated 6 days ago by
Trivas
★ 1.5k • written 6 days ago by
Mat
▴ 60
0
votes
2
replies
166
views
How can I compute energy from a protein PDB file?
pdb
protein
updated 13 hours ago by
Matthias Zepper
4.1k • written 1 day ago by
4fzcgueyp5
• 0
0
votes
1
reply
162
views
GO ENRICHMENT ANALYSIS- DESEQ
GO
updated 6 days ago by
Basti
★ 1.7k • written 7 days ago by
oduduabasi.isaiah
• 0
0
votes
0
replies
158
views
Convert from limma voom normalized matrix each gene to high/low
limma-voom
RNA-SEQ
updated 5 days ago by
Ram
40k • written 5 days ago by
Manuel Sokolov Ravasqueira
▴ 100
1
vote
1
reply
154
views
tensorQTL interaction issue
genomics
eqtl
genetics
qtl
25 minutes ago by
Solal
• 0
0
votes
2
replies
152
views
I need help with univariate logistic regression in a set of microarray data
R
microarray
odds-ratio
updated 7 hours ago by
Ram
40k • written 21 hours ago by
Pooria
• 0
0
votes
0
replies
151
views
Can optimal cofactors for arcsinh transformation be calculated in parallel?
parallel
R
flowcytometry
flowCore
flowVS
5 days ago by
gmiller
• 0
0
votes
0
replies
150
views
Is the concept of a cofactor in an arcsinh transformation specific to Flow Cytometry?
FlowCytometry
flowCore
FlowVS
5 days ago by
gmiller
• 0
0
votes
2
replies
149
views
Generating a 3D model from 2D slices of a nucleus
imaging
modeling
5 hours ago by
jachimowicz9002
▴ 10
0
votes
1
reply
146
views
Transfer harmony-integrated scRNA-seq data to scanpy
scRNA-seq
harmony
updated 2 days ago by
Radu Tanasa
▴ 60 • written 2 days ago by
fifty_fifty
▴ 60
0
votes
1
reply
143
views
Calculating haplotype and nucleotide diversity with deep amplicon sequencing data
haplotype
diversity
Pegas
Arlequin
HTS_data
6 days ago by
deorugz
• 0
0
votes
0
replies
140
views
Guide for ICD-10 to EFO conversion?
icd10
efo
5 days ago by
optimistsso4co3
▴ 100
0
votes
1
reply
138
views
Large fold change when analyzing expression profiling from microarray
limma
DEG
RNA
updated 1 day ago by
Ram
40k • written 1 day ago by
Yibin
• 0
0
votes
0
replies
137
views
Software for chimera detection of amplicon (e.g. 16S) nanopore reads
chimera
nanopore
amplicon
5 days ago by
rob_DNA
▴ 10
0
votes
0
replies
128
views
In silico testing of mouse cell line expression
mouse
gene
expression
2 days ago by
Hashirama
▴ 20
0
votes
0
replies
128
views
tidy_vcf function
tidy_vcf
manhattan
vcf
updated 2 days ago by
Pierre Lindenbaum
157k • written 2 days ago by
sooni
▴ 10
1
vote
0
replies
127
views
rMATS visualisation
R
rMATS
maser
updated 1 day ago by
Ram
40k • written 2 days ago by
Smriti
▴ 10
0
votes
0
replies
126
views
News:
Course - Gene Set Enrichment Analysis in R/Bioconductor
GeneSetEnrichmentAnalysis
R
Genomics
Bioconductor
GSEA
2 days ago by
carlopecoraro2
★ 2.4k
0
votes
1
reply
123
views
FEAST - Microbial Source Tracking
Source-Tracking
Microbiome
updated 1 day ago by
Ram
40k • written 1 day ago by
avinash.dhar
• 0
0
votes
0
replies
120
views
Select minimum set of SNPs from VCF file to identify a individual
selection
SNP
6 days ago by
Bioxbio
• 0
0
votes
1
reply
120
views
How to assign gene names after kallisto when I add GFP?
tximport
RNA-seq
kallisto
updated 1 day ago by
dsull
★ 4.8k • written 1 day ago by
bioinfo
▴ 110
0
votes
0
replies
119
views
Job:
Two Postdoctoral Positions in Spatial Proteomics at Berlin-BUCH | Max-Delbrück-Center
spatial_proteomics
Postdoc
MDC_Berlin
2 days ago by
alwayshope
▴ 30
0
votes
2
replies
115
views
Get discordant read pairs from bam
samtools
NGS
updated 7 hours ago by
benformatics
3.8k • written 8 hours ago by
paulaotero.sanchez
• 0
2
votes
3
replies
107
views
Forum:
How do you validate and verify your pipeline's software updates?
Validation
Verification
Quality-Assurance
updated 3 hours ago by
ATpoint
77k • written 4 hours ago by
kieran
• 0
0
votes
1
reply
107
views
Bam sort merge error?
bam
linux
sam
updated 16 hours ago by
Pierre Lindenbaum
157k • written 18 hours ago by
Athena
• 0
0
votes
0
replies
104
views
Problem with RNAseq MarkDuplicates(Picard)
MarkDuplicates
GATK
SNP
RNA-seq
updated 1 day ago by
Ram
40k • written 1 day ago by
Grace
• 0
0
votes
0
replies
103
views
How to obtain de pvalue of my DMRs using Bumphunter function from minfi
DMRs
6 days ago by
Irene
• 0
0
votes
0
replies
100
views
Problems encountered during the survival analysis with TCGA data
R
survival-analysis
TCGA
updated 1 day ago by
Ram
40k • written 1 day ago by
applepie
• 0
0
votes
1
reply
90
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 hours ago by
bk11
★ 1.4k • written 3 hours ago by
prietto
• 0
0
votes
4
replies
84
views
Understanding mother and father alleles in VCF file
snp
vcf
2 hours ago by
c.
• 0
3
votes
2
replies
89
views
Feature plot not applicable for RunTSNE object in seurat?
harmony
Seurat
single-cell
5 hours ago by
synat.keam
▴ 80
0
votes
1
reply
88
views
pheatmap
pheatmap
heatmap
differential-expression
RNA-seq
updated 8 hours ago by
Ram
40k • written 10 hours ago by
Sara
▴ 30
0
votes
0
replies
67
views
Algorithmic Solutions for Resolving Overlapping Sequences in Sanger Sequencing of PCR Segments
Sanger
pcr
updated 8 hours ago by
Ram
40k • written 19 hours ago by
Amior
• 0
0
votes
1
reply
63
views
WGCNA plotEigengeneNetworks error (coercion to logical)
WGCNA
plotEigengeneNetworks
RNA-seq
RStudio
updated 4 hours ago by
Ram
40k • written 5 hours ago by
Victor
• 0
0
votes
0
replies
61
views
Detection of CNVs with copy number greater than 4 by PennCNV
copy-number
PennCNV
updated 8 hours ago by
Ram
40k • written 14 hours ago by
yamamoto.yasuyuki.n6
• 0
0
votes
0
replies
57
views
DMRcate design
R
Epigenetics
EPIC
DMRcate
updated 8 hours ago by
Ram
40k • written 11 hours ago by
Bioinfonext
▴ 440
0
votes
0
replies
56
views
Adding means cluster from fviz_cluster on the PCA
fviz_cluster
updated 8 hours ago by
Ram
40k • written 10 hours ago by
ayaosama2111
▴ 10
0
votes
0
replies
44
views
Adding custom annotation to VEP output VCF
bcftools
VEP
vcf
4 hours ago by
avelarbio46
▴ 30
0
votes
0
replies
39
views
News:
Course :MACHINE LEARNING - A HANDS-ON INTRODUCTION IN R
R
Statistical-Learning
Omics
Machine-Learning
updated 3 hours ago by
Ram
40k • written 5 hours ago by
carlopecoraro2
★ 2.4k
0
votes
1
reply
30
views
Kimura% of calcDivergenceFromAlign output
repeatlandscape
repeatmasker
2 hours ago by
睿紘
• 0
0
votes
0
replies
28
views
Help on dendrimer building
dendrimer
gromacs
molecular-dynamics
4 hours ago by
v.berriosfarias
▴ 130
0
votes
0
replies
12
views
ATAC-Seq and RPKM
RPKM
ATAC-Seq
and
1 hour ago by
qudrat.nii
• 0
0
votes
0
replies
11
views
STAR Genome index Error
STAR
GenomeSAindex
54 minutes ago by
Prasanna
• 0
196 results • Page
4 of 4
Recent Votes
Answer: tensorQTL interaction issue
Answer: Script for getting summary statistic of any genome using GTF or GFF3 ?
Comment: How do you validate and verify your pipeline's software updates?
Comment: How do you validate and verify your pipeline's software updates?
Answer: GSEA with GO and KEGG datasets
GSEA with GO and KEGG datasets
Answer: Exporting DEGs obtained from DESeq2
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Teacher
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★ 1.4k
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★ 2.7k
Popular Question
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v.berriosfarias
▴ 130
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avelarbio46
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Bioinfonext
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GenoMax
135k
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hemantcnaik
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Recent Replies
Answer: tensorQTL interaction issue
by
Solal
• 0
Writing a solution for anyone interested. The issue stems from a dosage error, some variant contains only heterozygous individuals and no h…
Answer: The Biostar Handbook. A bioinformatics e-book for beginners.
by
Qboy
• 0
Great book! I love using it to help my mentees to learn bioinformatics better. It would be also fantastic to compile all other necessary Pr…
Comment: Rockhoppper - Suspiciously low percentage of perfectly aligned reads
by
langziv
▴ 50
Thanks. I'll try.
Comment: How to get sample names and genotype for SNP in multi-sample VCF file
by
avelarbio46
▴ 30
Hi! I'm trying to parallelize your code (to run on a bunch of files), but it is not working because of multiple processes spawning. Do you …
Comment: Rockhoppper - Suspiciously low percentage of perfectly aligned reads
by
GenoMax
135k
> so I don't think the genome size is available. Perhaps not for your specific strain but plenty of other Kpn genomes are available and th…
Comment: Kimura% of calcDivergenceFromAlign output
by
睿紘
• 0
For additional information, "Coverage for each repeat class and divergence (Kimura)" is also the result from calcDivergenceFromAlign.pl
Comment: Rockhoppper - Suspiciously low percentage of perfectly aligned reads
by
langziv
▴ 50
By the way, I run Rockhopper on the untrimmed files, and the full match percentage grew to 20%-30%, and there are 1552 transcripts in the u…
Comment: Rockhoppper - Suspiciously low percentage of perfectly aligned reads
by
langziv
▴ 50
Here are the total bases in 4 fastq files (after adapter removal): 1,027,852,411, 1,041,895,083, 1,121,786,520, 1,299,721,929. I just rem…
Comment: Understanding mother and father alleles in VCF file
by
c.
• 0
actually they didn't tell me which relatives were from mother side and which from father side, you are right. But how can you find related …
Comment: Rockhoppper - Suspiciously low percentage of perfectly aligned reads
by
GenoMax
135k
Correct. Data that went into the assembly.
Comment: Rockhoppper - Suspiciously low percentage of perfectly aligned reads
by
langziv
▴ 50
Total bases (number of reads * read length) should be calculated after removal of adapters, right?
Comment: Getting BLAST to give output whilst running
by
Ken
• 0
If I understand correctly, Blast can tell you how many results it has gotten but it can't tell you how many it is going to get, therefore i…
Comment: Understanding mother and father alleles in VCF file
by
Ram
40k
I don't understand your logic. You don't know what phasing is but are confident it is not required, and your proof is that relatives were d…
Comment: Understanding mother and father alleles in VCF file
by
c.
• 0
It's from Nebula genomics. It must be possible to deduce parental alleles, since I converted the VCF file into a Myheritage VCF file and th…
Comment: Deseq2 error
by
sgadila
• 0
Sorry, I just edited my post.
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