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
Post does not exist.
Limit : all time
all time
today
this week
this month
this year
116,903 results • Page
1 of 2339
Sort: Rank
Rank
Views
Votes
Replies
0
votes
0
replies
8
views
reference-free assembly error assessment tools
assembly
27 minutes ago by
lagartija
▴ 160
1
vote
2
replies
75
views
Benchmarking RNASeq Variant Calling Pipeline (Short Reads)
rna-seq
vcf
variant-calling
updated 36 minutes ago by
lagartija
▴ 160 • written 5 hours ago by
Esraa
• 0
0
votes
0
replies
14
views
Duplicated sequence samtools
bowtie2
samtools
35 minutes ago by
Moinuddin
• 0
0
votes
0
replies
14
views
Extracting only 4-fold degenerate sites from gene sequences/alignments?
alignments
1 hour ago by
J.
• 0
0
votes
0
replies
17
views
Herald:
The Biostar Herald for Monday, May 13, 2024
herald
1 hour ago by
Biostar
2.7k
795
votes
167
replies
143k
views
109 follow
News:
The Biostar Handbook. A bioinformatics e-book for beginners.
training
handbook
updated 3 months ago by
Biostar
2.7k • written 7.4 years ago by
Istvan Albert
100k
0
votes
1
reply
30
views
Splitting Seurat object by sample layers
split
seuratobject
seurat
layers
updated 1 hour ago by
bk11
★ 2.4k • written 2 hours ago by
kilcdincer
▴ 10
0
votes
2
replies
37
views
Galaxy StringTie error
stringtie
troubleshoot
galaxy
error
1 hour ago by
trkfs
• 0
0
votes
0
replies
31
views
dbNSFP sift scores integration
SIFT
VEP
dbNSFP
3 hours ago by
atariw
▴ 10
0
votes
0
replies
62
views
How to interpret infinite odds ratio?
statistics
4 hours ago by
Lukas
• 0
0
votes
1
reply
82
views
Mouse ribosome sequences in fasta format
fasta
mm10
rRNA
updated 4 hours ago by
GenoMax
142k • written 14 hours ago by
octpus616
▴ 100
0
votes
1
reply
60
views
Getting the coding_sequence.fasta from the .gff file from the AUGUSTUS gene prediction.
augustus
annotation
assembly
genome
updated 4 hours ago by
Juke34
8.6k • written 5 hours ago by
Vijith
▴ 30
0
votes
1
reply
56
views
consensus sequence calling
consensus
updated 1 hour ago by
bk11
★ 2.4k • written 5 hours ago by
Ghada
• 0
0
votes
3
replies
101
views
Single-cell RNA-seq FindMarker and EnhancedVolcano Plot: most genes are low -log10P value
Seurat
R
single-cell
RNA-seq
bioinformatics
6 hours ago by
yau
• 0
3
votes
2
replies
161
views
imputation through beagle
panel
beagle
reference
imputation
10 minutes ago by
analyst
▴ 50
0
votes
0
replies
34
views
Empty kernel in SEACells model
single-cell
scanpy
seacells
python
anndata
5 hours ago by
JACKY
▴ 140
0
votes
1
reply
315
views
Using samtools with GCS (google cloud storage) on a docker container seems to give "Protocol Not Supported" error
samtools
gcs
updated 6 hours ago by
aw7
▴ 280 • written 23 days ago by
abhishekghadge
• 0
1
vote
1
reply
156
views
Long reads and fixing of mate-pair issues/marking duplicates with samtools
mate-pair
samtools
alignment
updated 6 hours ago by
aw7
▴ 280 • written 4 days ago by
Zeng Hao
▴ 40
0
votes
0
replies
51
views
Reference panel of normals for ensembl named refgenome
Mutect2
7 hours ago by
gernophil
▴ 80
0
votes
0
replies
44
views
Producing sequence for splicing isoforms
isoform
rMATs
splicing
alternative
SplAdder
7 hours ago by
tomas4482
▴ 390
2
votes
3
replies
186
views
BWA alignment
Samtools
bam
8 hours ago by
Vahid
• 0
3
votes
2
replies
110
views
Publish a Letter in higher impact vs Research article in lower impact
Article
Letter
Journal
updated 8 hours ago by
ATpoint
82k • written 8 hours ago by
jennyp0706
• 0
0
votes
1
reply
115
views
Manual Assembly and Protein Translation, HELP, assignment revision
sequence
university
assembly
protein
genomics
updated 9 hours ago by
Philipp Bayer
8.4k • written 1 day ago by
samRayne
• 0
0
votes
1
reply
198
views
Two-Sample Mendelian Randomization: Association between Instrumental Variable and Outcome
Randomization
Mendelian
two-sample
updated 9 hours ago by
Zeng Jingyu
▴ 60 • written 3 days ago by
Nikki
• 0
2
votes
13
replies
2.8k
views
6 follow
CNVKIT - unable to produce scatter and diagram pdfs
cnvkit
updated 11 hours ago by
Anitha
• 0 • written 4.8 years ago by
ww22runner
▴ 60
0
votes
1
reply
152
views
Generating .bed file and .map file for polyploid vcf file through plink
bed
polyploid
map
plink
updated 11 hours ago by
chrchang523
10k • written 5 days ago by
analyst
▴ 50
0
votes
0
replies
66
views
lncRNA
tcga
lncrna
12 hours ago by
jain72744
▴ 10
0
votes
1
reply
197
views
Nomalization - TCGA, RNA-seq and Microarray
TCGA
RNA-seq
Nomalization
Microarray
updated 18 hours ago by
Zhenyu Zhang
★ 1.2k • written 3 days ago by
jain72744
▴ 10
2
votes
5
replies
498
views
Tissue-specific DEG analysis with DEseq2
DEseq2
RNA-seq
DEG
R
updated 23 hours ago by
arctic
▴ 40 • written 10 days ago by
M.
▴ 30
1
vote
2
replies
285
views
How to remove multiple batch effects from RNA-seq data before limma differential gene expression analysis?
ComBat-seq
limma
RNA-seq
removeBatchEffect
batch-effect
updated 2 hours ago by
Ram
43k • written 1 day ago by
t.fortunato.asquini
• 0
1
vote
1
reply
205
views
Practical Haplotype Graph v2 not finding correct paths
Pangenome
PHG
graph
updated 1 day ago by
pjb39
▴ 210 • written 2 days ago by
beantkapoor16
• 0
0
votes
2
replies
169
views
Output file of samtools flagstat empty
samtools-flagstat
updated 8 hours ago by
colindaven
6.4k • written 1 day ago by
ramendra.sarma
• 0
0
votes
0
replies
81
views
How can I create a eigencorplot of pca created from deseq2 object with PCAtools
eigencorplot
PCAtools
deseq2
pca
1 day ago by
BioinfGuru
★ 1.7k
2
votes
8
replies
293
views
joint callset and vcf sorting, unknown TAG issue
sort
bcftools
GLNexus
merge
VCF
updated 1 day ago by
Pierre Lindenbaum
161k • written 1 day ago by
Matteo Ungaro
▴ 100
0
votes
0
replies
97
views
News:
Online course: An Introduction to Nanopore Direct RNA Sequencing
Nanopore
RNAseq
1 day ago by
carlopecoraro2
★ 2.5k
0
votes
1
reply
204
views
input file in rmats
rmats
updated 1 day ago by
Mathew
▴ 120 • written 3 days ago by
Lambodarswain316
• 0
2
votes
2
replies
240
views
Kraken2 database
kraken
microbialdb
database
krakendb
kraken2
4 hours ago by
Christopher
• 0
6
votes
7
replies
321
views
Longest transcript variant per gene
transcript
longest
variant
orthofinder
22 hours ago by
sansan_96
▴ 90
2
votes
3
replies
223
views
error in fun(x((i)), ...) : only defined on a data frame with all numeric alike variables
studio
Cibersort
R
7 hours ago by
Azra
▴ 10
2
votes
1
reply
197
views
Failed to open VCF file
GATK
sentieon
BWA-MEM
updated 2 days ago by
Pierre Lindenbaum
161k • written 2 days ago by
melissachua90
▴ 70
9
votes
7
replies
7.1k
views
Align paired and unpaired reads simultaneously using Bowtie2?
alignment
updated 2 days ago by
Ruqaiya
• 0 • written 5.7 years ago by
xiaozhongzhiping
▴ 20
0
votes
4
replies
340
views
Adata.raw.X in LIANA, something wrong with conversion from Seurat to adata in python.
k
9 hours ago by
beginner123
• 0
6
votes
4
replies
13k
views
Trimmomatic: What is the difference between paired and unpaired output files in paired-end mode
trimmomatic
paired-end
updated 2 days ago by
Ruqaiya
• 0 • written 6.4 years ago by
dllopezr
▴ 130
0
votes
2
replies
200
views
java.nio.bufferunderflowexception haplotypecaller error for bqsr reads
deducplicated
java.nio.bufferunderflowexception
haplotypecaller
bqsr
10 hours ago by
analyst
▴ 50
0
votes
6
replies
361
views
Is it Possible to "Merge" data from Replicates within a VCF SNP File
snp
vcf
plink
bioinformatics
genomics
updated 1 day ago by
Pierre Lindenbaum
161k • written 2 days ago by
ajbarrett98
• 0
0
votes
11
replies
463
views
In IGV is this a heterogeneous mutation or false call?
mutations
IGV
heterogeneous
22 hours ago by
Tuck898
• 0
3
votes
3
replies
243
views
what is another word for a BLAST "hit"?
blast
alignment
2 days ago by
dec986
▴ 380
0
votes
1
reply
184
views
extract viral protein of interest from 10k whole viral genomes
nBLAST
viral-genome
updated 2 days ago by
Ram
43k • written 2 days ago by
Shwetha
• 0
0
votes
0
replies
154
views
Marker Features variance by cluster, sample, and treatment group
Seurat
scATAC-seq
ArchR
updated 2 days ago by
Ram
43k • written 3 days ago by
naomiboldon
• 0
1
vote
3
replies
259
views
How to format "I" and "D" in vcf version 4.2 for liftover analysis in GATK
gatk
vcf
liftover
updated 2 days ago by
Ram
43k • written 3 days ago by
Omics data mining
▴ 260
116,903 results • Page
1 of 2339
Recent Votes
Answer: imputation through beagle
Answer: imputation through beagle
Answer: imputation through beagle
Comment: Publish a Letter in higher impact vs Research article in lower impact
Comment: Publish a Letter in higher impact vs Research article in lower impact
Answer: Practical Haplotype Graph v2 not finding correct paths
A: Looking For A Way To Count Total Length Of Regions Of Bed File
Recent Locations •
All
United States,
just now
United States,
2 minutes ago
Israel,
3 minutes ago
University Park, USA,
7 minutes ago
Canada,
7 minutes ago
Portugal,
8 minutes ago
United States,
9 minutes ago
Recent Awards •
All
Commentator
to
Santosh Anand
5.7k
Popular Question
to
lagartija
▴ 160
Popular Question
to
bioinfo
▴ 150
Popular Question
to
Sara
▴ 30
Popular Question
to
anasjamshed
▴ 120
Popular Question
to
pablo
▴ 300
Scholar
to
Bastien Hervé
5.3k
Recent Replies
Comment: imputation through beagle
by
analyst
▴ 50
Thank you so much dthorbur. Yes I am new to imputation analysis. I will follow your kind suggestions. Thanks again!
Answer: Benchmarking RNASeq Variant Calling Pipeline (Short Reads)
by
lagartija
▴ 160
I don't know but another way of doing it would be to combine different datasets of different strains that you know are clonal. Then you kno…
Comment: consensus sequence calling
by
bk11
★ 2.4k
Please check out these posts https://www.biostars.org/p/367626/
Comment: Galaxy StringTie error
by
trkfs
• 0
will do, thank you
Answer: Splitting Seurat object by sample layers
by
bk11
★ 2.4k
You can do the following- Idents(SeuratObj) <- "orig.ident" control_set <- subset(SeuratObj, idents = c("counts.control","data.…
Comment: Galaxy StringTie error
by
GenoMax
142k
> I have sent a bug report to the Galaxy administrator If you have not done so please post this in Galaxy help forum for directed help: h…
Comment: 44% Successfully Assigned Fragments with featureCounts after 85% uniquely mapped
by
Thind amarinder
▴ 340
Wondering, if it was total RNAseq data? or ployA
Comment: RNA seq analysis
by
Matthias Zepper
4.6k
It is still obscure to me how many different tissues you would like to include into your comparison and what your intended design is. To …
Comment: Getting the coding_sequence.fasta from the .gff file from the AUGUSTUS gene pred
by
Juke34
8.6k
You can get a look here https://www.biostars.org/p/9465973/
Answer: Mouse ribosome sequences in fasta format
by
GenoMax
142k
A version of the mouse rDNA repeat can be found here: https://www.ncbi.nlm.nih.gov/nuccore/BK000964 Use the dropdown menu at top-left t…
Comment: Kraken2 database
by
Christopher
• 0
Hello, Mathew. Firstly, thank you for answering my question. **Sorry, what analysis are you trying to perform with these databases?** I a…
Comment: Benchmarking RNASeq Variant Calling Pipeline (Short Reads)
by
GenoMax
142k
As long as it is the same GIAB sample you could compare your SNP with the SNP's available for the whole genome set.
Comment: Single-cell RNA-seq FindMarker and EnhancedVolcano Plot: most genes are low -log
by
yau
• 0
Dear Mensur, Thanks so much for your reply!! In my case, I got 1 control(healthy) and 2 disease mouse Single cell RNA-sew data, so I …
Comment: BWA alignment
by
ATpoint
82k
The relevant code line is precisely the same as in the question.
Answer: imputation through beagle
by
dthorbur
★ 2.0k
Building a reference panel from the samples you intend to impute seems like a very circular approach. Plus, GBS is a reduced representation…
Traffic: 2519 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