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311 results • Page
3 of 7
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1
vote
2
replies
279
views
Dotplot error: subscript out of bound
R
scRNA-seq
seurat
6 days ago by
Xuhao
• 0
0
votes
2
replies
293
views
miRNAseq - over-presented sequence in negative control
miRNAseq
adaptor
dimer
18 days ago by
MH85
• 0
0
votes
2
replies
248
views
Segmentation fault error in CONTROL-FREEC
copy-number-variants
FREEC
18 days ago by
DdogBoss
• 0
0
votes
2
replies
179
views
Detect STRs in illumina library
repeats
annotation
STR
2 days ago by
kirillkirilenko
▴ 20
0
votes
2
replies
303
views
NCBI Genome Workbench Sequence ID edit
NCBI
Workbench
Genome
Sequence
24 days ago by
Paige
• 0
0
votes
2
replies
315
views
Sample size estimation with ssizeRNA in R
transcriptomics
power-analysis
RNA-seq
sample-size-estimation
24 days ago by
Nana
• 0
2
votes
2
replies
224
views
Clustering algorithm based on grouping sequences into gene families
gene-families
clustering
updated 11 days ago by
Ram
40k • written 12 days ago by
francesco
• 0
0
votes
2
replies
1.6k
views
Question about REDItools
REDItools
updated 14 days ago by
Ethan Lee
• 0 • written 4.1 years ago by
tujuchuanli
▴ 100
0
votes
2
replies
235
views
NCBI nt seqid2taxid.map
ncbi
kraken2
kraken
database
16 days ago by
Gio
• 0
0
votes
2
replies
282
views
Gene Ontology - How to do Transcript Ontology?
gene-ontology
GO
transcripts
updated 18 days ago by
Ram
40k • written 20 days ago by
Lakritz the LabRat
• 0
0
votes
2
replies
277
views
STAR mapping two pass mode for multiple samples with split steps or one step ?
STAR
RNA-seq
19 days ago by
octpus616
▴ 90
2
votes
2
replies
276
views
Pangenome using Orthofinder
OrthoFinder
Pangenome
bacteria
12 days ago by
kirankumareripogu
▴ 10
0
votes
2
replies
384
views
log2fC from limma on methylation analysis
methylation
limma
minfi
fold-change
updated 14 days ago by
Ram
40k • written 11 months ago by
adeizadavid
▴ 10
0
votes
2
replies
204
views
Identify genes for mapped reads with combined human-7HPV genome index
star
samtools
updated 11 days ago by
Ram
40k • written 11 days ago by
r.j.lock
• 0
0
votes
2
replies
339
views
How to load a galaxy DESeq results table into R so I can continue my workflow there
r
RNA-seq
deseq2
18 days ago by
Nicolas
• 0
0
votes
2
replies
241
views
Is it okay to just average the log2FC values across different cell types in pseudobulk scRNA-seq data?
scrna-seq
rna-seq
log2fc
9 days ago by
JLee
• 0
0
votes
2
replies
246
views
Volunteer projects in 2023 for new bioinformaticians
junior
volunteer
projects
22 days ago by
gallardodiazmiriam
▴ 20
2
votes
2
replies
362
views
Currently lost between contigs, scaffolds and chromosomes due to positionally sorted scRNAseq bam files
bam
contigs
scRNAseq
updated 25 days ago by
ATpoint
77k • written 25 days ago by
nyxtoviopouli
• 0
1
vote
2
replies
424
views
Ranked fold changes for non-replicated data
expression
metagenomics
LogFC
fold-change
updated 14 days ago by
Ram
40k • written 18 months ago by
Tom
▴ 540
0
votes
2
replies
301
views
ClusterProfiler GeneRatio demoninator not the same for all values
enrichment-analysis
clusterprofiler
RNA-seq
deseq2
23 days ago by
Lily
• 0
3
votes
2
replies
194
views
Program for Overlapping DMRs (Differentially Methylated Regions) Between Groups
methylation
DMR
updated 4 days ago by
Basti
★ 1.7k • written 4 days ago by
epianalysis
• 0
0
votes
2
replies
696
views
RSEM not giving .genes.results and isoforms.results ; Plase check if you provide correct parameters/options for the pipeline!
genomics
transcriptome
rsem
ngs
2 days ago by
kat.bi
• 0
1
vote
2
replies
237
views
Searching a tool to modify annotation files.
annotation
updated 19 days ago by
GenoMax
134k • written 19 days ago by
Charles Plessy
★ 2.9k
4
votes
2
replies
442
views
Recommended way to normalize SmartSeq2 gene expression matrix to better match 10X expression data
rna-seq
smartseq2
r
updated 10 days ago by
yhdist
▴ 70 • written 12 days ago by
Cookin
▴ 10
0
votes
2
replies
203
views
how to create a loop in R
R
offtopic
updated 3 days ago by
Ram
40k • written 4 days ago by
mthm
▴ 50
0
votes
2
replies
698
views
pal2nal -nogap -nomismatch options not working
pal2nal
updated 14 days ago by
wangjb702
• 0 • written 10 months ago by
pkfsantos
• 0
1
vote
2
replies
256
views
Understanding TCGA barcodes with dot in the fieldname
tcga
updated 4 days ago by
Zhenyu Zhang
▴ 980 • written 7 days ago by
Tahsin
• 0
0
votes
2
replies
317
views
Sentrix Array Genotyping
Illumina
22 days ago by
joo
• 0
1
vote
2
replies
317
views
Converting scMultiome data to loom using SEURAT
scMultiome
CCAF
Seurat
21 days ago by
halimaakhter014
• 0
1
vote
2
replies
227
views
Problem with Mageck paired analysis
Mageck
updated 18 days ago by
Meisam
▴ 200 • written 18 days ago by
toma.85
• 0
0
votes
2
replies
278
views
Modify the code to take most abundant reads from a cluster and process it.
cd-hit-est
clustering
6 days ago by
Mo
▴ 40
1
vote
2
replies
279
views
Multiple testing adjustment for stepwise model selection
statistics
12 days ago by
mel22
▴ 100
0
votes
2
replies
276
views
circRNA isolation
circular-RNA
circRNA
cDNA
15 days ago by
dbagmerve
• 0
0
votes
2
replies
251
views
Picking parameters for QC of long-read data?
long-read
nanopore
qc
qualiy-control
23 days ago by
Gio
• 0
0
votes
2
replies
298
views
Deseq2 colData for single condition
RNA-seq
14 days ago by
Petesview
• 0
0
votes
2
replies
224
views
I am interested in creating bar graphs from the outcomes of my BLAST analysis
Blastn
updated 23 days ago by
Ram
40k • written 24 days ago by
hashim.rana11
▴ 20
0
votes
2
replies
556
views
Network analysis for two Factors
chip-seq
network-analysis
updated 28 days ago by
Ram
40k • written 7 months ago by
Ankit
▴ 390
0
votes
2
replies
248
views
How to run TRUST4 for BCR/TCR detection using 10X data?
immunology
trust4
illumina
10x
17 days ago by
O.rka
▴ 680
1
vote
2
replies
156
views
Is it normal if regress out the cell cycle effects but the DEGs are quite the similar (no big changes)
regress_out
Cell_cycle
Seurat
5 days ago by
alwayshope
▴ 30
1
vote
2
replies
292
views
functional analysis prediction
functionalanalysis
metabarcoding
16S
12 days ago by
safeassli
• 0
0
votes
2
replies
342
views
What is happening in the Zuker-Algorithm
R
folding
RNA
updated 28 days ago by
4galaxy77
2.8k • written 28 days ago by
Serij´s
• 0
0
votes
2
replies
268
views
Extract reference and alternate SNPs for different samples
vcftools
bcftools
SNPs
updated 22 days ago by
GenoMax
134k • written 22 days ago by
gubrins
▴ 270
0
votes
1
reply
187
views
Replace ambiguous characters in fasta MSA
maximum-likelihood
DNA
updated 23 days ago by
Joe
21k • written 23 days ago by
Alexandre
• 0
0
votes
1
reply
183
views
How to generate a consensus sequence from BAM file with bcftools?
bam
bcftools
consensus
updated 17 days ago by
GenoMax
134k • written 17 days ago by
marongiu.luigi
▴ 690
1
vote
1
reply
108
views
Imputation server failing to see samples in VCF files
imputation
VCF
updated 19 hours ago by
Ram
40k • written 22 hours ago by
Ben
• 0
0
votes
1
reply
213
views
Counting Isoforms from Sam File
Samtools
updated 21 days ago by
Ram
40k • written 23 days ago by
serodyc
▴ 20
0
votes
1
reply
211
views
Esearch, Epost, and Efetch for Large Datasets in Biopython
eutils
biopython
entrez
updated 8 days ago by
Ram
40k • written 9 days ago by
Salem
• 0
0
votes
1
reply
177
views
vg rna pantranscriptome
rna
vg
updated 10 days ago by
Jordan M Eizenga
▴ 360 • written 11 days ago by
z
• 0
0
votes
1
reply
1.7k
views
error when running local chlorop1.1
chlorop
updated 4 days ago by
Ram
40k • written 7.3 years ago by
gerrychang1985
▴ 40
0
votes
1
reply
188
views
IPYRAD - Step 3
IPYRAD
updated 24 days ago by
Pierre Lindenbaum
157k • written 24 days ago by
Mariana
• 0
311 results • Page
3 of 7
Recent Votes
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
Comment: ncbi error report log for validate fastq issue
A: Bowtie2 MAPQ difference using local vs end-to-end alignment
C: Bowtie2 MAPQ difference using local vs end-to-end alignment
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77k
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Recent Replies
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 …
Comment: Weirdness in annotation (missing allele frequencies)
by
Can Abdullah
• 0
Thank you so much, I decided to move forward as you suggested. Initially, I thought using the most up-to-date databases and positions would…
Comment: Getting the overlap between two GTF files
by
GenoMax
134k
Something in `AGAT` should work: https://agat.readthedocs.io/en/latest/?badge=latest
Answer: Automate the Splitting of a VCF File by Sample (bcftools)
by
Pierre Lindenbaum
157k
> My problem has been with trying to loop the process. ok here is a **nextflow** based solution,(NOT tested) workflow { …
Comment: Assessing Rockhopper's output
by
langziv
▴ 50
I see. I tried using the GUI Rockhopper for RNA-seq analysis of a K. pneumoniae strain, but the program didn't find the strain's assembly…
Answer: Getting the overlap between two GTF files
by
Pierre Lindenbaum
157k
bedtools intersect \ -a <(awk '/^[^#]/ {printf("%s\t%d\t%s\t%s\n",$1,int($4)-1,$5,$0);}' file1.gtf | sort -t $'\t' -k1,1 -k2…
Comment: Assessing Rockhopper's output
by
shelkmike
▴ 980
I used Rockhopper only for bacterial genomes assembled into circular contigs or circular scaffolds.
Comment: Unable to install HorvathMammalMethylChip40manifest packages
by
ATpoint
77k
There is no package of that name in CRAN or Bioconductor. Where do you have it from, so which tutorial you follow?
Comment: Subclustering of intergated cells from scRNA-seq data
by
fifty_fifty
▴ 60
thank you. This is exactly what I was looking for
Answer: Search RCSB with a list of protein names?
by
Mensur Dlakic
★ 25k
This is not the most elegant solution, but it should work with previous suggestions. In this remote directory: http://ftp.wwpdb.org/p…
Answer: Automate the Splitting of a VCF File by Sample (bcftools)
by
Ram
40k
The manual says you can split samples out at once using the `+split` plugin. So, `bcftools +split -Oz -o <PATH> file.vcf.gz` should do the …
Comment: differences between trajectories in conditions with Monocle3 or other tools
by
Amitm
★ 2.2k
Phate (or Monocle) doesn't do UMAP. If you have done UMAP already (using seurat) then you could use the cell barcode to UMAP cluster label …
Comment: Error: cannot open file 2 for reading From Cufflinks Version 2.2.1 When Attempti
by
Y
• 0
I figured out how to make it work. The bams have to be comma separated not just by space: cd "${input_directory_with_associated_bam_fi…
Comment: Search RCSB with a list of protein names?
by
Joseph
• 0
Hey, this is so close to what I'm looking for - I clarified in my edit. This is a great way to batch download lots of PDBs in RCSB by their…
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