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121,831 results • Page
597 of 2437
Sort: Rank
Rank
Views
Votes
Replies
0
votes
0
replies
801
views
Download COG Database
database
COG
4.1 years ago by
gaurav.iari
• 0
3
votes
2
replies
2.0k
views
How to interpret bimodal distribution of GC-content for RNAseq and can it be remedied ?
RNA-Seq
GCcontent
FastQC
RNAseq
updated 4.1 years ago by
GenoMax
153k • written 4.1 years ago by
Alexander
▴ 220
5
votes
3
replies
2.2k
views
AnnotationHub::mapIds() cannot find existing ENSG (GEO supplemental data cross-referenced with ensembl.org)
ensg
annotationhub
mapping
4.1 years ago by
mk
▴ 310
1
vote
5
replies
2.2k
views
De novo genome assembly
De
novo
Assembly
Genome
Minimap2
Mother
updated 4.1 years ago by
GenoMax
153k • written 4.1 years ago by
rodriguez.migs10
• 0
1
vote
0
replies
1.2k
views
hisat2 compatibility for long read
Long-read
hisat2
updated 2.2 years ago by
Ram
45k • written 4.1 years ago by
kishorssf91
▴ 20
2
votes
1
reply
3.2k
views
illumina adapter specifying and removing using fastp
adapter
index
illumina
fastp
fastq
updated 4.1 years ago by
GenoMax
153k • written 4.1 years ago by
Mehmet
▴ 820
0
votes
2
replies
1.2k
views
Extremely low number of variants in VCF file after filtering MIN(FORMAT/DP)>10
bcftools
snp
vcf
calling
updated 4.1 years ago by
cpad0112
21k • written 4.1 years ago by
Linda
▴ 80
0
votes
1
reply
2.1k
views
extract list of SNPs from multiple chr{1:22}.bgen files using plink2
subset
of
extract
maf
SNPs
cutoff
plink2
updated 4.1 years ago by
chrchang523
11k • written 4.1 years ago by
Sharad
▴ 10
1
vote
3
replies
2.6k
views
formatting error: Calculate LD matrix from bgen file
plink
ld_matrix
updated 14 months ago by
Ram
45k • written 4.1 years ago by
chrisclarkson100
▴ 160
0
votes
0
replies
693
views
Mixed model analysis using lme4
mixed-model
fixed-effect
lme4
random-effect
lmer
updated 12 months ago by
Ram
45k • written 4.1 years ago by
b.g.tamang
▴ 20
12
votes
8
replies
4.3k
views
7 follow
Highly used R packages with no Python equivalent
package
python
r
software
updated 4.1 years ago by
seidel
11k • written 4.1 years ago by
t
• 0
1
vote
2
replies
3.6k
views
install ensembl-vep
ensembl-vep
install
4.1 years ago by
yueli7
▴ 250
2
votes
3
replies
1.3k
views
How to separate sub-families from transposons sequence based fasta files?
fasta
transposons
updated 2.5 years ago by
Ram
45k • written 4.1 years ago by
ANAM
• 0
2
votes
1
reply
1.0k
views
calculating fold change from dataframe
fold
frame
change
data
updated 4.1 years ago by
ATpoint
89k • written 4.1 years ago by
Gil Rodriguez
• 0
1
vote
4
replies
1.4k
views
Variant calling from 5 MB regions coming from contrasting cultivars
calling
alignment
variant
4.1 years ago by
VenGeno
▴ 100
0
votes
0
replies
542
views
variant filtration with gene names or position
variant-filtration
4.1 years ago by
ziziqolo
▴ 10
0
votes
1
reply
830
views
How does find the sequence of each oligonucleotide in microarray probe?
Affymetrics
technology
probe
microarray
updated 4.1 years ago by
cpad0112
21k • written 4.1 years ago by
modarzi
▴ 170
2
votes
3
replies
2.7k
views
How to subset vcf by sample and write?
bcftools
vcf
updated 4.1 years ago by
sbstevenlee
▴ 480 • written 4.1 years ago by
lincaijin1994
▴ 50
0
votes
4
replies
2.3k
views
Can RNA-Seq be used for TMB calculation?
RNA-Seq
tmb
updated 4.1 years ago by
Kevin Blighe
89k • written 4.8 years ago by
rotemkat
▴ 10
0
votes
5
replies
8.5k
views
bcftools consensus still returns "Could not parse the header" error
bcftools
samtools
4.1 years ago by
shpak.max
▴ 60
1
vote
1
reply
1.6k
views
Detecting and masking repeats with EDTA: Low threshold vs complete masking
repeat
masker.
annotation
genome
EDTA
updated 4.1 years ago by
jaredbernard
▴ 30 • written 4.2 years ago by
zhtsandres
• 0
7
votes
5
replies
1.7k
views
Why does Txdb transcript length not always match to transcript end-start position?
biomart
transcript
Txdb
length
transcription
updated 4.1 years ago by
i.sudbery
22k • written 4.1 years ago by
Sora Yoon
▴ 20
0
votes
5
replies
2.8k
views
printing volcano plot
bioinfokit
python
gene_expression
volcano_plot
updated 4.1 years ago by
Ram
45k • written 4.1 years ago by
Gil Rodriguez
• 0
1
vote
0
replies
492
views
Myeloma Data Search
myeloma
updated 2.7 years ago by
Ram
45k • written 4.1 years ago by
anasjamshed
▴ 140
2
votes
4
replies
5.4k
views
Interpreting bcftools isec output
bcftools
isec
intersection
vcf
updated 3.7 years ago by
Ram
45k • written 4.1 years ago by
pabe
▴ 30
5
votes
4
replies
3.0k
views
How do we process Kallisto output (continuous real values) for DESEQ2 analysis (which strictly require discrete count values)?
read-counts
DESEQ2
differential-gene-expression
kallisto
updated 17 months ago by
Ram
45k • written 4.1 years ago by
mrj
▴ 180
0
votes
0
replies
951
views
Job:
Product Manager for Online Bioinformatics Resources for Online Bioinformatics Resources
Resources
Product-Manager
updated 2.5 years ago by
Ram
45k • written 4.1 years ago by
jyu
▴ 90
0
votes
2
replies
2.4k
views
[pysam] How to find both both primary and supplementary read?
NGS
pysam
bam
python
SAM
4.1 years ago by
octpus616
▴ 120
1
vote
2
replies
1.5k
views
question about Mutation Annotation Format (MAF) variant classifications
annotation
ICGC
MAF
R
4.1 years ago by
Charles Murtaugh
▴ 50
0
votes
1
reply
755
views
Cytogenetics Database
database
ISCN
Cytogenetics
4.1 years ago by
Jng
• 0
0
votes
3
replies
1.5k
views
KCCG /ClinSV issue with hg38
variation
human
genome
wgs
4.1 years ago by
Ishak
▴ 20
13
votes
15
replies
13k
views
6 follow
Where To Find Annotation File For Agilent Microarray?
annotation
updated 4.1 years ago by
smrutimayipanda
▴ 20 • written 12.1 years ago by
jobinv
★ 1.1k
0
votes
0
replies
623
views
Find causal mutation for a special trait in one population
Detecting
SV
SNP
4.1 years ago by
dominik.lagler
▴ 30
0
votes
0
replies
698
views
Genbank submission problem
tbl
genbank
gbff
submission
4.1 years ago by
hs
• 0
0
votes
1
reply
1.2k
views
errors installing HTSeq
HTSeq
RNAseq
updated 4.1 years ago by
GenoMax
153k • written 4.1 years ago by
rhksgudbc
• 0
2
votes
3
replies
1.1k
views
Genotyping variants from BAM (human)
genotyping
updated 4.1 years ago by
GenoMax
153k • written 4.1 years ago by
German.M.Demidov
★ 3.0k
0
votes
0
replies
559
views
Getting the average of pdb structure from only one trajectory
PBD
Trajectory
updated 4.1 years ago by
Michael
56k • written 4.1 years ago by
aaggencc
• 0
3
votes
1
reply
4.0k
views
Issues with enricher() function from clusterProfiler
clusterProfiler
enrichment
updated 4.1 years ago by
Guangchuang Yu
★ 2.6k • written 4.6 years ago by
luca.marisaldi
▴ 10
0
votes
13
replies
3.4k
views
Default CNV call thresholds for haplotype chromosome s
haplotype
cnvkit
mal
calling
cnv
updated 4.1 years ago by
German.M.Demidov
★ 3.0k • written 4.1 years ago by
enes
▴ 40
0
votes
0
replies
901
views
Job:
PostDoc in Bioinformatics / Machine Learning (Luxembourg, Europe)
PostDoc
machine-learning
updated 2.5 years ago by
Ram
45k • written 4.1 years ago by
Rainer
▴ 130
4
votes
4
replies
2.7k
views
How do I export a KaryoploteR plot or insert it into a grid/lattice? Can I assign a KaryoploteR plot to a variable?
karyoploteR
grid
ideograms
updated 4.1 years ago by
Lisa Ha
▴ 120 • written 4.1 years ago by
Andrew
▴ 20
2
votes
3
replies
1.7k
views
Cannot compile Lumpy-SV.
structural
KCCG
ClinSV
variation
4.1 years ago by
Ishak
▴ 20
6
votes
5
replies
1.8k
views
How to Append numbers on ALL headers in FASTA (e.g., >gene#1)?
FASTA
perl
Python
updated 4.1 years ago by
cpad0112
21k • written 4.1 years ago by
sasa
▴ 10
0
votes
2
replies
1.4k
views
How do you perform in silico PCR ?
taxonomy
PCR
NCBI
updated 4.1 years ago by
brunobsouzaa
▴ 840 • written 4.1 years ago by
Camp
• 0
4
votes
2
replies
2.4k
views
convert GenBank formatted sequence file to FASTA format
fasta
python
genback
updated 4.0 years ago by
Ram
45k • written 4.1 years ago by
lauren
▴ 20
6
votes
6
replies
5.4k
views
SRA-tools fasterq-dump and cellranger issues
cellranger
updated 2.9 years ago by
dhkwnr95
▴ 20 • written 4.1 years ago by
vishvak2000
▴ 10
0
votes
4
replies
1.7k
views
Functional enrichment and visualization of metatranscriptomics data
clusterProfiler
4.1 years ago by
shail.nair05
▴ 20
1
vote
0
replies
634
views
question about integrating snRNA seq data from different batch and different experimental conditions
Seurat
batch
integrate
4.1 years ago by
Wonjae
▴ 10
0
votes
0
replies
1.1k
views
Job:
Bioinformatics Postdoctoral Research Associate
postdoc
multi-omics
Python
Matlab
updated 2.5 years ago by
Ram
45k • written 4.1 years ago by
jobs
• 0
0
votes
1
reply
1.4k
views
Popgenome nvalid sites
vcf
Popgenome
4.1 years ago by
shinken123
▴ 150
121,831 results • Page
597 of 2437
Recent Votes
C: DiffBind error when calling dba.count
Answer: CBioPortal: What does Mutation type: Targeted_Region means?
Answer: CBioPortal: What does Mutation type: Targeted_Region means?
Comment: how to start
Comment: how to start
Answer: how to start
Comment: Perform Hierarchical Clustering in R with ggdendro Visualization
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Recent Replies
Comment: Parabricks : Number of GPUs requested (2) is more than number of GPUs (0) in the
by
Mensur Dlakic
★ 29k
For posterity, here is `nvidia-smi` output for our cluster: ``` +-------------------------------------------------------------------------…
Answer: Parabricks : Number of GPUs requested (2) is more than number of GPUs (0) in the
by
Mensur Dlakic
★ 29k
How often do we get a chance to help @yokofakun after all the help Pierre has provided? I feel like we have to make a serious effort here. …
Comment: DiffBind error when calling dba.count
by
Irene
• 0
I am having the same issue with the same situation, so i do not understand what could be the problem...i do not know if you finally figure …
Comment: Parabricks : Number of GPUs requested (2) is more than number of GPUs (0) in the
by
Pierre Lindenbaum
166k
@genomax I'm using the 'GPU' queue of my cluster (SLURM). The very same config was used with another parabrick subtool and I got not probl…
Comment: Parabricks : Number of GPUs requested (2) is more than number of GPUs (0) in the
by
GenoMax
153k
Are you running this under a job scheduler? Is there a separate partition for the GPU's/are they accessible to the scheduler?
Comment: Learning Bioinformatics doing Projects
by
Anjali
• 0
thank you.
Comment: Statistical test of difference between two conditions and account for the batch
by
ATpoint
89k
Are the batches biological replicates?
Comment: how to start
by
shelkmike
★ 1.7k
If you want to save time at the cost of having a lesser understanding of how bioinformatic programs work, you may study through the BioStar…
Answer: how to start
by
shelkmike
★ 1.7k
I would recommend, in the following order:<br> 1) Go through Bioinformatics Algorithms, either as a video course or as a book, and do all e…
Comment: Perform Hierarchical Clustering in R with ggdendro Visualization
by
Bastien Hervé
6.4k
For what is worth, in a previous project, I have done some tests on different hierarchical clustering methods for single cell RNAseq. I had…
Answer: how to start
by
yura.grabovska
▴ 820
* Get some data - either your own or from a paper / GEO / ArrayExpress / SRA / TCGA / cBioPortal etc etc. * Look at the methods of papers…
Comment: Perform Hierarchical Clustering in R with ggdendro Visualization
by
ATpoint
89k
"ward.D2" -- top of the pops in terms of interpretatble clusters from gene expression data in my hands, the rest is...often crytpic.
Comment: High percentage of intronic/intergenic reads in RNA-seq
by
i.sudbery
22k
I'd expect to see more or less what they see in your reference. Somewhere between half and two thirds of reads mapping to exons. The low fr…
Comment: Perform Hierarchical Clustering in R with ggdendro Visualization
by
Bastien Hervé
6.4k
As the whole presentation relies on a distance matrix and elements aggregation by hierarchical clustering, it would be helpful to better un…
Comment: Perform Hierarchical Clustering in R with ggdendro Visualization
by
GenoMax
153k
> Read in data Add an example of what is in `data.csv`.
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