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771 results • Page
1 of 16
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Views
Votes
Replies
0
votes
0
replies
10
views
DEG gene list and find common TF from public ChlP-Seq data
chip-seq
TF
50 minutes ago by
Joshua
• 0
0
votes
3
replies
109
views
Encountering Error while Running 'make vcf' in Biostar Handbook
bugfix
biostarhandbook
vcf
1 hour ago by
Tully
• 0
0
votes
5
replies
206
views
Getting the overlap between two GTF files
file
RNA-seq
GTF
updated 19 hours ago by
GenoMax
134k • written 21 hours ago by
feather-W
• 0
0
votes
1
reply
68
views
vcf.gz to vcf
VCF
updated 2 hours ago by
Mark
★ 1.3k • written 4 hours ago by
sooni
▴ 10
2
votes
6
replies
274
views
Search RCSB with a list of protein names?
RCSB
protein
updated 3 hours ago by
Jiyao Wang
▴ 340 • written 1 day ago by
Joseph
• 0
0
votes
1
reply
68
views
How to get ncol = nrow?
ncol
nrow
DESeq2
updated 3 hours ago by
Mark
★ 1.3k • written 5 hours ago by
Suha
• 0
0
votes
1
reply
84
views
bedtools intersect by position & stand not working even with common regions
bedtools
genomic
intersect
bedops
intervals
updated 2 hours ago by
rfran010
▴ 830 • written 9 hours ago by
Alewa
▴ 130
0
votes
1
reply
103
views
How to import bigwig files into igvR
bigwig
igvr
updated 12 hours ago by
Trivas
★ 1.5k • written 16 hours ago by
ntsopoul
▴ 50
0
votes
1
reply
96
views
MAKER: WARNING: Could not get initialization lock. Trying Again...
gene
annotation
MAKER
prediction
updated 9 hours ago by
GenoMax
134k • written 16 hours ago by
memy
▴ 20
0
votes
0
replies
73
views
TPM from STAR output without re-allign the file using RSEM or Salmon
bulkRNASEQ
STAR
RSEM
16 hours ago by
camillab.
▴ 140
2
votes
4
replies
291
views
Automate the Splitting of a VCF File by Sample (bcftools)
bcftools
vcf
updated 19 hours ago by
Pierre Lindenbaum
157k • written 2 days ago by
RogueBiochemist
• 0
0
votes
1
reply
117
views
Unable to install HorvathMammalMethylChip40manifest packages
r
programming
updated 21 hours ago by
ATpoint
77k • written 23 hours ago by
Nibedita
• 0
0
votes
0
replies
86
views
TEtranscripts Tool in Galaxy
RNAseq
Transposable_Elements
TE_Transcripts
1 day ago by
gorizwango
▴ 30
0
votes
0
replies
84
views
rMats Run Does Not Generate More Than One Output Row Per File
Singularity
rMats
sif
1 day ago by
Y
• 0
2
votes
4
replies
241
views
Subclustering of intergated cells from scRNA-seq data
scRNA-seq
Seurat
1 day ago by
fifty_fifty
▴ 60
1
vote
1
reply
134
views
Imputation server failing to see samples in VCF files
imputation
VCF
updated 1 day ago by
Ram
40k • written 1 day ago by
Ben
• 0
2
votes
1
reply
170
views
TPM RNA-seq data for differential expression analysis
RNA-seq
updated 1 day ago by
Ram
40k • written 1 day ago by
Catalin-George
• 0
2
votes
4
replies
236
views
Snakemake alignment script
snakemake
alignment
1 day ago by
Begonia_pavonina
▴ 110
0
votes
1
reply
158
views
Issues with featureCounts
featurecounts
rna-seq
differential-expression
updated 1 day ago by
Ram
40k • written 1 day ago by
Aime
• 0
1
vote
7
replies
321
views
biomaRT doesn't report uniprot id
R
Uniprot
biomaRt
updated 1 day ago by
Ram
40k • written 1 day ago by
H.Hasani
▴ 990
0
votes
1
reply
146
views
Quality Control of VCFs that used different genotyping arrays
bcftools
VCF
updated 1 day ago by
bk11
★ 1.3k • written 1 day ago by
Shane
• 0
1
vote
4
replies
289
views
How to perform hypothesis testing on contingency tables and compare with the null distribution?
hypothesis-testing
contingency-table
1 day ago by
RK
• 0
0
votes
1
reply
150
views
QC of genetic data
PLINK
updated 1 day ago by
bk11
★ 1.3k • written 1 day ago by
kl
▴ 10
1
vote
3
replies
214
views
differences between trajectories in conditions with Monocle3 or other tools
trajectory
scRna-seq
monocle3
single-cell
updated 1 day ago by
Amitm
★ 2.2k • written 1 day ago by
Chironex
▴ 40
2
votes
5
replies
434
views
6 follow
How to convert data in r?
R
offtopic
updated 1 day ago by
Ram
40k • written 2 days ago by
star
▴ 350
8
votes
9
replies
2.4k
views
Why should ATAC-seq mapped reads be shifted +4 and -5 for +strand and -strand, respectively
ATAC-seq
updated 1 day ago by
benformatics
3.8k • written 2.8 years ago by
progistar
▴ 40
7
votes
6
replies
6.0k
views
7 follow
ATAC-seq +4 -5 shift
atac-seq
updated 1 day ago by
ATpoint
77k • written 3.5 years ago by
Jingyue
▴ 70
0
votes
4
replies
307
views
Assessing Rockhopper's output
transcriptome
Rockhopper
RNA-seq
de-novo-assembly
19 hours ago by
langziv
▴ 50
0
votes
1
reply
320
views
Recommendations for extending contigs from denovo assembly to identify SV insertion sites on chromosome
Nanopore
WGS
Long-Read
SV
Assembly
1 day ago by
dk0319
▴ 70
3
votes
4
replies
245
views
How to get the gft file to run velocyto for velocity analysis?
velocity
1 day ago by
Chris
▴ 200
0
votes
1
reply
147
views
Lower alignment rate when using collapsed reads
short_rna
RNA-Seq_mapping
collapsed_reads
updated 2 days ago by
LChart
3.4k • written 2 days ago by
blz
▴ 30
1
vote
5
replies
1.3k
views
Unmapped Reads in Kallisto
Kallisto
RNA-Seq
alignment
bustools
updated 2 days ago by
dsull
★ 4.8k • written 3.6 years ago by
msutennis23
• 0
0
votes
0
replies
108
views
Can optimal cofactors for arcsinh transformation be calculated in parallel?
parallel
R
flowcytometry
flowCore
flowVS
2 days ago by
gmiller
• 0
0
votes
0
replies
110
views
Is the concept of a cofactor in an arcsinh transformation specific to Flow Cytometry?
FlowCytometry
flowCore
FlowVS
2 days ago by
gmiller
• 0
1
vote
1
reply
178
views
Comparing multiple RNASeq studies
RNASeq
updated 2 days ago by
Zhenyu Zhang
▴ 980 • written 2 days ago by
Luke
▴ 10
0
votes
1
reply
152
views
Issue with merging in plink and eigensoft.
Eigensoft
Eigenstrat
Plink
updated 2 days ago by
bk11
★ 1.3k • written 2 days ago by
Jd
• 0
3
votes
4
replies
311
views
Network analysis with cytoscape
RNA-seq
cytoscape
2 days ago by
Chris
▴ 200
3
votes
3
replies
236
views
Clustering in single cell
seurat
single-cell
2 days ago by
Chris
▴ 200
0
votes
0
replies
123
views
Convert from limma voom normalized matrix each gene to high/low
limma-voom
RNA-SEQ
updated 2 days ago by
Ram
40k • written 2 days ago by
Manuel Sokolov Ravasqueira
▴ 100
0
votes
2
replies
1.3k
views
Converting hdf5 file to loom file
single-cell
python
scvelo
RNA
updated 2 days ago by
bk11
★ 1.3k • written 2.4 years ago by
sidrah.maryam
▴ 50
2
votes
4
replies
3.8k
views
Is there a way to use CNVkit without a reference from normal samples?
sequence
CNVkit
updated 2 days ago by
Matteo Schiavinato
★ 3.6k • written 5.5 years ago by
leandro.bispo.oliveira
• 0
4
votes
3
replies
268
views
Allele frequency calculation for genotype dosage value
plink
dosage
r
impute
updated 1 day ago by
zx8754
11k • written 2 days ago by
Sebastian
▴ 10
3
votes
15
replies
507
views
How to subset large BAM files specifically/ extract specific subsets?
bamtools
RNAseq
samtools
BAM
2 days ago by
ella
• 0
0
votes
0
replies
128
views
Guide for ICD-10 to EFO conversion?
icd10
efo
2 days ago by
optimistsso4co3
▴ 100
4
votes
5
replies
384
views
identify DEGs across all conditions and per specific conditions
R
DEseq2
2 days ago by
camillab.
▴ 140
0
votes
0
replies
129
views
Software for chimera detection of amplicon (e.g. 16S) nanopore reads
chimera
nanopore
amplicon
2 days ago by
rob_DNA
▴ 10
2
votes
2
replies
241
views
Get support value of MRCA given a list of tip.label in R newick trees
phylogeny
newick
R
ape
tree
2 days ago by
pl.terzian
• 0
0
votes
2
replies
217
views
Splitting VCF/BCF file into seperate gene files
genomics
bcftools
eqtl
gwas
updated 2 days ago by
Pierre Lindenbaum
157k • written 3 days ago by
Lynne-95
• 0
3
votes
3
replies
251
views
Have some issues in running prokka on WSL
prokka
updated 2 days ago by
Ram
40k • written 3 days ago by
Kirill
▴ 10
1
vote
3
replies
268
views
comparision of umap single cell
single-cell
2 days ago by
synat.keam
▴ 80
771 results • Page
1 of 16
Recent Votes
A: .gstmp extension on .bam files downloaded from google bucket; and EOF marker is
Comment: Significance testing of top vs. random SNPs
Answer: Search RCSB with a list of protein names?
A: running RAxML and MrBayes over concatinated multiple sequence alignments
Comment: Weirdness in annotation (missing allele frequencies)
Comment: Weirdness in annotation (missing allele frequencies)
Comment: ncbi error report log for validate fastq issue
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Recent Replies
Comment: Getting the overlap between two GTF files
by
Alex Reynolds
35k
What would that be?
Answer: Encountering Error while Running 'make vcf' in Biostar Handbook
by
Tully
• 0
@ialbert ,I am deeply immersed in the fog and request the help ,please
Comment: bedtools intersect by position & stand not working even with common regions
by
rfran010
▴ 830
are you sure bedtools can handle the non-standard location of strand information?
Answer: Getting the overlap between two GTF files
by
rfran010
▴ 830
Maybe somebody knows something I don't, but I feel like bedtools should be able to handle your gtf files directly. If it's not done alre…
Answer: vcf.gz to vcf
by
Mark
★ 1.3k
As the error says, the file is not compressed. In linux the file extension is essentially optional. The file could be named `my.vcf.txt` ye…
Answer: Search RCSB with a list of protein names?
by
Jiyao Wang
▴ 340
You can use NCBI esearch to search the protein names against the structure database to get the PDB IDs, then retrieve the structures.
Answer: How to get ncol = nrow?
by
Mark
★ 1.3k
Without your actual data, it's hard to assist. I think what you're asking is 'how do I rename the rows of my dataframe(s)'. Taking the …
Comment: MAKER: WARNING: Could not get initialization lock. Trying Again...
by
GenoMax
134k
What kind of hardware are you running this on? You need to have the right kind of hardware (multiple CPU's not just cores), MPI libraries a…
Answer: Getting the overlap between two GTF files
by
Alex Reynolds
35k
Using `bedops --intersect` and `gtf2bed` will get their common genomic space: ``` bedops --intersect <(gtf2bed < transcripts.gtf) <(gtf2be…
Comment: Encountering Error while Running 'make vcf' in Biostar Handbook
by
Tully
• 0
```bash # Obtain the makefile curl -s http://data.biostarhandbook.com/make/snpcall.mk > Makefile # Run the makefile make vcf ``` Error me…
Comment: Encountering Error while Running 'make vcf' in Biostar Handbook
by
Tully
• 0
> System Information: Ubuntu 22.04 (WSL2) > > Shell: zsh > > Installation Verification: Yes, doctor.py OK [1]: https://www.biostarhand…
Comment: Retrieve The Reads And Fastq From Bam File
by
Reem
• 0
Did it affect the bamtofastq output file? if so how did you solve the problem? Thanks
Answer: How to import bigwig files into igvR
by
Trivas
★ 1.5k
You could try seeing if this fixes your issue with rtracklayer: https://support.bioconductor.org/p/p133244/
Comment: Weirdness in annotation (missing allele frequencies)
by
Jeremy Leipzig
21k
0.60625 is 97/160 so if you have 80 individuals in your VCF that's an internal allele frequency, not gnomAD
Comment: Weirdness in annotation (missing allele frequencies)
by
Can Abdullah
• 0
Yes, I was confused as well. I think the same. Maybe Annovar uses some other resources besides gnomad, but it does not make sense. Also, I …
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