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484 results • Page
4 of 10
Sort: Views
Rank
Views
Votes
Replies
0
votes
2
replies
428
views
QC exclusion of A/T or G/C alleles to avoid strand issues
quality-control
SNV
QC
SNP
9 days ago by
_quantum_girl_
▴ 10
0
votes
0
replies
423
views
Correlation between cell type prediction scores and individual gene expression in spatial transcriptomic datasets
single-cell
Spatial-Transcriptomics
2 days ago by
biocellbio
• 0
1
vote
1
reply
421
views
Difference when using difference number of pathways score to compare between 3 groups
GSVA
Limma
updated 7 days ago by
Gordon Smyth
★ 7.0k • written 10 days ago by
Chris
▴ 260
0
votes
2
replies
418
views
miRNAs quantification using mirdeep2 tool
differential-expression
mirdeep2
miRNA
9 days ago by
Ashok
• 0
3
votes
5
replies
415
views
Very low RNA splicing rate for pulmonary AT2 cells
RNA-velocity
scVelo
scRNA-seq
splicing
updated 25 days ago by
GenoMax
141k • written 26 days ago by
e.r.zakiev
▴ 200
0
votes
0
replies
415
views
Pairwise alignment of two long chromosomes (~100Mbp) with lastz
lastz
alignment
updated 23 days ago by
Ram
43k • written 21 months ago by
vahe.galstyan
• 0
1
vote
1
reply
414
views
Long reads Annotation
long-reads
pacbio
updated 23 days ago by
Ram
43k • written 2.1 years ago by
Gerardo
• 0
2
votes
6
replies
412
views
create a gene count matrix csv file from seurat object
Seurat
sparseMatrix
20 days ago by
jkim
▴ 170
1
vote
1
reply
411
views
Load a full GFF3 into annotation track using arrow (Apollo)
arrow
python-apollo
Apollo
9 days ago by
renan.igor
• 0
0
votes
7
replies
408
views
DESeq: too low p-value for RNAseq
R
DESeq
p-value
RNA-seq
FDR
updated 23 days ago by
Papyrus
★ 2.9k • written 24 days ago by
doramora
▴ 10
2
votes
4
replies
404
views
Per Base Sequence Content - continuous raise of G%
fastqc
updated 18 days ago by
GenoMax
141k • written 19 days ago by
pl.terzian
• 0
0
votes
5
replies
404
views
Used featureCounts to generate a count matrix for sc RNA-seq and it has all 0s.
scRNA-seq
updated 18 days ago by
GenoMax
141k • written 19 days ago by
Shay
• 0
0
votes
1
reply
403
views
How to add rowLinks, rowTree in SummarizedExperiment manually.
phylogenetic-tree
microbiome
updated 10 days ago by
Ram
43k • written 19 months ago by
Muhammad
• 0
5
votes
6
replies
400
views
7 follow
Seeking Help with Unexpected MA Plot Output
MAplot
RNAseq
Rstudio
updated 26 days ago by
Istvan Albert
100k • written 27 days ago by
Pumla
• 0
0
votes
0
replies
399
views
BETA whether on the same scale when performing rank-based inverse normal transformation on the same type of phenotype data for two cohorts separately…
normal
inverse
transformation
17 days ago by
Isaac
• 0
1
vote
4
replies
398
views
what is the normal range of htseq-count output for homo sapiens RNA-Seq
Transcriptomics
htseq-count
RNA-Seq
NGS
hisat2
updated 15 days ago by
BioinfGuru
★ 1.7k • written 16 days ago by
Morteza
• 0
1
vote
3
replies
395
views
multiple sequence alignment
BLAST
multiple-sequence-alignment
clustal-omega
MSA
updated 20 days ago by
Ram
43k • written 23 days ago by
catherinemaria2728
• 0
0
votes
2
replies
381
views
error in coding potential calculator CPC2
cpc
CPC2
coding-potential
9 days ago by
Ashok
• 0
0
votes
0
replies
380
views
Realistic RNA-seq using Polyester + Differences between Hexamer bias and positional bias?
polyester
short-read
bias
updated 26 days ago by
Ram
43k • written 18 months ago by
shinyjj
▴ 50
0
votes
2
replies
377
views
How can I solve this error?
metal
10 days ago by
22211020193
• 0
0
votes
2
replies
375
views
I can't add VAF from population for all of my variants from VCF file
vaf
vcf
genomics
gnomad
allelicfrequency
28 days ago by
Samuel
▴ 20
0
votes
0
replies
375
views
The chromatin accessibility in regulatory regions of the rhodopsin gene RHO.
ATAC-Seq
updated 26 days ago by
Ram
43k • written 2.7 years ago by
madhubioinform
• 0
1
vote
4
replies
371
views
Molecular docking with Autodock
Docking
proteomics
updated 23 days ago by
Ram
43k • written 12 weeks ago by
shwetamgr1
▴ 10
1
vote
0
replies
368
views
Differential expression analysis on multiple integrated datasets
microarray
Z-score
limma
differential-gene-expression
meta-analysis
updated 19 days ago by
Ram
43k • written 2.4 years ago by
michael.s
▴ 10
4
votes
4
replies
367
views
Average expression of a sample in single-cell data
single-cell
rna-seq
26 days ago by
newuser2024
• 0
3
votes
4
replies
362
views
Single cell analysis with "meta".tsv.gz file
Single-cell
26 days ago by
Estevão
• 0
1
vote
3
replies
360
views
Ensembl gene id conversion
biomart
ensembl
updated 12 days ago by
ATpoint
82k • written 14 days ago by
naveedhasan2000
• 0
0
votes
0
replies
357
views
Looking for an explanation as to what the Peak Score is from HOMER, not finding any answers on Biostars yet
Homer
ATAC-seq
11 days ago by
Ronin
• 0
1
vote
3
replies
355
views
how to do the repeatability filtering of vcf files?
snp
vcf.
updated 27 days ago by
Pierre Lindenbaum
161k • written 28 days ago by
Max
• 0
1
vote
4
replies
348
views
How to get human-mouse conservation score from UCSC
conservation
mouse
IGV
human
score
23 days ago by
diqixiaoyaoer
▴ 10
1
vote
5
replies
345
views
samtools filtering
samtools
updated 17 days ago by
jkbonfield
★ 1.2k • written 25 days ago by
sansan_96
▴ 80
0
votes
3
replies
344
views
Resources regarding Proteomics (In-Silico)
molecular-simulation
docking
protein
proteomics
updated 26 days ago by
Ram
43k • written 5 weeks ago by
Saurabh
• 0
0
votes
4
replies
343
views
Compute bootstrap values on consensus tree
phylogeny
tree
raxml
13 days ago by
pablo
▴ 300
0
votes
4
replies
341
views
What is the samtools flag used in bamPEFragment?
deeptools
updated 17 days ago by
GenoMax
141k • written 19 days ago by
Soohyun
• 0
0
votes
5
replies
340
views
Incongruencies in GT assignment by Freebayes
depth
freebayes
heterozygous
genotype
23 days ago by
virginia.baraja
• 0
0
votes
0
replies
338
views
Looking to improve my understanding of Homer's mergePeaks function: unclear of how the merged file is created?
Homer
ATACseq
24 days ago by
Ronin
• 0
0
votes
5
replies
338
views
BUSCO analysis failed due to Duplicate of sequence in Input genome fasta. How to solve this problem ?
duplicate
BUSCO.
updated 24 days ago by
GenoMax
141k • written 24 days ago by
Sony
▴ 10
3
votes
3
replies
337
views
Volcano Plot Output Inquiry: Graphs Facing Down
rstudio
volcano-plot
29 days ago by
Pumla
• 0
1
vote
2
replies
335
views
BAM to CRAM and BAM recover with smaller size
BAM
samtools
CRAM
updated 25 days ago by
jkbonfield
★ 1.2k • written 6 weeks ago by
geocarvalho
▴ 360
0
votes
8
replies
335
views
Error in cnetplot enrichplot package
R
updated 6 days ago by
Ram
43k • written 6 days ago by
Farhad
• 0
0
votes
2
replies
331
views
Why are gene models from JGI non-sense when using AGAT to to extract proteins?
translation
models
gif
gene
cgi
27 days ago by
O.rka
▴ 710
0
votes
0
replies
330
views
How to convert dataframe properly to anndata?
single-cell
python
anndata
updated 24 days ago by
Ram
43k • written 6 months ago by
bioinfo
▴ 150
0
votes
5
replies
330
views
Is it possible to get a list of representative genomes from a past RefSeq release?
representative
ncbi
asembly
refseq
updated 3 days ago by
GenoMax
141k • written 4 days ago by
Bertalan_Takacs
▴ 90
0
votes
7
replies
329
views
Low mapping rate with Salmon
RNA-seq
Salmon
Quantification
updated 2 days ago by
GenoMax
141k • written 6 days ago by
Patadu94
• 0
0
votes
0
replies
328
views
GTEx long read data
short-read
long-read
gtex
updated 23 days ago by
Ram
43k • written 19 months ago by
shinyjj
▴ 50
0
votes
0
replies
327
views
How to import filtered_tf_bc_matrix and add it to my anndata object?
python
anndata
atac-seq
updated 24 days ago by
Ram
43k • written 6 months ago by
bioinfo
▴ 150
0
votes
0
replies
326
views
Finding the number of CpG sites in rainbow trout reference genome
reference-genome
CpG
updated 26 days ago by
Ram
43k • written 2.3 years ago by
marina.el-kamouh
• 0
0
votes
5
replies
326
views
different FeatureCounts output for the same data
fpkm
Counts
Rsubread
rna-seq
updated 1 day ago by
Istvan Albert
100k • written 4 days ago by
sehriban.buyukkilic
▴ 10
0
votes
4
replies
325
views
Questions about transfering wgs file to reference genome file
fasta
cram
genome
17 days ago by
me
• 0
0
votes
3
replies
325
views
10x GEX and ADT data analysis in Seurat
Seurat
scRNA-seq
ADT
Cite-seq
GEX
updated 15 days ago by
ATpoint
82k • written 17 days ago by
gdfsnkfns
• 0
484 results • Page
4 of 10
Recent Votes
Comment: NGS forensics: how to know if data is fabricated
A: Hard time trying to calculate Allele Frequency and DP from Platypus
Answer: NGS forensics: how to know if data is fabricated
Answer: NGS forensics: how to know if data is fabricated
Comment: NGS forensics: how to know if data is fabricated
Answer: NGS forensics: how to know if data is fabricated
Comment: NGS forensics: how to know if data is fabricated
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Answer: Differential Expression using Isoseq-supplemented reference transcriptome
by
Gordon Smyth
★ 7.0k
> What is the best method to test for differential abundance at the isoform level? Salmon returns TPM values instead of the counts which Li…
Answer: Finding batch and outlayers
by
Tigran
• 0
![enter image description here][1] [1]: /media/images/aa60b9ef-b08c-4093-9f0d-fb656a5c
Comment: NGS forensics: how to know if data is fabricated
by
benformatics
3.9k
Can you post an IGV screenshot of what this looks like?
Comment: NGS forensics: how to know if data is fabricated
by
benformatics
3.9k
Yeah some of the Illumina machines pre-trim adapters (not sure if this is still the standard). I've also definitely also seen quality-trimm…
Comment: PDB related issue
by
noodle
▴ 530
You can typically find much more useful info in the cif file, for example what you've found is called '_atom_site.pdbx_PDB_ins_code ' and d…
Comment: PDB related issue
by
Mensur Dlakic
★ 27k
The best way to find out is to read the original paper. My guess is that the residue has been crystallized in alternative conformations, wh…
Answer: NGS forensics: how to know if data is fabricated
by
Mensur Dlakic
★ 27k
I share the opinion by @philippbayer I have seen enough questionable things in life and in science to keep me permanently jaded, but there…
Comment: How many reads for WGS Sequencing?
by
Mensur Dlakic
★ 27k
I downloaded the data in two files from the link you provided. With this command: megahit -1 ERR072246_1.fastq.gz -2 ERR072246_2.fastq…
Comment: How many reads for WGS Sequencing?
by
Mensur Dlakic
★ 27k
If you have Linux the assembly should work on your system, but 8 GB is generally not enough for assembling larger genomes.
Comment: How many reads for WGS Sequencing?
by
Mensur Dlakic
★ 27k
I think you might be getting stuck on less relevant parts of my exercise. The most important point was that nothing is wrong with the data.…
Comment: What does it mean single base resolution in sequencing?
by
dsull
★ 5.9k
Great comprehensive explanation and overview of the technologies -- with regards to sequencing assays, the one thing I'd add is SNV identif…
Answer: What does it mean single base resolution in sequencing?
by
dsull
★ 5.9k
I think that term means slightly different things in different contexts. For example, it's useful to profile mRNA modifications (e.g. m6a) …
Comment: Cannot process all the reads in a fast5 file?
by
chujie
• 0
Hi, I met the same problem, have you found the solution?
Answer: What does it mean single base resolution in sequencing?
by
LauferVA
4.2k
Hi @fe3e6f65 , In a single sentence, the answer to your question can be summarized as, "*the resolution of a genomic technology refers to …
Comment: PCA plot
by
LauferVA
4.2k
Without more context, we cannot interpret this PCA plot. There are many possibilities. In addition, this question is basic enough that it w…
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