Latest
Open
Jobs
Tutorials
Tags
About
FAQ
Community
Planet
New Post
Log In
New Post
Latest
Open
News
Jobs
Tutorials
Forum
Tags
Planet
Users
Log In
Sign Up
About
Limit : all time
all time
today
this week
this month
this year
121,113 results • Page
8 of 2423
Sort: Rank
Rank
Views
Votes
Replies
4
votes
6
replies
599
views
Problem with Accession Number Changes in UniProt FASTA Sequences
FASTA
Accession
Uniprot
IdMapping
5 weeks ago by
bioinfo_enthusiast
• 0
1
vote
2
replies
522
views
PPI Network Analysis of Virulence Genes in Morganella morganii Using STRING Database
PPI
STRING
5 weeks ago by
bioinfo_enthusiast
• 0
21
votes
12
replies
1.2k
views
7 follow
Forum:
Reproducibility Crisis
R-Bioinformatics
updated 5 weeks ago by
i.sudbery
21k • written 6 weeks ago by
ParastooA
▴ 20
6
votes
13
replies
7.9k
views
7 follow
Getting sample information from GEO
GEO
NCBI
updated 6 weeks ago by
DareDevil
★ 4.4k • written 8.0 years ago by
Tom_L
▴ 360
0
votes
3
replies
427
views
How to Close a Phage Genome? Issues with PhageTerm and CheckV Completeness
phage
genome
assembly
PhageTerm
updated 5 weeks ago by
GenoMax
151k • written 6 weeks ago by
mail2steff
▴ 70
2
votes
2
replies
402
views
RepBase30.02.fasta.tar.gz
RepBase30.02.fasta.tar.gz
offtopic
updated 5 weeks ago by
Michael
55k • written 6 weeks ago by
jupitoy
• 0
1
vote
5
replies
1.4k
views
CIBERSORTx error (error in rep(2, size * length(cells) -1)) : invalid 'times' argument
deconvolution
RNA-seq
CIBERSORTx
CIBERSORT
updated 11 weeks ago by
zhbyrd
• 0 • written 10 months ago by
Mr. George
▴ 10
2
votes
2
replies
411
views
Differences in DEG results using RSEM with and without the --strandness reverse
rsem
DEG
STAR
transcriptomic
updated 5 weeks ago by
LauferVA
4.7k • written 6 weeks ago by
Emy Alade
• 0
3
votes
5
replies
620
views
Absolute vs. differential gene expression - which analysis is more informative?
Differential-gene-expression
Gene-expression
RNA-Seq
updated 5 weeks ago by
LauferVA
4.7k • written 6 weeks ago by
bioinfo1990
▴ 10
2
votes
3
replies
537
views
making psam file for plink2
plink2
5 weeks ago by
dec986
▴ 380
4
votes
4
replies
499
views
gtf file for canFam2 genome version
gtffile
6 weeks ago by
1769mkc
★ 1.3k
2
votes
2
replies
504
views
Bioinformatics
StringDB
updated 5 weeks ago by
Ram
45k • written 6 weeks ago by
ahmad79rezahay
• 0
0
votes
0
replies
237
views
News:
Epigenomics Data Analysis
Epigenomics
RNA-seq
ATAC-seq
Chip-seq
HI-C
6 weeks ago by
Physalia-courses
★ 2.6k
4
votes
8
replies
810
views
does any licenses needed to make experiments?
offtopic
updated 6 weeks ago by
Dunois
★ 2.9k • written 6 weeks ago by
suleyman
• 0
6
votes
5
replies
509
views
Strange overrepresented sequence
fastQC
adapter
rnaseq
6 weeks ago by
georomano
• 0
13
votes
6
replies
6.4k
views
Add metadata based on tree structure
R
ggtree
updated 6 weeks ago by
rsieber
▴ 10 • written 5.5 years ago by
Jack
▴ 50
0
votes
3
replies
341
views
Normalize RNAseq data on RT-dPCR or RT-qPCR
RNAseq
updated 6 weeks ago by
ATpoint
88k • written 6 weeks ago by
lagartija
▴ 160
0
votes
2
replies
331
views
Is there a way to import a large amount of regions of interest into IGV
sequencing
igv
genomics
ngs
updated 6 weeks ago by
GenoMax
151k • written 6 weeks ago by
Mark
▴ 30
4
votes
10
replies
884
views
Question about an alignment
ces
sequencing
alignment
5 weeks ago by
barslmn
★ 2.4k
0
votes
2
replies
327
views
Arioc (read mapping) ref sequence length error
mapping
gpu
arioc
read
6 weeks ago by
Michael
• 0
0
votes
0
replies
349
views
When I want to compare two groups at multiple time points in scRNA-seq datasets, the criteria for the genes to be analyzed
Seurat
scRNA-seq
6 weeks ago by
Apprentice
▴ 170
7
votes
6
replies
771
views
Heatmap problem in R
R
Heatmap
6 weeks ago by
ParastooA
▴ 20
3
votes
4
replies
526
views
Bacterial VCF file annotation using snpEff error
SnpEff
6 weeks ago by
1769mkc
★ 1.3k
1
vote
4
replies
554
views
Coverage depth using samtools
samtools
ngs
depth
sequencing
coverage
6 weeks ago by
slzr_
• 0
4
votes
4
replies
508
views
MarkDuplicates RNASeq: A few samples look weird. What could be the cause?
qc
markduplicates
picard
rnaseq
updated 6 weeks ago by
GenoMax
151k • written 6 weeks ago by
Davor
• 0
0
votes
2
replies
389
views
Data Integrity (NCBI SRA and TCGA)
clinic
metadata
updated 5 weeks ago by
Zhenyu Zhang
★ 1.3k • written 6 weeks ago by
umarfaruksahin
• 0
0
votes
0
replies
1.4k
views
concatenating 2 differently-imputed VCF files then filtering by imputation score to keep the higher imputation score imputed vaiant from duplicate v…
Imputation
filtration
score
duplicate
variants
6 weeks ago by
SalmaElShafie
• 0
0
votes
0
replies
233
views
loss of coverage using gargammel
gargammel.pl
ART
AdapterRemoval
6 weeks ago by
anna.utili
• 0
1
vote
2
replies
418
views
What is the stance on optical duplicates in RNASeq?
duplicates
rnaseq
optical-duplicates
5 weeks ago by
Davor
• 0
2
votes
4
replies
585
views
How to rank genes for GSEA using edgeR-LRT results ?
DEG
edgeR
updated 6 weeks ago by
dariober
15k • written 6 weeks ago by
Picasa
▴ 680
4
votes
3
replies
568
views
Using bulk RNA-seq DE results to perform PCA in single cell RNA-seq
Single-cell
scRNAseq
updated 6 weeks ago by
jared.andrews07
★ 18k • written 6 weeks ago by
Oli
• 0
3
votes
1
reply
324
views
Access to dbSnp137 (GRCh37)
dbSnp137
GRCh38
dbSnp
updated 6 weeks ago by
Marcellie87
▴ 10 • written 6 weeks ago by
Steven
▴ 50
0
votes
0
replies
222
views
How to convert RAP-DB/MSU IDS to RefSeq/Entrez Gene IDS?
IRGSP
Entrez
RAP-DB
RefSeq
6 weeks ago by
ChanderKant (CK) Chaudhary
▴ 10
4
votes
4
replies
2.0k
views
Annotating single cell data automatically
single-cell
updated 6 weeks ago by
S.Ghazala
▴ 60 • written 12 months ago by
Gerard
▴ 20
4
votes
0
replies
321
views
News:
Join the online/distributed nf-core Hackathon next week!
nf-core
nextflow
container
workflows
bioinformatics
6 weeks ago by
Matthias Zepper
5.1k
0
votes
3
replies
442
views
Non variants sites of the genome (gVCF file)
non
genome
variants
sites
gVCF
updated 6 weeks ago by
LauferVA
4.7k • written 6 weeks ago by
heureuse
▴ 10
1
vote
1
reply
332
views
Choosing the "right" sequence as an input control
input
control
chipseq
updated 6 weeks ago by
ATpoint
88k • written 6 weeks ago by
mark.pekarsky
▴ 20
1
vote
2
replies
456
views
Unable to parse config file
nextflow
nf-core
Pulled
form
github
updated 6 weeks ago by
Phil Ewels
★ 1.4k • written 6 weeks ago by
JieQY
• 0
0
votes
1
reply
326
views
Seeking Guidance on Selecting Control ChIP Sequences for nf-core/chipseq Pipeline
SRR
nf-core
chipseq
updated 5 weeks ago by
mark.ziemann
★ 2.0k • written 6 weeks ago by
mark.pekarsky
▴ 20
0
votes
0
replies
215
views
Problem with GSVA output
GSVA
RNAseq
6 weeks ago by
a.stef.44
▴ 10
0
votes
2
replies
374
views
Using UMI-tools on Smart-seq3 RNA-Seq data
rna-seq
UMI
UMI-tools
smart-seq3
updated 6 weeks ago by
Ram
45k • written 6 weeks ago by
Agastya
▴ 10
1
vote
5
replies
576
views
Remove site with only missing data
Fasta
updated 6 weeks ago by
Pierre Lindenbaum
166k • written 6 weeks ago by
Leane
• 0
0
votes
3
replies
435
views
Problems with Seaborn plots in Python
python
sns
plot
updated 6 weeks ago by
Wayne
★ 2.1k • written 6 weeks ago by
egascon
▴ 60
4
votes
4
replies
597
views
Downloading full list of Homo sapiens genes
Genes
6 weeks ago by
Nigussie
• 0
0
votes
1
reply
321
views
How to normalise Nanopore mRNA sequencing data between two cell lines
Nanopore
RNAseq
Normalization
updated 6 weeks ago by
lagartija
▴ 160 • written 6 weeks ago by
Mo
▴ 50
2
votes
5
replies
4.4k
views
Python library for parsing bcftools stats file
bcftools
updated 6 weeks ago by
Pierre Lindenbaum
166k • written 7.8 years ago by
William
★ 5.3k
0
votes
0
replies
235
views
Manta SV (specially Translocation)
manta
Structural-Variant
updated 6 weeks ago by
Ram
45k • written 6 weeks ago by
Nai
▴ 50
0
votes
3
replies
583
views
Cytoscape COLOUR EDGES
Reulatory
Cytoscape
Networks
updated 6 weeks ago by
Scooter
▴ 310 • written 7 weeks ago by
SKY
▴ 60
3
votes
3
replies
1.3k
views
How to perform PPI network analysis in STRING for newly sequenced bacterial genome ?
Proteomics
cytoscape
network
STRING
updated 5 weeks ago by
bioinfo_enthusiast
• 0 • written 3.9 years ago by
Kumar
▴ 120
0
votes
0
replies
243
views
How to perform burden test using plink /seq
plink-seq
Burden-Test
updated 6 weeks ago by
Ram
45k • written 6 weeks ago by
aiswaryabioinfo
▴ 30
121,113 results • Page
8 of 2423
Recent Votes
Comment: What are BED files?
Comment: Ggplot make boxplots more wide
Answer: Editing and Adding to a GTF file
Comment: Ggplot make boxplots more wide
A: what is the purpose of indexing a genome
Comment: Sample level genotype mapping in plink vcf output
Answer: When and why is bwa aln better then bwa mem?
Recent Locations •
All
France,
2 minutes ago
Ramat Gan,
2 minutes ago
Austria/Vienna,
3 minutes ago
Norway,
8 minutes ago
USA,
14 minutes ago
Italy,
14 minutes ago
India,
14 minutes ago
Recent Awards •
All
Popular Question
to
Nona
▴ 90
Popular Question
to
enee
▴ 20
Popular Question
to
genetixs
▴ 20
Popular Question
to
Basti
★ 2.1k
Scholar
to
Pierre Lindenbaum
166k
Popular Question
to
SomeOne
▴ 170
Popular Question
to
wonde2000
• 0
Recent Replies
Comment: What are BED files?
by
ATpoint
88k
The first and post important skill for a bioinformatician (or scientist in general) is to find available information online. This can be go…
Answer: What are BED files?
by
Pierre Lindenbaum
166k
BED format https://genome.ucsc.edu/FAQ/FAQformat.html#format1
Comment: ggplot make boxplots more wide
by
Nona
▴ 90
Thank you everyone.
Comment: Minimum number of samples for multi-omics data integration
by
manaswwm
▴ 560
If your analysis is aimed at comparing two groups (eg: treatment conditions), then you should probably have a look at power calculations to…
Answer: Editing and Adding to a GTF file
by
Juke34
9.2k
To add functional information (name or function) do not use attributes used to structure the file ( gene_id/ transcript_id for GTF and ID/P…
Comment: Warning in bcftools when subsetting a VCF by variant ID
by
Pierre Lindenbaum
166k
cross-posted: https://bioinformatics.stackexchange.com/questions/23393/
Comment: Sample level genotype mapping in plink vcf output
by
Pierre Lindenbaum
166k
0 : REF 1: first ALT 2: second ALT 3 : third ALT etc...
Comment: Sample level genotype mapping in plink vcf output
by
1769mkc
★ 1.3k
It works, how does this convert the binary to actual genotype?
Comment: Transcript identification and quantification
by
dsull
★ 7.5k
AH perfect!! Thanks -- that's exactly right! Here's the updated command (and links) for v3: pip install kb_python wget https://ra…
Comment: Gene Exons Painter
by
Mensur Dlakic
★ 29k
I am really not picking up on you - really. It just strikes me that if you want to get people to use your tools, a little bit more effort i…
Answer: Assigning a string variable on Visual Studio using python
by
GenoMax
151k
Not sure what you are trying to do here. How are the two lines you wrote above connected? You can't have a space in python variable names, …
Comment: Transcript identification and quantification
by
GenoMax
151k
There are some barcodes provided here --> https://github.com/mortazavilab/parse_pipeline/tree/main/barcodes Perhaps @dsull knows if there…
Comment: Ggplot make boxplots more wide
by
zx8754
12k
Set colour to Day as well: ```R ggplot( data = metadata, aes(x = location, y = gene, fill = Day, colour = Day)) + geom_boxplot() ``` To …
Comment: Transcript identification and quantification
by
dsull
★ 7.5k
Ooh, that's a bit tricky. I worked with v3 of the kit a while back but for some reason I can only find the R2/R3 barcodes. I'll let you kno…
Comment: The Biostar Herald for Monday, May 05, 2025
by
cmdcolin
★ 4.2k
BinSeq format from ArcInstitute also ! https://github.com/ArcInstitute/binseq ...the trio of binseq+xsra+https://github.com/ArcInstitute/SR…
Traffic: 2364 users visited in the last hour
Content
Search
Users
Tags
Badges
Help
About
FAQ
Access
RSS
API
Stats
Use of this site constitutes acceptance of our
User Agreement and Privacy Policy
.
Powered by the
version 2.3.6