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687 results • Page
2 of 14
Sort: replies
Rank
Views
Votes
Replies
4
votes
8
replies
775
views
Create a new bed file with all pairwise combinations between two other bed files, based on bp distance
SNPs
BED
eqtl
bedtools
updated 23 days ago by
Alex Reynolds
35k • written 24 days ago by
J
▴ 10
1
vote
8
replies
477
views
Overlapping Ranges within Granges object
Genomicranges
IRanges
GRanges
updated 2 days ago by
Alex Reynolds
35k • written 6 days ago by
ntsopoul
▴ 60
0
votes
8
replies
544
views
What does it mean single base resolution in sequencing?
SNP
sequencing
updated 19 days ago by
LauferVA
4.2k • written 21 days ago by
jinyu
▴ 10
3
votes
8
replies
6.6k
views
7 follow
GATK genomicsDBimport intervals for WGS
gatk
genomicsdbimport
updated 17 days ago by
Sd
• 0 • written 5.1 years ago by
Nicolas Rosewick
11k
3
votes
8
replies
640
views
How to access TCGA samples that were treated with a specific drug?
TCGA
RNA-seq
13 days ago by
Qroid
▴ 40
1
vote
8
replies
569
views
Downsampling fastq file
downsample
fastq
20 days ago by
marco.barr
▴ 130
2
votes
8
replies
401
views
joint callset and vcf sorting, unknown TAG issue
sort
bcftools
GLNexus
merge
VCF
updated 8 days ago by
Pierre Lindenbaum
161k • written 8 days ago by
Matteo Ungaro
▴ 100
0
votes
8
replies
479
views
Error in cnetplot enrichplot package
R
updated 27 days ago by
Ram
43k • written 27 days ago by
Farhad
• 0
5
votes
7
replies
526
views
RNA seq analysis
DESeq
RNA-seq
5 days ago by
Jacek
▴ 20
0
votes
7
replies
4.3k
views
B allele frequency (BAF)
snp
updated 2 days ago by
aidangcruickshank
▴ 10 • written 3.7 years ago by
rthapa
▴ 90
4
votes
7
replies
437
views
How does gene length effect the number of reads mapped
RNA-seq
CPM
sequencing
6 days ago by
Chen
• 0
4
votes
7
replies
640
views
Very low RNA splicing rate for pulmonary AT2 cells
RNA-velocity
scVelo
scRNA-seq
splicing
21 days ago by
e.r.zakiev
▴ 210
6
votes
7
replies
408
views
Longest transcript variant per gene
transcript
longest
variant
orthofinder
7 days ago by
sansan_96
▴ 90
3
votes
7
replies
425
views
FastQC Quality per tile and per sequence behaving strange after using Cutadapt
fastqc
cutadapt
illumina
tile
paired-end
21 days ago by
salias
• 0
2
votes
7
replies
1.4k
views
6 follow
Differential Expression using Isoseq-supplemented reference transcriptome
RNA-Seq
Salmon
Isoseq
updated 21 days ago by
Gordon Smyth
★ 7.2k • written 8 months ago by
Calum
▴ 10
1
vote
7
replies
620
views
gvcf joint calling
WES
GATK
VCF
gVCF
22 days ago by
zihanss
• 0
7
votes
7
replies
6.0k
views
6 follow
How to know synonymous and non-synonymous SNPs from transcriptome sequencing
RNA-Seq
SNP
updated 25 days ago by
rohitsatyam102
▴ 870 • written 6.2 years ago by
smallfish
▴ 10
1
vote
7
replies
580
views
Question regarding WGCNA
WGCNA
Network-construction
11 days ago by
deepak
• 0
4
votes
7
replies
536
views
In one PCA plot, can I calculate the percentage of different factors that contribute to the PCA?
PCA
R
VARIANCE
updated 3 days ago by
marco.barr
▴ 130 • written 5 days ago by
diqixiaoyaoer
▴ 20
9
votes
7
replies
7.2k
views
Align paired and unpaired reads simultaneously using Bowtie2?
alignment
updated 9 days ago by
Ruqaiya
• 0 • written 5.7 years ago by
xiaozhongzhiping
▴ 20
0
votes
7
replies
462
views
RNAseq one control two conditions, shared and exclusive genes
conditions
RNAseq
multiple
Rstudio
updated 7 days ago by
Mohamed Abderrahmane
▴ 20 • written 21 days ago by
matteo.levorato
• 0
4
votes
7
replies
620
views
To get p-values for the TPM
P-value
TPM
RSEM
updated 25 days ago by
dsull
★ 6.0k • written 26 days ago by
VITALA
• 0
1
vote
7
replies
521
views
Downsampling long-read BAM files
nanopore
BAM
QC
ONT
downsampling
17 days ago by
eebloom
▴ 80
1
vote
7
replies
622
views
ScRNA data question
scRNA
Vlnplot
Samples
updated 21 days ago by
bk11
★ 2.5k • written 25 days ago by
starswillfade
▴ 10
1
vote
7
replies
358
views
Add stats to the plot
R
stats
plotting
updated 8 hours ago by
marco.barr
▴ 130 • written 1 day ago by
Ghada
• 0
0
votes
7
replies
662
views
Post-imputation plot
michigan-imputation-server
quality-control
updated 17 days ago by
LChart
3.9k • written 21 days ago by
kl
▴ 10
0
votes
6
replies
463
views
How to slice a gvcf file with tabix?
Tabix
bed
gvcf
26 days ago by
Sd
• 0
4
votes
6
replies
1.2k
views
Soft-clipping read ends based on read group
ancient
molecule
at
bam
DNA
RG
ends
clipping
damage
updated 12 days ago by
chenl
▴ 10 • written 2.5 years ago by
Martyna
• 0
0
votes
6
replies
509
views
Use of Kraken output for functional analysis
metagenomics
kraken
shotgun
updated 26 days ago by
gv
• 0 • written 7 weeks ago by
Srinka
▴ 20
1
vote
6
replies
757
views
anRichment is missing
WGCNA
anRichment
updated 14 days ago by
GenoMax
142k • written 6 months ago by
michael.flower.14
▴ 180
0
votes
6
replies
500
views
Differential Expression Analysis using DESeq2 in R
deseq2
R
updated 16 days ago by
swbarnes2
14k • written 17 days ago by
Erina
• 0
1
vote
6
replies
1.5k
views
CellRanger output more cells than specified using --force-cells? Why?
scRNA-seq
cellranger
updated 1 day ago by
scideas
▴ 30 • written 8 months ago by
rohitsatyam102
▴ 870
2
votes
6
replies
1.9k
views
How can you *consistently* download BioProject IDs from NCBI's BioSample database using Entrez Direct?
XML
ncbi
entrez-direct
updated 4 days ago by
Ram
43k • written 3.9 years ago by
millere
• 0
3
votes
6
replies
769
views
Ciriquant not configuring hisat2 indexed files
ciriquant
28 days ago by
Atul K.
• 0
3
votes
6
replies
2.0k
views
7 follow
DNA methylation preprocessing
SWAN
DNA
methylation
Funnorm
updated 23 days ago by
Ram
43k • written 2.4 years ago by
SYOSY
▴ 10
0
votes
6
replies
361
views
ComplexHeatmap - How to change fontsize of rowAnnotation
ComplexHeatmap
2 days ago by
hannes.bongartz
• 0
3
votes
6
replies
526
views
install package: package ‘gmwm’ is not available for this version of R
r
updated 7 days ago by
Pine
▴ 20 • written 15 days ago by
snajafy
• 0
0
votes
6
replies
2.1k
views
Copy number Variation analysis using conumee
R
software error
sequencing
genome
updated 11 days ago by
GenoMax
142k • written 3.2 years ago by
gs000095
▴ 10
4
votes
6
replies
3.8k
views
How to interpret DEXseq results in therms of significance
DEXseq
RNA-Seq
exon
updated 14 days ago by
Sara
▴ 30 • written 6.7 years ago by
Lila M
★ 1.2k
7
votes
6
replies
616
views
Filtering sam or bam file with maximum matching region
crisper-edited
alignment
match
29 days ago by
analyst
▴ 50
5
votes
6
replies
614
views
Programmatically retrieving positions of protein active site residues
Uniprot
PDB
Proteins
updated 20 days ago by
me
▴ 760 • written 21 days ago by
Mariana
▴ 40
2
votes
6
replies
3.8k
views
Treatment VS Control in Single Cell RNAseq analysis
Single Cell
RNAseq
DE Analysis
Treatment
Control
updated 24 days ago by
ATpoint
82k • written 3.9 years ago by
grayapply2009
▴ 280
2
votes
6
replies
412
views
BWA alignment
Samtools
bam
updated 5 days ago by
a.alnawfal.1992
▴ 260 • written 7 days ago by
Vahid
• 0
1
vote
6
replies
421
views
Do I need to go back and filter my long-reads?
alignment
nanopore
filtering
QC
ONT
updated 17 days ago by
GenoMax
142k • written 5 weeks ago by
eebloom
▴ 80
6
votes
6
replies
1.8k
views
agilent human all exon sureselct v7 bed file
exon
human
bed
v7
agilent
all
sureselect
updated 15 days ago by
MiladAD
▴ 10 • written 2.0 years ago by
soheil
• 0
10
votes
6
replies
10k
views
6 follow
CDS vs cDNA vs transcript for mapping RNA-Seq reads
Assembly
rna-seq
alignment
updated 24 days ago by
Antonio R. Franco
★ 5.1k • written 6.1 years ago by
williamsbrian5064
▴ 520
4
votes
6
replies
818
views
7 follow
Heatmap and rna-seq
RNA-Seq
Heatmap
updated 23 days ago by
dsull
★ 6.0k • written 27 days ago by
qudrat.nii
▴ 10
1
vote
6
replies
2.8k
views
Segmentation fault using gemma
gemma
gwas
updated 21 days ago by
dimpleadiwal050896
• 0 • written 5.0 years ago by
ggman
▴ 90
4
votes
6
replies
3.9k
views
Taking the difference of two VCFs (or removing singletons)
genome
sequencing
singleton
SNP
filter
updated 20 days ago by
Andres
▴ 20 • written 9.7 years ago by
hermathena
▴ 40
2
votes
5
replies
2.5k
views
identifying transgene insertion site in WGS
WGS
insertion site
trangene
de-novo
soap
updated 12 days ago by
Cameron.walker9900
• 0 • written 5.1 years ago by
Assa Yeroslaviz
★ 1.8k
687 results • Page
2 of 14
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Answer: Generating Group/Cluster Lists from fastq files
The Biostar Herald for Monday, May 20, 2024
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A: ClusterProfiler : What is GeneRatio and BgRatio?
A: ClusterProfiler : What is GeneRatio and BgRatio?
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Comment: Filter Genome for Specific Sites
by
Pierre Lindenbaum
161k
> My sites are in an Excel file right now ![enter image description here][1] <!-- was an American educator and academic administrator…
Comment: Filter Genome for Specific Sites
by
GenoMax
142k
> I have a list of ~1,300 single bp sites Convert your file to plain text [**BED format**][1] (three fields required). Use `bedtools slo…
Comment: How to generate an Upset plot in R to plot the shared variants between cell free
by
sainavyav22
• 0
It worked, Thank you very much!
Comment: What marks a De-Novo Genome assembly as FAILED?
by
dthorbur
★ 2.0k
I'm unsure you'll be able to identify whole chromosomes that are not core from illumina reads alone. That might be easier to do with a micr…
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by
Mohamed Samir
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Dear marco, We need to ask ourselves why it is not working for all bioprojects ? I have looked into this, and observed that as long as the…
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43k
You ***want*** ~3000 DE genes?<a href="" title="Text added because biostars parser needs it"></a>
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by
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142k
> I was hoping to just do this in galaxy This is not a galaxy option but `clumpify.sh ` from BBMap suite can cluster sequences/dedupe th…
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by
beantkapoor16
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Hello, just wanted to check in if the code has been fixed yet? Thank you.
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jared.andrews07
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Based on the [source code](https://bitbucket.org/young_computation/rose/src/feb35cb1d9556a76f8ac1f51521539bb30651343/ROSE_utils.py?at=maste…
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by
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43k
They're not addressing the actual question, just saying something tangentially related. It looks like their understanding of both consensus…
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by
Oburah
• 0
Hello, i encountered this problem when running ROSE, Do anyone know how to solve it? python2.7 ROSE_main.py -g HG38 -i /home/hesborn/…
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Try this example: library(UpSetR) #example input, 4 samples, 250 variants set.seed(1); d <- data.frame(matrix(sample…
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We have been using SeSAMe, it works well for the most part. They have an enrichment tool called KnowYourCG. You can check it out their vign…
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I think you have set a filter to get these pahways upstream from the DEG results. You should extract the IDs or names of the genes that you…
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