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122,009 results • Page
607 of 2441
Sort: Rank
Rank
Views
Votes
Replies
2
votes
2
replies
904
views
Nanopore dRNA - view unmapped segments of mapped reads
nanopore
sequencing
directRNA
updated 4.2 years ago by
GenoMax
154k • written 4.2 years ago by
yryan
▴ 10
0
votes
0
replies
641
views
What should I write after --operation in ANNOVAR for my interest database ?
ANNOVAR
CIViC
annotation
DoCM
VCF
4.2 years ago by
Zahra
▴ 110
4
votes
7
replies
3.6k
views
Download all Becteria and protist fasta protein sequences from UNIPROT proteomes
uniprot
fetch
fasta
proteome
bash
4.2 years ago by
Chvatil
▴ 140
0
votes
0
replies
731
views
Job:
Bioinformatician (f/m/d)
Hamburg
genomics
Germany
4.2 years ago by
gasta88
▴ 50
0
votes
0
replies
791
views
Job:
Software Engineer / Software Developer (f / m / d) for software in the context of DNA sequencing-based cancer diagnostics
Hamburg
genomics
Germany
4.2 years ago by
gasta88
▴ 50
0
votes
1
reply
762
views
Choosing the right sample among GEO datasets
GEOdatasets
chipsamples
celllinesamples
chipseq
chipseqanalysis
updated 4.2 years ago by
ATpoint
89k • written 4.2 years ago by
buffealo
▴ 130
6
votes
3
replies
6.6k
views
K-means for RNA seq gene clustering
kmeans
updated 4.2 years ago by
Kevin Blighe
89k • written 4.2 years ago by
curiousmind007
▴ 30
3
votes
6
replies
6.7k
views
How do I detect deletions?
bcftools
DNA-seq
calling
variant
updated 4.2 years ago by
bernatgel
★ 3.4k • written 4.2 years ago by
gt
▴ 30
1
vote
3
replies
2.4k
views
Can I use All Peaks (MACS2 -q 1) for analysis?
Peak
DiffBind
MACS2
4.2 years ago by
Tian
▴ 50
0
votes
0
replies
848
views
Job:
UK PhD Opportunity: Text mining the impact of SARS-CoV-2 mutations from the research literature at University of Glasgow
bionlp
sars-cov-2
text-mining
4.2 years ago by
jake.lever
▴ 50
1
vote
4
replies
1.5k
views
How to get from annotated sequences to UniProt IDs
annotation
updated 4.2 years ago by
Tm
★ 1.1k • written 4.2 years ago by
robert.murphy
▴ 110
0
votes
2
replies
1.6k
views
Low read counts in one of three biological replicates. Remove?
RNA-Seq
4.2 years ago by
nadal-t
▴ 20
0
votes
5
replies
1.9k
views
Considering the multiple test correction for the analysis of polygenic risk score association
association
allele
polygenic
score
Bonferroni
updated 4.2 years ago by
German.M.Demidov
★ 3.0k • written 4.2 years ago by
seta
★ 1.9k
0
votes
0
replies
1.6k
views
Job:
Post-doctoral Fellow in Cancer Biology and Immunology
biology
immunology
Cancer
molecular
4.2 years ago by
waihungh
▴ 20
0
votes
0
replies
1.5k
views
Job:
Pacific Biosciences: Senior Bioinformatics Software Engineer (remote)
software-engineer
updated 2.6 years ago by
Ram
45k • written 4.2 years ago by
Armin
• 0
0
votes
1
reply
1.6k
views
annotation parameter in ChIPQC
ChIP-Seq
ChIPQC
updated 4.2 years ago by
384306874
• 0 • written 5.3 years ago by
chaudharyc61
▴ 110
0
votes
0
replies
946
views
Motif finding HOMER results
interpretation
finding
HOMER
motif
4.2 years ago by
c.heininger
▴ 10
5
votes
12
replies
3.8k
views
How do you limit the result from the BLAST executable?
blast
updated 4.2 years ago by
gb
★ 2.2k • written 4.2 years ago by
adhamzul
▴ 20
0
votes
1
reply
866
views
EnsemblVEP could not generate any output for a list of frameshift insertion input
Frame_Shift_Insertion
EnsemblVEP
4.2 years ago by
nazaninhoseinkhan
▴ 530
0
votes
1
reply
889
views
How do I extract predicted genes from annotation from MAKER-P?
MAKER-P
updated 4.1 years ago by
Ram
45k • written 4.2 years ago by
eennadi
▴ 40
0
votes
0
replies
910
views
Renaming ggplot heatmap x-axis from gene names to number of genes
axes
ggplot2
heatmap
4.2 years ago by
Anand
▴ 40
3
votes
1
reply
1.7k
views
genome assembly in org.Mm.eg.db
R
updated 2.6 years ago by
Ram
45k • written 4.2 years ago by
anithaslvn
▴ 10
0
votes
1
reply
1.1k
views
How to find the names of elements while parsing PDB files via biopython?
Biopython
PDB
4.2 years ago by
Tzunami
▴ 10
1
vote
1
reply
1.2k
views
Best current tool for deconvolution of bulk sample
cibersort
updated 4.2 years ago by
Evan
▴ 250 • written 4.2 years ago by
changxu.fan
▴ 80
2
votes
3
replies
1.4k
views
plant viruses sequences
alignment
gene
updated 4.2 years ago by
GenoMax
154k • written 4.2 years ago by
Ric
▴ 440
0
votes
0
replies
860
views
ichorCNA mouse reference files for calling copy number
copynumber
4.2 years ago by
heskett
▴ 110
0
votes
8
replies
1.8k
views
use a list of id to extract sequence from different genomics
sequence
perl
4.2 years ago by
LZH289
• 0
0
votes
0
replies
729
views
Job:
postdoctoral position in bioinformatics/computational proteomics
BionformaticsPostdocUTMB
4.2 years ago by
Rovshan
• 0
0
votes
0
replies
544
views
PoolSNP RuntimeError: dictionary changed size during iteration
Poolsnp
4.2 years ago by
shpak.max
▴ 60
1
vote
1
reply
1.1k
views
What is the right way to merge multiple patient samples in scrna-seq?
Seurat
scrna-seq
cell
processing
updated 4.2 years ago by
ATpoint
89k • written 4.2 years ago by
cogen859
• 0
1
vote
3
replies
1.7k
views
How to filter VEP results of "missing values"
filter
VEP
updated 4.2 years ago by
GenoMax
154k • written 4.2 years ago by
YL
▴ 10
2
votes
2
replies
1.5k
views
Tool:
miRAnno—network-based functional microRNA annotation
pathways
miRNA
annotation
microRNA
4.2 years ago by
tomastokar
▴ 50
0
votes
0
replies
462
views
Determining the effect of dataset size in results
R
4.2 years ago by
a_confused_biologist
• 0
21
votes
14
replies
12k
views
Tool:
trackplot: Fast and minimal dependency standalone R script to generate IGV style locus tracks from bigWig files
visualization
igv
ChIP-Seq
R
bigwigs
updated 2.3 years ago by
Ram
45k • written 4.9 years ago by
poisonAlien
★ 3.2k
1
vote
3
replies
2.2k
views
SSPACE bowtie and bwa error
Assembly
next-gen
software error
genome
updated 4.2 years ago by
hnt001
▴ 10 • written 6.3 years ago by
milady81
▴ 70
0
votes
1
reply
1.3k
views
EdgeR - Input for Analysis Functions (estimateDisp, exactTest, glmQLFit)
edgeR
R
4.2 years ago by
Noah E.
▴ 20
1
vote
1
reply
1.2k
views
How to change CpG methylation cutoffs in edgeR
R
updated 4.2 years ago by
iraia.munoa
▴ 130 • written 5.5 years ago by
embueno
• 0
1
vote
5
replies
2.6k
views
MUSCLE alignment - aligning whole genome with gene sequences
alignment
mega
updated 4.2 years ago by
GenoMax
154k • written 4.2 years ago by
manaswwm
▴ 570
5
votes
4
replies
3.2k
views
Error when using UpSetR package
UpSetR
R
4.2 years ago by
peter.berry5
▴ 60
18
votes
15
replies
21k
views
9 follow
Tools Parsing Ncbi Blast -M 7 Xml Output Format?
blast
xml
parsing
updated 4.2 years ago by
Yoann Pageaud
• 0 • written 14.5 years ago by
Lhl
▴ 760
0
votes
8
replies
2.0k
views
print only columns with data from every line
unix
awk
4.2 years ago by
HL
▴ 10
2
votes
12
replies
3.6k
views
Bowtie2 aligner
Bowtie2
alignment
updated 4.2 years ago by
GenoMax
154k • written 4.2 years ago by
priya.bmg
▴ 70
1
vote
2
replies
1.1k
views
Determine relative copy numbers of plasmids
mapping
bowtie2
samtools
coverage
4.2 years ago by
rororo
▴ 10
0
votes
1
reply
1.0k
views
SNP density plot of aedes genome using bed file
density
Variant
ideograms
4.2 years ago by
anithanagaraj93
▴ 10
1
vote
0
replies
777
views
What is the importance of removing reads mapped to repetitive elements for downstream enrichment in RNAseq/CLIPseq?
Repetitive_elements
alignment
CLIPseq
RNAseq
updated 4.2 years ago by
GenoMax
154k • written 4.2 years ago by
Patrick
▴ 10
1
vote
1
reply
1.2k
views
How to get uniform data yields per barcode in nanopore sequencing
ONT
nanopore
updated 4.2 years ago by
samuel.a.odonnell
▴ 600 • written 4.2 years ago by
Irsan
★ 7.8k
0
votes
0
replies
1.1k
views
Job:
PhD student, PostDoc and Software Developer Positions at the interface of Mathematics and Life Science
postdoc
phd
Computational-Biology
Mathematics
updated 2.6 years ago by
Ram
45k • written 4.2 years ago by
emad-24
• 0
0
votes
0
replies
752
views
somatic variant calling with Mutect2
calling
somatic
Mutect2
variant
4.2 years ago by
Elisa
• 0
0
votes
0
replies
683
views
Forum:
Poll about a structured description of a tool, a pipeline
survey
pipeline
updated 2.3 years ago by
Ram
45k • written 4.2 years ago by
Anastasiya M
• 0
1
vote
11
replies
3.1k
views
How to merge folders that have similar (not the same) names, in a folder keeping as its name the common part of the name of the two folders
folders
merge
name-based
updated 4.2 years ago by
cpad0112
21k • written 4.2 years ago by
Mania
• 0
122,009 results • Page
607 of 2441
Recent Votes
Manual Genome Curation using PretextView course
Answer: How to get proteins from GFF file resulted from MAKER annotation
Comment: DESeq2 on metagenome KO counts
Answer: DESeq2 on metagenome KO counts
Answer: DESeq2 on metagenome KO counts
Answer: DESeq2 on metagenome KO counts
Comment: GUI commercial software for 10x single cell gene expression analysis
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Recent Awards •
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Teacher
to
andres.firrincieli
3.9k
Teacher
to
Aleksandra
▴ 180
Popular Question
to
vernonlim98
• 0
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to
GenoMax
154k
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11k
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Recent Replies
Comment: DESeq2 on metagenome KO counts
by
ATpoint
89k
This statement makes zero sense in response to what I wrote.
Comment: DESeq2 on metagenome KO counts
by
Aleksandra
▴ 180
I focused on the fact that DESeq2 models overdispersion, but overlooked its implicit assumption: normalisation works when the main source o…
Comment: DESeq2 on metagenome KO counts
by
Aleksandra
▴ 180
Thank you very much. I mistakenly drew a superficial analogy. I equated KO counters with gene counters.
Comment: DESeq2 on metagenome KO counts
by
ATpoint
89k
Both vst or logcpm will favor expression level (magnitude of counts) rather than differences in a hclust/heatmap. For differences you need …
Comment: DESeq2 on metagenome KO counts
by
ATpoint
89k
The DESeq2 developer has advised many times against DESeq2 for metagenomics. Please search for related posts over at support.bioconductor.o…
Answer: DESeq2 on metagenome KO counts
by
andres.firrincieli
3.9k
I wouldn’t use DESeq2 on aggregated raw counts per KO, because doing so means accepting two pretty big assumptions: 1. All genes with t…
Comment: DESeq2 on metagenome KO counts
by
Aleksandra
▴ 180
(I apologise for my previous reply; I wanted to be as detailed as possible) DESeq2 handles KO counts perfectly well. For a time-series des…
Comment: DESeq2 on metagenome KO counts
by
Aleksandra
▴ 180
I apologise for how that sounded; I wanted to be as detailed as possible.
Comment: GUI commercial software for 10x single cell gene expression analysis
by
Istvan Albert
103k
A comment on: "*Wonky analysis is possible even with open-source R libraries.*" True - and arguably, the risk of a wonky analysis is actua…
Comment: GUI commercial software for 10x single cell gene expression analysis
by
GenoMax
154k
`Trailmaker` likely only supports Parse's evercode data. <br> `BioTuring` does not appear to have published pricing. <br> `Rosalind` appear…
Answer: GUI commercial software for 10x single cell gene expression analysis
by
firestar
★ 1.7k
Found a few more when I asked around. I have no idea how good or bad these are. If anyone has used these or knows more about these, feel fr…
Comment: How to handle TrEMBL proteins without gene annotation in plasma proteomics?
by
GenoMax
154k
> I performed a standard proteomics screening workflow What database did you use to search against? Perhaps you are using an old (not so c…
Answer: FACS quality control based on size and doublet detection in scRNA-seq
by
ATpoint
89k
No, it's unrelated. Doublets in 10x happen if two cells get enclosed into the same GEM droplet. This has nothing to do with how flow cytome…
Answer: How to handle TrEMBL proteins without gene annotation in plasma proteomics?
by
Elisabeth Gasteiger
★ 2.4k
Apparently you are working with human proteins? I would strongly recommend looking only at proteins that are part of the human reference pr…
Comment: Tools to simulate Illumina short read sequences and ONT long reads with a refere
by
colindaven
8.0k
Wow, thats too long. How much RAM does your machine have, it is likely swapping
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