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90 results • Page
1 of 2
Sort: Votes
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Views
Votes
Replies
6
votes
3
replies
263
views
How can I adjust Y-axis scale when making relative abundance box plot ?
statistics
box-plot
R
scale_adjustment
logarithm
updated 6 days ago by
Jeremy
▴ 860 • written 7 days ago by
ohtang7
▴ 40
4
votes
2
replies
269
views
KEGG DATABASE
DATABASE
KEGG
updated 1 day ago by
jv
★ 1.3k • written 4 days ago by
Sijjil
• 0
3
votes
6
replies
466
views
scRNA-seq: Consistent low number of cells and low fraction reads across the samples
scRNA-seq
cells
mRNA
expression
gene
updated 5 days ago by
jv
★ 1.3k • written 7 days ago by
newbee
▴ 40
3
votes
1
reply
144
views
GEO dataset Microarray data analysis help
R
microarray
NCBI
GEO
updated 1 day ago by
Ram
41k • written 1 day ago by
Confused_human
▴ 20
2
votes
4
replies
259
views
error when installing gistic2 using conda
conda
gistic2
updated 1 day ago by
Ram
41k • written 2 days ago by
luckyday1661
• 0
2
votes
2
replies
207
views
4 Fastq files for a single run generated by 10X
scRNA-Seq
Fastq
SRA
10X
1 day ago by
hkarakurt
▴ 180
2
votes
11
replies
693
views
Data preparation for a ML model
machine-learning
RNA-Seq
R
python
biomarkers
6 days ago by
sil_bioinfo
▴ 40
2
votes
2
replies
215
views
R script in docker
R
Visual_studio_code
Docker
6 days ago by
mrashad
▴ 70
2
votes
4
replies
284
views
An issue with gtf file (ballgownrsem)
Ballgown
RNA-seq
GTF
RSEM
8 hours ago by
cucindarko51
• 0
2
votes
5
replies
231
views
kallisto index build difference according to version
index
version
kallisto
updated 2 days ago by
dsull
★ 5.1k • written 2 days ago by
estilo
• 0
1
vote
2
replies
225
views
How can I amend the output of a DIAMOND python script?
Python
Diamond
COG_analysis
6 days ago by
eamaunders
• 0
1
vote
5
replies
1.5k
views
BLAST: overflow error
BLAST
updated 2 days ago by
GenoMax
136k • written 19 months ago by
antoinefelden
▴ 60
1
vote
1
reply
1.0k
views
How to interpret the discrepancy of assignment rate in featurecounts using forward and reverse strand protocols
RNAseq
updated 17 hours ago by
charles.feigin
• 0 • written 6 weeks ago by
xinrantian
▴ 20
1
vote
3
replies
333
views
Bam files generated with STAR cause a segmentation fault core dump error when used with another tool
RNA-Seq
mapping
updated 2 days ago by
GenoMax
136k • written 3 days ago by
bkffadia
• 0
1
vote
1
reply
125
views
ANNOVAR Download Failing
ANNOVAR
updated 1 day ago by
Ram
41k • written 1 day ago by
tony
• 0
1
vote
4
replies
199
views
Feasibility of Enrichment Analysis from RTqPCR results
GO
RT-qPCR
Enrichment-Analysis
updated 17 hours ago by
GenoMax
136k • written 1 day ago by
Javier
• 0
1
vote
1
reply
366
views
Trinity 'genes' too much
Trinity
RNA-seq
updated 1 day ago by
Ram
41k • written 2.1 years ago by
Hou
• 0
0
votes
0
replies
131
views
Compute matrix skipping many regions stating not found in compute matrix output
computematrix
Deeptools
5 days ago by
Mehwish
▴ 10
0
votes
0
replies
146
views
is there a way to set colors pallets for glMDSPlot(x)?
Glimma
glMDSPlot
5 days ago by
James
• 0
0
votes
3
replies
811
views
"MethylKit" package for WGBS data
MethylKit
WGBS
updated 5 days ago by
viveksomya123
• 0 • written 2.3 years ago by
shrinka.genetics
▴ 20
0
votes
2
replies
1.5k
views
Does GNOMAD use all LOFTEE LoF filters?
loftee
gnomad
LOF
ensembl
vep
updated 4 days ago by
AMARU
• 0 • written 3.8 years ago by
brismiller
▴ 50
0
votes
0
replies
125
views
bootstraped treemix show no migration event
Treemix
Bootstrap
4 days ago by
reza
▴ 300
0
votes
0
replies
112
views
BioSQL Unable to remove database using server.remove_database
BioSQL
biopython
Mysql
Python
4 days ago by
Navindu
• 0
0
votes
1
reply
214
views
Issue with genetic QC sex check
plink
4 days ago by
kl
▴ 10
0
votes
0
replies
115
views
Should I perform eQTL colocalization for just one of eGenes at a time?
colocalization
coloc
eCaviar
eQTL
3 days ago by
maximal_life
▴ 20
0
votes
2
replies
517
views
Understanding gene level copy number data from TCGAbiolinks
CNV
TCGA
updated 2 days ago by
Zhenyu Zhang
★ 1.1k • written 13 months ago by
billyK
• 0
0
votes
1
reply
100
views
Funannotate iprscan Creates empty file
funannotate
interproscan
fungus
annotation
2 days ago by
Umer
▴ 50
0
votes
2
replies
253
views
How to identify CG, CHG, or CHH from MeDIP data
MethylationStudy
CHG
CHH
CG
MeDIP
2 days ago by
Tm
★ 1.1k
0
votes
0
replies
86
views
extracting Uniprot IDs for Kegg pathways
mapping
uniprot
R
kegg
clusterprofiler
2 days ago by
Assa Yeroslaviz
★ 1.8k
0
votes
0
replies
202
views
How to find promoters (such as GC box and TATA box) in set of genes using bioinformatics analysis ?
promoter
motif
updated 2 days ago by
Ram
41k • written 5 days ago by
shome
▴ 10
0
votes
3
replies
306
views
Can FPKM be used to create bar graphs for DEGs?
RNA-seq
updated 2 days ago by
Ram
41k • written 20 days ago by
junli1988
• 0
0
votes
0
replies
196
views
Trouble Adding Log Fold Changes to KEGG Pathway Visualization
KEGG
RStudio
updated 2 days ago by
Ram
41k • written 26 days ago by
ramirj49
• 0
0
votes
0
replies
80
views
How do I pick the best conditions for scATAC-Seq after a series of bulk test runs?
ATAC-seq
2 days ago by
cyril-cros
▴ 940
0
votes
5
replies
293
views
calculate nucleotide diversity from whole-genome-sequence data for individual genes
genomics
nucleotide_diversity
vcf
updated 2 days ago by
manaswwm
▴ 490 • written 6 days ago by
J
• 0
0
votes
3
replies
1.0k
views
Error with Ice normalization when running HiC-Pro
Hi-C
HiChIP
HiC-Pro
updated 2 days ago by
Ram
41k • written 2.1 years ago by
Amina
• 0
0
votes
0
replies
92
views
Comparing 16S rRNA (culture) sequences with metagenome
metagenome
shotgun
rRNA_culture
16S
updated 2 days ago by
Ram
41k • written 2 days ago by
aswin
• 0
0
votes
0
replies
94
views
Differing output: vcftools' --weir-fst-pop and R hierfstats package's varcomp.glob()
vcftools
hierfstats
fst
2 days ago by
S
• 0
0
votes
0
replies
109
views
Expression differs when running plotTranscripts vs boxplot of FPKM or coverage values (R)?
R
updated 2 days ago by
Ram
41k • written 2 days ago by
boone5jones
• 0
0
votes
1
reply
144
views
Annotation GTF/GFF Arabidopsis thaliana
Arabidopsis
GFF
GTF
Annotation
2 days ago by
enriquesan
• 0
0
votes
1
reply
145
views
Java error while running HiCDC overview code
R
Juicer
HiC
HiCDCPlus
updated 1 day ago by
Brian Bushnell
20k • written 2 days ago by
isMM
• 0
0
votes
0
replies
93
views
GAPIT p-value significance threshold
GAPIT
p-value
GWAS
1 day ago by
Clayton
• 0
0
votes
1
reply
137
views
Microbial gene coverage from blast result
gene
coverage
1 day ago by
aanchal.yadav
• 0
0
votes
2
replies
199
views
what should I do if I get a compromised sample of scRNA-seq data?
scRNA-seq
data
snRNA-seq
updated 1 day ago by
ATpoint
78k • written 2 days ago by
wangjb702
• 0
0
votes
0
replies
86
views
Need to PrepSCTfindMarker again after subset if the original object has already been normalized?
FindMarker
Seurat
1 day ago by
Adrian
• 0
0
votes
0
replies
89
views
RNA secondary structure for GRCH38 transcriptome
dot-bracket-notation
human
RNA-secondary-structure
GRCH38
1 day ago by
Saad Khan
▴ 420
0
votes
0
replies
99
views
Classification ML model using different type of data
machine-learning
transcriptomics
R
python
biomarkers
1 day ago by
sil_bioinfo
▴ 40
0
votes
1
reply
398
views
How to determine E. coli MLST (Multi Locus Sequence Typing ) from the sequencing of the PCR product of 7 housekeeping genes
MLST
phylogenetic
nanopre
updated 1 day ago by
Joe
21k • written 1 day ago by
Ralph
• 0
0
votes
1
reply
506
views
Problems separating and converting molecule files with openbabel
openbabel
updated 1 day ago by
mthm
▴ 50 • written 16 months ago by
smithk
• 0
0
votes
0
replies
92
views
WGCNA for different tissues
WGCNA
Worms
RNA-Seq
1 day ago by
kdca
• 0
0
votes
1
reply
140
views
How to remove 3rd codon positions in a multiple sequence allignment?
i
updated 1 day ago by
Ram
41k • written 1 day ago by
francesco.degiglio
• 0
90 results • Page
1 of 2
Recent Votes
A: difference between GSEA and Gene Ontology
Answer: Does the Minion demultiplex when basecalling?
the difference between the positions called by somatic caller (MuTect2) and the position called by germline caller (UnifiedGenotyper)?
A: Extract somatic mutations and germline mutations from variant calling files?
C: visualizing mutational data using Maftools for reference genome hg19
Answer: Ambient RNA removal method that generates whole (integer) counts
Answer: Ambient RNA removal method that generates whole (integer) counts
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Recent Awards •
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Scholar
to
jared.andrews07
★ 16k
Popular Question
to
Mr Locuace
▴ 150
Popular Question
to
benjamin.pyenson
• 0
Popular Question
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Malachi Griffith
19k
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awhale01
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hkarakurt
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Recent Replies
Comment: Resolving over clustered NGS with Q-scores
by
sam.himes92
• 0
The system that we used was [Aviti][1]. Our sequencing core was the one who quantified the loading/library concentration. Sorry I don't hav…
Comment: Where can I get a list of SNPs mapping overlapping genes in humans?
by
Alex Reynolds
35k
I modified the answer with an approach for that use case.
Comment: Where can I get a list of SNPs mapping overlapping genes in humans?
by
Ram
41k
OP is looking for overlapping genes - genes with presumably different gene IDs that share some loci. I think the `genes.bed` creation logic…
Comment: Where can I get a list of SNPs mapping overlapping genes in humans?
by
Alex Reynolds
35k
Note: The file `snps.bed` will be very large. You'll need sufficient disk space for this step.
Answer: Where can I get a list of SNPs mapping overlapping genes in humans?
by
Alex Reynolds
35k
Given files `genes.bed` and `snps.bed`, you could do something like: ``` $ bedmap --echo --echo-map-id --delim '\t' genes.bed snps.bed > a…
Answer: How to add exon annotations to genome annotation
by
alex.zaccaron
▴ 380
You can use [AGAT][1] to process your annotation file to add the missing exons. I believe `agat_convert_sp_gxf2gxf.pl -g no_exons.gff -o wi…
Comment: Annotation Visualization IGV
by
Pierre Lindenbaum
158k
and you got answer that should be validate (green tick), or people asked you questions but got no answers.
Comment: Annotation Visualization IGV
by
awhale01
• 0
Correct I have asked those questions before.
Comment: Annotation Visualization IGV
by
Pierre Lindenbaum
158k
you asked questions before: review, comment and/or validate them please: https://www.biostars.org/p/9530777/ ; https://www.biostars.org/p/9…
Comment: Ambient RNA removal method that generates whole (integer) counts
by
EK
• 0
Thanks, Jared. Sounds like rounding counts is the simplest approach for now. :)
Comment: Resolving over clustered NGS with Q-scores
by
Trivas
★ 1.5k
Could you tell us which sequencer you used, how you quantified your library size and concentration, and what your loading concentration was…
Comment: Resolving over clustered NGS with Q-scores
by
sam.himes92
• 0
I should have mentioned, we ran both Read 1 and 2 well past the points of interest. For each read we ran 75 cycles.
Answer: Resolving over clustered NGS with Q-scores
by
Trivas
★ 1.5k
It might be because Illumina recommends 26 cycles for Read 1: https://knowledge.illumina.com/instrumentation/general/instrumentation-genera…
Comment: Resolving over clustered NGS with Q-scores
by
sam.himes92
• 0
Yes at 5%.
Comment: Resolving over clustered NGS with Q-scores
by
ATpoint
78k
Has phiX been spiked in to increase nucleotide diversity.
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