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122,009 results • Page
1 of 2441
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Votes
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0
votes
0
replies
64
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Should differential expression analysis be incorporated in cross validation for training machine learning models?
RNA-seq
DEA
TCGA
Learning
Machine
5 hours ago by
yordany.perdigon
• 0
1
vote
0
replies
64
views
News:
Manual Genome Curation using PretextView course
Genome-Assembly
PretextView
HI-C
Manuel-Curation
15 hours ago by
Physalia-courses
★ 2.6k
4
votes
9
replies
415
views
DESeq2 on metagenome KO counts
abundance
KEGG
KO
deseq
metagenome
gene
updated 19 hours ago by
Aleksandra
▴ 180 • written 1 day ago by
young_bioinformatician
▴ 240
0
votes
0
replies
94
views
News:
Introduction to Processing and Analysis of Spatial Multiplexed Proteomics Data
Spatial
Proteomics
omics
updated 23 hours ago by
GenoMax
154k • written 1 day ago by
oliverhooker
▴ 110
846
votes
170
replies
215k
views
112 follow
News:
The Biostar Handbook. A bioinformatics e-book for beginners.
handbook
training
updated 10 days ago by
Biostar
3.6k • written 8.9 years ago by
Istvan Albert
103k
17
votes
12
replies
826
views
6 follow
GUI commercial software for 10x single cell gene expression analysis
single-cell
software
commercial
gui
updated 1 day ago by
Istvan Albert
103k • written 5 days ago by
firestar
★ 1.7k
2
votes
1
reply
138
views
FACS quality control based on size and doublet detection in scRNA-seq
sequencing
FACS
detection
rna
doublet
cell
scRNA-seq
single
updated 1 day ago by
ATpoint
89k • written 1 day ago by
carolofharvest
▴ 50
0
votes
0
replies
100
views
combine VCF from diploid reference/haplotypes for the same sample
bcftools
combine
VCF
1 day ago by
Matteo Ungaro
▴ 130
4
votes
4
replies
236
views
How to handle TrEMBL proteins without gene annotation in plasma proteomics?
biomarker
uniprot
proteomics
annotation
trembl
updated 1 day ago by
Elisabeth Gasteiger
★ 2.4k • written 1 day ago by
Luwell
• 0
6
votes
2
replies
175
views
Recommendations for 200 SNP markers genotyping
sequencing
DNA
genotyping
marker
updated 1 day ago by
Aleksandra
▴ 180 • written 1 day ago by
PolenP
▴ 10
0
votes
2
replies
235
views
Interpreting genomic features distribution for CUT&RUN peaks
cut_and_run
genomic
features
1 day ago by
Rozita
▴ 40
0
votes
1
reply
134
views
hisat2 error-Paired end reads not equal or lack of RAM/disk space?
end
fastq
paired
updated 1 day ago by
lieven.sterck
16k • written 1 day ago by
aj123
▴ 130
0
votes
1
reply
141
views
Reasonable number of SNPs in a bacterial genome.
SNP
bacteria
updated 1 day ago by
dthorbur
★ 3.1k • written 1 day ago by
yesquokkan
• 0
2
votes
6
replies
489
views
Difficulty running FoldX in linux
DDG
foldx
updated 1 day ago by
strayeroliver
• 0 • written 3 days ago by
strayeroliver
▴ 10
0
votes
2
replies
220
views
Active site using castpfold
activesite
castpfold
Docking
updated 1 day ago by
Mensur Dlakic
★ 30k • written 2 days ago by
Ria
• 0
5
votes
12
replies
1.0k
views
6 follow
Differences between published differential gene expression results and own analysis on RNA-seq data
R
TCGA
LIMMA
updated 2 days ago by
Zhenyu Zhang
★ 1.3k • written 9 days ago by
vernonlim98
• 0
1
vote
4
replies
319
views
Problems with PacBio's Improved Phased Assembler (IPA)
pacbio
hifi
assembly
genome
1 day ago by
Panos
★ 1.8k
0
votes
6
replies
367
views
downloading raw bam files from pacbio sequencer
raw
bam_file
raw_subreads
reads
updated 2 days ago by
GenoMax
154k • written 3 days ago by
pranavdatar01
• 0
0
votes
0
replies
125
views
Best way to map biological pathways to cancer hallmarks using PLMs (without building models)?
PLM
mapping
LLM
extraction
Relation
2 days ago by
DEPANSHI
• 0
0
votes
2
replies
316
views
installation of package ‘DESeq2’ had non-zero exit status
Bioinformatics
updated 2 days ago by
GenoMax
154k • written 2 days ago by
Sarita
• 0
0
votes
1
reply
170
views
Checkm results differ from database info
How-to-solve
Checkm
Error
updated 2 days ago by
Mensur Dlakic
★ 30k • written 2 days ago by
alevbozan18
• 0
0
votes
2
replies
1.0k
views
Transverse data
EXCEL
Unix
updated 2 days ago by
basu
• 0 • written 2.7 years ago by
Sidra
• 0
0
votes
0
replies
138
views
Is this the correct order of steps in GATK germline cohort variant calling (VQSR workflow)?
gVCF
VCF
GATK
VQSR
2 days ago by
Ramnaresh
• 0
0
votes
0
replies
164
views
How to select background metabolite sets for differential metabolite enrichment analysis?
enrichment
ORA
2 days ago by
Edward
• 0
0
votes
2
replies
240
views
Pseudogene - scarce info
pseudogene
mastersdegree
2 days ago by
mf810
• 0
2
votes
3
replies
306
views
SNP calling ONT sequenced files
ONT
SNPs
updated 3 days ago by
cfos4698
★ 1.2k • written 3 days ago by
blur
▴ 280
0
votes
4
replies
1.7k
views
HIV NL4-3 transcriptome fasta
rna-seq
CLIP-seq
updated 3 days ago by
Ales
▴ 70 • written 5.5 years ago by
xiaoleiusc
▴ 140
1
vote
1
reply
226
views
Doubt on docking
docking
active
site
bioinformatics
updated 3 days ago by
Mensur Dlakic
★ 30k • written 3 days ago by
Ria
• 0
0
votes
0
replies
158
views
News:
Online course: RNA sequencing data analysis using R and Bioconductor - 3–14 November
R
DifferentialExpressionAnalysis
RNAseq
Bioconductor
3 days ago by
Physalia-courses
★ 2.6k
6
votes
3
replies
329
views
Nextflow MultiQC runs multiple times due to FASTQC zip name collisions
fastqc
nextflow
multiqc
updated 3 days ago by
Phil Ewels
★ 1.5k • written 4 days ago by
DdogBoss
▴ 30
0
votes
1
reply
4.9k
views
News:
::Last Call:: In-Person Workshop - NGS Epigenomics Data Analysis (November 3-5 in Munich) - BS-Seq, ChIP-Seq, ATAC-Seq, ...
chip-seq
atac-seq
bs-seq
3 days ago by
ecSeq Bioinformatics
▴ 20
0
votes
2
replies
5.5k
views
Best set of tools / workflows for predicting the biosynthesis pathways of complex organic molecules
ngs
pathways
bioinformatics
updated 3 days ago by
ehaag
▴ 100 • written 19 days ago by
Mark
▴ 60
12
votes
14
replies
3.3k
views
6 follow
Tools to simulate Illumina short read sequences and ONT long reads with a reference genome
simulate
reads
bioinformatics
short
short-read
updated 1 day ago by
colindaven
8.0k • written 11 days ago by
PolenP
▴ 10
1
vote
1
reply
227
views
Corresponding BAM files
BAM
SRA
GEO
FASTQ
updated 3 days ago by
GenoMax
154k • written 3 days ago by
aj123
▴ 130
0
votes
1
reply
236
views
scVI vs Harmony, which is better for cell type based clustering in brain tissue?
harmony
scVI
single
cell
updated 3 days ago by
Arup Ghosh
3.4k • written 4 days ago by
biotrekker
▴ 110
0
votes
2
replies
1.7k
views
Analyzing CRISPR and RNAi genome wide screens
CRISPR
RNAi
meta analysis
updated 4 days ago by
Meisam
▴ 250 • written 7.3 years ago by
spacemorrissey
▴ 280
0
votes
3
replies
2.7k
views
meta data analysis for clustering
meta-analysis
clustering
functional genomics
updated 4 days ago by
Meisam
▴ 250 • written 7.7 years ago by
jiwpark00
▴ 230
2
votes
9
replies
3.4k
views
GTF file for HIV strain pNL4-3
HIV
annotation
mapping
updated 4 days ago by
Ales
▴ 70 • written 7.3 years ago by
caggtaagtat
★ 1.9k
0
votes
1
reply
212
views
Diffbind or DESEQ2 Chipseq data
Chipseq
DESEQ2
Diffbind
4 days ago by
Irene
• 0
0
votes
0
replies
173
views
Job:
Postdoctoral Fellowship at the American Museum of Natural History's Richard Gilder Graduate School
Postdoctoral
Fellowship
4 days ago by
Info-rggs
▴ 20
0
votes
0
replies
178
views
News:
Autumn School in Bioinformatics - online, 20–24 October
NGS
Phylogenomics
RNAseq
Singularity
Docker
4 days ago by
Physalia-courses
★ 2.6k
1
vote
4
replies
411
views
Dorado in PowerShell on Windows
Windows
on
PowerShell
in
Dorado
updated 3 days ago by
jared.andrews07
★ 19k • written 4 days ago by
sbissi102
▴ 10
1
vote
0
replies
192
views
Is this an appropriate command for estimating contaminatin in a germline WGS sample using GATK?
gatk
4 days ago by
curious
▴ 900
1
vote
4
replies
444
views
Which aligner is more suitable for ONT R10.4.1 Dorado-corrected reads: minimap2 or winnowmap?
winnowmap
minimap2
R10.4.1
Nanopore
4 days ago by
tungsega
▴ 10
2
votes
2
replies
346
views
Nextflow: How to format input tuple for STAR_ALIGN process with STAR index directory
nextflow
5 days ago by
DdogBoss
▴ 30
4
votes
4
replies
443
views
how to respond that my research does not have experimental validation
rebuttal
updated 5 days ago by
Mensur Dlakic
★ 30k • written 5 days ago by
nuorain
▴ 40
6
votes
6
replies
545
views
Quantification using salmon in alignment-based mode after minimap2 run
nanopore
ont
salmon
updated 4 days ago by
Rob
7.2k • written 5 days ago by
Assa Yeroslaviz
★ 1.9k
1
vote
1
reply
294
views
infercnv error at STEP 18 - file descriptor is too large for select()
R
10x
singlecell
infercnv
5 days ago by
yura.grabovska
▴ 840
0
votes
0
replies
214
views
News:
online course - Environmental Metagenomics
Illumina
Metagenomics
Nanopore
MAGs
5 days ago by
Physalia-courses
★ 2.6k
0
votes
1
reply
275
views
Need Help : JGI IMG Bulk Download
Bioinformatics
updated 5 days ago by
GenoMax
154k • written 5 days ago by
Ananaya
• 0
122,009 results • Page
1 of 2441
Recent Votes
Manual Genome Curation using PretextView course
Answer: How to get proteins from GFF file resulted from MAKER annotation
Comment: DESeq2 on metagenome KO counts
Answer: DESeq2 on metagenome KO counts
Answer: DESeq2 on metagenome KO counts
Answer: DESeq2 on metagenome KO counts
Comment: GUI commercial software for 10x single cell gene expression analysis
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Recent Replies
Comment: DESeq2 on metagenome KO counts
by
ATpoint
89k
This statement makes zero sense in response to what I wrote.
Comment: DESeq2 on metagenome KO counts
by
Aleksandra
▴ 180
I focused on the fact that DESeq2 models overdispersion, but overlooked its implicit assumption: normalisation works when the main source o…
Comment: DESeq2 on metagenome KO counts
by
Aleksandra
▴ 180
Thank you very much. I mistakenly drew a superficial analogy. I equated KO counters with gene counters.
Comment: DESeq2 on metagenome KO counts
by
ATpoint
89k
Both vst or logcpm will favor expression level (magnitude of counts) rather than differences in a hclust/heatmap. For differences you need …
Comment: DESeq2 on metagenome KO counts
by
ATpoint
89k
The DESeq2 developer has advised many times against DESeq2 for metagenomics. Please search for related posts over at support.bioconductor.o…
Answer: DESeq2 on metagenome KO counts
by
andres.firrincieli
3.9k
I wouldn’t use DESeq2 on aggregated raw counts per KO, because doing so means accepting two pretty big assumptions: 1. All genes with t…
Comment: DESeq2 on metagenome KO counts
by
Aleksandra
▴ 180
(I apologise for my previous reply; I wanted to be as detailed as possible) DESeq2 handles KO counts perfectly well. For a time-series des…
Comment: DESeq2 on metagenome KO counts
by
Aleksandra
▴ 180
I apologise for how that sounded; I wanted to be as detailed as possible.
Comment: GUI commercial software for 10x single cell gene expression analysis
by
Istvan Albert
103k
A comment on: "*Wonky analysis is possible even with open-source R libraries.*" True - and arguably, the risk of a wonky analysis is actua…
Comment: GUI commercial software for 10x single cell gene expression analysis
by
GenoMax
154k
`Trailmaker` likely only supports Parse's evercode data. <br> `BioTuring` does not appear to have published pricing. <br> `Rosalind` appear…
Answer: GUI commercial software for 10x single cell gene expression analysis
by
firestar
★ 1.7k
Found a few more when I asked around. I have no idea how good or bad these are. If anyone has used these or knows more about these, feel fr…
Comment: How to handle TrEMBL proteins without gene annotation in plasma proteomics?
by
GenoMax
154k
> I performed a standard proteomics screening workflow What database did you use to search against? Perhaps you are using an old (not so c…
Answer: FACS quality control based on size and doublet detection in scRNA-seq
by
ATpoint
89k
No, it's unrelated. Doublets in 10x happen if two cells get enclosed into the same GEM droplet. This has nothing to do with how flow cytome…
Answer: How to handle TrEMBL proteins without gene annotation in plasma proteomics?
by
Elisabeth Gasteiger
★ 2.4k
Apparently you are working with human proteins? I would strongly recommend looking only at proteins that are part of the human reference pr…
Comment: Tools to simulate Illumina short read sequences and ONT long reads with a refere
by
colindaven
8.0k
Wow, thats too long. How much RAM does your machine have, it is likely swapping
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