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1,000 results • Page
1 of 20
Sort: Rank
Rank
Views
Votes
Replies
0
votes
0
replies
14
views
RNA seq analysis
DESeq
RNA-seq
analysis
14 minutes ago by
prifa
• 0
0
votes
0
replies
29
views
Chance for trained without experience
bio
updated 46 minutes ago by
ATpoint
82k • written 1 hour ago by
shehab
• 0
0
votes
0
replies
21
views
How can I analysis Nomalized expression data?
DEseq2
RNA-seq
1 hour ago by
mnx0723
• 0
0
votes
0
replies
31
views
Xenium multi sample data
batch
annotation
cell
Xenium
effect
2 hours ago by
Omics data mining
▴ 260
0
votes
2
replies
53
views
Phasing a mixture of two individuals' DNA with long reads
long-reads
phasing
50 minutes ago by
njornet
▴ 20
0
votes
1
reply
61
views
Exploring Diet Effects in Single-Cell RNA Sequencing
batch_effect
scRNA
seurat
integration
updated 2 hours ago by
ATpoint
82k • written 3 hours ago by
Darya
• 0
0
votes
4
replies
80
views
Percentage coverage of reference genome by de novo genome
SAMtools
BWA
alignment
ddRAD
updated 2 hours ago by
Michael
54k • written 3 hours ago by
Lemonhope
• 0
0
votes
0
replies
41
views
Why does my Hi-C contact map show large regions making little to no contact?
BWA-MEM2
Hi-C
PretextMap
3 hours ago by
Winter
• 0
0
votes
0
replies
43
views
Error in plotting PCA plot in seurat
PCA
single-cell
seurat
scRNA
RNA
4 hours ago by
Sumeet
• 0
0
votes
0
replies
33
views
Generating .bed file and .map file for polyploid vcf file through plink
bed
polyploid
map
plink
6 hours ago by
analyst
▴ 50
0
votes
0
replies
49
views
meffil.snp.concordance
meffil
methylation
snp_concordance
11 hours ago by
kyj222637
• 0
0
votes
0
replies
48
views
PseudobulkExpression.Seurat error
Seurat
pseudo-bulk
11 hours ago by
sooni
▴ 20
0
votes
2
replies
117
views
STAR aligner error
RNA-seq
STAR
slurm
3 hours ago by
M.
▴ 30
0
votes
0
replies
52
views
monocle 3-- Could not get node in small cluster
monocle3
14 hours ago by
synat.keam
▴ 100
0
votes
1
reply
100
views
Correlating Bulk Differential Expression with quantitative
Differential-Expression
DESeq2
updated 10 hours ago by
Ram
43k • written 15 hours ago by
Nicholas
• 0
0
votes
3
replies
207
views
Filtering Multi-sample VCF file for all except one Genotype
variant
SNP
VCF
updated 16 hours ago by
Ram
43k • written 20 hours ago by
schmince
• 0
0
votes
1
reply
105
views
ERROR: Duplicate entry "..." in sam header; samtools view: failed to add PG line to the header
sort.
SAMtools.
BAM.
SAM.
updated 21 hours ago by
GenoMax
142k • written 21 hours ago by
Sony
▴ 10
5
votes
5
replies
224
views
Error in dimnames(x) <- dn : length of 'dimnames' [2] not equal to array extent
EGSEA
8 hours ago by
Chris
▴ 280
0
votes
1
reply
108
views
Differentail gene expression results
differential
expression
gene
rna-seq
Deseq2
updated 23 hours ago by
ATpoint
82k • written 1 day ago by
ahmad.sajad4541
• 0
1
vote
5
replies
175
views
UMI-Tools knee-method has great influence on the results of white list
single-cell
whitelist
UMI
RNA
UMI-Tools
updated 21 hours ago by
i.sudbery
19k • written 1 day ago by
Assa Yeroslaviz
★ 1.8k
1
vote
1
reply
128
views
student
epitranscriptomics
updated 1 day ago by
ATpoint
82k • written 1 day ago by
useriwa
• 0
0
votes
0
replies
82
views
Imputation of missing genotypes
panel
beagle
imputation
1 day ago by
analyst
▴ 50
0
votes
3
replies
143
views
trying to count a pattern in my fastq file using bbduk
java
bbduk
bbmap
fastq
updated 21 hours ago by
GenoMax
142k • written 1 day ago by
Assa Yeroslaviz
★ 1.8k
0
votes
1
reply
89
views
Correlation Analysis
statistics
methylation
NGS
expression
updated 1 hour ago by
manaswwm
▴ 510 • written 1 day ago by
Researcher
▴ 30
1
vote
2
replies
150
views
Repeated testing/data mining in RNA Seq
repeated
RNA-Seq
mining
testing
data
20 hours ago by
robert.flynn.21
• 0
0
votes
0
replies
97
views
Get Paired TCRa/b from MIXCR
python
r
mixcr
tcr_seq
1 day ago by
Scott McKay
▴ 30
0
votes
0
replies
98
views
Cellphonedb results
cpdb
visulization
cellphonedb
1 day ago by
piotto
▴ 20
0
votes
0
replies
106
views
Cox Model with interaction item interpretation
Cox
1 day ago by
Bine
▴ 60
0
votes
0
replies
92
views
how to downlad slices of CRAM fro ICGC ARGO
icgc
samtools
cram
1 day ago by
Javier
• 0
1
vote
6
replies
420
views
Question regarding WGCNA
WGCNA
Network-construction
updated 21 hours ago by
andres.firrincieli
3.6k • written 4 days ago by
deepak
• 0
0
votes
0
replies
99
views
vdjtools
vdjtools
1 day ago by
yueli7
▴ 250
0
votes
1
reply
178
views
16S rRNA microbiome differential abundance analysis with DESeq2 finds same microbial Genus in both groups.
microbiome
16S
DESeq2
updated 1 day ago by
andres.firrincieli
3.6k • written 1 day ago by
Antonio
• 0
0
votes
0
replies
109
views
Error while loading model of Spatial data deconvolution using cell2location
Python
cell2location
updated 1 day ago by
Ram
43k • written 2 days ago by
sidrah.maryam
▴ 50
0
votes
0
replies
96
views
Normalizing AMR gene count data
abundance
RGI
updated 1 day ago by
Ram
43k • written 2 days ago by
arshad1292
▴ 100
0
votes
0
replies
107
views
Help with VG Toolkit: VCF Output is Empty
vg
updated 2 days ago by
Pierre Lindenbaum
161k • written 2 days ago by
sarumonsus
• 0
0
votes
0
replies
113
views
How to implement an IGV to streamlit app?
python
streamlit
igv
2 days ago by
avigail.shnaider
• 0
0
votes
0
replies
121
views
Mitogenomes gap closure and making circular genome
gapclosure
Mitogenomes
validation
circulargenome
2 days ago by
KHURRAM SHAHZAD
• 0
0
votes
0
replies
111
views
Looking for phytopathogenic, Nitrogen-Fixing, and Growth-Promoting databases for Metagenomic Analysis
Bacteria
Metagenomics
Database
2 days ago by
Christopher
• 0
0
votes
0
replies
114
views
Clarification on StringTie's `--merge` parameters
stringtie
stringtie-merge
3 days ago by
DGTool
• 0
0
votes
0
replies
122
views
Seurat V5 integration
Seurat
samples
integration
combine
3 days ago by
starswillfade
▴ 10
0
votes
1
reply
180
views
Problem with Seurat package in PercentageFeatureSet function
cell
single
updated 1 day ago by
bk11
★ 2.4k • written 3 days ago by
Yoosef
▴ 60
0
votes
1
reply
256
views
creating batch colum for batch correction
batch-correction
combat
2 days ago by
Expert
▴ 10
0
votes
1
reply
212
views
Help with DGEList function
DGEList
R
updated 2 days ago by
marco.barr
▴ 90 • written 4 days ago by
Natali
• 0
0
votes
0
replies
150
views
Homer motif analysis
Homer
4 days ago by
daffodil
▴ 10
0
votes
1
reply
197
views
fastq screen aligner no specified.
BWA
Bowtie2
FastqScreen
updated 4 days ago by
GenoMax
142k • written 4 days ago by
Ximena
• 0
0
votes
1
reply
192
views
filtering before dada2
bbduk
qiime2
dada2
metagenomic
updated 4 days ago by
Ram
43k • written 4 days ago by
Valentina
• 0
0
votes
6
replies
419
views
Differential Expression Analysis using DESeq2 in R
deseq2
R
updated 4 days ago by
swbarnes2
14k • written 4 days ago by
Erina
• 0
1
vote
3
replies
279
views
TaxID mapping file
annotation
blobtools
RNAseq
decontamination
transcriptomes
2 days ago by
Lada
▴ 30
1
vote
0
replies
145
views
.lgen file has 3+ different alleles
PLINK
lgen
ped
updated 2 days ago by
zx8754
11k • written 4 days ago by
Emilie
▴ 10
0
votes
0
replies
137
views
vcf procesing for ML antigen prediction
formats
vcf
fastaq
HLA_imputation
HLA_typing
4 days ago by
Javier
• 0
1,000 results • Page
1 of 20
Recent Votes
Answer: TFs and Gene databases
Answer: java out of memory error through beagle for imutation
A: Could you explain the difference between STAR, KALLISTO, SALMON etc. to experime
Could you explain the difference between STAR, KALLISTO, SALMON etc. to experimental Biologist/non-bioinformatician
Comment: Microarray pbrobe ID to gene ID problem
Answer: Microarray pbrobe ID to gene ID problem
Answer: How do I change the title font size in ViolinPlot (Seurat)
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Recent Replies
Comment: Soft-clipping read ends based on read group
by
chenl
▴ 10
Hi, Can you please share how did you clip both ends of the reads with ClipReads? Clipping form the start with `-CT "1-3"` for instance wor…
Comment: Phasing a mixture of two individuals' DNA with long reads
by
njornet
▴ 20
This is related to that other question but for now, the only thing I'm interested in is separating the three unique chromosomes, without as…
Comment: A question about reference genome for creating the consensus sequence
by
GenoMax
142k
> I wonder how to adjust the base genome. If you are looking to make changes to the reference you used for alignment then look into http…
Comment: Phasing a mixture of two individuals' DNA with long reads
by
GenoMax
142k
We had a related discussion in a prior thread by OP: https://www.biostars.org/p/9593780/ Do you have genotype (or independent sequence) da…
Answer: TFs and Gene databases
by
b.contreras.moreira
▴ 180
I can also suggest <https://footprintdb.eead.csic.es> which links TFs to their DNA motifs, not their gene targets.
Comment: Correlation Analysis
by
manaswwm
▴ 510
How many methylation and expression values do you have per gene? If per gene you have a table named - *gene_corr*; which has two columns - …
Comment: How do I change the title font size in ViolinPlot (Seurat)
by
Assa Yeroslaviz
★ 1.8k
thx for the explanation. I did look at the function and I also read in the help page, that you get a patchwork object, only when using `co…
Comment: Percentage coverage of reference genome by de novo genome
by
Lemonhope
• 0
Thank you, I'll check out Quast!
Answer: How do I change the title font size in ViolinPlot (Seurat)
by
ATpoint
82k
Looking at the source code of the function it seems that they make individual plots with ggplot when `features` is `> 1` and then use patch…
Comment: Percentage coverage of reference genome by de novo genome
by
Lemonhope
• 0
Thank you for the response to answer you question, no, the ddRADseq data (short paired end illumina reads) for all the samples were used …
Comment: Percentage coverage of reference genome by de novo genome
by
Michael
54k
minimap2 can do this too, mummer (nucmer) is more accurate but slightly slower. If you want to do this as part of generating assembly stati…
Comment: TFs and Gene databases
by
ijarne
• 0
Thank you so much @jaredandrews07 it looks like I will be able to get what I intended with these sources !!
Comment: Percentage coverage of reference genome by de novo genome
by
Joe
21k
If you have contigs for assemblies, using read-based approaches like samtools is probably not the way to go. As you're interested in % cov…
Comment: Exploring Diet Effects in Single-Cell RNA Sequencing
by
ATpoint
82k
Has data been generated in the same batch, so same day, in the same 10x runs?
Answer: Comparative Analysis of Algorithms for Implementing the FM-Index: Correctness, C
by
Michael
54k
So I am assuming you have calculated a Burrows-Wheeler transform, then add the FM-index for the first and last column of the BW-matrix. I r…
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