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327 results • Page
3 of 7
Sort: Votes
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Views
Votes
Replies
0
votes
0
replies
597
views
Contig extension using PRICE
price
updated 12 days ago by
Ram
40k • written 3.0 years ago by
A_heath
▴ 140
0
votes
1
reply
162
views
GO ENRICHMENT ANALYSIS- DESEQ
GO
updated 6 days ago by
Basti
★ 1.7k • written 7 days ago by
oduduabasi.isaiah
• 0
0
votes
0
replies
57
views
DMRcate design
R
Epigenetics
EPIC
DMRcate
updated 8 hours ago by
Ram
40k • written 11 hours ago by
Bioinfonext
▴ 440
0
votes
0
replies
125
views
Reverse complement only sequences resulted from BLASTN minus
DNA
fasta
bash
updated 27 days ago by
Ram
40k • written 27 days ago by
Oscar
▴ 30
0
votes
0
replies
132
views
Install packages in old version Julia
package
Julia
22 days ago by
sooni
▴ 10
0
votes
0
replies
12
views
ATAC-Seq and RPKM
RPKM
ATAC-Seq
and
1 hour ago by
qudrat.nii
• 0
0
votes
0
replies
118
views
Running Funannotate on Fungal Genome
funannotate
assembly
genomeassembly
denovo
annotation
22 days ago by
Umer
▴ 50
0
votes
1
reply
123
views
FEAST - Microbial Source Tracking
Source-Tracking
Microbiome
updated 1 day ago by
Ram
40k • written 1 day ago by
avinash.dhar
• 0
0
votes
0
replies
176
views
Current landscape of approaches to scRNA-seq with nanopore sequencers?
scRNA-seq
nanopore
single-cell
9 days ago by
LauferVA
3.7k
0
votes
2
replies
299
views
miRNAseq - over-presented sequence in negative control
miRNAseq
adaptor
dimer
21 days ago by
MH85
• 0
0
votes
2
replies
255
views
Segmentation fault error in CONTROL-FREEC
copy-number-variants
FREEC
22 days ago by
DdogBoss
• 0
0
votes
0
replies
127
views
How to compare degradation rate or half-life
degradation-rate
half-life
updated 27 days ago by
Ram
40k • written 27 days ago by
g744695539
• 0
0
votes
3
replies
358
views
Seeking Assistance for Interpreting a Network Representation on String-DB.org
gene-ontology
GO
enrichment
Proteome
stringdb
updated 24 days ago by
rfran010
▴ 840 • written 25 days ago by
Biomed-jeh
• 0
0
votes
0
replies
180
views
High pvalues when using clusterProfiler for seurat
clusterProfiler
12 days ago by
Ahmed
• 0
0
votes
0
replies
157
views
Find reference genome regions spanned by only mapping quality 0 reads in multiple WGS samples
mapping-quality
BAM
FASTA
29 days ago by
William
★ 5.2k
0
votes
1
reply
190
views
Replace ambiguous characters in fasta MSA
maximum-likelihood
DNA
updated 26 days ago by
Joe
21k • written 27 days ago by
Alexandre
• 0
0
votes
0
replies
151
views
Converting the TCGA ID to the Cohort ID
tcga
depmap
tcgabiolinks
29 days ago by
tyasird
▴ 10
0
votes
1
reply
199
views
Merge microbiota data
microbiota
OTU
updated 26 days ago by
Ram
40k • written 26 days ago by
shamila.ismael
• 0
0
votes
1
reply
193
views
Drawing label around clusters
cells
Single
updated 22 days ago by
Mensur Dlakic
★ 25k • written 22 days ago by
synat.keam
▴ 80
0
votes
11
replies
770
views
Normalization for microarrays >1000+ samples?
microarray
normalization
oligo
13 days ago by
evmae
• 0
0
votes
0
replies
193
views
TCGAbiolinks not working anymore
R
TCGAbiolinks
GDC
updated 25 days ago by
Ram
40k • written 25 days ago by
master chief
• 0
0
votes
9
replies
199
views
Deseq2 error
R
deseq2
2 hours ago by
sgadila
• 0
0
votes
0
replies
139
views
Issue in creating Gene Regulatory Network links using CellOracle
Python
CellOracle
GRN
18 days ago by
Debashish
• 0
0
votes
0
replies
162
views
simuations with sim1000g
snps
simulation
sim1000G
chromosome
24 days ago by
Eliza
▴ 30
0
votes
0
replies
103
views
How to obtain de pvalue of my DMRs using Bumphunter function from minfi
DMRs
6 days ago by
Irene
• 0
0
votes
1
reply
220
views
Long read filtering based on reference
Long-read
ONT
updated 25 days ago by
Ram
40k • written 25 days ago by
Link
• 0
0
votes
3
replies
2.0k
views
extraction of original gene iDs from reference annotation file
rna-seq
updated 13 days ago by
aishwarya
• 0 • written 5.3 years ago by
blooming.daisy333
▴ 110
0
votes
1
reply
184
views
PyMOL: how to list all selection names?
pymol
updated 15 days ago by
Wayne
★ 1.8k • written 16 days ago by
Ondina
▴ 90
0
votes
0
replies
158
views
Convert from limma voom normalized matrix each gene to high/low
limma-voom
RNA-SEQ
updated 5 days ago by
Ram
40k • written 5 days ago by
Manuel Sokolov Ravasqueira
▴ 100
0
votes
2
replies
247
views
Is it okay to just average the log2FC values across different cell types in pseudobulk scRNA-seq data?
scrna-seq
rna-seq
log2fc
13 days ago by
JLee
• 0
0
votes
1
reply
195
views
Geo2r rna seq analysis
Geo2r
RNA-seq
updated 22 days ago by
Ram
40k • written 22 days ago by
angiannak
• 0
0
votes
1
reply
147
views
DESeq2 error - converting result object into dataframe
R
DESeq2
Shiny
updated 7 days ago by
Ram
40k • written 7 days ago by
shasabhi1
• 0
0
votes
1
reply
169
views
GO analysis after DESeq2
GO
updated 8 days ago by
Ram
40k • written 8 days ago by
oduduabasi.isaiah
• 0
0
votes
0
replies
282
views
GTF/Reference genome adjustments? Gene-based differential expression analysis of genetically modified mouse line
RNA-seq
DGE
updated 15 days ago by
Ram
40k • written 15 days ago by
alex
• 0
0
votes
0
replies
141
views
ADNI DATASET
ADNI
23 days ago by
karthivalarmathi99
▴ 10
0
votes
3
replies
193
views
Bug of vg surject
vg
updated 6 days ago by
Jordan M Eizenga
▴ 360 • written 6 days ago by
Qi
• 0
0
votes
3
replies
275
views
Errors while trying to run Scenic
Scenic
updated 14 days ago by
GenoMax
135k • written 14 days ago by
Stavroula
• 0
0
votes
0
replies
120
views
Select minimum set of SNPs from VCF file to identify a individual
selection
SNP
6 days ago by
Bioxbio
• 0
0
votes
3
replies
298
views
Extracting/assembling organellar reads from RNAseq data
transcriptome
star
alignment
mapping
updated 15 days ago by
LChart
3.4k • written 22 days ago by
Miles
• 0
0
votes
13
replies
610
views
STAR Intron Motif Script Gives Segmentation fault Error
STAR
Linux
10 days ago by
Y
• 0
0
votes
1
reply
1.7k
views
error when running local chlorop1.1
chlorop
updated 8 days ago by
Ram
40k • written 7.3 years ago by
gerrychang1985
▴ 40
0
votes
1
reply
129
views
Running Ibex on both BCR chains?
BCR
ibex
single-cell
updated 8 days ago by
Ram
40k • written 8 days ago by
actinia94
• 0
0
votes
2
replies
302
views
Deseq2 colData for single condition
RNA-seq
17 days ago by
Petesview
• 0
0
votes
3
replies
297
views
Assigning GO ids to blast hits
Linux
GO
blast
updated 7 days ago by
gv
• 0 • written 27 days ago by
Mousumi Akter
• 0
0
votes
1
reply
200
views
quantifying splicing transcripts for nanopore RNAseq
RNAseq
splicing
nanopore
updated 20 days ago by
GenoMax
135k • written 21 days ago by
jshen
• 0
0
votes
0
replies
138
views
Genetic distance in cM from VCF of non-reference species to run Beagle
plink
beagle
vcf
updated 14 days ago by
Ram
40k • written 14 days ago by
AndrMod
• 0
0
votes
1
reply
203
views
TCGAbiolinks MSI data
msi
updated 22 days ago by
bk11
★ 1.4k • written 24 days ago by
Elizabeth
▴ 10
0
votes
0
replies
120
views
Molecular Docking, Sars-cov-2
Molecular-docking
updated 27 days ago by
Ram
40k • written 27 days ago by
frogfrapper
• 0
0
votes
2
replies
246
views
Quality Control of VCFs that used different genotyping arrays
bcftools
VCF
1 day ago by
Shane
• 0
0
votes
4
replies
642
views
CAZy database has multiple family sequence...
metagenomics
cazy
annotation
updated 27 days ago by
JyiYeung
• 0 • written 9 months ago by
GYUDAE
• 0
327 results • Page
3 of 7
Recent Votes
Answer: tensorQTL interaction issue
Answer: Script for getting summary statistic of any genome using GTF or GFF3 ?
Comment: How do you validate and verify your pipeline's software updates?
Comment: How do you validate and verify your pipeline's software updates?
Answer: GSEA with GO and KEGG datasets
GSEA with GO and KEGG datasets
Answer: Exporting DEGs obtained from DESeq2
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Popular Question
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avelarbio46
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Bioinfonext
▴ 440
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Recent Replies
Answer: tensorQTL interaction issue
by
Solal
• 0
Writing a solution for anyone interested. The issue stems from a dosage error, some variant contains only heterozygous individuals and no h…
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.
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