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184 results • Page
2 of 4
Sort: replies
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Views
Votes
Replies
2
votes
5
replies
1.8k
views
How to make alpha diversity boxplot?
alpha_diversity
taxa
ASV
box_plot
shannon
updated 5 days ago by
yeah
• 0 • written 10 months ago by
Amr
▴ 140
2
votes
5
replies
375
views
ATAC-seq troubleshoot - Just Noise
ATAC-seq
updated 4 days ago by
ATpoint
77k • written 8 days ago by
vk
▴ 40
0
votes
5
replies
459
views
genome data downloads for various strains
gisaid
hass-marr
updated 4 days ago by
Ram
40k • written 8 days ago by
iftikharmaryam123
• 0
2
votes
5
replies
353
views
How to check RNAseq support for annotated genes?
gene
RNA-seq
annotation
updated 3 days ago by
Michael
53k • written 8 days ago by
BioinfoBee
• 0
1
vote
5
replies
219
views
bcftools error merging two VCFs: REF prefixes differ
bcftools
VCF
3 days ago by
Shane
• 0
4
votes
5
replies
1.9k
views
ChIP-seq heatmap input bed file
bed
chip-seq
deeptools
heatmap
updated 2 days ago by
Miao Zhang
• 0 • written 23 months ago by
buffealo
▴ 90
4
votes
5
replies
352
views
identify DEGs across all conditions and per specific conditions
R
DEseq2
2 days ago by
camillab.
▴ 140
1
vote
5
replies
490
views
Number of accessible regions included by DESeq2 to generate the PCA plot with the nf-core ATACseq pipeline ?
nf-core
atac-seq
PCA
DESeq2
updated 1 day ago by
Michael Love
★ 2.5k • written 2 days ago by
Alexandre Eeckhoutte
• 0
1
vote
5
replies
276
views
CollectRnaSeqMetrics (Picard) output to convert FeatureCounts into TPM
R
Picard
CollectRnaSeqMetrics
updated 1 day ago by
Ram
40k • written 2 days ago by
camillab.
▴ 140
2
votes
5
replies
276
views
Mapping SNP rsIds/ positions to genes coding for proteins
SNP
rsid
2 days ago by
Harsh
• 0
1
vote
5
replies
373
views
Complex multifactorial DE analysis with limma/edgeR based on rnaseq data
R
edgeR
limma
RNA-seq
updated 1 day ago by
LChart
3.4k • written 2 days ago by
svlachavas
▴ 780
1
vote
5
replies
1.3k
views
Unmapped Reads in Kallisto
Kallisto
RNA-Seq
alignment
bustools
updated 1 day ago by
dsull
★ 4.8k • written 3.6 years ago by
msutennis23
• 0
1
vote
5
replies
191
views
Search RCSB with a list of protein names?
RCSB
protein
updated 13 hours ago by
Mensur Dlakic
★ 25k • written 17 hours ago by
Joseph
• 0
8
votes
5
replies
322
views
Frustrated with DEA results
microarray
differential-expression
updated 1 day ago by
dsull
★ 4.8k • written 2 days ago by
jopadrosa
• 0
1
vote
5
replies
286
views
Enrichment of mitochondrial and ribosomal pathways - an artifact?
Pathway
Mitochondria
Ribosome
scRNA-seq
Enrichment
3 days ago by
omer.shomrat
• 0
0
votes
5
replies
740
views
Can vg take MUMmer output as input?
vg
updated 3 days ago by
Ram
40k • written 2.8 years ago by
ac2278
▴ 20
2
votes
5
replies
395
views
6 follow
How to convert data in r?
R
offtopic
updated 21 hours ago by
Ram
40k • written 1 day ago by
star
▴ 350
2
votes
4
replies
192
views
Subclustering of intergated cells from scRNA-seq data
scRNA-seq
Seurat
10 hours ago by
fifty_fifty
▴ 60
2
votes
4
replies
269
views
Integrated Seurat object change name of the two conditions
R
integrated
Seurat
4 days ago by
camillab.
▴ 140
0
votes
4
replies
248
views
Assessing Rockhopper's output
transcriptome
Rockhopper
RNA-seq
de-novo-assembly
2 hours ago by
langziv
▴ 50
0
votes
4
replies
344
views
Hugo_Symbol to Entrez ID
hugo
bioinformatics
entrez
ids
symbols
updated 5 days ago by
Kevin Blighe
86k • written 7 days ago by
shakyaram079
• 0
1
vote
4
replies
273
views
geom_signif() uses t-test to compare between more than 3 groups... Isn't this wrong?
ggplot2
ANOVA
t-test
4 days ago by
RM123
▴ 10
2
votes
4
replies
197
views
Snakemake alignment script
snakemake
alignment
21 hours ago by
Begonia_pavonina
▴ 110
3
votes
4
replies
297
views
Dotplot : how to self-define the range of legend
analysis
seq
RNA
updated 5 days ago by
GenoMax
134k • written 6 days ago by
Xuhao
• 0
1
vote
4
replies
251
views
How to perform hypothesis testing on contingency tables and compare with the null distribution?
hypothesis-testing
contingency-table
18 hours ago by
RK
• 0
3
votes
4
replies
205
views
How to get the gft file to run velocyto for velocity analysis?
velocity
16 hours ago by
Chris
▴ 200
0
votes
4
replies
731
views
Is there a way to get a list of all homogygous sites for each sample with plink (regardless if they are in a run)
plink
updated 5 days ago by
chrchang523
10k • written 20 days ago by
curious
▴ 730
2
votes
4
replies
275
views
Which function is best for pathway analysis?
pathway
2 days ago by
Chris
▴ 200
0
votes
4
replies
209
views
BED files
BED
NGS
Chromosomes
updated 3 days ago by
Ram
40k • written 4 days ago by
adarsh_pp
▴ 30
3
votes
4
replies
278
views
Network analysis with cytoscape
RNA-seq
cytoscape
1 day ago by
Chris
▴ 200
0
votes
4
replies
240
views
Comparing multiple columns from two files using AWK
awk
updated 3 days ago by
Ram
40k • written 3 days ago by
emiliomastriani
▴ 30
1
vote
4
replies
221
views
How to filter vcf file by MAF using bcftools?
bcftools
vcf
updated 2 days ago by
Ram
40k • written 2 days ago by
_quantum_girl_
▴ 10
1
vote
4
replies
247
views
Running Rockhopper from a command-line
rockhopper
java
3 days ago by
langziv
▴ 50
2
votes
4
replies
3.8k
views
Is there a way to use CNVkit without a reference from normal samples?
sequence
CNVkit
updated 1 day ago by
Matteo Schiavinato
★ 3.6k • written 5.5 years ago by
leandro.bispo.oliveira
• 0
0
votes
4
replies
228
views
Sequence quality drops in the 3' end of the left sequence in paired end. What could be the cause?
sequencing
updated 3 days ago by
GenoMax
134k • written 3 days ago by
eggrandio
▴ 40
0
votes
4
replies
261
views
Saving the output of LD pruning from SNPRelate package as a new GDS file
LD-pruning
SNPRelate
updated 3 days ago by
DBScan
▴ 200 • written 4 days ago by
Patrick
• 0
3
votes
4
replies
216
views
Unable to build applet in DNAnexus, .jar file not found
dnanexus
applet
updated 4 days ago by
LChart
3.4k • written 4 days ago by
_quantum_girl_
▴ 10
2
votes
4
replies
304
views
Using STAR aligner to build index of hg38
hg38
STAR
alignment
RNAseq
index
6 days ago by
Grace
• 0
1
vote
4
replies
260
views
How to sort cd-hit-est cluster file
sort
cd-hit-est
4 days ago by
Mo
▴ 40
2
votes
4
replies
352
views
Ties in reranked list
fgsea
GSEA
6 days ago by
Hamza
• 0
2
votes
4
replies
239
views
Automate the Splitting of a VCF File by Sample (bcftools)
bcftools
vcf
updated 2 hours ago by
Pierre Lindenbaum
157k • written 1 day ago by
RogueBiochemist
• 0
1
vote
3
replies
282
views
How to find out what adapters to remove after FastQC of RNAseq data?
Trimmomatic
FastQC
NGS
RNA-seq
5 days ago by
ella
• 0
0
votes
3
replies
720
views
to annotate BEDPE files
bedtools
annotate
updated 3 days ago by
Lhl
▴ 760 • written 2.6 years ago by
Bogdan
★ 1.4k
3
votes
3
replies
223
views
Have some issues in running prokka on WSL
prokka
updated 1 day ago by
Ram
40k • written 2 days ago by
Kirill
▴ 10
1
vote
3
replies
240
views
comparision of umap single cell
single-cell
1 day ago by
synat.keam
▴ 80
1
vote
3
replies
243
views
miRDeep2 - identifying miRNAs from deep sequencing data
microRNA
miRDeep2
updated 4 days ago by
Ram
40k • written 4 days ago by
Hasan
• 0
3
votes
3
replies
278
views
Chip-Seq and correlation of bam file
Chip-Seq
updated 1 day ago by
jared.andrews07
★ 15k • written 2 days ago by
qudrat.nii
• 0
0
votes
3
replies
203
views
What is the correct procedure to generate a consensus bacterial sequence?
consensus
samtools
illumina
fastq
1 day ago by
marongiu.luigi
▴ 690
3
votes
3
replies
226
views
Fetch Fastq files directly for SRA data
NCBI
FASTQ
SRA
updated 3 days ago by
GenoMax
134k • written 3 days ago by
Chintan
• 0
4
votes
3
replies
234
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
184 results • Page
2 of 4
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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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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