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122,009 results • Page
608 of 2441
Sort: Rank
Rank
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Votes
Replies
4
votes
5
replies
1.4k
views
6 follow
Gene prediction methods
Gene
prediction
updated 4.2 years ago by
GenoMax
154k • written 4.3 years ago by
Pratheep
▴ 150
1
vote
4
replies
2.4k
views
cellranger count aggregated to transcripts
cellranger
gtf
10x
updated 4.2 years ago by
benformatics
4.2k • written 4.2 years ago by
jomo018
▴ 730
1
vote
4
replies
2.1k
views
Paired-end to Single-end
bam
updated 4.2 years ago by
Kevin Blighe
89k • written 4.2 years ago by
kstangline
▴ 110
1
vote
4
replies
2.4k
views
extracting fasta sequence from fasta file with multiple genomes
bedtools
fasta
grep
updated 4.2 years ago by
cpad0112
21k • written 4.2 years ago by
ss3943
• 0
0
votes
0
replies
739
views
Repeat masking custom library not reading
masking
repeat
ngs
repeatmasker
4.2 years ago by
Shri hari
▴ 40
8
votes
10
replies
3.0k
views
FASTA of translated amino acid sequences in their six reading frames, which one is the optimal?
aminoacid
protein
peptide
Reading
optimal
frames
4.2 years ago by
Luis999
▴ 20
0
votes
4
replies
2.3k
views
kissplice2reftranscriptome interpreting output
RNA-Seq
kissplice2reftranscriptome
kissplice
updated 4.2 years ago by
944908620
• 0 • written 7.7 years ago by
rares_lucaciu
• 0
0
votes
0
replies
975
views
PSMC parameter choosing (-t, -p)
psmc
updated 2.5 years ago by
Ram
45k • written 4.2 years ago by
clinnaeus
▴ 30
9
votes
5
replies
30k
views
7 follow
DESeq2 analysis for multiple conditions
RNA-Seq
DESeq2
updated 2.8 years ago by
Ram
45k • written 10.4 years ago by
eager_learner
▴ 60
0
votes
1
reply
1.5k
views
Help with installing Bayescan (Big Sur)
Installation
commandline
Bayescan
updated 4.2 years ago by
ATpoint
89k • written 4.2 years ago by
8bde229f
• 0
2
votes
2
replies
1.3k
views
Functional annotation by blast
trembl
Blast
nr
Functional_annotation
Blast2GO
4.2 years ago by
GenesisBio
• 0
0
votes
0
replies
1.6k
views
Job:
Senior Postdoctoral Research Fellow at Big Data Institute, University of Oxford
big
postdoc
genomics
data
4.2 years ago by
Shicheng Guo
★ 9.6k
0
votes
1
reply
1.5k
views
What does betaPrior do in DESEQ?
DESeq
RNAseq
updated 4.2 years ago by
i.sudbery
22k • written 4.2 years ago by
kirby199
• 0
0
votes
0
replies
942
views
Herald:
The Biostar Herald for Monday, July 26, 2021
herald
4.2 years ago by
Biostar
3.6k
0
votes
1
reply
961
views
Handling cultivars in transcriptome de novo assembly
transcriptomic
trinity
DGE
updated 4.2 years ago by
h.mon
35k • written 4.2 years ago by
DaneLukin
• 0
0
votes
1
reply
826
views
Quantify the effects of a gene list between datasets
scRNA-Seq
Comparison
RNA-Seq
4.2 years ago by
bioinf.questions
• 0
4
votes
4
replies
2.1k
views
RNA-seq for samples with RIN<3
RIN
Low
updated 8 months ago by
Emilie
▴ 10 • written 4.2 years ago by
mariam28071993
• 0
1
vote
1
reply
783
views
How can I extract duplicated rows for the same value and write them down in one row
bash
updated 4.2 years ago by
Ram
45k • written 4.2 years ago by
amal.elzemrany
▴ 30
3
votes
3
replies
2.1k
views
How do you split metagenomic bins/MAGs into eukaryotic and prokaryotic?
protist
metagenomics
prokaryotic
eukaryotic
gtdbtk
updated 4.2 years ago by
Mensur Dlakic
★ 30k • written 4.2 years ago by
O.rka
▴ 750
2
votes
2
replies
1.2k
views
Helper packages for differential gene expression analysis in R
dge
deseq2
RNA-seq
r
updated 4.2 years ago by
GenoMax
154k • written 4.2 years ago by
Dunois
★ 2.9k
0
votes
0
replies
636
views
How can I conduct GO/Pathway analysis in EdgeR when there is >1 value for each gene?
edgeR
R
4.2 years ago by
Noah E.
▴ 20
1
vote
0
replies
682
views
GO Term analysis
GO
updated 4.2 years ago by
Ram
45k • written 4.2 years ago by
snehu.sambare
▴ 10
1
vote
2
replies
1.9k
views
Merge regions in bedgraph file
bedgraph
4.2 years ago by
eoneill627
▴ 20
0
votes
0
replies
920
views
Paired Analysis in EdgeR
EdgeR
PairedAnalysis
4.2 years ago by
bryan.yankee27
• 0
1
vote
2
replies
1.0k
views
Low similarity gene alignment
analysis
align
gene
updated 4.2 years ago by
Dunois
★ 2.9k • written 4.2 years ago by
Hsiangnan Cheng
• 0
0
votes
1
reply
1.0k
views
metascape
list
gene
input
metascape
updated 4.2 years ago by
Ram
45k • written 4.2 years ago by
fionajcunningham
• 0
5
votes
5
replies
4.3k
views
Visualiation of samtools depth output in a plot
plot
depth
samtools
updated 4.0 years ago by
Carlo Yague
9.0k • written 4.2 years ago by
dominik.lagler
▴ 30
1
vote
3
replies
1.2k
views
ALT-aware autodetection of hg38.p13 in DRAGEN
alt
patch
alt-aware
dragen
hg38
updated 4.2 years ago by
GenoMax
154k • written 4.2 years ago by
Tal
• 0
0
votes
0
replies
1.1k
views
Error with CONVERTF mergeit program
plink
convertf
eigenstrat
4.2 years ago by
harmadikemil
• 0
2
votes
2
replies
1.2k
views
Filter vcf file based on the GTs of a single sample
bcftools
vcf
samtools
bcf
updated 4.2 years ago by
sbstevenlee
▴ 480 • written 4.2 years ago by
miguellarrazlopezdenovales
▴ 20
4
votes
6
replies
2.7k
views
6 follow
What is the best annotation tool?
VCF
annotation
updated 4.2 years ago by
colindaven
8.0k • written 4.2 years ago by
Sonia
• 0
0
votes
0
replies
997
views
Job:
Postdoctoral Fellowship in Bioinformatics and Liver Cancer Genomics
Cancer
NGS
Single-cell
genomics
updated 2.6 years ago by
Ram
45k • written 4.2 years ago by
waihungh
▴ 20
0
votes
0
replies
1.6k
views
Job:
PhD Scholarship in Bioinformatics and Liver Cancer Genomics
Cancer
NGS
Single-cell
genomics
updated 2.6 years ago by
Ram
45k • written 4.2 years ago by
waihungh
▴ 20
0
votes
0
replies
898
views
Job:
research assistant in bioinformatics at Essen University Hospital
metadata
Germany
Essen
updated 2.6 years ago by
Ram
45k • written 4.2 years ago by
christina.klaere
• 0
1
vote
6
replies
7.6k
views
How to write a .pdb file using Python
python
PDB
output
updated 4.2 years ago by
Nitin Narwade
★ 1.7k • written 4.2 years ago by
Jingtong
• 0
3
votes
36
replies
7.6k
views
inquiry related to snpsift
rsid
snp
vcf
updated 4.2 years ago by
Kevin Blighe
89k • written 4.2 years ago by
rheab1230
▴ 150
2
votes
3
replies
1.2k
views
Kallisto quantification
kallisto
RNA-Seq
updated 4.2 years ago by
Ram
45k • written 4.2 years ago by
shubhamvermauoh
• 0
0
votes
0
replies
2.6k
views
How to control the order of cells in dittoHeatmap for scRNAseq data analysis?
Cell
scRNA
dittoHeatmap
Single
4.2 years ago by
FantasticAI
▴ 60
0
votes
5
replies
1.9k
views
Multivariable Design in EdgeR (Design matrix / model.matrix) - Tilde Use
edgeR
R
4.2 years ago by
Noah E.
▴ 20
14
votes
7
replies
5.7k
views
Difference between a bin and a MAG
metagenomics
mags
binning
updated 3.8 years ago by
v.berriosfarias
▴ 140 • written 4.2 years ago by
Maria Laura
▴ 30
9
votes
5
replies
3.8k
views
Analysis of shRNA/CRISPR screens in 2021
crispr
shrna
updated 4.1 years ago by
dsull
★ 7.7k • written 4.2 years ago by
ATpoint
89k
9
votes
9
replies
2.7k
views
Forum:
Opinions on publishing Research as a Blog?
bioinformatics
publishing
4.2 years ago by
ponganta
▴ 590
1
vote
3
replies
2.2k
views
Running Salmon RNA quantification with pre-computed index
salmon
RNAseq
4.2 years ago by
saipra003
▴ 20
0
votes
1
reply
935
views
Retrieve reads overlapping indels
variants
reads
indel
updated 4.2 years ago by
Medhat
9.8k • written 4.2 years ago by
yliueagle
▴ 290
0
votes
0
replies
690
views
Criteria to be used to select top 10 hub genes for salt tolerance in rice using cytohubba
analysis
cytohubba
hubgenes
criteria
updated 4.2 years ago by
GenoMax
154k • written 4.2 years ago by
suvethamagudapathi
• 0
15
votes
8
replies
4.5k
views
8 follow
Would this laptop be sufficient for small dataset/sequence analysis?
DeSEQ2
tcga
Xena
laptop
4.2 years ago by
BioinformaticsEnthusiast
• 0
15
votes
6
replies
12k
views
Matplotlib comprehensive chromosome drawing
matplotlib
python
updated 2.8 years ago by
Ram
45k • written 10.3 years ago by
Sakti
▴ 530
3
votes
3
replies
3.1k
views
When to merge sequencing data from multiple lanes (FastQToSam, SamToFastq, BWA, MergeBamFiles, or additional step)?
alignment
pipeline
ngs
picard
sequencing
updated 4.2 years ago by
lieven.sterck
16k • written 4.2 years ago by
Jordi
▴ 60
0
votes
2
replies
1.8k
views
fineRADstructure file error
finestructure
fineradstucture
structure
SNP
RADseq
updated 4.2 years ago by
alexis.diaz
• 0 • written 6.0 years ago by
Whirlingdaf
▴ 60
2
votes
3
replies
2.5k
views
How to fill taxonomy informations from NCBI?
Taxonomy
NCBI
updated 4.2 years ago by
shenwei356
8.7k • written 4.2 years ago by
Camp
• 0
122,009 results • Page
608 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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andres.firrincieli
3.9k
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▴ 180
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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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