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1,000 results • Page
4 of 20
Sort: Rank
Rank
Views
Votes
Replies
0
votes
0
replies
117
views
LEfSe
LEfSe
14 days ago by
benkosta
• 0
0
votes
0
replies
96
views
How should I handle read counts derived from SGSeq when I want to build DEXSeqDataSet object
DEXSeq
DEXSeqDataSet
SGSeq
14 days ago by
Sara
▴ 30
0
votes
2
replies
175
views
Longitudinal analysis of subpopulations: which approach is better?
differential-expression
DEG
model
14 days ago by
Lluís R.
★ 1.2k
0
votes
0
replies
110
views
Comparing peptide sequences with MS/MS peptide data using MaxQuant
Transcriptomics
Mass-spectrometry
Proteins
updated 4 hours ago by
Ram
43k • written 14 days ago by
atharvakarkare14
▴ 30
0
votes
2
replies
221
views
What should I consider as FASTA for dataset?
PDB
FASTA
14 days ago by
Nafi
• 0
0
votes
0
replies
601
views
Differential accessibility using DiffBinf
diffbind
14 days ago by
Shloka
• 0
0
votes
0
replies
105
views
vg call vs vg surject
vg
variation
graphs
updated 14 days ago by
GenoMax
142k • written 14 days ago by
aliraza3119
• 0
0
votes
1
reply
227
views
Finding batch and outlayers
Pca
updated 14 days ago by
christopher medway
▴ 460 • written 15 days ago by
Tigran
• 0
2
votes
2
replies
221
views
PDB related issue
rcsb
pdb
updated 15 days ago by
noodle
▴ 580 • written 15 days ago by
Nafi
• 0
0
votes
9
replies
2.6k
views
6 follow
Cannot process all the reads in a fast5 file?
metagenome
base-calling
fastq
nanopore
updated 14 days ago by
Ram
43k • written 8 months ago by
Gio
• 0
1
vote
2
replies
258
views
Downloading full alignments from Pfam
pfam
8 days ago by
bef1
• 0
0
votes
0
replies
135
views
adjusting for confounders in LMER in R
confounders
LMER
R
updated 14 days ago by
dariober
14k • written 15 days ago by
rene.j.erhardt
▴ 20
1
vote
3
replies
355
views
How to assign cell types after integration in scRNA
scRNA-seq
updated 15 days ago by
ATpoint
82k • written 16 days ago by
Francesco
▴ 10
0
votes
0
replies
151
views
STAR total splices (in Log.final) vs collapsed splice junctions (in SJ.out.tab)
STAR
16 days ago by
tnminh89
▴ 10
0
votes
0
replies
155
views
Filter low express genes in microarray data
microarray
16 days ago by
Chris
▴ 280
0
votes
0
replies
582
views
Correlation between cell type prediction scores and individual gene expression in spatial transcriptomic datasets
single-cell
Spatial-Transcriptomics
17 days ago by
biocellbio
• 0
0
votes
0
replies
217
views
Phasing VCF Files and Analyzing Reads with Multiple Variants
haplotypes
vcf
phasing
17 days ago by
HarperReed
• 0
1
vote
0
replies
169
views
Simulation of label-free bottom-up proteomics expression dataset
label-free
bottom-up
lc-ms
proteomics
17 days ago by
KABILAN
▴ 70
0
votes
0
replies
188
views
Running Phylogenetic Analysis With NCBI Genome
population-genetics
phylogenetic
updated 17 days ago by
Ram
43k • written 17 days ago by
SineWave
• 0
0
votes
0
replies
188
views
RNA-seq: full length gene
RNA-seq
updated 17 days ago by
Ram
43k • written 17 days ago by
Nargis
• 0
0
votes
0
replies
169
views
Haplotype Phased Assembly Contigs to Chromosome Annotations
Assembly
phased
Haplotype
Annotation
17 days ago by
turcoa1
• 0
0
votes
0
replies
180
views
Designing single-stable RNA molecules
structure
RNA
18 days ago by
Edna
• 0
0
votes
0
replies
191
views
How to visualize/predict the final transcript from Delly output?
WGS
DELLY
18 days ago by
simplitia
▴ 130
1
vote
1
reply
260
views
Normalize scRNAseq data to housekeeping genes to compare several datasets
RNA-sequencing
housekeeping
Single-cell
normalization
updated 18 days ago by
ATpoint
82k • written 18 days ago by
AaronJaime
• 0
0
votes
0
replies
174
views
How to calculate correlation coefficient for chipseq?
chipseq
bigwigsummary
correlation
18 days ago by
Emily
▴ 20
1
vote
0
replies
188
views
How to calculate reliable Ka/Ks or dN/dS ratio for genes of interest from VCF file
dnds
kaks
VCF
18 days ago by
rohitsatyam102
▴ 860
0
votes
0
replies
171
views
how to read graph_test output of monocle 3
monocle3
18 days ago by
synat.keam
▴ 100
0
votes
1
reply
529
views
GAPIT p-value significance threshold
GAPIT
p-value
GWAS
updated 18 days ago by
ginellegrenier
• 0 • written 5 months ago by
Clayton
• 0
0
votes
0
replies
168
views
Why not use iBAQ for calculating differential abundance of proteins?
protein
maxquant
18 days ago by
Aspire
▴ 330
0
votes
4
replies
398
views
Highest variable features in single cell data
single-cell
6 days ago by
carolofharvest
▴ 40
1
vote
3
replies
436
views
PCA plot
DESeq2
PCAplot
updated 15 days ago by
LauferVA
4.2k • written 18 days ago by
Aaliya
▴ 10
0
votes
0
replies
165
views
Can you give me an example of a small globular protein (PDB) that has disordered alpha-carbons?
protein
pdb
alpha-carbon
19 days ago by
4fzcgueyp5
• 0
0
votes
2
replies
306
views
Annovar using R package
Annovar
gnomAD
R
18 days ago by
DKA
▴ 40
0
votes
5
replies
428
views
Is it possible to get a list of representative genomes from a past RefSeq release?
representative
ncbi
asembly
refseq
updated 18 days ago by
GenoMax
142k • written 19 days ago by
Bertalan_Takacs
▴ 90
0
votes
0
replies
163
views
One error problem occurred caused by data type during using GDCprepare to handle BRCA data
TCGA
GDCprepare
updated 19 days ago by
Ram
43k • written 19 days ago by
glaciya2018
• 0
0
votes
0
replies
324
views
roary not working with pgap output gff files with fasta sequence but works with prokka's gff outputs
pangenome
PGAP
NCBI
roary
Prokka
19 days ago by
pramach1
▴ 40
0
votes
1
reply
199
views
GEMMA GWAS how to specify factor or numerical for covariates
covariate
GEMMA
GWAS
updated 19 days ago by
Sofia
• 0 • written 19 days ago by
mawigoj318
• 0
0
votes
0
replies
163
views
Sequence BLAST in plus/minus and plus/plus
blast
CRISPR
strand
sequencing
19 days ago by
salias
• 0
0
votes
5
replies
443
views
different FeatureCounts output for the same data
fpkm
Counts
Rsubread
rna-seq
updated 16 days ago by
Istvan Albert
100k • written 19 days ago by
sehriban.buyukkilic
▴ 10
0
votes
0
replies
137
views
Alternative splicing analysis using SUPPA tool - how to normalise counts?
rna-seq
single-cell
suppa
alternative-splicing
updated 19 days ago by
Ram
43k • written 19 days ago by
newuser2024
• 0
1
vote
2
replies
274
views
alignment result
RNA-seq
samtools
hisat2
18 days ago by
ahmad.sajad4541
• 0
0
votes
0
replies
135
views
AttributeError: module 'scvelo' has no attribute 'pp
loomfile
scvelo
scipy
annData
numpy
20 days ago by
Kash
▴ 110
0
votes
1
reply
186
views
How to solve this RoseTTAFold colaboratory error?
modeling
Google
Colaboratory
RoseTTAFold
protein
updated 19 days ago by
Mensur Dlakic
★ 27k • written 20 days ago by
benguyarenbeyaz98
• 0
2
votes
2
replies
329
views
How to calculate identity percentage between proteins contained in a FASTA file?
protein
FASTA
alignment
updated 19 days ago by
Ram
43k • written 20 days ago by
v.berriosfarias
▴ 140
2
votes
9
replies
928
views
TCGA2STAT Error: Firehose connection
FIREHOSE
TCGA
updated 20 days ago by
LauferVA
4.2k • written 7 months ago by
Gnana
• 0
0
votes
11
replies
690
views
How do I use the STARSolo aligner with MGI DNBelab C series HT scRNAseq libraries?
STARSolo
scRNA-seq
STAR
snRNA-seq
MGI
18 days ago by
atowns21
• 0
0
votes
1
reply
207
views
Find subcluster under a cluster, find differential genes in one cluster between 2 samples??
clustering
subclustering
scRNAseq
updated 20 days ago by
bk11
★ 2.4k • written 20 days ago by
alphaflylizard
• 0
0
votes
0
replies
116
views
The concept of co-occurrence network structure
co-occurence
microbiome
network
20 days ago by
ohtang7
▴ 40
0
votes
1
reply
197
views
Plot DNA methylation level of DMR on the basis of certain genes
rrbs
methylkit
updated 20 days ago by
GenoMax
142k • written 20 days ago by
Srinka
▴ 20
0
votes
5
replies
412
views
Should I remove unlocalized scaffols in reference genome before alignment?
qualimap
alignment
minimap2
GRCh38
assembly
19 days ago by
njornet
▴ 20
1,000 results • Page
4 of 20
Recent Votes
Comment: Kraken2 database
Comment: How does gene length effect the number of reads mapped
Comment: How does gene length effect the number of reads mapped
Comment: How does gene length effect the number of reads mapped
Comment: How does gene length effect the number of reads mapped
A: Filtering of VCF, INFO DP or FORMAT DP
What is the difference between GRCh37 and hs37? And hg19?
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Comment: What does the 'E%' represent in BUSCO results?
by
GenoMax
142k
According to ChatGPT: In BUSCO, the "E" category represents "End" or "Endof" gene fragments. These are orthologous groups for which the ge…
Comment: Help with IGV abbreviation
by
GeneC
• 0
Thank you for the link and details
Comment: Help with IGV abbreviation
by
GeneC
• 0
Thank you very much for helping with the details.
Comment: How does gene length effect the number of reads mapped
by
Chen
• 0
thank you :)
Answer: Filtering based on alternate allelic balance
by
Arton
• 0
I found the answer when using bcftools. Is there is a way to do this with FilterVcf? bcftools filter --include '(FMT/AD[0:1])/(FMT/A…
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by
GenoMax
142k
Those are SAM format fields. Check section 1.4 here: https://samtools.github.io/hts-specs/SAMv1.pdf > 1:2114:12111:13792 That is part of …
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▴ 130
Hi, here is a breakdown of each part that you asked about: **flag 99**: This indicates various properties of the read alignment. In this c…
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I don't see any databases with just pathogenic bacteria genomes from just a quick search, I would imagine that using the Standard-16 databa…
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Should be possible: https://www.biostars.org/p/430366/ Are you using an older version of `diamond`? Latest versions of `diamond` can use N…
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Hi, Below SNPEff database building error I am getting. "FATAL ERROR: Most Exons do not have sequences!" The headers are correct and sam…
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the last line of SeqIO.write(record.....'fasta') in a for loop will input the the last record into new fasta file and it will only contain …
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142k
You could use `sarek` (nf-core's exome pipeline) if you don't want to customize or reinvent : https://nf-co.re/sarek/3.4.2
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Please use the formatting bar (especially the `code` option) to present your post better. You can use backticks for inline code (\`text\` b…
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Two last seats have just become available. Apply now, if you want them.
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