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116,847 results • Page
1 of 2337
Sort: Rank
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Views
Votes
Replies
0
votes
4
replies
72
views
Different output for read length
samtools
BAM
2 minutes ago by
marco.barr
▴ 100
0
votes
1
reply
217
views
Snakemake fails to find conda in PBS
snakemake
updated 1 hour ago by
tim.booth
▴ 50 • written 27 days ago by
yixinzeng
• 0
0
votes
2
replies
58
views
Presence of unknown sites in ANNOVAR output file
ANNOVAR
updated 1 hour ago by
GenoMax
142k • written 2 hours ago by
sainavyav22
• 0
0
votes
0
replies
26
views
Truncated metadata file report from ENA Portal API
ena
python
updated 2 hours ago by
Ram
43k • written 2 hours ago by
Giulia
• 0
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
0
replies
25
views
What is workflow for de-novo assembling of nuclear and mito genomes of non-model organisms
de-novo
WGS
DNA-seq
assembling
2 hours ago by
Matvii Mykhailichenko
• 0
0
votes
3
replies
439
views
JASPAR2024_getMatrixSet error
JASPAR2024
getMatrixSet
updated 3 hours ago by
Ram
43k • written 11 weeks ago by
maplewj
▴ 10
0
votes
3
replies
96
views
How to convert normalized BigWig file to count matrix?
count-matrix
BigWig
updated 3 hours ago by
Ram
43k • written 5 hours ago by
feather-W
• 0
0
votes
3
replies
166
views
bcftools - reducing to "sites-only"?
sites-only
bcftools
updated 4 hours ago by
Pierre Lindenbaum
161k • written 19 hours ago by
Matthew
• 0
3
votes
4
replies
2.9k
views
Have you ever obtained user guide of ExomeCNV?
CNV
updated 4.4 years ago by
lffu_0032
▴ 90 • written 5.2 years ago by
oghzzang
▴ 50
0
votes
1
reply
48
views
input file for alternative splicing in rmats in linux
rmats
updated 2 hours ago by
Ram
43k • written 5 hours ago by
Lambodarswain316
• 0
0
votes
2
replies
120
views
Server or aws cloud- which one is better for gatk pipeline
aws
server
calling
gatk
cloud
updated 6 hours ago by
Michael
54k • written 12 hours ago by
ashaneev07
▴ 20
1
vote
1
reply
369
views
ComBat_Seq stuck adjusting the data
Batch-Effect
RNAseq
ComBat-Seq
updated 7 hours ago by
Jaïr
• 0 • written 4 months ago by
NorbertK
▴ 10
4
votes
3
replies
771
views
How to solve the error 'ERROR::MATE_NOT_FOUND:Found xxx unpaired mates' when run SamToFastq
samtofasq
picard
validatesamfile
updated 6 hours ago by
Pierre Lindenbaum
161k • written 8 hours ago by
Lila M
★ 1.2k
1
vote
3
replies
114
views
Nextflow: how to get the process work dir, within the process
nextflow
updated 7 hours ago by
Pierre Lindenbaum
161k • written 7 hours ago by
ScottDansk
▴ 10
1
vote
0
replies
64
views
What is Deepvariant default filtering values ?
vcf
calling
filter
variant
deepvariant
8 hours ago by
Shae
▴ 10
0
votes
1
reply
126
views
Enhanced Volcano-Cut off
foldchange
enhancedvolcano
updated 10 hours ago by
marco.barr
▴ 100 • written 19 hours ago by
odi
▴ 10
1
vote
4
replies
173
views
Importing a fastq file
Fastq
11 hours ago by
oumo
• 0
0
votes
6
replies
2.1k
views
Copy number Variation analysis using conumee
R
software error
sequencing
genome
updated 7 hours ago by
GenoMax
142k • written 3.2 years ago by
gs000095
▴ 10
1
vote
1
reply
92
views
Conda severely broken after attempting mamba install
biopython
conda
mamba
pycosat
updated 11 hours ago by
andres.firrincieli
3.6k • written 11 hours ago by
kacollier
▴ 30
1
vote
2
replies
1.5k
views
Seurat CellCycleScoring – confused about the proper order of operations when using SCTransform
CellCycleScoring
SCTransform
Seurat
updated 14 hours ago by
Li
• 0 • written 2.3 years ago by
GPM
▴ 10
0
votes
0
replies
65
views
Summary Statistics SNPs not found in Target data
SNP
plink
PRS
updated 15 hours ago by
Ram
43k • written 15 hours ago by
curious_butterfly
• 0
0
votes
0
replies
73
views
Long reads and fixing of mate-pair issues/marking duplicates with samtools
mate-pair
samtools
alignment
8 hours ago by
Zeng Hao
▴ 40
0
votes
2
replies
135
views
Contig assembly task, errors
genetics
contig
assembly
dna
bioinformatics
3 hours ago by
rackbersingh
• 0
1
vote
3
replies
142
views
Help with Biopython for Beginner
Python
ORF
FASTA
Biopython
updated 1 hour ago by
GenoMax
142k • written 19 hours ago by
cput
• 0
0
votes
0
replies
81
views
Annotate VCF via VEP for gnomAD annotation considering FILTER column
vep
vcf
gnomad
20 hours ago by
asalimih
▴ 60
0
votes
5
replies
324
views
Filtering Multi-sample VCF file for all except one Genotype
variant
SNP
VCF
updated 1 hour ago by
Jeremy Leipzig
22k • written 2 days ago by
schmince
• 0
0
votes
2
replies
193
views
featureCounts output summary assigned value higher than uniquely mapped reads from HISAT2
RNA-seq
featureCounts
HISAT
updated 8 hours ago by
i.sudbery
19k • written 22 hours ago by
Prawesh
• 0
0
votes
9
replies
1.5k
views
kinannote software installation problems
kinannote
updated 22 hours ago by
Emanoelle
• 0 • written 5.7 years ago by
Elizabeth
▴ 30
0
votes
1
reply
134
views
Obtaining Infinium Methylation450K manifest for hg38
TCGA
hg38
methylation
Illumina
updated 22 hours ago by
marco.barr
▴ 100 • written 1 day ago by
elisheva
▴ 120
0
votes
0
replies
73
views
Pathway analysis of Bacteria from denovo genome assembly
KEGG-KASS
WGS
Pathway
denovo
updated 21 hours ago by
Ram
43k • written 1 day ago by
mathavanbioinfo
▴ 90
0
votes
1
reply
224
views
Seurat V5 integration
Seurat
integration
updated 21 hours ago by
Ram
43k • written 4 days ago by
starswillfade
▴ 10
0
votes
2
replies
183
views
Error in plotting PCA plot in seurat
PCA
single-cell
seurat
scRNA
RNA
updated 21 hours ago by
Ram
43k • written 1 day ago by
Sumeet
• 0
0
votes
0
replies
90
views
News:
Online course: Introduction to Deep Learning
Python
Deep-Learning
Convolutional-Neural-Network
Machine-Learning
updated 21 hours ago by
Ram
43k • written 1 day ago by
carlopecoraro2
★ 2.5k
4
votes
5
replies
3.4k
views
How to compare compare two Sam files to check mapping
alignment
updated 1 day ago by
DavidStreid
▴ 90 • written 6.4 years ago by
madhu.9124
▴ 60
0
votes
2
replies
128
views
How/where can I get fungal mitogenome data for analysis?
fungal
mitogenome
updated 1 day ago by
GenoMax
142k • written 1 day ago by
madders73
• 0
4
votes
2
replies
226
views
How can I analyze normalized expression data?
DEseq2
RNA-seq
15 hours ago by
mnx0723
• 0
3
votes
4
replies
4.0k
views
FarmCPU - how to explain the reported 'effect'?
gwas
updated 1 day ago by
chloek88
• 0 • written 5.5 years ago by
Philipp Bayer
8.4k
2
votes
4
replies
230
views
RNA seq analysis
DESeq
RNA-seq
updated 10 minutes ago by
s.ghazala
• 0 • written 1 day ago by
prifa
▴ 10
10
votes
3
replies
270
views
TFs and Gene databases
Transcription-factor
Target
Regulatory-Networks
updated 1 day ago by
b.contreras.moreira
▴ 180 • written 2 days ago by
ijarne
• 0
0
votes
0
replies
120
views
Chance for trained without experience
bio
updated 1 day ago by
ATpoint
82k • written 1 day ago by
shehab
• 0
1
vote
2
replies
160
views
How do I change the title font size in ViolinPlot (Seurat)
Seurat
Violin-Plot
ggplot2
patchwork
1 day ago by
Assa Yeroslaviz
★ 1.8k
0
votes
0
replies
96
views
Xenium multi sample data
batch
annotation
cell
Xenium
effect
1 day ago by
Omics data mining
▴ 260
0
votes
2
replies
150
views
Phasing a mixture of two individuals' DNA with long reads
long-reads
phasing
1 day ago by
njornet
▴ 20
0
votes
2
replies
178
views
Exploring Diet Effects in Single-Cell RNA Sequencing
batch_effect
scRNA
seurat
integration
updated 1 day ago by
Adam
▴ 30 • written 1 day ago by
Darya
• 0
0
votes
5
replies
217
views
Percentage coverage of reference genome by de novo genome
SAMtools
BWA
alignment
ddRAD
updated 1 day ago by
Joe
21k • written 1 day ago by
Lemonhope
• 0
0
votes
0
replies
137
views
Why does my Hi-C contact map show large regions making little to no contact?
BWA-MEM2
Hi-C
PretextMap
10 hours ago by
Winter
• 0
0
votes
5
replies
261
views
A question about reference genome for creating the consensus sequence
fasta
fa
cram
genome
1 day ago by
me
• 0
2
votes
11
replies
2.6k
views
6 follow
CNVKIT - unable to produce scatter and diagram pdfs
cnvkit
updated 1 day ago by
DGTool
• 0 • written 4.8 years ago by
ww22runner
▴ 60
2
votes
1
reply
122
views
java out of memory error through beagle for imutation
beagle
java.out.of.memory
imputation
1 day ago by
analyst
▴ 50
116,847 results • Page
1 of 2337
Recent Votes
Comment: Spike-in control found in raw reads (16S amplicon seq) but not picked up by DADA
Network plot from expression data in R using igraph
Comment: RNA seq analysis
RNA seq analysis
Answer: WGCNA kME vs kWithin Hub Gene Disparities
WGCNA kME vs kWithin Hub Gene Disparities
Comment: Spike-in control found in raw reads (16S amplicon seq) but not picked up by DADA
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Comment: Different output for read length
by
GenoMax
142k
Post the data at pastebin.com and add a link here or you could a GitHub gist. You were suspended by biostars SPAM bot since you pasted link…
Comment: Different output for read length
by
GenoMax
142k
Post the data at pastebin.com and add the link here. You were suspended by biostars SPAM bot since you pasted these links in quick successi…
Comment: RNA seq analysis
by
s.ghazala
• 0
Could you clarify on what exactly you are referring to with "SRA data table". If you are retrieving fastq files (raw data), then you could …
Comment: Spike-in control found in raw reads (16S amplicon seq) but not picked up by DADA
by
sovrappensiero
▴ 100
Thanks, Chris. I really appreciate your help. This has clarified a lot for me!
Answer: Snakemake fails to find conda in PBS
by
tim.booth
▴ 50
Snakemake does not have support for micromamba. There is an open issue: https://github.com/snakemake/snakemake/issues/2322
Comment: absolute path for symbolic links in Snakefile
by
tim.booth
▴ 50
Further to this answer - if you are using GNU coreutils (ie. any modern Linux), there is a "-r" flag to fix this problem. I typically use "…
Answer: Different output for read length
by
Pierre Lindenbaum
161k
I supect your reads are hard clipped. Show us the first lines of samtools view /home/sorted.bam | cut -f 2,6,10 | head -n 20
Comment: Presence of unknown sites in ANNOVAR output file
by
sainavyav22
• 0
Here you go. 1.perl convert2annovar.pl -format vcf4old 1008_Tumor.vcf > 1008Tumor_variant.avinput 2.perl annotate_variation.pl 100…
Comment: Filtering Multi-sample VCF file for all except one Genotype
by
Jeremy Leipzig
22k
Those are samples. If a sample has a 0/1 or a 1/1 genotype for that variant, they have the variant. Your question is ambiguous because you…
Comment: Help with Biopython for Beginner
by
GenoMax
142k
> That turns it into a mess of paragraphs See above. Select (highlight with mouse) the part you want to represent as `code` and then click…
Comment: Help with Biopython for Beginner
by
cput
• 0
That turns it into a mess of paragraphs, but if it truly is more productive thanks for the tip!
Comment: Presence of unknown sites in ANNOVAR output file
by
Ram
43k
Please show us your full annovar command line.
Comment: input file for alternative splicing in rmats in linux
by
Ram
43k
I've done what I can to make your post more professional. Stick to outlining your problem, personal pleas do not really belong on a profess…
Comment: Contig assembly task, errors
by
rackbersingh
• 0
Hi Phillip, Thanks for providing an answer and clearing up some confusion, looking into what you said about older assemblers reverse comp…
Comment: How to analyze Infinium Mouse Methylation BeadChip array data?
by
Tawny
▴ 180
Did you get this figured out? I am having the same error in R.
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