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1,000 results • Page
2 of 20
Sort: Rank
Rank
Views
Votes
Replies
0
votes
1
reply
148
views
Pairwise Alignment
Pairwise-Alignment
updated 2 days ago by
Ram
39k • written 3 days ago by
Fatemeh
• 0
0
votes
0
replies
96
views
How to perform a phylogenetic analysis from a vcf file
variants
haplotyping
phylogeny
vcf
3 days ago by
rj.rezwan
• 0
0
votes
1
reply
162
views
Where to get the molecular subtype information of STAD sample in TCGA
TCGA
database
updated 3 days ago by
Hamid Ghaedi
2.9k • written 3 days ago by
younglin113
▴ 50
0
votes
0
replies
137
views
How to keep ComplexHeatmap from reordering annotations
Dendrogram
HeatmapAnnotations
R
Heatmap
ComplexHeatmap
4 days ago by
Manuel
• 0
1
vote
3
replies
227
views
Differential protein expression analysis
R
proteomic
statistics
updated 11 hours ago by
dsull
★ 4.2k • written 4 days ago by
Ribo
▴ 40
0
votes
3
replies
326
views
(ERR): "index/Trinity.fa" does not exist or is not a Bowtie 2 index Exiting now ...
bowtie2
align_stats
trinity
3 days ago by
eimanpharmacist
▴ 20
0
votes
4
replies
370
views
What are recommended parameters for the local protein alignment ?
protein
alignment
3 days ago by
Alexander
▴ 70
0
votes
0
replies
130
views
microsatellite, SSR, using Galaxy
Galaxy
SSR
using
microsatellite
4 days ago by
m.esmaeilpour
▴ 10
0
votes
0
replies
147
views
decoupleR & Transcription Factory Activity Inference: pvalue or padj?
pvalue
padj
decoupleR
4 days ago by
OST
▴ 10
2
votes
3
replies
342
views
Low mapping percentage
mapping
STAR
RNAseq
4 days ago by
Sib
▴ 40
0
votes
0
replies
174
views
Visualization App for RNASeq Differential Expression and Enrichment Analysis
differential
visualization
RNASeq
analysis
expression
enrichment
5 days ago by
Mark
• 0
0
votes
0
replies
160
views
busco id description
OrthoDB
BUSCO
updated 5 days ago by
Ram
39k • written 5 days ago by
angelina
• 0
0
votes
5
replies
392
views
how to Construct a Newick tree file from five large fasta files
tree
Newick
alignment
updated 5 days ago by
Joe
21k • written 5 days ago by
gunala.nikhil
• 0
0
votes
0
replies
164
views
NMDS plotting issue
NMDS
metagenomic
5 days ago by
arshad1292
▴ 90
0
votes
2
replies
243
views
featurecounts not working on mirbase annotation file
usegalaxy
miRNA-seq
2 days ago by
demoraesdiogo2017
▴ 90
0
votes
0
replies
142
views
IGV insertions
insertions
IGV
5 days ago by
christoph.schubart
• 0
1
vote
0
replies
155
views
Bayesian network for biological data using bnlearn
bnlearn
RNA-seq
bayesian-network
updated 5 days ago by
Ram
39k • written 5 days ago by
priyankamehta.1811
▴ 10
0
votes
0
replies
150
views
jellyfish options
kmer
jellyfish
5 days ago by
Tele
• 0
0
votes
3
replies
227
views
hardfilter error
bam
recall
5 days ago by
bestone
▴ 10
0
votes
0
replies
125
views
cnetplot enrichment graph to cytoscape
clusterprofiler
cnetplot
enrichplot
5 days ago by
Omics data mining
▴ 220
0
votes
0
replies
126
views
How to extract the surrogate variables from DNA methlation Data
sva
array
limma
methylation
updated 5 days ago by
GenoMax
130k • written 5 days ago by
Dablax
• 0
1
vote
1
reply
602
views
Reads with highest MAPQ values from SAM files are showing mismatches to reference sequence and IGV classified them as supplementary reads
minimap
Nanopore
IGV
updated 5 days ago by
GenoMax
130k • written 5 days ago by
Mohd
▴ 20
0
votes
0
replies
117
views
Convert tree into bifurcation table
Tree
Newick
ASR
Mutation
5 days ago by
Alexandre
• 0
0
votes
1
reply
186
views
Processing WES VCF for case control GWAS analysis
GWAS
PLINK
updated 5 days ago by
raphael.B
▴ 360 • written 5 days ago by
sonsunjirachote
• 0
4
votes
6
replies
1.5k
views
Why weblogo of biopython doesn't work?
Biopython
Weblogo
updated 5 days ago by
minakshiboruahassam
• 0 • written 9 months ago by
Plus
▴ 20
1
vote
2
replies
231
views
The famous WGS dataset, Ashkenazi Trio?
wgs
dataset
updated 5 days ago by
thadjudkins2
• 0 • written 5 days ago by
herh
• 0
1
vote
0
replies
145
views
Integrating mRNA and microRNA analysis results
mRNA
microRNA
6 days ago by
abba647
▴ 10
4
votes
4
replies
295
views
Does adding reads cause batch effects?
kallisto
RNAseq
updated 6 days ago by
ATpoint
72k • written 6 days ago by
bioinfo
▴ 80
0
votes
1
reply
165
views
Merge different vcf files
vcf
updated 5 days ago by
Ram
39k • written 6 days ago by
caique.manochio
• 0
0
votes
4
replies
281
views
Identification of genes involved in my pathway
KEGG
keggGet
6 days ago by
smanzano250800
• 0
0
votes
8
replies
350
views
The inchworm process failed. Trinity running error.
inchworm
transcriptome
trinity
updated 5 days ago by
GenoMax
130k • written 6 days ago by
Marta
• 0
1
vote
2
replies
209
views
Combination of ROC CURVE
roccurve
R
AUC
3 days ago by
Maria17
▴ 20
1
vote
0
replies
97
views
Considering gaps in calculating conservation score from MSA
multiple
alignment
sequence
conservation
python
6 days ago by
Jonathan Lefebre
▴ 70
0
votes
3
replies
180
views
DEGseq for multiple samples
DEGseq
DEG
updated 6 days ago by
Ram
39k • written 6 days ago by
ALOUSH ALI
• 0
0
votes
0
replies
80
views
Metabolomics Data Annotation
annotation
metabolomics
camera
updated 6 days ago by
Ram
39k • written 6 days ago by
Rishabh Jha
• 0
1
vote
3
replies
210
views
My kernel is killing the pairtools dedup script, how to prevent that?
ubuntu
hic
pairtools
aws
updated 6 days ago by
GenoMax
130k • written 6 days ago by
NikhilP
▴ 20
2
votes
2
replies
182
views
bioinformatic analysis protocol performed by CD Genomics
Genomics
analysis
CD
Protocol
updated 1 day ago by
Ram
39k • written 6 days ago by
linnet.roque6
▴ 10
3
votes
12
replies
2.2k
views
What is NCBI Gene ID, where to find it and how to convert to entrez ID?
RNA-Seq
updated 6 days ago by
Pegasus
▴ 90 • written 3.7 years ago by
mnazir
▴ 10
0
votes
0
replies
106
views
RRBS fastq - biased per base sequence content
fastqc
rrbs
6 days ago by
mbk0asis
▴ 670
0
votes
0
replies
303
views
What are the existing proposals for how to approach genomic coordinates in a pangenome reference environment?
coordinates
pangenome
genomic
6 days ago by
Vincent Laufer
★ 2.9k
0
votes
0
replies
106
views
Determining Cutoff for score in a bed file in ATAC-seq Data Analysis
bed
ATAC-seq
updated 7 days ago by
Ram
39k • written 7 days ago by
Mah
• 0
1
vote
3
replies
221
views
To call variants can I use my aligned WGS data as a reference genome
VCF
samtools
reference
genome
updated 7 days ago by
GenoMax
130k • written 7 days ago by
mls
• 0
0
votes
0
replies
109
views
snpEff error. No CDS checked
snpEff
gtf
WES
7 days ago by
fifty_fifty
▴ 40
0
votes
0
replies
111
views
Tool to align metagenomic data to reference genome
tool
metagenomics
alignment
7 days ago by
Maddie
• 0
1
vote
2
replies
209
views
how to look for interactions between different chromosomes
SNP
interactions
Gene
HiC
6 days ago by
rheab1230
▴ 140
2
votes
4
replies
239
views
Filter VCF file for variant alleles
VCF
variants
bcftools
vcftools
updated 7 days ago by
Ram
39k • written 7 days ago by
miguellarrazlopezdenovales
• 0
1
vote
0
replies
108
views
Linear models with limma: coefficients not estimatable, are the others OK?
limma
7 days ago by
fr
▴ 200
0
votes
2
replies
175
views
Ambient RNA expression correction
scRNAseq
SoupX
Seurat
updated 7 days ago by
rpolicastro
12k • written 7 days ago by
Pac314
▴ 10
0
votes
2
replies
167
views
readGenericHeader() error message Limma
rna
limma
microarray
genomics
normalization
6 days ago by
survive
• 0
1
vote
1
reply
131
views
mitochondrial genome, SRA PacBio sequencing.
Mitochondrial
PacBio
SRA
Mitogenome
updated 7 days ago by
GenoMax
130k • written 7 days ago by
hashim.rana11
▴ 20
1,000 results • Page
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Recent Votes
NM_transcript ID gene identification
Converting Genome Coordinates From One Genome Version To Another (Ucsc Liftover, Ncbi Remap, Ensembl Api)
Converting Genome Coordinates From One Genome Version To Another (Ucsc Liftover, Ncbi Remap, Ensembl Api)
A: Mouse promoter regions
Answer: How to get information about promoter from bulk-RNAseq?
A: Extracting Flanking Regions across TSS using R scripts
A: Mouse promoter regions
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Recent Replies
Comment: Creating a local version of Clustered NR database
by
GenoMax
130k
> One idea is to provide just the representative sequences as a first > pass. This seems reasonable since it should capture significant pa…
Comment: pal2nal -nogap -nomismatch options not working
by
Marie
• 0
Hi, did you end up solving this? I am running into the same issue. Marie
Comment: How to get information about promoter from bulk-RNAseq?
by
camillab.
▴ 130
and what about enhancer? is it possible to do it from a bulk-RNAseq?
Comment: How to get information about promoter from bulk-RNAseq?
by
camillab.
▴ 130
yes! clearly the terminology on my side needs to improved!
Comment: How to get information about promoter from bulk-RNAseq?
by
rpolicastro
12k
Generally speaking, most promoters only initiate transcription for a single gene, with a single gene potentially having multiple promoters …
Answer: How to get information about promoter from bulk-RNAseq?
by
Trivas
★ 1.2k
I'd probably select the genes of interest from your bulk RNA-seq results then use the UCSC table browser to get the sequence upstream of th…
Comment: How to add annotation columns with specific colors to the heatmap?
by
Ram
39k
Show us your exact code - it is quite easy to tweak colors in ComplexHeatmap with the `col=` argument.
Comment: VCF file CSQ flag
by
Ram
39k
True, but it's not technically impossible to annotate GVCFs, which is why I did not address that point.
Comment: Creating a local version of Clustered NR database
by
PeterC_NCBI
▴ 260
@genomax Sorry for the delay in reply. We're still working out the details of what exactly to provide. One idea is to provide just the rep…
Comment: Shannon's Entropy by Sliding Window in R
by
rohitsatyam102
▴ 690
Hi Were u able to achieve this?
Comment: Differences in GTF files hg19 and hg38
by
GenoMax
130k
Since this is not an answer to the original question do not add it as such. I moved your last comment to the correct spot it should have be…
Comment: VCF file CSQ flag
by
Pierre Lindenbaum
154k
if your talking about the gvcf produced by HaplotypeCaller with ERC=GVCF, you don't annote g.vcf files , you must first merge the g.vcf.f…
Comment: [python]sklearn.ensemble.RandomForestClassifier(TypeError: string indices must b
by
Ram
39k
https://www.biostars.org/u/127538/ : Please delete this question or it will be deleted by moderators in a few days.
Comment: VCF file CSQ flag
by
Ram
39k
A gvcf files has blocks for both variant loci and non-variant loci, so you won't see a CSQ for each record, only for those variant loci wit…
Comment: Differences in GTF files hg19 and hg38
by
heureuse
• 0
Thank you very much. I get it from UCSC.
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