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328 results • Page
1 of 7
Sort: Rank
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Views
Votes
Replies
0
votes
0
replies
8
views
STAR Genome index Error
STAR
GenomeSAindex
22 minutes ago by
Prasanna
• 0
0
votes
0
replies
12
views
ATAC-Seq and RPKM
RPKM
ATAC-Seq
and
36 minutes ago by
qudrat.nii
• 0
0
votes
1
reply
27
views
Kimura% of calcDivergenceFromAlign output
repeatlandscape
repeatmasker
1 hour ago by
睿紘
• 0
0
votes
4
replies
76
views
Understanding mother and father alleles in VCF file
snp
vcf
2 hours ago by
c.
• 0
0
votes
1
reply
78
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
0
replies
28
views
Help on dendrimer building
dendrimer
gromacs
molecular-dynamics
3 hours ago by
v.berriosfarias
▴ 130
0
votes
0
replies
44
views
Adding custom annotation to VEP output VCF
bcftools
VEP
vcf
4 hours ago by
avelarbio46
▴ 30
0
votes
9
replies
192
views
Deseq2 error
R
deseq2
2 hours ago by
sgadila
• 0
0
votes
1
reply
63
views
WGCNA plotEigengeneNetworks error (coercion to logical)
WGCNA
plotEigengeneNetworks
RNA-seq
RStudio
updated 3 hours ago by
Ram
40k • written 4 hours ago by
Victor
• 0
0
votes
1
reply
449
views
Low percentage of 'Fraction Antibody Reads Usable' in Feature Barcode Cell Ranger output
scCITE-seq
feature-barcode
10x
scRNA-seq
updated 3 hours ago by
Ram
40k • written 5 months ago by
rocio.castellanos
• 0
0
votes
10
replies
199
views
Rockhoppper - Suspiciously low percentage of perfectly aligned reads
Rockhopper
RNA-seq
35 minutes ago by
langziv
▴ 50
0
votes
0
replies
56
views
Adding means cluster from fviz_cluster on the PCA
fviz_cluster
updated 7 hours ago by
Ram
40k • written 10 hours ago by
ayaosama2111
▴ 10
0
votes
0
replies
57
views
DMRcate design
R
Epigenetics
EPIC
DMRcate
updated 8 hours ago by
Ram
40k • written 10 hours ago by
Bioinfonext
▴ 440
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 13 hours ago by
yamamoto.yasuyuki.n6
• 0
0
votes
1
reply
220
views
Determine kit used for library preparation for whole exome sequencing from fastq files
Agilent
NGS
library-preparation
updated 3 hours ago by
Ram
40k • written 18 hours ago by
Harinder
• 0
0
votes
1
reply
107
views
Bam sort merge error?
bam
linux
sam
updated 15 hours ago by
Pierre Lindenbaum
157k • written 18 hours ago by
Athena
• 0
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 18 hours ago by
Amior
• 0
0
votes
4
replies
194
views
counting from a single BAM file with multiple samples
cell-barcode
RNA-seq
updated 1 day ago by
LChart
3.4k • written 1 day ago by
dr-device
• 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
2
votes
6
replies
268
views
Match variants from RNAseq with known databases
dbsnp
SNP
vcf
bcftools
RNA-seq
1 day ago by
dilokef367
• 0
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
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
1
vote
2
replies
185
views
extract first and last n bp from fasta file from multiple fasta file in R
comparative-genomics
updated 1 day ago by
Ram
40k • written 1 day ago by
praasu
▴ 40
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
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
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
128
views
tidy_vcf function
tidy_vcf
manhattan
vcf
updated 2 days ago by
Pierre Lindenbaum
157k • written 2 days ago by
sooni
▴ 10
0
votes
1
reply
180
views
Pheatmap x must be numeric
deseq2
r
pheatmap
updated 1 day ago by
Ram
40k • written 2 days ago by
Hamza
• 0
0
votes
0
replies
128
views
In silico testing of mouse cell line expression
mouse
gene
expression
2 days ago by
Hashirama
▴ 20
2
votes
2
replies
292
views
bedtools intersect by position & stand not working even with common regions
bedtools
genomic
intersect
bedops
intervals
1 day ago by
Alewa
▴ 140
0
votes
1
reply
202
views
Unable to install HorvathMammalMethylChip40manifest packages
r
programming
updated 3 days ago by
ATpoint
77k • written 3 days ago by
Nibedita
• 0
0
votes
1
reply
199
views
TEtranscripts Tool in Galaxy
RNAseq
Transposable_Elements
TE_Transcripts
updated 10 hours ago by
biofalconch
★ 1.0k • written 3 days ago by
gorizwango
▴ 30
1
vote
1
reply
214
views
Imputation server failing to see samples in VCF files
imputation
VCF
updated 4 days ago by
Ram
40k • written 4 days ago by
Ben
• 0
0
votes
2
replies
269
views
Issues with featureCounts
featurecounts
rna-seq
differential-expression
updated 10 hours ago by
biofalconch
★ 1.0k • written 4 days ago by
Aime
• 0
0
votes
2
replies
246
views
Quality Control of VCFs that used different genotyping arrays
bcftools
VCF
1 day ago by
Shane
• 0
1
vote
4
replies
407
views
How to perform hypothesis testing on contingency tables and compare with the null distribution?
hypothesis-testing
contingency-table
4 days ago by
RK
• 0
0
votes
3
replies
285
views
QC of genetic data
PLINK
updated 5 hours ago by
bk11
★ 1.4k • written 4 days ago by
kl
▴ 10
1
vote
3
replies
285
views
differences between trajectories in conditions with Monocle3 or other tools
trajectory
scRna-seq
monocle3
single-cell
updated 4 days ago by
Amitm
★ 2.2k • written 4 days ago by
Chironex
▴ 40
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
1
vote
1
reply
226
views
Comparing multiple RNASeq studies
RNASeq
updated 5 days ago by
Zhenyu Zhang
▴ 980 • written 5 days ago by
Luke
▴ 10
0
votes
1
reply
196
views
Issue with merging in plink and eigensoft.
Eigensoft
Eigenstrat
Plink
updated 5 days ago by
bk11
★ 1.4k • written 5 days ago by
Jd
• 0
3
votes
3
replies
284
views
Clustering in single cell
seurat
single-cell
5 days ago by
Chris
▴ 200
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
3
votes
15
replies
563
views
How to subset large BAM files specifically/ extract specific subsets?
bamtools
RNAseq
samtools
BAM
5 days ago by
ella
• 0
0
votes
0
replies
140
views
Guide for ICD-10 to EFO conversion?
icd10
efo
5 days ago by
optimistsso4co3
▴ 100
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
1
vote
3
replies
280
views
comparision of umap single cell
single-cell
5 days ago by
synat.keam
▴ 80
0
votes
0
replies
144
views
tensorQTL interaction issue
genomics
eqtl
genetics
qtl
5 days ago by
Solal
• 0
1
vote
5
replies
401
views
Complex multifactorial DE analysis with limma/edgeR based on rnaseq data
R
edgeR
limma
RNA-seq
updated 4 days ago by
LChart
3.4k • written 6 days ago by
svlachavas
▴ 780
328 results • Page
1 of 7
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Comment: How do you validate and verify your pipeline's software updates?
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Answer: Exporting DEGs obtained from DESeq2
Answer: Exporting DEGs obtained from DESeq2
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Popular Question
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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.
Comment: Differentially Expressed Genes between two conditions (scRNA, single GEO dataset
by
bk11
★ 1.4k
You can simply do `Idents(seurat.integrated) <- "Type"` instead of `seurat.integrated <- SetIdent(seurat.integrated, value=seurat.integrate…
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