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121,832 results • Page
603 of 2437
Sort: Rank
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Votes
Replies
0
votes
0
replies
946
views
Clarifications about intercepts when fitting models with DESeq2
GLM
rnaseq
DESeq2
DEA
rna-seq
4.1 years ago by
Eisuan
▴ 20
0
votes
1
reply
1.1k
views
using a singualrity application ARGs-OAP
Data-Analysis
WholeShotgunMetagenome
AMR
Microbiome
Metagenomics
updated 4.1 years ago by
ATpoint
89k • written 4.1 years ago by
serene.s
• 0
4
votes
4
replies
2.9k
views
Single-stranded RNA-seq: strandedness of samples
rnaseq
4.1 years ago by
fr
▴ 220
3
votes
4
replies
3.1k
views
Choice of normalization method for spike-in data
spike-in
DiffBind
4.1 years ago by
eashby47
▴ 10
0
votes
1
reply
1.9k
views
Job:
Postdoctoral Position, Department of Biology , Colorado State University
postdoc
updated 2.5 years ago by
Ram
45k • written 4.1 years ago by
Anireddy
• 0
1
vote
6
replies
2.0k
views
How to group transcripts by "gene" from different transcript assemblies?
assembly
trinity
rnaspades
transcript
updated 4.1 years ago by
ponganta
▴ 590 • written 4.1 years ago by
O.rka
▴ 750
0
votes
7
replies
2.3k
views
How to get fold changes from MetaDE package in R?
R
MetaDE
updated 4.1 years ago by
ATpoint
89k • written 4.1 years ago by
humbertojirey
• 0
0
votes
1
reply
896
views
C. elegans WGS large portion of reads flagged as unmapped with Sam flag 133 and 165
sam
WGS
flag
133
165
unmapped
updated 4.1 years ago by
Tm
★ 1.1k • written 4.1 years ago by
tyler.j.kennedy
• 0
0
votes
0
replies
872
views
Help With Cbioportal expression data
rnaseq
TCGA
R
cbioportal
bioconductor
4.1 years ago by
daniela.paola.s.p
▴ 70
2
votes
2
replies
1.1k
views
Pathway Expression Analysis on Individual Cells?
seurat
sc-RNA-seq
4.1 years ago by
ospinae
• 0
0
votes
1
reply
961
views
Protein homolog query issue
transcriptom
blast
species
sequence
Related
updated 4.1 years ago by
Jean-Karim Heriche
27k • written 4.1 years ago by
jaqx008
▴ 110
0
votes
0
replies
572
views
variant impact on immune genes
Genes
Variant
SnpEff
4.1 years ago by
Adarsh Kuamr
▴ 60
0
votes
1
reply
780
views
Protein to gene name conversion
ID
R
updated 4.1 years ago by
GenoMax
153k • written 4.1 years ago by
mm2568
• 0
2
votes
2
replies
859
views
Nanopore dRNA - view unmapped segments of mapped reads
nanopore
sequencing
directRNA
updated 4.1 years ago by
GenoMax
153k • written 4.1 years ago by
yryan
▴ 10
0
votes
0
replies
619
views
What should I write after --operation in ANNOVAR for my interest database ?
ANNOVAR
CIViC
annotation
DoCM
VCF
4.1 years ago by
Zahra
▴ 110
4
votes
7
replies
3.3k
views
Download all Becteria and protist fasta protein sequences from UNIPROT proteomes
uniprot
fetch
fasta
proteome
bash
4.1 years ago by
Chvatil
▴ 140
0
votes
0
replies
713
views
Job:
Bioinformatician (f/m/d)
Hamburg
genomics
Germany
4.1 years ago by
gasta88
▴ 50
0
votes
0
replies
780
views
Job:
Software Engineer / Software Developer (f / m / d) for software in the context of DNA sequencing-based cancer diagnostics
Hamburg
genomics
Germany
4.1 years ago by
gasta88
▴ 50
0
votes
1
reply
726
views
Choosing the right sample among GEO datasets
GEOdatasets
chipsamples
celllinesamples
chipseq
chipseqanalysis
updated 4.1 years ago by
ATpoint
89k • written 4.1 years ago by
buffealo
▴ 130
6
votes
3
replies
6.5k
views
K-means for RNA seq gene clustering
kmeans
updated 4.1 years ago by
Kevin Blighe
89k • written 4.1 years ago by
curiousmind007
▴ 30
3
votes
6
replies
6.4k
views
How do I detect deletions?
bcftools
DNA-seq
calling
variant
updated 4.1 years ago by
bernatgel
★ 3.4k • written 4.1 years ago by
gt
▴ 30
1
vote
3
replies
2.3k
views
Can I use All Peaks (MACS2 -q 1) for analysis?
Peak
DiffBind
MACS2
4.1 years ago by
Tian
▴ 50
0
votes
0
replies
813
views
Job:
UK PhD Opportunity: Text mining the impact of SARS-CoV-2 mutations from the research literature at University of Glasgow
bionlp
sars-cov-2
text-mining
4.1 years ago by
jake.lever
▴ 50
1
vote
4
replies
1.4k
views
How to get from annotated sequences to UniProt IDs
annotation
updated 4.1 years ago by
Tm
★ 1.1k • written 4.1 years ago by
robert.murphy
▴ 110
0
votes
2
replies
1.5k
views
Low read counts in one of three biological replicates. Remove?
RNA-Seq
4.1 years ago by
nadal-t
▴ 20
0
votes
5
replies
1.8k
views
Considering the multiple test correction for the analysis of polygenic risk score association
association
allele
polygenic
score
Bonferroni
updated 4.1 years ago by
German.M.Demidov
★ 3.0k • written 4.1 years ago by
seta
★ 1.9k
0
votes
0
replies
1.5k
views
Job:
Post-doctoral Fellow in Cancer Biology and Immunology
biology
immunology
Cancer
molecular
4.1 years ago by
waihungh
▴ 20
0
votes
0
replies
1.4k
views
Job:
Pacific Biosciences: Senior Bioinformatics Software Engineer (remote)
software-engineer
updated 2.5 years ago by
Ram
45k • written 4.1 years ago by
Armin
• 0
0
votes
1
reply
1.6k
views
annotation parameter in ChIPQC
ChIP-Seq
ChIPQC
updated 4.1 years ago by
384306874
• 0 • written 5.2 years ago by
chaudharyc61
▴ 110
0
votes
0
replies
919
views
Motif finding HOMER results
interpretation
finding
HOMER
motif
4.1 years ago by
c.heininger
▴ 10
5
votes
12
replies
3.6k
views
How do you limit the result from the BLAST executable?
blast
updated 4.1 years ago by
gb
★ 2.2k • written 4.1 years ago by
adhamzul
▴ 20
0
votes
1
reply
820
views
EnsemblVEP could not generate any output for a list of frameshift insertion input
Frame_Shift_Insertion
EnsemblVEP
4.1 years ago by
nazaninhoseinkhan
▴ 530
0
votes
1
reply
856
views
How do I extract predicted genes from annotation from MAKER-P?
MAKER-P
updated 4.1 years ago by
Ram
45k • written 4.1 years ago by
eennadi
▴ 40
0
votes
0
replies
873
views
Renaming ggplot heatmap x-axis from gene names to number of genes
axes
ggplot2
heatmap
4.1 years ago by
Anand
▴ 40
3
votes
1
reply
1.7k
views
genome assembly in org.Mm.eg.db
R
updated 2.5 years ago by
Ram
45k • written 4.1 years ago by
anithaslvn
▴ 10
0
votes
1
reply
1.1k
views
How to find the names of elements while parsing PDB files via biopython?
Biopython
PDB
4.1 years ago by
Tzunami
▴ 10
1
vote
1
reply
1.2k
views
Best current tool for deconvolution of bulk sample
cibersort
updated 4.1 years ago by
Evan
▴ 250 • written 4.1 years ago by
changxu.fan
▴ 80
2
votes
3
replies
1.4k
views
plant viruses sequences
alignment
gene
updated 4.1 years ago by
GenoMax
153k • written 4.1 years ago by
Ric
▴ 440
0
votes
0
replies
819
views
ichorCNA mouse reference files for calling copy number
copynumber
4.1 years ago by
heskett
▴ 110
0
votes
8
replies
1.7k
views
use a list of id to extract sequence from different genomics
sequence
perl
4.1 years ago by
LZH289
• 0
0
votes
0
replies
710
views
Job:
postdoctoral position in bioinformatics/computational proteomics
BionformaticsPostdocUTMB
4.1 years ago by
Rovshan
• 0
0
votes
0
replies
524
views
PoolSNP RuntimeError: dictionary changed size during iteration
Poolsnp
4.1 years ago by
shpak.max
▴ 60
1
vote
1
reply
1.0k
views
What is the right way to merge multiple patient samples in scrna-seq?
Seurat
scrna-seq
cell
processing
updated 4.1 years ago by
ATpoint
89k • written 4.1 years ago by
cogen859
• 0
1
vote
3
replies
1.6k
views
How to filter VEP results of "missing values"
filter
VEP
updated 4.1 years ago by
GenoMax
153k • written 4.1 years ago by
YL
▴ 10
2
votes
2
replies
1.4k
views
Tool:
miRAnno—network-based functional microRNA annotation
pathways
miRNA
annotation
microRNA
4.1 years ago by
tomastokar
▴ 50
0
votes
0
replies
443
views
Determining the effect of dataset size in results
R
4.1 years ago by
a_confused_biologist
• 0
21
votes
14
replies
12k
views
Tool:
trackplot: Fast and minimal dependency standalone R script to generate IGV style locus tracks from bigWig files
visualization
igv
ChIP-Seq
R
bigwigs
updated 2.2 years ago by
Ram
45k • written 4.8 years ago by
poisonAlien
★ 3.2k
1
vote
3
replies
2.1k
views
SSPACE bowtie and bwa error
Assembly
next-gen
software error
genome
updated 4.1 years ago by
hnt001
▴ 10 • written 6.2 years ago by
milady81
▴ 70
0
votes
1
reply
1.3k
views
EdgeR - Input for Analysis Functions (estimateDisp, exactTest, glmQLFit)
edgeR
R
4.1 years ago by
Noah E.
▴ 20
1
vote
1
reply
1.1k
views
How to change CpG methylation cutoffs in edgeR
R
updated 4.1 years ago by
iraia.munoa
▴ 130 • written 5.4 years ago by
embueno
• 0
121,832 results • Page
603 of 2437
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Motif analysis of DMRs (Differentially Methylated Regions) by HOMER
Comment: Parabricks : Number of GPUs requested (2) is more than number of GPUs (0) in the
Answer: Parabricks : Number of GPUs requested (2) is more than number of GPUs (0) in the
Answer: Split chromosome into smaller fragments to save memory when build xg and gcsa in
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?
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Answer: Criteria for choosing variants
by
benformatics
4.2k
The whole question seems very confusing as if there is a substantial knowledge gap. Calling variants in tumor-normal pairs is relatively…
Comment: How to fix "Please indicate the file directory in 'setting' file?" for MaxBin2?
by
GenoMax
153k
> Cannot run FragGeneScan. Please indicate the file directory in 'setting' file. Looks like you will need to add the. directory containing…
Comment: How to fix "Please indicate the file directory in 'setting' file?" for MaxBin2?
by
Pallishree
• 0
i have run this command (maxbin2_env) [m5@mks1 FASTQ]$ /data/sms/home/m5/.conda/envs/maxbin2_env/bin/run_MaxBin.pl \ ? -contig /…
Comment: Parabricks : Number of GPUs requested (2) is more than number of GPUs (0) in the
by
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3.4k
The `--nv` flag for apptainer is there?
Comment: Parabricks : Number of GPUs requested (2) is more than number of GPUs (0) in the
by
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3.4k
The GPUs have 24 GB memory each but only worked with the flag.
Comment: Parabricks : Number of GPUs requested (2) is more than number of GPUs (0) in the
by
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166k
it doesn't work with `--htvc-low-memory` (same error with 4.5.0-1 )
Comment: Parabricks : Number of GPUs requested (2) is more than number of GPUs (0) in the
by
GenoMax
153k
`Parabrix` is not supported on multi-instance GPU's (MIG) so having that setting disabled is perfect.
Comment: Parabricks : Number of GPUs requested (2) is more than number of GPUs (0) in the
by
GenoMax
153k
That option is indicated for using a 16GB GPU. Was that the case or even though you had a >16 GB GPU, this option was needed to fix the err…
Comment: Parabricks : Number of GPUs requested (2) is more than number of GPUs (0) in the
by
Arup Ghosh
3.4k
I faced a similar issue with Parabricks and version 4.3.0; using `--htvc-low-memory` resolved the problem.
Comment: Parabricks : Number of GPUs requested (2) is more than number of GPUs (0) in the
by
Mensur Dlakic
★ 29k
Maybe this will help: https://stackoverflow.com/questions/67091056/gpu-allocation-in-slurm-gres-vs-gpus-per-task-and-mpirun-vs-srun
Comment: Split chromosome into smaller fragments to save memory when build xg and gcsa in
by
Jordan M Eizenga
▴ 750
GCSA2 indexing is fairly demanding on disk space, so that can happen. I would generally recommend having 1-2 TB of disk availability if you…
Comment: how to start
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shelkmike
★ 1.7k
If you plan to become a professional bioinformatician, I don't recommend the approach suggested by Joe and Yura Grabovska (learning bioinfo…
Comment: vg input and output files
by
GenoMax
153k
Have you looked at this page: https://github.com/vgteam/vg/wiki/Basic-Operations There is a pipeline illustration on this page that shows …
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by
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89k
To me knowledge, ensembl approach means that you run several tools and then run some sort of filtration and classification approach to deci…
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by
Pierre Lindenbaum
166k
vg is a toolkit containing different tools. What are you talking about when you want to use 'input' and 'output' files.
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