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122,027 results • Page
582 of 2441
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0
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News:
Online training - Genomic Prediction
Genomics
4.1 years ago by
Physalia-courses
★ 2.7k
1
vote
2
replies
1.1k
views
Plotting chromosomes and target capture baits
plotting
target_capture
Hyb-Seq
R
4.1 years ago by
Begonia_pavonina
▴ 210
1
vote
1
reply
775
views
Problem of visualizing results of PPI network
analyst
network
Cytoscape
updated 4.1 years ago by
Scooter
▴ 310 • written 4.1 years ago by
bookorg
▴ 20
0
votes
0
replies
666
views
Cutoffs for Proxy Identification: D' and R^2
plink2
4.1 years ago by
dec986
▴ 380
5
votes
15
replies
4.4k
views
7 follow
DESeq2 normalization - Found Difference in values when calculated manually
DESeq2
normalization
difference
4.1 years ago by
Sandhiya
▴ 20
0
votes
1
reply
994
views
getting different value list from GATK gc content and CANOES
CNV
GATK
CANOES
updated 4.1 years ago by
nicholasopoku24
• 0 • written 6.2 years ago by
a.tavallaie
• 0
0
votes
1
reply
895
views
How is better perform the analyze the somatic mutations? (the mutations of my interest gene)
somatic
VCF
annotation
Oncoplot
updated 4.1 years ago by
German.M.Demidov
★ 3.0k • written 4.1 years ago by
Sonia
• 0
1
vote
1
reply
962
views
How to load user-defined genome in IGV-webapp
IGV-WEBAPP
IGV
igv
updated 4.1 years ago by
GenoMax
154k • written 4.1 years ago by
Frieda
▴ 60
2
votes
6
replies
1.9k
views
Statistics on RNAseq data
on
Statistics
data
RNAseq
updated 4.1 years ago by
hafiz.talhamalik
▴ 350 • written 4.1 years ago by
margot.27.muller
▴ 30
0
votes
0
replies
886
views
Job:
Bioinformatics position at the spatial transcriptomics facility of Lyon (France)
single-cell
spatial-transcriptomics
updated 2.9 years ago by
Ram
45k • written 4.1 years ago by
yad.ghavi-helm
• 0
1
vote
2
replies
1.4k
views
Error when opening CEL files in python
python
updated 4.1 years ago by
Shred
★ 1.6k • written 4.1 years ago by
Paula
• 0
1
vote
2
replies
1.3k
views
Variant Allele Frequency
Cancer
updated 4.1 years ago by
German.M.Demidov
★ 3.0k • written 4.1 years ago by
adarsh
▴ 60
0
votes
4
replies
2.3k
views
Find NLS in list of proteins.
localization
nuclear
signal
updated 4.1 years ago by
Joe
22k • written 4.1 years ago by
qmarulfiz
▴ 60
1
vote
4
replies
1.6k
views
Multiple hypothesis correction with multiple gene sets
gene-set-enrichment
GO
multiple-test-correction
GO-enrichment
updated 4.1 years ago by
Gordon Smyth
★ 8.3k • written 4.1 years ago by
suragnair
• 0
0
votes
2
replies
1.7k
views
HRD score LST?
cnv
updated 4.1 years ago by
e.rempel
★ 1.1k • written 5.0 years ago by
vctrm67
▴ 90
2
votes
2
replies
1.1k
views
Sudden coverage increase in IGV
IGV
sequencing
coverage
updated 4.1 years ago by
GenomeXP
• 0 • written 4.1 years ago by
mrs97
• 0
1
vote
2
replies
1.3k
views
How to get all genes and their annotations within a LD block?
GWAS
haplotype
SNPs
genome
wheat
Ensembl
4.1 years ago by
b.g.tamang
▴ 20
0
votes
2
replies
3.8k
views
From Bismark to methylkit, which file is better to use?
Bisulfite sequencing
Bismark
methylkit
updated 12 months ago by
Lluís R.
★ 1.2k • written 4.9 years ago by
iraia.munoa
▴ 130
0
votes
1
reply
738
views
Regarding functional similarity analysis by GOSemSim package of R
GOSemSim
updated 4.1 years ago by
Jean-Karim Heriche
27k • written 4.1 years ago by
jyotsnap
• 0
0
votes
2
replies
1.9k
views
trinity run_DE_analysis.pl Failed with error: ‘package ‘limma’ could not be loaded’
run_DE_analysis.pl
trinity
4.1 years ago by
Rajesh
▴ 10
2
votes
4
replies
2.3k
views
Any suggestion on metagenomics pipelines for processing shotgun metagenomics whole genome sequencing samples?
metagenomics_pipelines
WGS
shotgun_metagenomics
antimicrobial_resistance
4.1 years ago by
eli_bayat
▴ 100
1
vote
3
replies
2.1k
views
WGCNA
Installation
WGCNA
updated 4.1 years ago by
tothepoint
▴ 940 • written 4.1 years ago by
Nithya
▴ 10
0
votes
0
replies
652
views
Neighboring index between clusters on a map
connectivity
clustering
4.1 years ago by
thejustpark
▴ 80
2
votes
3
replies
2.4k
views
GIAB Benchmark (High Confidence) Bed Filles
SNPS
GIAB
variants
updated 4.1 years ago by
desouzareis.r
▴ 290 • written 4.1 years ago by
bioinformatics2020
▴ 840
8
votes
10
replies
5.2k
views
UCSC knownCanonical hg19 vs. hg38
genome
UCSC
hg19
hg38
canonical
updated 4.1 years ago by
Luis Nassar
▴ 670 • written 4.6 years ago by
Sanjar
▴ 150
1
vote
2
replies
1.4k
views
Tool:
krust: a k-mer counter in Rust using the rust-bio and rayon crates
Rust
kmer-counting
fasta
kmer
updated 4.1 years ago by
Istvan Albert
103k • written 4.1 years ago by
jlivesey
▴ 10
0
votes
2
replies
1.0k
views
Can i estimate the hormone-receptor binding affinity ?
hormone
updated 2.6 years ago by
Ram
45k • written 4.1 years ago by
dmorfologia3
• 0
1
vote
2
replies
1.0k
views
Edit vcf file 0|0 to 0
linux
vcf
genomics
edit
4.1 years ago by
zoubda
• 0
2
votes
4
replies
2.0k
views
Problem with BAM file headers
SAM
GATK
BAM
4.1 years ago by
Lucas
• 0
0
votes
0
replies
875
views
Weird PCA plot using WGCNA results
cancer
PCA
expression
WGCNA
plot
4.1 years ago by
seta
★ 1.9k
0
votes
1
reply
1.2k
views
List of codon numbers in a panel
browser
codon
list
ucsc
genome
updated 4.1 years ago by
Luis Nassar
▴ 670 • written 4.5 years ago by
ines
• 0
2
votes
6
replies
4.5k
views
GenomeInfoDb (in R) and UCSC just stopped co-operating in terms of mm10
seqlevels
seqlevelsStyle
GenomeInfoDnb
R
UCSC
updated 4.1 years ago by
Alex Reynolds
36k • written 4.3 years ago by
sami.kilpinen
▴ 20
1
vote
3
replies
2.5k
views
clusterProfiler: number of GO terms in results
clusterProfiler
4.1 years ago by
thistleq777
▴ 10
2
votes
2
replies
1.9k
views
PRSice-2 without Ref SNP ID
Catalog
PGS
PRSice
PRS
4.1 years ago by
Jenish
▴ 20
0
votes
0
replies
563
views
How to do virtual screening and determining pharmacore
QSAR
Docking
4.1 years ago by
ashwing.kofficial
▴ 10
8
votes
3
replies
4.2k
views
Please help me understand linkage disequilibrium
LD
Linkage
disequilibrium
SNP
updated 4.1 years ago by
i.sudbery
22k • written 4.1 years ago by
?
▴ 60
0
votes
0
replies
1.2k
views
Job:
PhD student for a computational breast cancer research project
Cancer
PhD
Omics
updated 2.7 years ago by
Ram
45k • written 4.1 years ago by
s.vosberg
• 0
1
vote
1
reply
2.2k
views
Ensembl VEP Docker: cannot write to FASTA lockfile
Ensembl
Docker
VEP
updated 4.1 years ago by
Emily
24k • written 4.1 years ago by
PimPolacko
• 0
0
votes
0
replies
756
views
How to show intermolecular forces between two chains within the same protein in Pymol
protein
python
pymol
antibody
antigen
4.1 years ago by
Lucy
• 0
2
votes
2
replies
1.5k
views
network analysis for microbial amplicon sequencing data
plot
Network
igraph
R
4.1 years ago by
Bioinfonext
▴ 480
0
votes
2
replies
1.6k
views
Unicycler and GNU parallel
Unicycler
parallel
4.1 years ago by
emma.a
▴ 130
0
votes
1
reply
3.1k
views
PROVEAN input script
python
provean
variant effect prediction
updated 4.1 years ago by
TongZhou
• 0 • written 8.1 years ago by
s_herrera
▴ 10
0
votes
0
replies
706
views
GREAT genome ontology top hits criteria?
bed
GREAT
gene-ontology
go
updated 2.7 years ago by
Ram
45k • written 4.1 years ago by
a_bis
▴ 40
0
votes
0
replies
682
views
Job:
Postdoctoral Scientist in Statistical Bioinformatics and Software Development, WEHI, Melbourne, Australia
Australia
4.1 years ago by
Gordon Smyth
★ 8.3k
0
votes
0
replies
845
views
GREAT difference between 'mouse phenotype' and 'mouse phenotype single KO'
bed
gene-ontology
GREAT
go
updated 2.7 years ago by
Ram
45k • written 4.1 years ago by
a_bis
▴ 40
0
votes
1
reply
1.0k
views
Running htseq-count to "grab" long non coding gene_id names
lncRNA
htseq
updated 4.1 years ago by
GenoMax
154k • written 4.1 years ago by
dimitrischat
▴ 210
3
votes
3
replies
1.4k
views
Germline Cancer Mutations
Cancer
updated 4.1 years ago by
benformatics
4.2k • written 4.1 years ago by
adarsh
▴ 60
198
votes
46
replies
77k
views
34 follow
Tutorial:
Analysing Microarray Data In Bioconductor
microarray-analysis
bioconductor
updated 7 months ago by
Riley J
• 0 • written 13.1 years ago by
Obi Griffith
20k
0
votes
0
replies
725
views
Has anybody used RIP-MD tool for generation of RIN from MD trajectories?
Interaction
MD
simulation
VMD
Network
Residue
4.1 years ago by
Anjali
• 0
12
votes
5
replies
2.0k
views
Remove duplicates in fasta files based on a specific value with awk
sort
fasta
sed
awk
updated 4.1 years ago by
cpad0112
21k • written 4.1 years ago by
Mgs3
▴ 30
122,027 results • Page
582 of 2441
Recent Votes
A: What does BAF mean?
What does BAF mean?
Comment: VCF: Replacing RefSeq ID to chr in #CHROM
A: VCF: Replacing RefSeq ID to chr in #CHROM
Answer: Modeling/simulations using SNPs data
what is the output of 'samtools coverage'
Answer: Discrepancy in Q-score assessment of ONT reads in Nanopore and third-party softw
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Comment: Brave: Bioinformatics Reactive Analysis and Visualization Engine
by
Edward
• 0
Thanks for the reply and suggestions. This software is a bit similar to galaxy. Recently, I am adding an application store for pipelines, s…
Answer: Modeling/simulations using SNPs data
by
Dave Carlson
★ 2.2k
I would recommend looking into using [SLiM][1] for forward-time population genetic simulations. It's widely used and very well documented, …
Answer: Strugling on the 3'rule of HGVS
by
Jeremy Leipzig
23k
> chrM : m.57T>TC, but according to the 3'rule it should be named m.60T>TC (if I understood correctly). no that cannot be shifted, like yo…
Answer: Extract fastq sequences based on date/time (which is in the header)
by
zhanxw
▴ 20
This tool can be helpful: https://github.com/angelovangel/nanotimes
Answer: Filter nanopore fastq files by start time
by
zhanxw
▴ 20
This is an efficient tool: https://github.com/angelovangel/nanotimes
Answer: Choosing enrichment analysis tool
by
i.sudbery
22k
Standard enrichement tools, like Metascape, Enrichr or David assume that under a model of no pathway being particularly involved in what yo…
Answer: Discrepancy in Q-score assessment of ONT reads in Nanopore and third-party softw
by
k-tarasov
▴ 10
Thanks to colindaven answer, I managed to travel by hyperlinks to the source of the discrepancy. It seems that Nanopore tools compute *ave…
Answer: Discrepancy in Q-score assessment of ONT reads in Nanopore and third-party softw
by
colindaven
8.0k
I agree completely. I think the cause is well discussed here : https://github.com/OpenGene/fastplong/issues/20 `fastplong` currently sti…
Comment: Discrepancy in Q-score assessment of ONT reads in Nanopore and third-party softw
by
k-tarasov
▴ 10
Thank you for answer. No, I am looking at all reads before appllying any filters. There are 2,429,312 raw reads, and in 16s-wf pipeline I …
Comment: Discrepancy in Q-score assessment of ONT reads in Nanopore and third-party softw
by
GenoMax
154k
Are you only looking at reads that satisfy this filter (which is in your command line in GitHub post) in your `seqkit` and `fastqc` reports…
Comment: Configuration file for DSP WTA
by
GenoMax
154k
> data starting from Fastq Generally did this with the entire flowcell folder and not fastq files. The data needs to be demultiplexed in a…
Answer: How to create a consensus of a contig with samtools or bbmap?
by
jkbonfield
★ 1.3k
Your first command outputted SAM rather than BAM, and SAM without a header (no `-h`) option. If you used `-o contig_1.bam` it would have w…
Comment: Brave: Bioinformatics Reactive Analysis and Visualization Engine
by
ATpoint
89k
Seconding this, I also felt completely lost what this actually does. @OP, you need to learn to make sharp, concise bulletpoints advertising…
Answer: Validating snRNA-seq cell type by correlating with other datasets
by
ATpoint
89k
I would not do correlation analysis like this, I don't see how this makes any sense. Integration is possible but cumbersome. Instead, use `…
Comment: Choosing enrichment analysis tool
by
Marlene
• 0
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