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310 results • Page
3 of 7
Sort: Rank
Rank
Views
Votes
Replies
0
votes
0
replies
145
views
cosine simialrity of mutation signature analysis
similarity
Mutational
analysis
signature
cosine
12 days ago by
probioquestioner
• 0
0
votes
1
reply
225
views
Significance testing of top vs. random SNPs
SNPs
significance
variance
statistical
updated 8 days ago by
dthorbur
▴ 550 • written 12 days ago by
am29
▴ 30
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 9 days ago by
yhdist
▴ 70 • written 12 days ago by
Cookin
▴ 10
0
votes
0
replies
153
views
Why we are using filtering >0 for up and <0 for down after TopTags() to extract de genes ids?
EdgeR
logfc
DEG
12 days ago by
Ann
▴ 10
0
votes
1
reply
181
views
PyMOL: how to list all selection names?
pymol
updated 11 days ago by
Wayne
★ 1.8k • written 12 days ago by
Ondina
▴ 90
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
0
replies
148
views
Homozygous reference genotype for a GIAB genome
GIAB
IDs
reference
rs
Homozygous
12 days ago by
New2R
▴ 60
0
votes
0
replies
150
views
PRSice - Phenotype File Not Read Correctly
PRSice2
13 days ago by
V
• 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
1
vote
5
replies
519
views
Idat raw data conversion
idat
updated 12 days ago by
Giulio Genovese
▴ 330 • written 14 days ago by
Zi
• 0
1
vote
3
replies
361
views
What is "intersectional genetic strategy"? How does it work? What can it do?
cell-subtypes
13 days ago by
Ethan Lee
• 0
0
votes
0
replies
184
views
What metrics to use to calculate variant library evenness or uniformity or bias
library-bias
variant
updated 13 days ago by
Ram
40k • written 14 days ago by
eli_bayat
▴ 90
0
votes
0
replies
210
views
Tools to turn perfect phylogenetic matrix into a tree
parsimony
Phylogeny
tree
14 days ago by
Ritu_K
▴ 10
2
votes
4
replies
448
views
Help with celltype annotation
seurat
single-cell
13 days ago by
Chris
▴ 200
0
votes
1
reply
1.0k
views
Downstream analysis on multi-sample or single-sample VCF files?
next-gen
VCF
updated 14 days ago by
Ram
40k • written 2.8 years ago by
NGSCanBioinf
▴ 10
0
votes
1
reply
659
views
How to get enrichment of ERVs in differentially expressed peaks from ATAC-seq data?
ChIP-Seq
ERVs
ATAC-seq
updated 14 days ago by
pb11
▴ 10 • written 2.8 years ago by
fdemiguelsdp
• 0
3
votes
4
replies
374
views
Weighted analysis
RNA-seq
11 days ago by
Peter
• 0
1
vote
2
replies
279
views
Multiple testing adjustment for stepwise model selection
statistics
12 days ago by
mel22
▴ 100
0
votes
2
replies
298
views
Deseq2 colData for single condition
RNA-seq
14 days ago by
Petesview
• 0
0
votes
0
replies
177
views
PopGenome: there are missing regions when calculating Tajima's D per gene
PopGenome
12 days ago by
Bing
• 0
1
vote
2
replies
292
views
functional analysis prediction
functionalanalysis
metabarcoding
16S
12 days ago by
safeassli
• 0
0
votes
1
reply
232
views
Asymmetric/biased log2FC values for low-expressed genes in DESeq2
DESeq2
DEG
fold-change
updated 14 days ago by
Ram
40k • written 15 days ago by
chenzy
• 0
0
votes
9
replies
1.0k
views
Chipseq analysis on repeat genes
galaxy
repeatmasker
ChIP-seq
repeat-elements
ATAC-seq
updated 3 days ago by
rfran010
▴ 830 • written 15 days ago by
pb11
▴ 10
0
votes
5
replies
476
views
Convert gene id's to gene symbol preserving gene id's in deseq2
ensembl
r
DE
deseq2
updated 13 days ago by
Ram
40k • written 15 days ago by
dylannicoembros
• 0
1
vote
1
reply
250
views
Bioconductor Package Installation
bioconductor
updated 15 days ago by
Ram
40k • written 15 days ago by
oduduabasi.isaiah
• 0
0
votes
0
replies
206
views
External validation in bioinformatics analyses
External
validation
15 days ago by
Saeedeh Salehi
▴ 10
2
votes
4
replies
385
views
join the control replicates
RNA-seq
updated 15 days ago by
seidel
11k • written 15 days ago by
Jean Pierre
• 0
4
votes
5
replies
507
views
Pre-processing for single cell RNAseq: Hard thresholds, data (cluster)-driven or both?
scRNA-seq
12 days ago by
psm
▴ 100
0
votes
3
replies
324
views
RdRp scan - identifying/detecting viruses- metagenomic workflow- need help
RdRp
virus-detection
metagenomic
updated 11 days ago by
Ram
40k • written 15 days ago by
eric--carron
• 0
1
vote
1
reply
232
views
Is it possible to find the target bed file for TSO500 panel?
bed
illumina
target
updated 15 days ago by
GenoMax
134k • written 15 days ago by
Danchurova
• 0
0
votes
2
replies
276
views
circRNA isolation
circular-RNA
circRNA
cDNA
15 days ago by
dbagmerve
• 0
2
votes
2
replies
276
views
Pangenome using Orthofinder
OrthoFinder
Pangenome
bacteria
12 days ago by
kirankumareripogu
▴ 10
5
votes
3
replies
289
views
Visualisation of accessible regions in single cell atacseq data
visualization
scATAC-seq
single-cell
updated 15 days ago by
Ram
40k • written 16 days ago by
sarahmanderni
▴ 90
1
vote
2
replies
279
views
Dotplot error: subscript out of bound
R
scRNA-seq
seurat
6 days ago by
Xuhao
• 0
0
votes
0
replies
126
views
assembly: purge_dups removes too much sequence
purge_dups
assembly
nanopore
repeats
plants
16 days ago by
colindaven
5.5k
0
votes
7
replies
940
views
FACS (Fluorescence-activated cell sorting NOT cyTOF),Automating the removal of dead and duplicated cells
FACS
updated 3 days ago by
rfran010
▴ 830 • written 16 days ago by
ccbb7aab4
▴ 20
0
votes
0
replies
122
views
Paired vs Unpaired t-test: Compositional analysis in the Human snRNA-seq data
snRNA-seq
scRNA-seq
analysis
statistic
compositional
16 days ago by
joonhong kwon
▴ 50
0
votes
0
replies
125
views
how simply mutation annotation in R?
annotation
RNA-seq
Bioconductor
16 days ago by
octpus616
▴ 90
0
votes
2
replies
235
views
NCBI nt seqid2taxid.map
ncbi
kraken2
kraken
database
16 days ago by
Gio
• 0
0
votes
3
replies
259
views
CNV using GISTIC
CNV
GISTIC
updated 16 days ago by
Ram
40k • written 16 days ago by
ananta.kapoor
• 0
0
votes
0
replies
138
views
rDNA copy number variation (CNV) based on hg38
hg38
CNVkit
rDNA
CNV
genomics
16 days ago by
rbioinfo
▴ 10
0
votes
4
replies
308
views
Split reads along the genome in my samples
DNA
sequencing
17 days ago by
paulaotero.sanchez
• 0
0
votes
0
replies
135
views
Issue in creating Gene Regulatory Network links using CellOracle
Python
CellOracle
GRN
14 days ago by
Debashish
• 0
0
votes
0
replies
135
views
Cluster files from 2018-2020 archive of PDB
database
PDB
archive
Structural
17 days ago by
yhdist
▴ 70
0
votes
4
replies
286
views
Analyzing time-patterns in RNA Seq data only having results_apeglm
R
sequencing
17 days ago by
Paul
• 0
0
votes
0
replies
133
views
qtlseq oserror 38
qtlseq
15 days ago by
지헌
• 0
0
votes
1
reply
194
views
quantifying splicing transcripts for nanopore RNAseq
RNAseq
splicing
nanopore
updated 17 days ago by
GenoMax
134k • written 17 days ago by
jshen
• 0
0
votes
3
replies
333
views
Pearson correlation with different row numbers across two datasets?
perasoncorrelation
pearson
error
updated 17 days ago by
Kevin Blighe
86k • written 17 days ago by
siefeldin
▴ 30
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
0
votes
0
replies
112
views
OBITools - Problem with obiclean
python
OBITools
metabarcoding
obiclean
17 days ago by
Elise
• 0
310 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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3.8k
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• 0
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ATpoint
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Recent Replies
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…
Comment: Search RCSB with a list of protein names?
by
Joseph
• 0
This is a really neat package, but I don't think it does exactly what I want, so I've clarified my question. This seems like it grabs a PD…
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