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122,009 results • Page
279 of 2441
Sort: Rank
Rank
Views
Votes
Replies
13
votes
9
replies
11k
views
6 follow
How to find promoter sequence of a gene?
promoter
2.5 years ago by
sunyeping
▴ 110
1
vote
5
replies
1.4k
views
bash command to process a line
linux
command
updated 2.5 years ago by
Joe
22k • written 2.5 years ago by
saadleeshehreen
▴ 140
0
votes
0
replies
636
views
News:
Virtual RAD-seq Analysis Workshop!
workshops
popgen
genomics
rad-seq
2.5 years ago by
mia.nahom
▴ 10
4
votes
5
replies
1.9k
views
Centromere and telomere positions for Chm13v2 assembly
centromere
chm13v2
updated 2.2 years ago by
jleehan
▴ 120 • written 2.5 years ago by
arsala521
▴ 60
0
votes
5
replies
2.1k
views
featureCounts problem in reading Gff
featureCounts
GFF
RNA-seq
updated 2.5 years ago by
Ram
45k • written 2.5 years ago by
Beatrice
• 0
5
votes
0
replies
1.8k
views
Tool:
PyComplexHeatmap: a Python package to visualize multimodal genomics data
visualization
Python
ComplexHeatmap
PyComplexHeatmap
18 months ago by
Wubin
▴ 50
2
votes
2
replies
988
views
Retrieve hgnc_symbol from XM_ refseqs using BiomaRt
refseq_mrna_predicted
biomaRt
refseq
XM
2.5 years ago by
ladina.hoesli
• 0
0
votes
1
reply
811
views
Time change in expression vs time change in phenotype
RNA-Seq
DGE
DESeq2
2.5 years ago by
Ivan
• 0
0
votes
0
replies
656
views
How to perform a gsva assessing for the directonality of the genes.
gsva
2.5 years ago by
roybatty269
• 0
7
votes
7
replies
3.0k
views
Nextflow rnaseq finishing early
RNA-seq
nextflow
updated 2.5 years ago by
Ram
45k • written 2.5 years ago by
Raygozak
★ 1.4k
6
votes
6
replies
5.5k
views
ClusterProfiler enrichKEGG – remove organism name in plots?
KEGG
ggplot2
enrichKEGG
ClusterProfiler
updated 2.5 years ago by
jv
★ 1.9k • written 2.6 years ago by
Sian
▴ 30
2
votes
0
replies
1.0k
views
Herald:
The Biostar Herald for Tuesday, March 28, 2023
herald
2.5 years ago by
Biostar
3.6k
1
vote
4
replies
1.6k
views
Retrieve protein sequence from Mgnify given only accession code
Mgnify
API
updated 2.5 years ago by
biomarco
▴ 50 • written 3.3 years ago by
jscience
▴ 10
1
vote
1
reply
1.3k
views
Browsing MGnify IDs and clusters
metagenomics
mgnify
ebi
2.5 years ago by
biomarco
▴ 50
0
votes
0
replies
450
views
calculation of calibration factors using impuation reference panel and ethnicity
GWAS
Calibration
factor
2.5 years ago by
parveenkayenat
• 0
2
votes
4
replies
1.7k
views
Artificial reads - remove multiple mapped reads against reference genome, and only keep reads that completely match without any mismatches - samtools
samtools
2.5 years ago by
Jalil Sharif
▴ 80
0
votes
0
replies
670
views
Haploview linkage format .ped and .info file error
plink
Haploview
vcftools
updated 2.3 years ago by
Ram
45k • written 2.5 years ago by
Nai
▴ 50
6
votes
1
reply
1.1k
views
what is IGV visualization lighter color variants stand for
visualization
vcf
IGV
updated 2.5 years ago by
Jorge Amigo
14k • written 2.5 years ago by
octpus616
▴ 120
0
votes
2
replies
2.5k
views
Error when changing the database for minfi dropLociWithSnps
SNP
minfi
methylationEPIC
illumina
methylation
updated 2.5 years ago by
Satu
• 0 • written 8.3 years ago by
Ellen O
▴ 20
0
votes
0
replies
771
views
Bcftools consensus generates mismatched consensus sequence
Consensus
sequence
2.5 years ago by
Duy
• 0
0
votes
0
replies
475
views
Is there a function to get the number of aligned sites between pairs of sequences in a multiple sequence alignment in R?
msa
R
2.5 years ago by
audrey
• 0
0
votes
0
replies
1.2k
views
Nucleotide substitution model and neighbor-joining tree
phylogeny
substitution
mega
neighbor-joining
modeltest
2.5 years ago by
poecile.pal
▴ 50
5
votes
9
replies
4.4k
views
6 follow
Most efficient way to run Diamond against a very very large database (i.e., NCBI's NR)?
protein
annotation
alignment
diamond
nr
updated 2.2 years ago by
GenoMax
154k • written 2.5 years ago by
O.rka
▴ 750
0
votes
0
replies
551
views
Octopus advanced vcf guide: Example of overlapping vcf calls with *
vcf
spanning
alleles
octopus
2.5 years ago by
penington.j
• 0
3
votes
3
replies
5.0k
views
Editing fasta headers
fasta
updated 2.5 years ago by
Ram
45k • written 2.5 years ago by
Zoe
• 0
0
votes
0
replies
633
views
Link products to their genes
RNA-SEQ
GO
edgeR
2.5 years ago by
Pegasus
▴ 130
0
votes
0
replies
1.0k
views
Trajectory analysis using Monocle3 with Seurat sub-clustering
scRNA-seq
Trajectory
Seurat
analysis
Monocle3
2.5 years ago by
joonhong kwon
▴ 70
0
votes
0
replies
1.0k
views
News:
The Canadian Bioinformatics Workshops are back for summer 2023
CBW
training
workshop
2.5 years ago by
bioinformatics.ca
• 0
0
votes
1
reply
1.5k
views
Error parsing strand (?) from GFF line
assembly
updated 2.5 years ago by
cmdcolin
★ 4.3k • written 2.5 years ago by
hafiz.talhamalik
▴ 350
0
votes
3
replies
1.2k
views
Sample size for population genetics
Population-genetics
sample-size
updated 2.5 years ago by
Jeremy Leipzig
23k • written 2.5 years ago by
zimmer.schweiz
• 0
1
vote
0
replies
580
views
List of Ongoing and Planned Long Read Sequencing studies?
long-read-sequencing
third-generation
updated 2.5 years ago by
Ram
45k • written 2.5 years ago by
LauferVA
4.8k
4
votes
8
replies
6.7k
views
counting the unmapped reads
RNA-Seq
updated 2.5 years ago by
chemkhi.ali13
▴ 10 • written 10.4 years ago by
zizigolu
★ 4.4k
0
votes
0
replies
596
views
how to plot distribution of SNPs across a set of genes based on distance between snp and gene
snp
genes
updated 2.5 years ago by
Ram
45k • written 2.5 years ago by
rheab1230
▴ 150
0
votes
1
reply
995
views
Discordinant aligment
Paired-end
HISAT2
updated 2.5 years ago by
Istvan Albert
103k • written 2.5 years ago by
ali
• 0
0
votes
1
reply
774
views
Using multimaping reads or unique reads on featurecounts?
featurecounts
HISAT2
updated 2.5 years ago by
GenoMax
154k • written 2.5 years ago by
omargmc.tak
• 0
1
vote
3
replies
3.2k
views
module and trait correlation for WGCNA
treatment
WGCNA
relation
microarray
module-treatment
updated 2.0 years ago by
andres.firrincieli
3.9k • written 2.6 years ago by
Shriyansh
• 0
3
votes
7
replies
3.8k
views
1000 genomes hg38 with dbSNP rsid
1000genomes
dbsnp
updated 2.5 years ago by
Ram
45k • written 2.5 years ago by
Vince
▴ 150
0
votes
0
replies
568
views
How to import impute2.dosage files to analyse it in R (GWAS)
regression
GWAS
impute2
dosage
2.5 years ago by
Sebastian
▴ 10
5
votes
3
replies
3.3k
views
What's the correct way to map to hg38 with alternative contigs?
NGS
bwa
2.4 years ago by
PeterWu
▴ 20
6
votes
4
replies
1.2k
views
Download NCBI compiled protein database for specific genus
protein
NCBI
updated 2.5 years ago by
GenoMax
154k • written 2.5 years ago by
saadleeshehreen
▴ 140
0
votes
0
replies
503
views
MD simulation error
MD
schrodinger
updated 2.5 years ago by
Ram
45k • written 2.5 years ago by
mixmatchey
• 0
0
votes
0
replies
559
views
File has zero value indivuals
Haploview
updated 2.5 years ago by
Ram
45k • written 2.5 years ago by
Nai
▴ 50
1
vote
6
replies
1.8k
views
Kallisto bustools for scRNA-seq
Kallisto
updated 2.5 years ago by
dsull
★ 7.7k • written 2.5 years ago by
t.ru
▴ 20
0
votes
0
replies
613
views
KEGGList Error in R
KEGGList
2.5 years ago by
GiV17
▴ 50
0
votes
1
reply
754
views
How to analyze RepeatProteinMask results
RepeatProteinMask
2.5 years ago by
zijian
• 0
0
votes
2
replies
1.1k
views
how to look at interaction between SNP and gene
SNP
Gene
Hi-C
2.5 years ago by
rheab1230
▴ 150
1
vote
2
replies
1.0k
views
Remove part of headers in FASTA file
Fasta
updated 2.5 years ago by
Mark
★ 1.7k • written 2.6 years ago by
fatemeh
• 0
5
votes
2
replies
1.1k
views
How to get a list of genes information for a pathway?
pathway
updated 2.5 years ago by
ATpoint
89k • written 2.5 years ago by
WUSCHEL
▴ 860
0
votes
0
replies
640
views
GATK VariantAnnotator -A PossibleDeNovo
VariantAnnotator
GATK
2.5 years ago by
zihanss
• 0
0
votes
0
replies
619
views
Tool:
BioLabImage - Mac program for DNA/RNA/protein gel/blot, cells/colonies image analysis
image-analysis
gel
blot
cells
colonies
updated 2.5 years ago by
Ram
45k • written 2.5 years ago by
vytarasov
▴ 180
122,009 results • Page
279 of 2441
Recent Votes
Comment: GUI commercial software for 10x single cell gene expression analysis
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
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Recent Replies
Comment: DESeq2 on metagenome KO counts
by
Aleksandra
▴ 180
I just wrote that I misunderstood your initial question.
Comment: DESeq2 on metagenome KO counts
by
Aleksandra
▴ 180
What exactly did I not get?
Comment: Interpreting genomic features distribution for CUT&RUN peaks
by
rfran010
★ 1.7k
If I understand correctly, you see increased signal at TSS sites compared to control (taller peaks in browser). However, 92% of the 450 siS…
Comment: combine VCF from diploid reference/haplotypes for the same sample
by
cmdcolin
★ 4.3k
this question is a little similar to your previous question (https://www.biostars.org/p/9614638/). just as added info, here is a tool calle…
Comment: hisat2 error-Paired end reads not equal or lack of RAM/disk space?
by
aj123
▴ 130
As mentioned above, I just got the raw fastq files from the ftp site listed.
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…
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