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328 results • Page
4 of 7
Sort: Votes
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Votes
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0
votes
0
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155
views
Why we are using filtering >0 for up and <0 for down after TopTags() to extract de genes ids?
EdgeR
logfc
DEG
16 days ago by
Ann
▴ 10
0
votes
1
reply
237
views
Asymmetric/biased log2FC values for low-expressed genes in DESeq2
DESeq2
DEG
fold-change
updated 18 days ago by
Ram
40k • written 18 days ago by
chenzy
• 0
0
votes
7
replies
792
views
Mugsy error -directory must be a directory
Mugsy
updated 12 days ago by
Ram
40k • written 2.8 years ago by
A_heath
▴ 140
0
votes
0
replies
153
views
PRSice - Phenotype File Not Read Correctly
PRSice2
16 days ago by
V
• 0
0
votes
1
reply
196
views
Issue with merging in plink and eigensoft.
Eigensoft
Eigenstrat
Plink
updated 5 days ago by
bk11
★ 1.4k • written 5 days ago by
Jd
• 0
0
votes
0
replies
126
views
How to find commutation using plink?
commutation
plink
28 days ago by
_quantum_girl_
▴ 10
0
votes
0
replies
137
views
Software for chimera detection of amplicon (e.g. 16S) nanopore reads
chimera
nanopore
amplicon
5 days ago by
rob_DNA
▴ 10
0
votes
3
replies
361
views
RSubread DESeq2
RNA-seq
subread
differential-expression
deseq2
updated 15 days ago by
Ram
40k • written 24 days ago by
Beyza
• 0
0
votes
2
replies
344
views
How to load a galaxy DESeq results table into R so I can continue my workflow there
r
RNA-seq
deseq2
21 days ago by
Nicolas
• 0
0
votes
0
replies
209
views
External validation in bioinformatics analyses
External
validation
19 days ago by
Saeedeh Salehi
▴ 10
0
votes
2
replies
284
views
circRNA isolation
circular-RNA
circRNA
cDNA
18 days ago by
dbagmerve
• 0
0
votes
0
replies
128
views
how simply mutation annotation in R?
annotation
RNA-seq
Bioconductor
19 days ago by
octpus616
▴ 90
0
votes
0
replies
110
views
RepeatMasker format in SQuIRE Fetch
SQuIRE
RepeatMasker
updated 28 days ago by
Ram
40k • written 28 days ago by
Javier
• 0
0
votes
1
reply
143
views
Calculating haplotype and nucleotide diversity with deep amplicon sequencing data
haplotype
diversity
Pegas
Arlequin
HTS_data
6 days ago by
deorugz
• 0
0
votes
0
replies
151
views
Can optimal cofactors for arcsinh transformation be calculated in parallel?
parallel
R
flowcytometry
flowCore
flowVS
5 days ago by
gmiller
• 0
0
votes
0
replies
187
views
What metrics to use to calculate variant library evenness or uniformity or bias
library-bias
variant
updated 17 days ago by
Ram
40k • written 17 days ago by
eli_bayat
▴ 90
0
votes
1
reply
227
views
How to extract gene lists following DEG analysis?
extract
gene
lists
updated 29 days ago by
seidel
11k • written 29 days ago by
hellokwmin
• 0
0
votes
1
reply
219
views
how to calculate TM-score to p-value?
tmscore
pdb
protein
structure
updated 8 days ago by
kvcsnandi
• 0 • written 23 days ago by
Xylanaser
▴ 80
0
votes
5
replies
489
views
Convert gene id's to gene symbol preserving gene id's in deseq2
ensembl
r
DE
deseq2
updated 17 days ago by
Ram
40k • written 19 days ago by
dylannicoembros
• 0
0
votes
3
replies
332
views
RdRp scan - identifying/detecting viruses- metagenomic workflow- need help
RdRp
virus-detection
metagenomic
updated 15 days ago by
Ram
40k • written 19 days ago by
eric--carron
• 0
0
votes
4
replies
297
views
Analyzing time-patterns in RNA Seq data only having results_apeglm
R
sequencing
20 days ago by
Paul
• 0
0
votes
3
replies
268
views
CNV using GISTIC
CNV
GISTIC
updated 20 days ago by
Ram
40k • written 20 days ago by
ananta.kapoor
• 0
0
votes
1
reply
187
views
Bowtie2 Error: reads file does not look like a FASTQ file
bowtie2
alignment
updated 27 days ago by
Ram
40k • written 27 days ago by
SO_Bio
• 0
0
votes
0
replies
165
views
Fastest way to find private SNPs for each sample
SNP
24 days ago by
Axzd
▴ 10
0
votes
1
reply
179
views
vg rna pantranscriptome
rna
vg
updated 14 days ago by
Jordan M Eizenga
▴ 360 • written 14 days ago by
z
• 0
0
votes
2
replies
231
views
I am interested in creating bar graphs from the outcomes of my BLAST analysis
Blastn
updated 27 days ago by
Ram
40k • written 27 days ago by
hashim.rana11
▴ 20
0
votes
0
replies
118
views
Spike-in normalization in ATAC-Seq with DiffBind
ATAC-Seq
spike-in
DiffBind
8 days ago by
frueher
• 0
0
votes
0
replies
126
views
Long-reads assembly using Miniasm in NanoGalaxy
assembly
Galaxy
metabarcoding
Nanopore
21 days ago by
Cedrick
• 0
0
votes
1
reply
154
views
Download an example of fully-imputed VCF files ?
VCF
impute
updated 7 days ago by
barslmn
★ 1.9k • written 8 days ago by
Ben
• 0
0
votes
0
replies
124
views
Paired vs Unpaired t-test: Compositional analysis in the Human snRNA-seq data
snRNA-seq
scRNA-seq
analysis
statistic
compositional
19 days ago by
joonhong kwon
▴ 50
0
votes
1
reply
382
views
Close genome comparison
Mauve
Mugsy
genome-comparison
GSAlign
updated 12 days ago by
Ram
40k • written 19 months ago by
A_heath
▴ 140
0
votes
1
reply
232
views
Any alternatives to DrugBank?
DrugBank
updated 24 days ago by
GenoMax
135k • written 24 days ago by
Clay
• 0
0
votes
5
replies
607
views
Bowtie2 with secondary alignment option produces multiple mapping with offset and varying alignment scores
bowtie2
score
alignment
multiple-alignment
29 days ago by
polag01
▴ 10
0
votes
0
replies
248
views
How can I identity Branch point sequence from Intron?
DNA-seq
splicing
RNA-seq
updated 1 day ago by
Ram
40k • written 20 months ago by
praasu
▴ 40
0
votes
0
replies
161
views
Coverage of domains
hmmer
protein
domains
24 days ago by
unknownunknown
• 0
0
votes
2
replies
285
views
Modify the code to take most abundant reads from a cluster and process it.
cd-hit-est
clustering
10 days ago by
Mo
▴ 40
0
votes
0
replies
28
views
Help on dendrimer building
dendrimer
gromacs
molecular-dynamics
3 hours ago by
v.berriosfarias
▴ 130
0
votes
0
replies
66
views
Algorithmic Solutions for Resolving Overlapping Sequences in Sanger Sequencing of PCR Segments
Sanger
pcr
updated 8 hours ago by
Ram
40k • written 18 hours ago by
Amior
• 0
0
votes
0
replies
107
views
How to remove chimera from 16S Sanger contigs
sanger-sequencing
chimera
uchime
updated 7 days ago by
Ram
40k • written 7 days ago by
eimanpharmacist
▴ 20
0
votes
1
reply
215
views
Merging the filename with tsv files for master file
genomics
updated 7 days ago by
barslmn
★ 1.9k • written 10 days ago by
smrutimayipanda
▴ 20
0
votes
1
reply
60
views
WGCNA plotEigengeneNetworks error (coercion to logical)
WGCNA
plotEigengeneNetworks
RNA-seq
RStudio
updated 3 hours ago by
Ram
40k • written 4 hours ago by
Victor
• 0
0
votes
1
reply
78
views
Differentially Expressed Genes between two conditions (scRNA, single GEO dataset with multiple samples and no cell annotations)
scRNA-seq
RNA-Seq
Seurat
updated 2 hours ago by
bk11
★ 1.4k • written 3 hours ago by
prietto
• 0
0
votes
1
reply
200
views
Identify parent of each read in a GAF
gaf
vgteam
vg
updated 13 days ago by
Jordan M Eizenga
▴ 360 • written 14 days ago by
cfourps
▴ 10
0
votes
1
reply
663
views
How to get enrichment of ERVs in differentially expressed peaks from ATAC-seq data?
ChIP-Seq
ERVs
ATAC-seq
updated 18 days ago by
pb11
▴ 10 • written 2.8 years ago by
fdemiguelsdp
• 0
0
votes
1
reply
180
views
Pheatmap x must be numeric
deseq2
r
pheatmap
updated 1 day ago by
Ram
40k • written 2 days ago by
Hamza
• 0
0
votes
1
reply
207
views
Is it okay to normalize data once more?
scRNA
normalization
updated 21 days ago by
biofalconch
★ 1.0k • written 21 days ago by
le93jk
• 0
0
votes
2
replies
385
views
log2fC from limma on methylation analysis
methylation
limma
minfi
fold-change
updated 18 days ago by
Ram
40k • written 11 months ago by
adeizadavid
▴ 10
0
votes
0
replies
314
views
Can plantiSMASH be used with a transcriptome instead of a genome?
plantiSMASH
updated 1 day ago by
Ram
40k • written 22 months ago by
kristina.mahan
▴ 160
0
votes
5
replies
474
views
genome data downloads for various strains
gisaid
hass-marr
updated 8 days ago by
Ram
40k • written 12 days ago by
iftikharmaryam123
• 0
0
votes
1
reply
910
views
Issue interpreting plasmidSPAdes output
plasmidSPAdes
updated 12 days ago by
Ram
40k • written 2.9 years ago by
A_heath
▴ 140
328 results • Page
4 of 7
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Answer: Script for getting summary statistic of any genome using GTF or GFF3 ?
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Answer: GSEA with GO and KEGG datasets
GSEA with GO and KEGG datasets
Answer: Exporting DEGs obtained from DESeq2
Answer: Exporting DEGs obtained from DESeq2
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Answer: The Biostar Handbook. A bioinformatics e-book for beginners.
by
Qboy
• 0
Great book! I love using it to help my mentees to learn bioinformatics better. It would be also fantastic to compile all other necessary Pr…
Comment: Rockhoppper - Suspiciously low percentage of perfectly aligned reads
by
langziv
▴ 50
Thanks. I'll try.
Comment: How to get sample names and genotype for SNP in multi-sample VCF file
by
avelarbio46
▴ 30
Hi! I'm trying to parallelize your code (to run on a bunch of files), but it is not working because of multiple processes spawning. Do you …
Comment: Rockhoppper - Suspiciously low percentage of perfectly aligned reads
by
GenoMax
135k
> so I don't think the genome size is available. Perhaps not for your specific strain but plenty of other Kpn genomes are available and th…
Comment: Kimura% of calcDivergenceFromAlign output
by
睿紘
• 0
For additional information, "Coverage for each repeat class and divergence (Kimura)" is also the result from calcDivergenceFromAlign.pl
Comment: Rockhoppper - Suspiciously low percentage of perfectly aligned reads
by
langziv
▴ 50
By the way, I run Rockhopper on the untrimmed files, and the full match percentage grew to 20%-30%, and there are 1552 transcripts in the u…
Comment: Rockhoppper - Suspiciously low percentage of perfectly aligned reads
by
langziv
▴ 50
Here are the total bases in 4 fastq files (after adapter removal): 1,027,852,411, 1,041,895,083, 1,121,786,520, 1,299,721,929. I just rem…
Comment: Understanding mother and father alleles in VCF file
by
c.
• 0
actually they didn't tell me which relatives were from mother side and which from father side, you are right. But how can you find related …
Comment: Rockhoppper - Suspiciously low percentage of perfectly aligned reads
by
GenoMax
135k
Correct. Data that went into the assembly.
Comment: Rockhoppper - Suspiciously low percentage of perfectly aligned reads
by
langziv
▴ 50
Total bases (number of reads * read length) should be calculated after removal of adapters, right?
Comment: Getting BLAST to give output whilst running
by
Ken
• 0
If I understand correctly, Blast can tell you how many results it has gotten but it can't tell you how many it is going to get, therefore i…
Comment: Understanding mother and father alleles in VCF file
by
Ram
40k
I don't understand your logic. You don't know what phasing is but are confident it is not required, and your proof is that relatives were d…
Comment: Understanding mother and father alleles in VCF file
by
c.
• 0
It's from Nebula genomics. It must be possible to deduce parental alleles, since I converted the VCF file into a Myheritage VCF file and th…
Comment: Deseq2 error
by
sgadila
• 0
Sorry, I just edited my post.
Comment: Differentially Expressed Genes between two conditions (scRNA, single GEO dataset
by
bk11
★ 1.4k
You can simply do `Idents(seurat.integrated) <- "Type"` instead of `seurat.integrated <- SetIdent(seurat.integrated, value=seurat.integrate…
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