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448 results • Page
4 of 9
Sort: Votes
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Views
Votes
Replies
0
votes
0
replies
113
views
Databases with GoF (Gain of Function) annotations.
gof
lof
gain-of-function
28 days ago by
_quantum_girl_
▴ 10
0
votes
0
replies
740
views
Creating a stable batch-corrected scRNA-Seq data with multiple datasets and multiple integrations
RNA-Seq
scRNA-Seq
batch-effect
updated 19 days ago by
Ram
43k • written 3.4 years ago by
hkarakurt
▴ 180
0
votes
2
replies
253
views
How to update R on ubuntu
installation
update
R
apt-get
8 days ago by
Bosberg
▴ 50
0
votes
0
replies
162
views
Input into WGCNA and Error on constructNetworks on RNA-Seq data - unique rownames
rownames
RNA-Seq
WGCNA
unique
20 days ago by
shasabhi1
• 0
0
votes
1
reply
205
views
Help with DGEList function
DGEList
R
updated 1 day ago by
marco.barr
▴ 90 • written 3 days ago by
Natali
• 0
0
votes
0
replies
164
views
how to read graph_test output of monocle 3
monocle3
12 days ago by
synat.keam
▴ 100
0
votes
0
replies
139
views
How can I plot the PCA with the raw count mRNA seq data?
PCA
normalization
updated 29 days ago by
Ram
43k • written 29 days ago by
Yoomi
▴ 20
0
votes
0
replies
113
views
Clarification on StringTie's `--merge` parameters
stringtie
stringtie-merge
2 days ago by
DGTool
• 0
0
votes
2
replies
289
views
Annovar using R package
Annovar
gnomAD
R
11 days ago by
DKA
▴ 40
0
votes
4
replies
556
views
How to reduce the variation of CIBERSORTx results?
CIBERSORTx
deconcolution
19 days ago by
feather-W
• 0
0
votes
0
replies
106
views
Tools to circularise the ion torrent bacterial genome assembly
iontorrent
bacteria
circularise
6 days ago by
VITALA
• 0
0
votes
2
replies
324
views
Merging Outputs from plink --assoc and --hardy to Produce Table
PLINK
PANDAS
R
20 days ago by
Koketso
• 0
0
votes
0
replies
45
views
Correlation Analysis
statistics
methylation
NGS
expression
8 hours ago by
Researcher
▴ 30
0
votes
0
replies
284
views
Different rsID for the same chromsome, position, ref & alt allele depending on different data sources. Which one should I use?
UKB
rsID
UKB-PPP
ensembl-vep
dbsnp
27 days ago by
lsy9
▴ 20
0
votes
0
replies
79
views
Normalizing AMR gene count data
abundance
RGI
updated 1 day ago by
Ram
43k • written 1 day ago by
arshad1292
▴ 100
0
votes
0
replies
147
views
Homer motif analysis
Homer
3 days ago by
daffodil
▴ 10
0
votes
0
replies
212
views
Phasing VCF Files and Analyzing Reads with Multiple Variants
haplotypes
vcf
phasing
11 days ago by
HarperReed
• 0
0
votes
2
replies
285
views
WGCNA
PCA
WGCNA
EIGENGENE
25 days ago by
rajasekargutha
▴ 60
0
votes
0
replies
1.8k
views
Differential expression using Scran batch corrected data
single-cell
Batch-effect
RNA-Seq
Scran
updated 19 days ago by
Ram
43k • written 5.5 years ago by
baldissera152
▴ 10
0
votes
1
reply
294
views
assembly using CCS, CLR, CCS_CLR sequences together?
assembly
updated 19 days ago by
GenoMax
142k • written 19 days ago by
ycts
• 0
0
votes
1
reply
146
views
Displaced fragment length distribution in ATAC-seq
ATAC-seq
nucleosome
fragment
updated 15 days ago by
ATpoint
82k • written 15 days ago by
enanoide
• 0
0
votes
1
reply
179
views
How to solve this RoseTTAFold colaboratory error?
modeling
Google
Colaboratory
RoseTTAFold
protein
updated 13 days ago by
Mensur Dlakic
★ 27k • written 13 days ago by
benguyarenbeyaz98
• 0
0
votes
0
replies
120
views
Blast2GO Fisher test
Fisher-test
Go-annotation
Blast2GO
updated 29 days ago by
Ram
43k • written 29 days ago by
BlackM
• 0
0
votes
3
replies
220
views
Software to separate reads from different individuals
software
development
nanopore
updated 7 days ago by
GenoMax
142k • written 8 days ago by
njornet
▴ 20
0
votes
1
reply
1.1k
views
Ensembl assembly choice for RNA-Seq reference mapping
RNA-Seq
ensembl
STAR
alignment
Assembly
updated 26 days ago by
AHerik
▴ 20 • written 5.0 years ago by
eoin
▴ 30
0
votes
8
replies
408
views
Error in cnetplot enrichplot package
R
updated 14 days ago by
Ram
43k • written 14 days ago by
Farhad
• 0
0
votes
0
replies
234
views
Using samtools with GCS (google cloud storage) on a docker container seems to give "Protocol Not Supported" error
samtools
gcs
17 days ago by
abhishekghadge
• 0
0
votes
0
replies
228
views
Variant Generation Using Longshot
long-reads
variant-calling
ONT
minion
longshot
updated 19 days ago by
Ram
43k • written 19 days ago by
samuelkalandarov2002
▴ 10
0
votes
0
replies
103
views
Issue while using circle_dat function from GOplot in R
GOplot
R
27 days ago by
ckelly96
• 0
0
votes
0
replies
203
views
filter the most significant ligand and receptors in netVisual_bubble in cell chat
cellchat
19 days ago by
synat.keam
▴ 100
0
votes
1
reply
228
views
Subsetting and merging back Seurat Object brings different results
Seurat
5 days ago by
Bine
▴ 60
0
votes
2
replies
307
views
bam merging for archaic samples
samtools
bam
updated 16 days ago by
Ram
43k • written 17 days ago by
Matteo Ungaro
▴ 100
0
votes
0
replies
187
views
Protein stability analysis
mutation
analysis
25 days ago by
marco.barr
▴ 90
0
votes
1
reply
836
views
How to compare differentially expressed genes among different affymatrix dataset
microarray
batch-effect
R
updated 20 days ago by
Ram
43k • written 4.8 years ago by
Calangoa
▴ 30
0
votes
5
replies
5.9k
views
Calculate Radius of Gyration [python 3]
biopython
PDB
Radius of Gyration
python
protein
updated 17 days ago by
ndm1096
• 0 • written 6.5 years ago by
ac.research
▴ 30
0
votes
0
replies
134
views
DESeq2 LRT divergent DEGs ?
interaction
LRT
deseq2
28 days ago by
klervi-lugue
• 0
0
votes
1
reply
183
views
RNA-seq bacteria contamination
RNA-seq
updated 15 days ago by
GenoMax
142k • written 15 days ago by
sh
• 0
0
votes
1
reply
219
views
Pattern of GC content across reads from fastp
multiqc
ddRAD
updated 28 days ago by
GenoMax
142k • written 29 days ago by
jberg
• 0
0
votes
1
reply
208
views
GATK won't produce figures while analyzing covariates to generate 'recal_plots.pdf'
GATK
recalibration
updated 5 days ago by
GenoMax
142k • written 5 days ago by
mgranada3
▴ 30
0
votes
3
replies
1.1k
views
Batch effect for SNP array
sva
combat
batch-effect
SNP
updated 22 days ago by
Ram
43k • written 4.3 years ago by
Taylor95
▴ 10
0
votes
0
replies
109
views
Trimming best practices for SNP calling
trimming
SNP
trimmomatic
15 days ago by
Enrique
• 0
0
votes
0
replies
173
views
Designing single-stable RNA molecules
structure
RNA
11 days ago by
Edna
• 0
0
votes
1
reply
220
views
Annotating a dataset with gnomAD v4 using Hail
Python
Sequencing
Hail
Exome
Annotation
updated 20 days ago by
DKA
▴ 40 • written 20 days ago by
james.melhorn
• 0
0
votes
0
replies
154
views
Diffbind and DESeq2 comparison for differential sites
diffbind
deseq2
updated 28 days ago by
Ram
43k • written 4 weeks ago by
Ankit
▴ 500
0
votes
1
reply
588
views
Basic stats in hierfstat
Fst
stats
hierfstat
updated 5 days ago by
mdav
• 0 • written 18 months ago by
Zoe
• 0
0
votes
5
replies
394
views
Should I remove unlocalized scaffols in reference genome before alignment?
qualimap
alignment
minimap2
GRCh38
assembly
13 days ago by
njornet
▴ 20
0
votes
6
replies
1.0k
views
Considering that the basal expression level is not 0 for the calculation of the differential expression
DESEQ2
RNA-Seq
Differential-gene-Expression
updated 28 days ago by
Ram
43k • written 5.8 years ago by
Pin.Bioinf
▴ 340
0
votes
1
reply
310
views
Monotonic genes in results of differential gene expression analysis
differential-expression
RNA-seq
monotonic-genes
updated 28 days ago by
Ram
43k • written 3 months ago by
Shaimaa Gamal
▴ 10
0
votes
1
reply
829
views
Bulk RNAseq MACS Sort Quality Contamination
EdgeR
Batch-effect
RNA-Seq
updated 19 days ago by
Ram
43k • written 3.7 years ago by
jordan15
• 0
0
votes
0
replies
1.8k
views
Accounting for hidden batch effects in differential expression analysis with DEXseq and Slueth
Batch-effect
RNA-Seq
Differential-Expression
updated 20 days ago by
Ram
43k • written 7.2 years ago by
vakul.mohanty
▴ 270
448 results • Page
4 of 9
Recent Votes
Comment: Spike-in control found in raw reads (16S amplicon seq) but not picked up by DADA
Answer: TFs and Gene databases
Answer: TFs and Gene databases
Answer: TFs and Gene databases
Answer: Understanding STAR output (Aligned.out.sam file)
Comment: High Malat-1 expression in single cell data
Comment: removeBatchEffect explained using base R linear models
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Comment: Spike-in control found in raw reads (16S amplicon seq) but not picked up by DADA
by
sovrappensiero
▴ 90
Thanks again. Hmm...this makes me suspicious of whether this normalization is actually possible. In case you'd like to take a look, [here]…
Comment: Filtering Multi-sample VCF file for all except one Genotype
by
Jeremy Leipzig
22k
The seven genotypes being 58025AA, 58025AG, 58051TT, 58051TC, 58051CC, 58057TT, 58057TC
Answer: TFs and Gene databases
by
jared.andrews07
★ 16k
See [TFlink](https://tflink.net/), [KnockTF2](https://bio.liclab.net/KnockTFv2/index.php), [TFBSDB](https://tfbsdb.systemsbiology.net/), an…
Comment: Filtering Multi-sample VCF file for all except one Genotype
by
GenoMax
142k
> Seven genotpyes have been sampled and all variants, which belong to one of those genotpyes are to be "erased" (or every other variant exc…
Comment: Filtering Multi-sample VCF file for all except one Genotype
by
Pierre Lindenbaum
161k
> , filter a multisample VCF file for all genotypes except one of them filter for what ?
Answer: Applying the metacell2 algorithm using python
by
Wayne
★ 2.0k
I had hoped things like [this Jupyter notebook for the rabbit data analysis](https://nbviewer.org/github/tanaylab/rabembflow/blob/master/2-…
Comment: Help with running egsea()
by
1769mkc
★ 1.2k
please provide the design matrix mean the metadata of the model fit2 which is there in the code . i guess other users can help
Comment: Applying the metacell2 algorithm using python
by
JACKY
▴ 140
The repo does not provide any valuable information unfortunately. The Metacell algorithm they provide in the vignette is missing the metagr…
Comment: Repeated testing/data mining in RNA Seq
by
robert.flynn.21
• 0
Thanks! I'll give it a go.
Comment: Applying the metacell2 algorithm using python
by
Wayne
★ 2.0k
Yes, they are very clear about this. The page about the Vignettes says: >"They are not meant as a comprehensive documentation of all the fe…
Comment: Gene density plot
by
dthorbur
★ 1.9k
This sounds like it would be a simple task in either python or R. Read data in, potentially with a library like `data.table` in `R`, depend…
Answer: HLA-HD tool for genomic imputation
by
Javier
• 0
Hi, I just solved the same error. In my case, it was because I misunderstood the instructions. hlahd.sh -t 4 *-f ~/hlahd.1.7.0/fr…
Comment: Question regarding WGCNA
by
andres.firrincieli
3.6k
Ok, then. You likely have a scale free topology that look like this: [link][1] In this situation you should pick the power value with an …
Comment: Bioinformatics Analyst - Laboratory Medicine and Pathology
by
Ram
43k
Why did you add this as an answer to a random post? I'm moving this to a comment. To answer your question, read this post: https://www.bio…
Comment: ERROR: Duplicate entry "..." in sam header; samtools view: failed to add PG lin
by
GenoMax
142k
> I don't understand why SAM header has "Duplicate entry" and what should I do in this case. Your reference sequence must have fasta head…
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